Page last updated: 2024-11-07

pilocarpine and Cystic Fibrosis

pilocarpine has been researched along with Cystic Fibrosis in 117 studies

Pilocarpine: A slowly hydrolyzed muscarinic agonist with no nicotinic effects. Pilocarpine is used as a miotic and in the treatment of glaucoma.
(+)-pilocarpine : The (+)-enantiomer of pilocarpine.

Cystic Fibrosis: An autosomal recessive genetic disease of the EXOCRINE GLANDS. It is caused by mutations in the gene encoding the CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR expressed in several organs including the LUNG, the PANCREAS, the BILIARY SYSTEM, and the SWEAT GLANDS. Cystic fibrosis is characterized by epithelial secretory dysfunction associated with ductal obstruction resulting in AIRWAY OBSTRUCTION; chronic RESPIRATORY INFECTIONS; PANCREATIC INSUFFICIENCY; maldigestion; salt depletion; and HEAT PROSTRATION.

Research Excerpts

ExcerptRelevanceReference
"Twenty-one children receiving topiramate and 20 healthy controls with no signs or symptoms of pulmonary or gastrointestinal disease and a negative family history for cystic fibrosis (CF) underwent bilateral pilocarpine iontophoresis and sweat collection via Macroduct® system."7.78Elevated sweat chloride concentration in children without cystic fibrosis who are receiving topiramate therapy. ( Guglani, L; Kurland, G; Lower, D; Sitwat, B; Weiner, DJ, 2012)
" Chest computed tomography showed the diffuse bronchiectasis in both lungs, and their diagnosis was confirmed by the repeated analysis of a quantitative pilocarpine iontophoresis test (QPIT)."7.73Cystic fibrosis in Korean children:a case report identified by a quantitative pilocarpine iontophoresis sweat test and genetic analysis. ( Ahn, KM; Kang, IJ; Kim, JH; Lee, JH; Lee, MG; Lee, SI; Park, HY, 2005)
"The chronically pilocarpine-treated rat has been proposed as an animal model for the disease cystic fibrosis, a generalized exocrinopathy."7.67The chronically pilocarpine-treated rat in the study of cystic fibrosis: investigations on submandibular gland and pancreas. ( Bardon, A; Ceder, O; Kuijpers, GA; Müller, RM; Roomans, GM, 1985)
"Collection of sweat via pilocarpine iontophoresis is commonly used to diagnose cystic fibrosis (CF), with thousands of tests performed each day."5.17Skin pretreatment with microneedles prior to pilocarpine iontophoresis increases sweat production. ( Buono, MJ; Prausnitz, MR; Wing, D, 2013)
" The sweat obtained from patients with cystic fibrosis has been compared with that from normal children: the concentrations of cyclic AMP and cyclic GMP are the same."5.05Is salt reabsorption in the human sweat duct subject to control? ( Schwarz, V; Simpson, IM, 1985)
"Twenty-one children receiving topiramate and 20 healthy controls with no signs or symptoms of pulmonary or gastrointestinal disease and a negative family history for cystic fibrosis (CF) underwent bilateral pilocarpine iontophoresis and sweat collection via Macroduct® system."3.78Elevated sweat chloride concentration in children without cystic fibrosis who are receiving topiramate therapy. ( Guglani, L; Kurland, G; Lower, D; Sitwat, B; Weiner, DJ, 2012)
" Chest computed tomography showed the diffuse bronchiectasis in both lungs, and their diagnosis was confirmed by the repeated analysis of a quantitative pilocarpine iontophoresis test (QPIT)."3.73Cystic fibrosis in Korean children:a case report identified by a quantitative pilocarpine iontophoresis sweat test and genetic analysis. ( Ahn, KM; Kang, IJ; Kim, JH; Lee, JH; Lee, MG; Lee, SI; Park, HY, 2005)
"Describe and define limitations of early pilocarpine iontophoresis (sweat testing) for cystic fibrosis (CF) newborn screening (NBS)."3.73Sweat testing infants detected by cystic fibrosis newborn screening. ( Comeau, AM; Dorkin, HL; Dovey, M; Gerstle, R; Martin, T; O'Sullivan, BP; Parad, RB, 2005)
"Two methods for the determination of sodium in the sweat after stimulation by pilocarpine-iontophoresis were compared in 227 patients, among them 27 with a known cystic fibrosis."3.67[Diagnosis of mucoviscidosis by examination of sweat: value of conductometry]. ( Bergmann, S; Hoffmann, C; Sprössig, C; Wunderlich, P, 1989)
"Elemental distribution and ultrastructure of the submandibular gland, the parotid gland and the pancreas were investigated in three suggested animal models of the disease cystic fibrosis: the chronically reserpinized rat, the chronically isoproterenol-treated rat, and the chronically pilocarpine-treated rat."3.67X-ray microanalysis of exocrine glands in animal models for cystic fibrosis. ( Müller, RM; Roomans, GM, 1985)
") for cystic fibrosis (CF) features a compact, portable configuration of electrodes that dispense pilocarpine for iontophoresis."3.67Evaluation of a cystic fibrosis screening system incorporating a miniature sweat stimulator and disposable chloride sensor. ( Brown, I; Cherian, AG; Duhon, G; Hill, JG; Huang, NN; Stejskal-Lorenz, E; Strominger, D; Waring, WW; Warwick, WJ; Yeung, WH, 1986)
"The chronically pilocarpine-treated rat has been proposed as an animal model for the disease cystic fibrosis, a generalized exocrinopathy."3.67The chronically pilocarpine-treated rat in the study of cystic fibrosis: investigations on submandibular gland and pancreas. ( Bardon, A; Ceder, O; Kuijpers, GA; Müller, RM; Roomans, GM, 1985)
"In order to study the disposition which is thought to be latent in chronic pancreatitis, we investigated the sweat chloride concentration of 95 normal subjects, 43 cases of chronic pancreatitis, 12 cases of cholelithiasis, 15 cases of peptic ulcers, 16 cases of hepatic diseases and 23 cases of diabetes mellitus with the sweat test, using the method of pilocarpine iontophoresis."3.66The significance of the sweat test in chronic pancreatitis. ( Endo, K; Hanawa, M; Koizumi, M; Takahashi, S; Takebe, T, 1978)
"Rats treated for 7 days with reserpine develop structural changes in the submaxillary gland that resemble those that have been reported in cystic fibrosis."3.65The chronically reserpinized rat as a possible model for cystic fibrosis. I. Submaxillary gland morphology and ultrastructure. ( Adelstein, E; Barbero, GJ; Martinez, JR; Quissel, D, 1975)
"Submaxillary saliva from reserpine-treated rats was found to have alterations in composition similar to those reported in the same secretion from patients with cystic fibrosis."3.65The chronically reserpinized rat as a possible model for cystic fibrosis. II. Comparison and cilioinhibitory effects of submaxillary saliva. ( Adshead, PC; Barbero, GJ; Martinez, JR; Quissell, DO, 1975)
"Cystic fibrosis is a genetic disease occurring more frequently in Caucasians."2.41[Diagnosis and management of cystic fibrosis in children]. ( Clement, A; Fauroux, B; Tamalet, A, 2000)
"Cystic fibrosis is a genetic recessive disorder caused by mutations in the gene that encodes the CFTR protein."2.41[Diagnosis of cystic fibrosis in adults]. ( Chinet, T; Fajac, I; Ferec, C; Garcia Carmona, T; Nguyen-Khoa, T, 2000)
"Pilocarpine was used at a concentration ∼130-times lower than that used in the classical Gibson and Cooke sweat test."1.72Needle-free iontophoresis-driven β-adrenergic sweat rate test. ( Frédérick, R; Gohy, S; Leal, T; Lebecque, P; Mottais, A; Reynaerts, A; Vanbever, R; Vermeulen, F, 2022)
"Cystic fibrosis is a chronic progressive autosomal recessive disorder caused by the CFTR gene mutations."1.35[Standardized sweat chloride analysis for the diagnosis of cystic fibrosis in Korea]. ( Ahn, KM; Cha, SI; Ki, CS; Kim, JH; Kim, SJ; Lee, M; Park, HY, 2008)
"We found no patients with severe acute pancreatitis who had CFTR gene mutations, suggesting that these alterations are not a risk factor for the disease in our population."1.31CFTR gene mutations in patients suffering from acute pancreatitis. ( Kostuch, M; Kulczycki, L; Rudzki, S; Semczuk, A, 2002)

