iodine has been researched along with Pancreatic Insufficiency in 33 studies
Iodine: A nonmetallic element of the halogen group that is represented by the atomic symbol I, atomic number 53, and atomic weight of 126.90. It is a nutritionally essential element, especially important in thyroid hormone synthesis. In solution, it has anti-infective properties and is used topically.
diiodine : Molecule comprising two covalently bonded iodine atoms with overall zero charge..
| Excerpt | Relevance | Reference |
|---|---|---|
| "Cystic fibrosis is the most common lethal genetic disease in Caucasians, manifesting as progressive lung dysfunction, pancreatic insufficiency, and intestinal disease." | 2.44 | Cystic fibrosis: newborn screening in America. ( Kleven, DT; McCudden, CR; Willis, MS, 2008) |
| "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) |
| "Cystic fibrosis is the most common autosomal recessive genetic defect of one gene CFTR, where a variety of mutations were revealed." | 1.33 | [Genotype and phenotype of gastrointestinal symptoms analysis in children with cystic fibrosis]. ( Iwańczak, F; Mowszet, K; Pawłowicz, J; Sasiadek, M; Smigiel, R; Stawarski, A; Stembalska, A, 2005) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 10 (30.30) | 18.7374 |
| 1990's | 5 (15.15) | 18.2507 |
| 2000's | 11 (33.33) | 29.6817 |
| 2010's | 5 (15.15) | 24.3611 |
| 2020's | 2 (6.06) | 2.80 |
| Authors | Studies |
|---|---|
| CHINN, AB | 1 |
| LAVIK, PS | 1 |
| STITT, RM | 1 |
| BUCKALOO, GW | 1 |
| Semple, A | 1 |
| Clark, T | 1 |
| Allen, NM | 1 |
| Krishnananthan, T | 1 |
| Nwokoro, C | 1 |
| Girodon, E | 1 |
| Porzio, M | 1 |
| Herzig, M | 1 |
| Pagin, A | 1 |
| Sermet-Gaudelus, I | 1 |
| Burgel, PR | 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 |
| Shen, Y | 1 |
| Liu, J | 1 |
| Zhong, L | 1 |
| Mogayzel, PJ | 1 |
| Zeitlin, PL | 2 |
| Sosnay, PR | 1 |
| Zhao, S | 1 |
| Souza Dos Santos Simon, MI | 1 |
| Forte, GC | 1 |
| da Silva Pereira, J | 1 |
| da Fonseca Andrade Procianoy, E | 1 |
| Drehmer, M | 1 |
| Kleven, DT | 1 |
| McCudden, CR | 1 |
| Willis, MS | 1 |
| Rose, JB | 1 |
| Ellis, L | 2 |
| John, B | 1 |
| Martin, S | 1 |
| Gonska, T | 3 |
| Solomon, M | 1 |
| Tullis, E | 3 |
| Corey, M | 3 |
| Adeli, K | 1 |
| Durie, PR | 4 |
| 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 |
| Ooi, CY | 1 |
| Dorfman, R | 1 |
| Cipolli, M | 1 |
| Castellani, C | 1 |
| Keenan, K | 1 |
| Freedman, SD | 1 |
| Zielenski, J | 2 |
| Berthiaume, Y | 1 |
| Schibli, S | 1 |
| ROMANO, C | 1 |
| BERTOLOTTI, E | 1 |
| DEPRA, M | 1 |
| Munck, A | 1 |
| Iwańczak, F | 1 |
| Smigiel, R | 1 |
| Stawarski, A | 1 |
| Pawłowicz, J | 1 |
| Stembalska, A | 1 |
| Mowszet, K | 1 |
| Sasiadek, M | 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 |
| Dalcin, Pde T | 1 |
| Abreu E Silva, FA | 1 |
| Paranjape, SM | 1 |
| Eichenhorn, MS | 1 |
| Lüthi, M | 1 |
| Zurbrügg, RP | 1 |
| Forsyth, JS | 1 |
| Gillies, DR | 1 |
| Wilson, SG | 1 |
| Evensen, SA | 1 |
| Davis, PB | 1 |
| Hubbard, VS | 1 |
| Di Sant'Agnese, PA | 1 |
| Nowakowska, A | 1 |
| Bal, J | 1 |
| Obersztyn, E | 1 |
| Sands, D | 1 |
| Maciejko, D | 1 |
| Mazurczak, T | 1 |
| De Braekeleer, M | 1 |
| Allard, C | 1 |
| Leblanc, JP | 1 |
| Simard, F | 1 |
| Aubin, G | 1 |
| Gilfillan, A | 1 |
| Warner, JP | 1 |
| Kirk, JM | 1 |
| Marshall, T | 1 |
| Greening, A | 1 |
| Ho, LP | 1 |
| Hargreave, T | 1 |
| Stack, B | 1 |
| McIntyre, D | 1 |
| Davidson, R | 1 |
| Dean, JC | 1 |
| Middleton, W | 1 |
| Brock, DJ | 1 |
| Wilson, DC | 1 |
| Ip, WF | 1 |
| Tsui, LC | 1 |
| Knowles, MR | 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 |
| Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
|---|---|---|---|---|---|---|---|
| A Phase II Study to Establish the Efficacy of Synthetic Human SecretiN in Human Acute Pancreatitis (SNAP) Study[NCT03686618] | Phase 2 | 40 participants (Anticipated) | Interventional | 2018-10-01 | Recruiting | ||
| [information is prepared from clinicaltrials.gov, extracted Sep-2024] | |||||||
5 reviews available for iodine and Pancreatic Insufficiency
| Article | Year |
|---|---|
Genetic diagnosis in practice: From cystic fibrosis to CFTR-related disorders.
