chlorine and Exocrine Pancreatic Insufficiency
chlorine has been researched along with Exocrine Pancreatic Insufficiency in 27 studies
chloride : A halide anion formed when chlorine picks up an electron to form an an anion.
Exocrine Pancreatic Insufficiency: A malabsorption condition resulting from greater than 10% reduction in the secretion of pancreatic digestive enzymes (LIPASE; PROTEASES; and AMYLASE) by the EXOCRINE PANCREAS into the DUODENUM. This condition is often associated with CYSTIC FIBROSIS and with chronic PANCREATITIS.
Research Excerpts
Excerpt | Relevance | Reference |
---|---|---|
"Cystic fibrosis is a monogenic disease considered to affect at least 100 000 people worldwide." | 2.72 | Cystic fibrosis. ( Davies, JC; Haq, IJ; Polineni, D; Shteinberg, M, 2021) |
"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 lethal autosomal recessive disorder usually associated with lung disease, pancreatic insufficiency and high sweat chloride levels." | 1.35 | Clinical and molecular characterization of S1118F-CFTR. ( Conoley, VG; Frederick, CA; Kappes, J; Li, C; Naren, AP; Nekkalapu, S; Penmatsa, H; Stokes, DC; Zhang, W, 2009) |
Research
Studies (27)
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 8 (29.63) | 18.7374 |
1990's | 3 (11.11) | 18.2507 |
2000's | 9 (33.33) | 29.6817 |
2010's | 4 (14.81) | 24.3611 |
2020's | 3 (11.11) | 2.80 |
Authors
Authors | Studies |
---|---|
Phadke, MY | 1 |
Sellers, ZM | 1 |
Procianoy, EDFA | 1 |
de Abreu E Silva, FA | 1 |
Maróstica, PJC | 1 |
Quinton, PM | 1 |
Shteinberg, M | 1 |
Haq, IJ | 1 |
Polineni, D | 1 |
Davies, JC | 1 |
de Winter-de Groot, KM | 1 |
Janssens, HM | 1 |
van Uum, RT | 1 |
Dekkers, JF | 1 |
Berkers, G | 1 |
Vonk, A | 1 |
Kruisselbrink, E | 1 |
Oppelaar, H | 1 |
Vries, R | 1 |
Clevers, H | 1 |
Houwen, RHJ | 1 |
Escher, JC | 1 |
Elias, SG | 1 |
de Jonge, HR | 1 |
de Rijke, YB | 1 |
Tiddens, HAWM | 1 |
van der Ent, CK | 1 |
Beekman, JM | 1 |
Bagheri-Behrouzi, A | 1 |
Steiß, JO | 1 |
Zimmer, KP | 1 |
Nährlich, L | 1 |
Najafi, M | 1 |
Alimadadi, H | 1 |
Rouhani, P | 1 |
Kiani, MA | 1 |
Khodadad, A | 1 |
Motamed, F | 1 |
Moraveji, A | 1 |
Hooshmand, M | 1 |
Haghi Ashtıani, MT | 1 |
Rezaei, N | 1 |
Voter, KZ | 1 |
Ren, CL | 1 |
Rose, JB | 1 |
Ellis, L | 2 |
John, B | 1 |
Martin, S | 1 |
Gonska, T | 2 |
Solomon, M | 1 |
Tullis, E | 1 |
Corey, M | 1 |
Adeli, K | 1 |
Durie, PR | 3 |
Ip, W | 1 |
Turner, D | 1 |
Han, WS | 1 |
Rose, J | 1 |
Durie, P | 1 |
Quinton, P | 1 |
Penmatsa, H | 1 |
Frederick, CA | 1 |
Nekkalapu, S | 1 |
Conoley, VG | 1 |
Zhang, W | 1 |
Li, C | 1 |
Kappes, J | 1 |
Stokes, DC | 1 |
Naren, AP | 1 |
Stormon, MO | 1 |
Ip, WF | 1 |
Schibli, S | 1 |
Rommens, JM | 1 |
Munck, A | 1 |
Augarten, A | 2 |
Ben Tov, A | 1 |
Madgar, I | 1 |
Barak, A | 1 |
Akons, H | 2 |
Laufer, J | 1 |
Efrati, O | 1 |
Aviram, M | 2 |
Bentur, L | 1 |
Blau, H | 2 |
Paret, G | 1 |
Wilschanski, M | 1 |
Kerem, BS | 1 |
Yahav, Y | 2 |
Paranjape, SM | 1 |
Zeitlin, PL | 1 |
Adelson, JW | 1 |
Forsyth, JS | 1 |
Gillies, DR | 1 |
Wilson, SG | 1 |