Research

Studies (117)

TimeframeStudies, this research(%)All Research%
pre-199085 (72.65)18.7374
1990's8 (6.84)18.2507
2000's15 (12.82)29.6817
2010's8 (6.84)24.3611
2020's1 (0.85)2.80

Authors

AuthorsStudies
Reynaerts, A1
Vermeulen, F1
Mottais, A1
Gohy, S1
Lebecque, P1
Frédérick, R1
Vanbever, R1
Leal, T1
Wing, D1
Prausnitz, MR1
Buono, MJ1
Aqil, B1
West, A1
Dowlin, M1
Tam, E1
Nordstrom, C1
Buffone, G1
Devaraj, S1
Gomez, CC1
Servidoni, Mde F1
Marson, FA1
Canavezi, PJ1
Vinagre, AM1
Costa, ET1
Ribeiro, AF1
Ribeiro, MA1
Toro, AA1
Pavan, CR1
Rondon, MV1
Lorena, SL1
Vieria, FU1
Ribeiro, JD1
Toltzis, P1
Kim, SJ1
Lee, M1
Cha, SI1
Park, HY2
Ahn, KM2
Ki, CS1
Kim, JH2
Klebanova, Y1
LeGrys, V1
Cooper, D1
Levy, D1
Santora, D1
Schwindt, C1
Gonska, T1
Ip, W1
Turner, D1
Han, WS1
Rose, J1
Durie, P1
Quinton, P1
Sermet-Gaudelus, I1
Munck, A1
Rota, M1
Roussey, M1
Feldmann, D1
Nguyen-Khoa, T2
Sands, D1
Ołtarzewski, M1
Nowakowska, A2
Zybert, K1
Guglani, L1
Sitwat, B1
Lower, D1
Kurland, G1
Weiner, DJ1
Laguna, TA1
Lin, N1
Wang, Q1
Holme, B1
McNamara, J1
Regelmann, WE1
Kostuch, M1
Rudzki, S1
Semczuk, A1
Kulczycki, L1
van den Bergh, FA1
Martens, A1
GIBSON, LE3
COOKE, RE1
SCHULTZE-JENA, BS1
COLTMAN, CA1
ATWELL, RJ1
ETHERIDGE, JE1
BIRDSONG, M1
ZELLMER, R1
HOKIN, LE1
HOKIN, MR1
LOBECK, CC2
LIEBERMAN, J1
KELLOGG, F1
PRUITT, A1
RICHTERICH, R1
FRIOLET, B1
JIRKA, M3
TROUTMAN, EG2
STANDLEY, ET1
RUIZ LOPEZ, A1
GORDON DE CAMIN, D1
ALEJANDRO AMPUERO, P1
DE LA ROSA DE AMPUERO, SI1
Gowda, V1
Roberts, M1
Wolfe, R1
Klaustermeyer, WB1
Thiagarajah, JR2
Song, Y2
Haggie, PM2
Verkman, AS2
Salinas, D1
Rosbe, K1
Finkbeiner, WE1
Nielson, DW1
Lee, JH1
Lee, MG1
Kang, IJ1
Lee, SI1
Beauchamp, M1
Lands, LC1
Parad, RB1
Comeau, AM1
Dorkin, HL1
Dovey, M1
Gerstle, R1
Martin, T1
O'Sullivan, BP1
Rock, MJ1
Hoffman, G1
Laessig, RH1
Kopish, GJ1
Litsheim, TJ1
Farrell, PM3
Kowalski, S2
Singer, Z2
Machalski, M2
Shwachman, H5
Mahmoodian, A2
McSherry, NR2
Mangos, JA1
Hansen, L2
Buechele, M1
Koroshec, J1
Warwick, WJ6
Houstĕk, J1
Morton, D1
Parker, A1
Estrada, P1
Martinez, JR5
McCurdy, RE1
Martinez, R1
Warren, RH1
Jones, B1
Heffington, R1
Webster, HL2
Coury, AJ1
Fogt, EJ1
Norenberg, MS1
Untereker, DF1
Blythe, SA1
Nielsen, OH1
Flensborg, EW1
Rosenstein, BJ2
Langbaum, TS2
Mawhinney, TP2
Feather, MS2
Barbero, GJ4
Denning, CR1
Huang, NN2
Cuasay, LR1
Tocci, P1
Barlow, WK1
Koscik, RE1
Rattenbury, JM1
Worthy, E1
Luk'ianova, EG1
LeGrys, VA1
Retsch-Bogart, GZ1
Chernick, CV1
Tamalet, A1
Fauroux, B1
Clement, A1
Chinet, T1
Fajac, I1
Ferec, C1
Garcia Carmona, T1
Hansen, LG1
Brown, IV1
Laine, WC1
Hansen, KL1
Jensen, O1
Adelstein, E1
Quissel, D1
Helwich, E1
Zöllner, H2
Hanawa, M1
Takebe, T1
Takahashi, S1
Koizumi, M1
Endo, K1
Gordes, E1
Brusilow, SW1
Mohmoodian, A1
Stephan, U3
Busch, EW1
Kollberg, H1
Hellsing, K1
Götz, M1
Stur, O1
Tárnoky, AL2
Bayliss, VM1
Bowen, HJ1
Burnow, RN1
Sherington, J1
Tocci, PM1
McKey, RM1
Adshead, PC1
Quissell, DO1
Shapiro, BL1
Pence, TV1
Smith, QT1
Rotter, J1
Kaiser, D2
Zucollo, A1
Martiarena, J1
Luna, C1
Pivetta, O1
Villagra, A1
Catanzaro, O1
Riedler, J1
Arrer, E1
Ferrer Calvete, J1
Ribes Koninckx, C1
Montero Brens, C1
Baxter, PS1
Wilson, AJ1
Read, NW1
Hardcastle, J1
Hardcastle, PT1
Taylor, CJ1
Sprössig, C1
Wunderlich, P1
Bergmann, S1
Hoffmann, C1
Müller, RM2
Roomans, GM3
Schwarz, V2
Simpson, IM1
Scarlett, SM1
Sagström, S1
Sagulin, GB1
Waring, WW1
Cherian, AG1
Brown, I1
Stejskal-Lorenz, E1
Yeung, WH1
Duhon, G1
Hill, JG1
Strominger, D1
Borowitz, SM1
Ghishan, FK1
Kuijpers, GA1
Bardon, A1
Ceder, O1
Gottschalk, B2
Fabricius, EM1
Pätzug, U1
Palombini, BC1
Souza, PR1
Szabo, LV1
Kenny, MA1
Lee, W1
Sturgess, J1
Reid, L1
Coleman, RL1
Lichtenstein, S1
MacLean, WC1
Tripp, RW1
Amendt, P2
Blanicky, P1
Colombo, ML1
De Candussio, G1
Baravalle, A1
Stock, HJ1
Stock, W1
Giese, U1
Prasad, LS1
Sinha, KP1
Rahman, A1
Jutzi, E1
Drack, E1
Slegers, JF1
Devi, CS1
Rao, NR1
Ramaiah, Y1
Berg, T1
Wranne, L1
Boniver, R1
Geubelle, F1
Rosenow, EC1
Lee, RA1
Sutcliffe, CH1
Style, PP1
Gebala, A1
Zytkiewicz, A1
Kopito, L1
Brehm, G1
De Haller, R1
De Haller, J1
Siegenthaler, P1
Sawyer, CJ1
Scott, AV1
Summer, GK1