Topics: Algorithms; Bronchiectasis; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Ex | 2020 |
Cystic fibrosis: newborn screening in America.
Topics: Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; DNA Mutational Analysis; Exocr | 2008 |
Cystic fibrosis in adults: diagnostic and therapeutic aspects.
Topics: Adult; Anti-Bacterial Agents; Anti-Inflammatory Agents; Cystic Fibrosis; Diagnosis, Differential; Dr | 2008 |
Atypical cystic fibrosis and CFTR-related diseases.
Topics: Adolescent; Adult; Airway Obstruction; Aspergillosis, Allergic Bronchopulmonary; Aspergillus fumigat | 2008 |
[Diagnosis and management of cystic fibrosis in children].
Topics: Adult; Age Factors; Anti-Bacterial Agents; Child; Chlorides; Cystic Fibrosis; Cystic Fibrosis Transm | 2000 |
28 other studies available for iodine and Pancreatic Insufficiency
| Article | Year |
|---|---|
Use of I131-labeled protein in the diagnosis of pancreatic insufficiency.
Topics: Disease; Exocrine Pancreatic Insufficiency; Humans; Iodine; Iodine Radioisotopes; Pancreas; Pancreat | 1952 |
Identification of a novel cystic fibrosis mutation in three patients of South Asian descent.
Topics: Adolescent; Adult; Asian People; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulato | 2020 |
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 |
Clinical Phenotypes and Genotypic Spectrum of Cystic Fibrosis in Chinese Children.
Topics: 3' Untranslated Regions; Adolescent; Asian People; Aspergillosis, Allergic Bronchopulmonary; Bronchi | 2016 |
Validation of a Nutrition Screening Tool for Pediatric Patients with Cystic Fibrosis.
Topics: Adolescent; Body Mass Index; Body Weight; Child; Cross-Sectional Studies; Cystic Fibrosis; Energy In | 2016 |
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 |
Type of CFTR mutation determines risk of pancreatitis in patients with cystic fibrosis.
Topics: Adult; Cohort Studies; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Exocrin | 2011 |
[ON THE ASSOCIATION OF A CHRONIC BRONCHOPNEUMOPATHY, PANCREATIC INSUFFICIENCY AND A NORMAL SWEAT TEST. INTERPRETATIVE CONSIDERATIONS].
Topics: Bronchiectasis; Bronchitis; Bronchopneumonia; Child; Cystic Fibrosis; Diagnosis; Electrolytes; Exocr | 1963 |
Heat wave and acute pancreatitis: very unusual cystic fibrosis presentation.
Topics: Acute Disease; Child; Child, Preschool; Chlorides; Cystic Fibrosis; Diagnostic Errors; Exocrine Panc | 2004 |
[Genotype and phenotype of gastrointestinal symptoms analysis in children with cystic fibrosis].
Topics: Adolescent; Adult; Child; Child, Preschool; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductan | 2005 |
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 |
Diagnosis and treatment of cystic fibrosis in adults.
Topics: Adrenal Cortex Hormones; Adult; Age Factors; Anti-Bacterial Agents; Cholelithiasis; Cystic Fibrosis; | 1984 |
A puzzling triad: anorexia nervosa, high sweat electrolytes and indication to partial exocrine pancreatic insufficiency.
Topics: 4-Aminobenzoic Acid; Adolescent; Anorexia Nervosa; Cystic Fibrosis; Diagnosis, Differential; Electro | 1983 |
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 |
[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 |
Genotype-phenotype correlation in cystic fibrosis patients compound heterozygous for the A455E mutation.
Topics: Adolescent; Adult; Canada; Child; Child, Preschool; Cystic Fibrosis; Cystic Fibrosis Transmembrane C | 1997 |
P67L: a cystic fibrosis allele with mild effects found at high frequency in the Scottish population.
Topics: Adolescent; Adult; Alleles; Child; Cystic Fibrosis; DNA; Exocrine Pancreatic Insufficiency; Female; | 1998 |
Uncertainty in the diagnosis of cystic fibrosis: possible role of in vivo nasal potential difference measurements.
Topics: Adolescent; Adult; Case-Control Studies; Child; Cystic Fibrosis; Cystic Fibrosis Transmembrane Condu | 1998 |
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 |