Evensen, SA | 1 |
Davis, PB | 1 |
Hubbard, VS | 1 |
Di Sant'Agnese, PA | 1 |
McKinney, PE | 1 |
Brent, J | 1 |
Kulig, K | 1 |
Nowakowska, A | 1 |
Bal, J | 1 |
Obersztyn, E | 1 |
Sands, D | 1 |
Maciejko, D | 1 |
Mazurczak, T | 1 |
Durieu, I | 1 |
Durupt, S | 1 |
Josserand, RN | 1 |
Durand, DV | 1 |
Bey-Omar, F | 1 |
Shmilovich, H | 1 |
Doolman, R | 1 |
Ben Tur, L | 1 |
Kerem, E | 1 |
Rivlin, J | 1 |
Sela, BA | 1 |
Szeinberg, A | 1 |
Tamalet, A | 1 |
Fauroux, B | 1 |
Clement, A | 1 |
Beaudry, PH | 1 |
Beck, R | 1 |
Goldberg, E | 1 |
Levison, H | 1 |
Foulston, C | 1 |
Gall, G | 1 |
Mitchell, I | 1 |
Cooper, DM | 1 |
Scott, RB | 1 |
Steinsapir, KD | 1 |
Vinters, HV | 1 |
Clinical Trials (1)
Trial Overview
Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
---|---|---|---|---|---|---|---|
Development a Core Set for Adults With Cystic Fibrosis Based on the International Classification of Functioning, Disability, and Health (ICF)[NCT06128499] | 30 participants (Anticipated) | Observational | 2023-12-20 | Not yet recruiting | |||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
Reviews
5 reviews available for chlorine and Exocrine Pancreatic Insufficiency
Article | Year |
---|---|
Cystic fibrosis.
Topics: Bicarbonates; Chlorides; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Disea | 2021 |
Diagnosis of cystic fibrosis.
Topics: Bronchiectasis; Chlorides; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Dia | 2008 |
Atypical cystic fibrosis and CFTR-related diseases.
Topics: Adolescent; Adult; Airway Obstruction; Aspergillosis, Allergic Bronchopulmonary; Aspergillus fumigat | 2008 |
Pathophysiology of the pancreas in cystic fibrosis.
Topics: Animals; Bicarbonates; Biological Transport; Chlorides; Cystic Fibrosis; Exocrine Pancreatic Insuffi | 1984 |
[Diagnosis and management of cystic fibrosis in children].
Topics: Adult; Age Factors; Anti-Bacterial Agents; Child; Chlorides; Cystic Fibrosis; Cystic Fibrosis Transm | 2000 |
Other Studies
22 other studies available for chlorine and Exocrine Pancreatic Insufficiency
Article | Year |
---|---|
Current clinical opinion on CFTR dysfunction and patient risk of pancreatitis: diagnostic and therapeutic considerations.
Topics: Chlorides; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Exocrine Pancreatic | 2022 |
Chloride Conductance, Nasal Potential Difference and Cystic Fibrosis Pathophysiology.
Topics: Adolescent; Adult; Child; Child, Preschool; Chlorides; Cystic Fibrosis; Cystic Fibrosis Transmembran | 2020 |
Stratifying infants with cystic fibrosis for disease severity using intestinal organoid swelling as a biomarker of CFTR function.
Topics: Biomarkers; Chlorides; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Exocrin | 2018 |
Misdiagnosis of cystic fibrosis based on transient pancreatic insufficiency and elevated sweat chloride.
Topics: Child; Child, Preschool; Chlorides; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regul | 2015 |
Genotype-phenotype relationship in Iranian patients with cystic fibrosis.