Reviews

7 reviews available for pilocarpine and Cystic Fibrosis

ArticleYear
[Diagnosis of cystic fibrosis; simple genotyping to rule out the disease preferable to starting with the sweat test].
    Nederlands tijdschrift voor geneeskunde, 2003, May-24, Volume: 147, Issue:21

    Topics: Cystic Fibrosis; DNA; Genotype; Humans; Iontophoresis; Mutation; Pancreatic Function Tests; Pilocarp

2003
Sweat-testing: a review of current technical requirements.
    Pediatric pulmonology, 2005, Volume: 39, Issue:6

    Topics: Chlorides; Cystic Fibrosis; Electrolytes; False Positive Reactions; Humans; Infant, Newborn; Iontoph

2005
Laboratory diagnosis of cystic fibrosis.
    Critical reviews in clinical laboratory sciences, 1983, Volume: 18, Issue:4

    Topics: Adolescent; Adult; Aging; Child; Child, Preschool; Chlorides; Cystic Fibrosis; Disease; Electric Con

1983
Development of a screening system for cystic fibrosis.
    Clinical chemistry, 1983, Volume: 29, Issue:9

    Topics: Adolescent; Adult; Child; Child, Preschool; Chlorides; Clinical Trials as Topic; Cystic Fibrosis; Hu

1983
Advances in the diagnosis and management of cystic fibrosis.
    Clinical biochemistry, 1984, Volume: 17, Issue:5

    Topics: Adolescent; Anti-Bacterial Agents; Child; Child, Preschool; Chlorides; Cystic Fibrosis; Humans; Infa

1984
[Diagnosis and management of cystic fibrosis in children].
    Revue des maladies respiratoires, 2000, Volume: 17, Issue:3 Pt 2

    Topics: Adult; Age Factors; Anti-Bacterial Agents; Child; Chlorides; Cystic Fibrosis; Cystic Fibrosis Transm

2000
[Diagnosis of cystic fibrosis in adults].
    Revue des maladies respiratoires, 2000, Volume: 17, Issue:3 Pt 2

    Topics: Adolescent; Adult; Age Factors; Chlorides; Chronic Disease; Cystic Fibrosis; Cystic Fibrosis Transme

2000

Trials

3 trials available for pilocarpine and Cystic Fibrosis

ArticleYear
Skin pretreatment with microneedles prior to pilocarpine iontophoresis increases sweat production.
    Clinical physiology and functional imaging, 2013, Volume: 33, Issue:6

    Topics: Administration, Cutaneous; Adult; California; Cystic Fibrosis; Electric Impedance; Equipment Design;

2013
Development of a screening system for cystic fibrosis.
    Clinical chemistry, 1983, Volume: 29, Issue:9

    Topics: Adolescent; Adult; Child; Child, Preschool; Chlorides; Clinical Trials as Topic; Cystic Fibrosis; Hu

1983
Is salt reabsorption in the human sweat duct subject to control?
    Clinical science (London, England : 1979), 1985, Volume: 68, Issue:4

    Topics: Absorption; Adolescent; Child; Cyclic AMP; Cyclic GMP; Cystic Fibrosis; Humans; Pilocarpine; Potassi

1985

Other Studies

108 other studies available for pilocarpine and Cystic Fibrosis

ArticleYear
Needle-free iontophoresis-driven β-adrenergic sweat rate test.
    Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society, 2022, Volume: 21, Issue:3

    Topics: Adrenergic Agents; Aminophylline; Ascorbic Acid; Child; Chlorides; Cystic Fibrosis; Cystic Fibrosis

2022
Implementation of a quality improvement program to improve sweat test performance in a pediatric hospital.
    Archives of pathology & laboratory medicine, 2014, Volume: 138, Issue:7

    Topics: Chlorides; Cystic Fibrosis; Hospitals, Pediatric; Humans; Infant; Infant, Newborn; Iontophoresis; Ma

2014
Pulsed direct and constant direct currents in the pilocarpine iontophoresis sweat chloride test.
    BMC pulmonary medicine, 2014, Dec-13, Volume: 14

    Topics: Adult; Biopsy; Chlorides; Cystic Fibrosis; Electric Impedance; Electrodiagnosis; Female; Humans; Ion

2014
50 Years Ago in TheJournal ofPediatrics: The Sweat Test in Cystic Fibrosis: A Comparison of Overnight Sweat Collection versus the Pilocarpine Iontophoresis Method.
    The Journal of pediatrics, 2016, Volume: 175

    Topics: Chlorides; Cystic Fibrosis; Diagnostic Tests, Routine; History, 20th Century; Humans; Iontophoresis;

2016
[Standardized sweat chloride analysis for the diagnosis of cystic fibrosis in Korea].
    The Korean journal of laboratory medicine, 2008, Volume: 28, Issue:4

    Topics: Adolescent; Adult; Child; Child, Preschool; Chlorides; Cystic Fibrosis; Female; Humans; Infant; Iont

2008
A case of localized adrenergic urticaria mimicking an allergic reaction to a sweat chloride test.
    Pediatric pulmonology, 2009, Volume: 44, Issue:9

    Topics: Child; Cystic Fibrosis; Humans; Male; Norepinephrine; Pilocarpine; Skin Tests; Sweating; Urticaria

2009
Sweat gland bioelectrics differ in cystic fibrosis: a new concept for potential diagnosis and assessment of CFTR function in cystic fibrosis.
    Thorax, 2009, Volume: 64, Issue:11

    Topics: Adrenergic beta-Agonists; Adult; Biomarkers; Chlorides; Cystic Fibrosis; Cystic Fibrosis Transmembra

2009
[French guidelines for sweat test practice and interpretation for cystic fibrosis neonatal screening].
    Archives de pediatrie : organe officiel de la Societe francaise de pediatrie, 2010, Volume: 17, Issue:9

    Topics: Administration, Cutaneous; Chlorides; Cystic Fibrosis; Humans; Infant; Infant, Newborn; Iontophoresi

2010
Bilateral sweat tests with two different methods as a part of cystic fibrosis newborn screening (CF NBS) protocol and additional quality control.
    Folia histochemica et cytobiologica, 2010, Sep-30, Volume: 48, Issue:3

    Topics: Case-Control Studies; Chlorides; Cystic Fibrosis; Electric Conductivity; False Positive Reactions; H

2010
Elevated sweat chloride concentration in children without cystic fibrosis who are receiving topiramate therapy.
    Pediatric pulmonology, 2012, Volume: 47, Issue:5

    Topics: Adolescent; Analgesics; Anticonvulsants; Bronchi; Cells, Cultured; Child; Chlorides; Cystic Fibrosis

2012
Comparison of quantitative sweat chloride methods after positive newborn screen for cystic fibrosis.
    Pediatric pulmonology, 2012, Volume: 47, Issue:8

    Topics: Chlorides; Cystic Fibrosis; Female; Humans; Infant; Infant, Newborn; Iontophoresis; Male; Muscarinic

2012
CFTR gene mutations in patients suffering from acute pancreatitis.
    Medical science monitor : international medical journal of experimental and clinical research, 2002, Volume: 8, Issue:9

    Topics: Adult; Aged; Alleles; Chlorine; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator

2002
A test for concentration of electrolytes in sweat in cystic fibrosis of the pancreas utilizing pilocarpine by iontophoresis.
    Pediatrics, 1959, Volume: 23, Issue:3

    Topics: Chlorides; Cystic Fibrosis; Electrolytes; Humans; Iontophoresis; Pilocarpine; Sodium; Sodium, Dietar

1959
[Determination of sweat electrolytes after pilocarpin iontophoresis].
    Monatsschrift fur Kinderheilkunde, 1961, Volume: 109

    Topics: Cystic Fibrosis; Electrolytes; Humans; Iontophoresis; Pilocarpine; Sweat

1961
Sweat collection in cystic fibrosis. Report of a simplified method employing pilocarpine iontophoresis and cellulose sponge.
    The Ohio State medical journal, 1962, Volume: 58

    Topics: Animals; Cellulose; Cystic Fibrosis; Humans; Iontophoresis; Pilocarpine; Porifera; Sweat; Sweating

1962
Pilocarpine iontophoresis as a method of obtaining sweat for electrolyte determinations; a preliminary report.
    Virginia medical monthly, 1962, Volume: 89

    Topics: Cystic Fibrosis; Electrolytes; Humans; Iontophoresis; Pilocarpine; Sweat

1962
[ON METHODS OF SWEAT PRODUCTION FOR THE DIAGNOSIS OF MUCOVISCIDOSIS].
    Monatsschrift fur Kinderheilkunde, 1963, Volume: 111

    Topics: Baths; Child; Cystic Fibrosis; Humans; Iontophoresis; Pilocarpine; Sweat; Sweating

1963
EFFECTS OF ACETYLCHOLINE ON THE INCORPORATION OF P32 INTO THE PHOSPHOLIPIDS IN SLICES OF SKIN FROM CHILDREN WITH AND WITHOUT CYSTIC FIBROSIS OF THE PANCREAS.
    The Journal of clinical investigation, 1963, Volume: 42

    Topics: Acetylcholine; Biopsy; Child; Cystic Fibrosis; Humans; Inositol; Iontophoresis; Lipid Metabolism; Ph

1963
EVALUATION OF THE SWEAT CHLORIDE ASSAY IN ADULTS: USE OF PILOCARPINE IONTOPHORESIS.
    The American journal of the medical sciences, 1963, Volume: 246

    Topics: Adolescent; Adult; Aging; Child; Chlorides; Cystic Fibrosis; Humans; Infant; Iontophoresis; Lung Dis

1963
THE EFFECT OF ACETAZOLAMIDE ON SWEAT ELECTROLYTES IN MUCOVISCIDOSIS.
    Metabolism: clinical and experimental, 1963, Volume: 12

    Topics: Acetazolamide; Carbonic Anhydrases; Child; Chlorides; Cystic Fibrosis; Electrolytes; Humans; Iontoph

1963
[IMMUNOELECTROPHORESIS OF PROTEINS IN SWEAT AND ON THE PROBLEM OF ITS USE IN THE LABORATORY DIAGNOSIS OF MUCOVISCIDOSIS].
    Acta Universitatis Carolinae. Medica, 1964, Volume: 10

    Topics: Antigens; Clinical Laboratory Techniques; Cystic Fibrosis; Humans; Immunoelectrophoresis; Pilocarpin

1964
A NEW METHOD OF IONTOPHORESIS AND ANALYSIS OF SWEAT ELECTROLYTE.
    The American review of respiratory disease, 1964, Volume: 90