Topics: Age of Onset; Asian People; Chlorides; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Re | 2015 |
Does the Macroduct collection system reliably define sweat chloride concentration in subjects with intermediate results?
Topics: Adolescent; Adult; Child; Child, Preschool; Chlorides; Clinical Laboratory Techniques; Cystic Fibros | 2009 |
Sweat gland bioelectrics differ in cystic fibrosis: a new concept for potential diagnosis and assessment of CFTR function in cystic fibrosis.
Topics: Adrenergic beta-Agonists; Adult; Biomarkers; Chlorides; Cystic Fibrosis; Cystic Fibrosis Transmembra | 2009 |
Clinical and molecular characterization of S1118F-CFTR.
Topics: Blotting, Western; Cells, Cultured; Chlorides; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conduc | 2009 |
Evidence of a generalized defect of acinar cell function in Shwachman-Diamond syndrome.
Topics: Adolescent; Adult; Bone Marrow Diseases; Breath Tests; Case-Control Studies; Child; Child, Preschool | 2010 |
Heat wave and acute pancreatitis: very unusual cystic fibrosis presentation.
Topics: Acute Disease; Child; Child, Preschool; Chlorides; Cystic Fibrosis; Diagnostic Errors; Exocrine Panc | 2004 |
The changing face of the exocrine pancreas in cystic fibrosis: the correlation between pancreatic status, pancreatitis and cystic fibrosis genotype.
Topics: Acute Disease; Adolescent; Adult; Child; Child, Preschool; Chlorides; Cohort Studies; Cystic Fibrosi | 2008 |
Cystic fibrosis presenting with chronic electrolyte depletion, metabolic alkalosis and hyperaldosteronism.
Topics: Alkalosis; Chlorides; Cystic Fibrosis; Exocrine Pancreatic Insufficiency; Humans; Hyperaldosteronism | 1982 |
A 69-year-old man with chronic obstructive pulmonary disease, pancreatic insufficiency and elevated sweat electrolytes.
Topics: Age Factors; Aged; Chlorides; Cystic Fibrosis; Diagnosis, Differential; Exocrine Pancreatic Insuffic | 1981 |
Low sweat electrolytes in a patient with cystic fibrosis.
Topics: Adult; Chlorides; Cystic Fibrosis; Electrolytes; Exocrine Pancreatic Insufficiency; Female; Humans; | 1980 |
Zinc chloride ingestion in a child: exocrine pancreatic insufficiency.
Topics: Chlorides; Exocrine Pancreatic Insufficiency; Humans; Infant; Male; Poisoning; Zinc Compounds | 1995 |
[A study evaluating the correlation between the phenotype and genotype among 65 cystic fibrosis patients].
Topics: Adolescent; Child; Child, Preschool; Chlorides; Cystic Fibrosis; Exocrine Pancreatic Insufficiency; | 1995 |
Increased sweat chloride concentrations in adult patients with pancreatic insufficiency: cystic fibrosis phenotype or lack of specificity of sweat test?
Topics: Adult; Chlorides; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Exocrine Pan | 1999 |
Serum lipase levels as a diagnostic marker in cystic fibrosis patients with normal or borderline sweat tests.
Topics: Adult; Child; Chlorides; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Exocr | 2000 |
Cystic fibrosis--clinical viewpoint--a disease that doesn't make sense.
Topics: Chlorides; Cystic Fibrosis; Exocrine Pancreatic Insufficiency; Humans; Infant, Newborn; Intestinal O | 1987 |
Elevated sweat chloride levels in anorexia nervosa.
Topics: Adolescent; Anorexia Nervosa; Child; Chlorides; Exocrine Pancreatic Insufficiency; Female; Humans; M | 1986 |
Transient neutral fat steatorrhea, elevated sweat chloride concentration, and hypoparathyroidism in a child with celiac disease.
Topics: Celiac Disease; Child, Preschool; Chlorides; Exocrine Pancreatic Insufficiency; Humans; Hypocalcemia | 1985 |
Central pontine myelinolysis in a child with the Shwachman-Diamond syndrome.
Topics: Anemia; Brain Diseases; Child; Chlorides; Demyelinating Diseases; Exocrine Pancreatic Insufficiency; | 1985 |