    Topics: Chemistry Techniques, Analytical; Cystic Fibrosis; Electrolytes; Genetics, Medical; Humans; Iontopho

1964
SWEAT CHLORIDE BY IONTOPHORESIS.
    Southern medical journal, 1964, Volume: 57

    Topics: Chlorides; Clinical Laboratory Techniques; Cystic Fibrosis; Humans; Infant; Iontophoresis; Pilocarpi

1964
A NEW METHOD OF IONTOPHORESIS AND ANALYSIS OF SWEAT ELECTROLYTE: A SURVEY OF SEVERAL KINDRED WITH CYSTIC FIBROSIS.
    Southern medical journal, 1965, Volume: 58

    Topics: Child; Cystic Fibrosis; Data Collection; Electrolytes; Genetics, Medical; Geriatrics; Humans; Iontop

1965
[The sweat test with intradermal injection of pilocarpine nitrate].
    El Dia medico, 1961, Volume: 33(Special)

    Topics: Cystic Fibrosis; Humans; Injections, Intradermal; Pilocarpine; Sweat; Sweating

1961
Recurrent cough and normal sweat chloride test.
    Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology, 2003, Volume: 91, Issue:6

    Topics: Adolescent; Bronchiectasis; Cough; Cystic Fibrosis; Diagnosis, Differential; Forced Expiratory Volum

2003
A small molecule CFTR inhibitor produces cystic fibrosis-like submucosal gland fluid secretions in normal airways.
    FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2004, Volume: 18, Issue:7

    Topics: Animals; Benzoates; Body Fluids; Bronchi; Cells, Cultured; Chlorides; Cholinergic Agents; Colforsin;

2004
Submucosal gland dysfunction as a primary defect in cystic fibrosis.
    FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2005, Volume: 19, Issue:3

    Topics: Adolescent; Adult; Biopsy; Child; Child, Preschool; Cystic Fibrosis; Cystic Fibrosis Transmembrane C

2005
Cystic fibrosis in Korean children:a case report identified by a quantitative pilocarpine iontophoresis sweat test and genetic analysis.
    Journal of Korean medical science, 2005, Volume: 20, Issue:1

    Topics: Blood Pressure; Bronchiectasis; Child; Cough; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conduct

2005
Sweat testing infants detected by cystic fibrosis newborn screening.
    The Journal of pediatrics, 2005, Volume: 147, Issue:3 Suppl

    Topics: Age Factors; Algorithms; Chlorides; Cystic Fibrosis; Decision Trees; DNA Mutational Analysis; Early

2005
Newborn screening for cystic fibrosis in Wisconsin: nine-year experience with routine trypsinogen/DNA testing.
    The Journal of pediatrics, 2005, Volume: 147, Issue:3 Suppl

    Topics: Age Factors; Chlorides; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; DNA Mu

2005
[Adult diabetes and mucoviscidosis].
    Polskie Archiwum Medycyny Wewnetrznej, 1967, Volume: 38, Issue:2

    Topics: Adolescent; Adult; Aged; Cystic Fibrosis; Diabetes Complications; Female; Humans; Iontophoresis; Mal

1967
[Sodium level in the sweat of patients with gastric and duodenal ulcer, and the value of sweat electrolyte determination in detecting of mucoviscidosis in adults].
    Polskie Archiwum Medycyny Wewnetrznej, 1967, Volume: 38, Issue:2

    Topics: Adolescent; Adult; Aged; Cystic Fibrosis; Female; Humans; Iontophoresis; Male; Middle Aged; Peptic U

1967
Pilocarpine iontophoresis sweat testing results of seven years' experience.
    Bibliotheca paediatrica, 1967, Volume: 86

    Topics: Adolescent; Adult; Child; Child, Preschool; Cystic Fibrosis; Female; Humans; Infant; Infant, Newborn

1967
The ionic composition of pilocarpine induced sweat in relation to gland output during aging and in cystic fibrosis.
    Bibliotheca paediatrica, 1967, Volume: 86

    Topics: Adolescent; Adult; Aging; Calcium; Child; Child, Preschool; Chlorides; Cystic Fibrosis; Female; Huma

1967
Sodium transport: inhibitory factor in sweat of patients with cystic fibrosis.
    Science (New York, N.Y.), 1967, Oct-06, Volume: 158, Issue:3797

    Topics: Absorption; Animals; Antimetabolites; Biological Transport, Active; Cystic Fibrosis; Humans; Parotid

1967
Sweat chloride assay for cystic fibrosis. Using pilocarpine iontophoresis stimulation, filter paper collection and cotlove chloridometer analysis.
    Minnesota medicine, 1967, Volume: 50, Issue:8

    Topics: Chlorides; Cystic Fibrosis; Humans; Pilocarpine; Sweat

1967
[Sweat composition changes in mucoviscidosis following pilocarpine and adrenalin iontophoresis].
    Vnitrni lekarstvi, 1967, Volume: 13, Issue:7

    Topics: Adolescent; Child; Child, Preschool; Cystic Fibrosis; Epinephrine; Female; Humans; Iontophoresis; Ma

1967
Exocrine pancreatic secretion in rats treated with reserpine after stimulation with pilocarpine, dopamine, and caerulein.
    Pediatric research, 1980, Volume: 14, Issue:1

    Topics: Amylases; Animals; Bicarbonates; Ceruletide; Chlorides; Cystic Fibrosis; Disease Models, Animal; Dop

1980
The chronically reserpinized rat as a model for cystic fibrosis: alterations in pancreatic enzyme secretion and storage.
    Pediatric research, 1981, Volume: 15, Issue:9

    Topics: Amylases; Animals; Cholecystokinin; Chymotrypsin; Cystic Fibrosis; Disease Models, Animal; Male; Pan

1981
Diagnostic testing in cystic fibrosis.
    The Journal of the Arkansas Medical Society, 1983, Volume: 79, Issue:12

    Topics: Adolescent; Adult; Child; Chlorides; Cystic Fibrosis; Humans; Iontophoresis; Pilocarpine; Sweat

1983
[Sweat electrolyte analysis by pilocarpine iontophoresis].
    Ugeskrift for laeger, 1981, Aug-31, Volume: 143, Issue:36

    Topics: Adolescent; Adult; Child; Child, Preschool; Cystic Fibrosis; Female; Humans; Infant; Infant, Newborn

1981
Incidence of meconium abnormalities in newborn infants with cystic fibrosis.
    American journal of diseases of children (1960), 1980, Volume: 134, Issue:1

    Topics: Child, Preschool; Cystic Fibrosis; Humans; Infant; Infant, Newborn; Intestinal Diseases; Intestinal

1980
Composition of pulmonary lavage fluid in control and reserpine-treated rats following chronic isoproterenol and pilocarpine administration.
    Pediatric research, 1980, Volume: 14, Issue:7

    Topics: Animals; Body Fluids; Carbohydrates; Cystic Fibrosis; Disease Models, Animal; Isoproterenol; Lipids;

1980
Cooperative study comparing three methods of performing sweat tests to diagnose cystic fibrosis.
    Pediatrics, 1980, Volume: 66, Issue:5

    Topics: Child; Cystic Fibrosis; Electrodes; False Negative Reactions; False Positive Reactions; Humans; Iont

1980
New approach to cystic fibrosis diagnosis by use of an improved sweat-induction/collection system and osmometry.
    Clinical chemistry, 1981, Volume: 27, Issue:3

    Topics: Chlorides; Cystic Fibrosis; Humans; Iontophoresis; Osmolar Concentration; Pilocarpine; Specimen Hand

1981
Sweat chloride concentrations in infants homozygous or heterozygous for F508 cystic fibrosis.
    Pediatrics, 1996, Volume: 97, Issue:4

    Topics: Age Factors; Alleles; Base Composition; Chlorides; Codon; Cystic Fibrosis; DNA; Follow-Up Studies; G

1996
Is the sweat test safe? Some instances of burns received during pilocarpine iontophoresis.
    Annals of clinical biochemistry, 1996, Volume: 33 ( Pt 5)

    Topics: Burns; Cystic Fibrosis; Humans; Infant; Infant, Newborn; Informed Consent; Iontophoresis; Pilocarpin

1996
[A method of sampling material for the determination of chlorides in sweat].
    Klinicheskaia laboratornaia diagnostika, 1997, Issue:2

    Topics: Chlorides; Cystic Fibrosis; Electrophoresis, Paper; Forearm; Humans; Pilocarpine; Specimen Handling;

1997
Urticaria associated with the pilocarpine iontophoresis sweat test.
    Pediatric pulmonology, 1997, Volume: 24, Issue:4

    Topics: Child; Chlorides; Cystic Fibrosis; Female; Histamine H1 Antagonists; Humans; Iontophoresis; Pilocarp

1997
Test for the concentration of electrolytes in cystic fibrosis of the pancreas utilizing pilocarpine by iontophoresis, by Lewis E. Gibson and Robert E. Cooke, Pediatrics; 1959;24:545-549.
    Pediatrics, 1998, Volume: 102, Issue:1 Pt 2

    Topics: Cystic Fibrosis; Electrolytes; History, 20th Century; Humans; Iontophoresis; Pilocarpine; Sweat

1998
Sweat chloride: quantitative patch for collection and measurement.
    Clinical laboratory science : journal of the American Society for Medical Technology, 2001,Summer, Volume: 14, Issue:3

    Topics: Adolescent; Adult; Aged; Child; Child, Preschool; Chlorides; Cystic Fibrosis; Humans; Infant; Iontop

2001
'Rusters'. The corrosive action of palmar sweat: I. Sodium chloride in sweat.
    Acta dermato-venereologica, 1979, Volume: 59, Issue:2

    Topics: Administration, Topical; Adolescent; Adult; Aluminum; Chlorides; Corrosion; Cystic Fibrosis; Dermato

1979
The chronically reserpinized rat as a possible model for cystic fibrosis. I. Submaxillary gland morphology and ultrastructure.
    Pediatric research, 1975, Volume: 9, Issue:5

    Topics: Animals; Body Weight; Cell Nucleus; Cystic Fibrosis; Cytoplasm; Disease Models, Animal; Endoplasmic

1975
[A new type of sweat test and its use in children].
    Problemy medycyny wieku rozwojowego, 1979, Volume: 8

    Topics: Adolescent; Age Factors; Child; Child, Preschool; Chlorides; Cystic Fibrosis; Electrodes; Humans; In

1979
The chronically reserpinized rat as an animal model for cystic fibrosis: I. Acute effect of isoproterenol and pilocarpine upon pulmonary lavage fluid.
    Pediatric research, 1979, Volume: 13, Issue:6

    Topics: Animals; Carbohydrate Metabolism; Cholesterol; Cystic Fibrosis; Isoproterenol; Lipid Metabolism; Lun

1979
[Improvement of the sweat test in diagnosis of mucoviscidosis].
    Zeitschrift fur medizinische Laboratoriumsdiagnostik, 1979, Volume: 20, Issue:2

    Topics: Child; Cystic Fibrosis; Humans; Mass Screening; Pilocarpine; Secretory Rate; Sweat

1979
The significance of the sweat test in chronic pancreatitis.
    The Tohoku journal of experimental medicine, 1978, Volume: 125, Issue:1

    Topics: Adolescent; Adult; Age Factors; Aged; Child; Chronic Disease; Cystic Fibrosis; Eating; Female; Human

1978
Cystic fibrosis. Problems encountered with sweat testing.
    JAMA, 1978, Oct-27, Volume: 240, Issue:18

    Topics: Chlorides; Cystic Fibrosis; False Negative Reactions; False Positive Reactions; Humans; Iontophoresi

1978
Measurement of chloride in sweat with the chloride-selective electrode.
    Clinical chemistry, 1978, Volume: 24, Issue:11

    Topics: Chlorides; Cystic Fibrosis; Electrodes; Humans; Infant, Newborn; Methods; Pilocarpine; Sweat

1978
Quality of sweat test performance in the diagnosis of cystic fibrosis.
    Clinical chemistry, 1979, Volume: 25, Issue:1

    Topics: Adolescent; Adult; Child; Child, Preschool; Cystic Fibrosis; Humans; Infant; Pilocarpine; Sweat; Swe

1979
[Mucoviscidosis (cystic fibrosis)].
    Der Internist, 1976, Volume: 17, Issue:7

    Topics: Celiac Disease; Child; Child, Preschool; Cystic Fibrosis; Diagnosis, Differential; Humans; Infant; I

1976
Cystic fibrosis detection by means of a test-strip.
    Pediatrics, 1975, Volume: 55, Issue:1

    Topics: Albumins; Cystic Fibrosis; Evaluation Studies as Topic; False Negative Reactions; False Positive Rea

1975
[Current use of the sweat test (author's transl)].
    Padiatrie und Padologie, 1977, Volume: 12, Issue:4

    Topics: Cystic Fibrosis; Humans; Infant, Newborn; Iontophoresis; Methods; Pilocarpine; Sweat

1977
The use of electrolyte measurements in the detection of cystic fibrosis.
    Clinica chimica acta; international journal of clinical chemistry, 1976, Jun-15, Volume: 69, Issue:3

    Topics: Adolescent; Adult; Child; Child, Preschool; Chlorides; Cystic Fibrosis; Female; Heterozygote; Humans

1976
Laboratory confirmation of the diagnosis of cystic fibrosis.
    Clinical chemistry, 1976, Volume: 22, Issue:11

    Topics: Adolescent; Adult; Child; Child, Preschool; Chlorides; Clinical Laboratory Techniques; Cystic Fibros

1976
The chronically reserpinized rat as a possible model for cystic fibrosis. II. Comparison and cilioinhibitory effects of submaxillary saliva.
    Pediatric research, 1975, Volume: 9, Issue:5

    Topics: Animals; Biological Assay; Bivalvia; Calcium; Carbohydrates; Cilia; Cystic Fibrosis; Disease Models,

1975
Insulin iontophoresis in cystic fibrosis.
    Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.), 1975, Volume: 149, Issue:3

    Topics: Chlorides; Cystic Fibrosis; Heterozygote; Humans; Insulin; Iontophoresis; Pilocarpine; Sweat

1975
[Simple measurement of skin chloride activity for diagnosis of cyste fibrosis (author's transl)].
    Zeitschrift fur Kinderheilkunde, 1975, Aug-11, Volume: 120, Issue:2

    Topics: Child; Child, Preschool; Chlorides; Cystic Fibrosis; Electrodes; Humans; Infant; Methods; Pilocarpin

1975
The kallikrein-kinin system of sweat in normal and cystic fibrosis subjects.
    Agents and actions. Supplements, 1992, Volume: 38 ( Pt 3)

    Topics: Child; Cystic Fibrosis; Female; Humans; Isoproterenol; Kallikreins; Male; Pilocarpine; Prekallikrein

1992
[Comparison of the classical Gibson-Cooke methods and the chloride-sensitive electrode in sweat testing for diagnosis of cystic fibrosis].
    Padiatrie und Padologie, 1991, Volume: 26, Issue:4

    Topics: Adolescent; Child; Child, Preschool; Chlorides; Cystic Fibrosis; Electrodes; Female; Humans; Infant;

1991
[The form of crystallization of perspiration in pancreatic cystic fibrosis].
    Anales espanoles de pediatria, 1990, Volume: 32, Issue:6

    Topics: Crystallization; Cystic Fibrosis; Electrolytes; Humans; Iontophoresis; Pilocarpine; Sweat

1990
Abnormal jejunal potential difference in cystic fibrosis.
    Lancet (London, England), 1989, Mar-04, Volume: 1, Issue:8636

    Topics: Action Potentials; Adolescent; Adult; Cystic Fibrosis; Dinoprostone; Female; Glucose; Humans; Jejunu

1989
[Diagnosis of mucoviscidosis by examination of sweat: value of conductometry].
    Kinderarztliche Praxis, 1989, Volume: 57, Issue:10

    Topics: Adolescent; Child; Child, Preschool; Cystic Fibrosis; Flame Ionization; Galvanic Skin Response; Huma

1989
X-ray microanalysis of exocrine glands in animal models for cystic fibrosis.
    Scanning electron microscopy, 1985, Issue:Pt 4

    Topics: Adrenergic beta-Agonists; Animals; Cystic Fibrosis; Cytoplasmic Granules; Disease Models, Animal; El

1985
Effects of chronic furosemide treatment on rat exocrine glands.
    Experimental and molecular pathology, 1988, Volume: 48, Issue:2

    Topics: Animals; Biological Transport; Cations; Chlorides; Cystic Fibrosis; Disease Models, Animal; Exocrine

1988
Evaluation of a cystic fibrosis screening system incorporating a miniature sweat stimulator and disposable chloride sensor.
    Clinical chemistry, 1986, Volume: 32, Issue:5

    Topics: Adolescent; Adult; Child; Child, Preschool; Chlorides; Cystic Fibrosis; Electrodes; False Negative R

1986
Advances in cystic fibrosis.
    Comprehensive therapy, 1986, Volume: 12, Issue:2

    Topics: Cystic Fibrosis; Humans; Pilocarpine; Sodium Chloride; Sweat

1986
The chronically pilocarpine-treated rat in the study of cystic fibrosis: investigations on submandibular gland and pancreas.
    Experimental and molecular pathology, 1985, Volume: 43, Issue:1

    Topics: Animals; Carbachol; Cystic Fibrosis; Disease Models, Animal; Electron Probe Microanalysis; Energy Me

1985
[Nightsweat collection for simple diagnosis of mucoviscidosis (author's transl)].
    Padiatrie und Padologie, 1974, Volume: 9, Issue:1

    Topics: Child; Chlorides; Cystic Fibrosis; Humans; Iontophoresis; Methods; Pilocarpine; Specimen Handling; S

1974
Cystic fibrosis: an improved diagnostic method utilizing constant current iontophoresis.
    Revista brasileira de biologia, 1972, Volume: 32, Issue:2

    Topics: Chlorides; Cystic Fibrosis; Humans; Iontophoresis; Methods; Pilocarpine; Sodium; Sweat

1972
Direct measurement of chloride in sweat with an ion-selective electrode.
    Clinical chemistry, 1973, Volume: 19, Issue:7

    Topics: Adolescent; Bicarbonates; Child; Child, Preschool; Chlorides; Cystic Fibrosis; Diagnosis, Differenti

1973
The effect of isoprenaline and pilocarpine on (a) bronchial mucus-secreting tissue and (b) pancreas, salivary glands, heart, thymus, liver and spleen.
    British journal of experimental pathology, 1973, Volume: 54, Issue:4

    Topics: Animals; Bronchi; Cystic Fibrosis; Glycoproteins; Heart; Isoproterenol; Liver; Mucous Membrane; Mucu

1973
Letter: Screening for cystic fibrosis by specific ion electrode.
    Clinical chemistry, 1973, Volume: 19, Issue:11

    Topics: Chlorides; Cystic Fibrosis; Evaluation Studies as Topic; Humans; Mass Screening; Methods; Pilocarpin

1973
Cystic fibrosis with edema and falsely negative sweat test.
    The Journal of pediatrics, 1973, Volume: 83, Issue:1

    Topics: Chlorides; Cystic Fibrosis; Edema; False Negative Reactions; Humans; Hypoproteinemia; Infant, Newbor

1973
[Necessity and possibilities of mass screening in mucoviscidosis].
    Kinderarztliche Praxis, 1973, Volume: 41, Issue:9

    Topics: Adolescent; Age Factors; Bronchitis; Child; Child, Preschool; Chlorides; Chronic Disease; Cystic Fib

1973
[Diabetes mellitus and mucoviscidosis].
    Kinderarztliche Praxis, 1973, Volume: 41, Issue:12

    Topics: Adolescent; Child; Child, Preschool; Chlorides; Cystic Fibrosis; Diabetes Complications; Glucose Tol

1973
Micro-isoelectric focusing of proteins in pilocarpine-induced sweat.
    Clinica chimica acta; international journal of clinical chemistry, 1971, Volume: 31, Issue:2

    Topics: Adult; Animals; Child; Child, Preschool; Cystic Fibrosis; Glycoproteins; Horses; Humans; Immune Sera

1971
[Personal experience and general considerations concerning the determination of sweat electrolyte levels by means of pilocarpine iontophoresis].
    Minerva pediatrica, 1972, Mar-17, Volume: 24, Issue:9

    Topics: Child; Child, Preschool; Cystic Fibrosis; Electrolytes; Female; Humans; Infant; Iontophoresis; Male;

1972
[Diagnosis of mucoviscidosis. Gibson's and Cook's apparatus without batteries for sweat collection using pilocarpine iontophoresis].
    Das Deutsche Gesundheitswesen, 1972, Feb-10, Volume: 27, Issue:6

    Topics: Cystic Fibrosis; Humans; Iontophoresis; Pilocarpine; Sodium Chloride; Sweat

1972
[Mucoviscidosis in childhood. Optimal sweat production and analysis].
    Das Deutsche Gesundheitswesen, 1972, Feb-17, Volume: 27, Issue:7

    Topics: Adolescent; Child; Child, Preschool; Cystic Fibrosis; Female; Humans; Infant; Infant, Newborn; Ionto

1972
Some observations on sweat test by Pilocarpine Iontophoresis.
    Indian pediatrics, 1971, Volume: 8, Issue:7

    Topics: Child; Child, Preschool; Cystic Fibrosis; Diagnosis, Differential; Humans; Infant; Iontophoresis; Nu

1971
[Sweat analysis following pilocarpine iontophoresis. Normal values of chloride in sweat, saliva and tears in relation to the child's age].
    Kinderarztliche Praxis, 1971, Volume: 39, Issue:4

    Topics: Adult; Age Factors; Child; Cystic Fibrosis; Diagnosis, Differential; Humans; Iontophoresis; Methods;

1971
[Sweating in the newborn infant. Studies on the pilocarpine stimulated single sweat gland].
    Helvetica paediatrica acta, 1971, Volume: 26, Issue:5

    Topics: Cystic Fibrosis; Female; Humans; Infant, Newborn; Male; Pilocarpine; Potassium; Sodium; Sweat; Sweat

1971
Sweat tests in cystic fibrosis: a comparison of the thermal test with pilocarpine stimulation at two dose levels.
    Clinical biochemistry, 1971, Volume: 4, Issue:1

    Topics: Adolescent; Adult; Aged; Child; Child, Preschool; Chlorides; Cystic Fibrosis; Evaluation Studies as

1971
[The sweat test].
    Maandschrift voor kindergeneeskunde, 1969, Volume: 37, Issue:4

    Topics: Cystic Fibrosis; Humans; Iontophoresis; Pilocarpine; Sweat

1969
Cystic fibrosis of pancreas in adults. A report of 4 cases.
    The Indian journal of chest diseases, 1969, Volume: 11, Issue:3

    Topics: Adolescent; Adult; Child; Chlorides; Cystic Fibrosis; Female; Humans; Iontophoresis; Male; Pilocarpi

1969
Pilocarpin iontophoresis--practical aspects.
    Acta paediatrica Scandinavica, 1967

    Topics: Burns, Electric; Cystic Fibrosis; Humans; Iontophoresis; Pilocarpine; Sweating

1967
[Value of a simple method for collecting perspiration].
    Revue medicale de Liege, 1967, May-01, Volume: 22, Issue:9

    Topics: Adolescent; Child; Child, Preschool; Chlorides; Cystic Fibrosis; Electrodes; Humans; Infant; Iontoph

1967
The effect of adrenergic stimulation upon sweating in normal children and cystic fibrosis patients.
    Pediatrics, 1968, Volume: 42, Issue:3

    Topics: Adolescent; Adult; Atropine; Child; Child, Preschool; Cystic Fibrosis; Epinephrine; Humans; Iontopho

1968
Cystic fibrosis and pregnancy.
    JAMA, 1968, Jan-15, Volume: 203, Issue:3

    Topics: Adult; Cystic Fibrosis; Diagnosis, Differential; Female; Humans; Infant, Newborn; Iontophoresis; Pil

1968
Some hazards of the sweat test.
    Archives of disease in childhood, 1968, Volume: 43, Issue:232

    Topics: Blister; Burns, Chemical; Burns, Electric; Child; Cystic Fibrosis; Electrodiagnosis; Humans; Hydroch

1968
Sweat electrolytes in mature and premature neonates after normal and pathological gestations and births.
    Polish medical science and history bulletin, 1968, Volume: 11, Issue:1

    Topics: Calcium; Cystic Fibrosis; Female; Humans; Infant, Newborn; Infant, Premature; Iontophoresis; Pilocar

1968
Studies in cystic fibrosis: determination of sweat electrolytes in situ with direct reading electrodes.
    Pediatrics, 1969, Volume: 43, Issue:5

    Topics: Child; Child, Preschool; Chlorides; Cystic Fibrosis; Electrodes; Hot Temperature; Humans; Infant; In

1969
[On the diagnosis of mucoviscidosis (cystic fibrosis)].
    Deutsche medizinische Wochenschrift (1946), 1969, Aug-22, Volume: 94, Issue:34

    Topics: Child; Child, Preschool; Chlorides; Cystic Fibrosis; Humans; Indicators and Reagents; Infant; Iontop

1969
Accuracy of the sweat test: advantage of a micromethod.
    Archives of disease in childhood, 1965, Volume: 40, Issue:214

    Topics: Cystic Fibrosis; Humans; In Vitro Techniques; Iontophoresis; Pilocarpine; Sweat

1965
Cystic fibrosis of the pancreas: a study of sweat electrolyte levels in thirty-six families using pilocarpine iontophoresis.
    Southern medical journal, 1966, Volume: 59, Issue:2

    Topics: Adult; Child; Cystic Fibrosis; Electrolytes; Humans; Iontophoresis; Pilocarpine; Sweat

1966
The sweat test in cystic fibrosis. A comparison of overnight sweat collection versus the pilocarpine iontophoresis method.
    The Journal of pediatrics, 1966, Volume: 69, Issue:2

    Topics: Adolescent; Adult; Child; Child, Preschool; Cystic Fibrosis; Electrolytes; Humans; Infant; Infant, N

1966