251 related articles for article (PubMed ID: 20052365)
1. Novel CFTR mutations in a Korean infant with cystic fibrosis and pancreatic insufficiency.
Choe YJ; Ko JS; Seo JK; Han JJ; Shim JO; Koh YY; Lee R; Ki CS; Kim JW; Kim JH
J Korean Med Sci; 2010 Jan; 25(1):163-5. PubMed ID: 20052365
[TBL] [Abstract][Full Text] [Related]
2. Diagnosis of cystic fibrosis.
Voter KZ; Ren CL
Clin Rev Allergy Immunol; 2008 Dec; 35(3):100-6. PubMed ID: 18506640
[TBL] [Abstract][Full Text] [Related]
3. Identification of a novel mutation of CFTR gene in a Korean patient with cystic fibrosis.
Ko JM; Kim GH; Kim KM; Hong SJ; Yoo HW
J Korean Med Sci; 2008 Oct; 23(5):912-5. PubMed ID: 18955805
[TBL] [Abstract][Full Text] [Related]
4. [Relation between gene mutations and pancreatic exocrine function in patients with cystic fibrosis].
Radivojević D; Guć-Sćekić M; Djurisić M; Lalić T; Minić P; Kanavakis E
Srp Arh Celok Lek; 2001; 129 Suppl 1():6-9. PubMed ID: 15637983
[TBL] [Abstract][Full Text] [Related]
5. Early decline of pancreatic function in cystic fibrosis patients with class 1 or 2 CFTR mutations.
Walkowiak J; Sands D; Nowakowska A; Piotrowski R; Zybert K; Herzig KH; Milanowski A
J Pediatr Gastroenterol Nutr; 2005 Feb; 40(2):199-201. PubMed ID: 15699697
[TBL] [Abstract][Full Text] [Related]
6. Acute Recurrent and Chronic Pancreatitis as Initial Manifestations of Cystic Fibrosis and Cystic Fibrosis Transmembrane Conductance Regulator-Related Disorders.
Baldwin C; Zerofsky M; Sathe M; Troendle DM; Perito ER
Pancreas; 2019 Aug; 48(7):888-893. PubMed ID: 31268981
[TBL] [Abstract][Full Text] [Related]
7. Pancreatitis among patients with cystic fibrosis: correlation with pancreatic status and genotype.
De Boeck K; Weren M; Proesmans M; Kerem E
Pediatrics; 2005 Apr; 115(4):e463-9. PubMed ID: 15772171
[TBL] [Abstract][Full Text] [Related]
8. Genetic diagnosis in practice: From cystic fibrosis to CFTR-related disorders.
Pagin A; Sermet-Gaudelus I; Burgel PR
Arch Pediatr; 2020 Feb; 27 Suppl 1():eS25-eS29. PubMed ID: 32172933
[TBL] [Abstract][Full Text] [Related]
9. The L441P mutation of cystic fibrosis transmembrane conductance regulator and its molecular pathogenic mechanisms in a Korean patient with cystic fibrosis.
Gee HY; Kim CK; Kim SW; Lee JH; Kim JH; Kim KH; Lee MG
J Korean Med Sci; 2010 Jan; 25(1):166-71. PubMed ID: 20052366
[TBL] [Abstract][Full Text] [Related]
10. A novel CFTR mutation found in a Chinese patient with cystic fibrosis.
Li N; Pei P; Bu DF; He B; Wang GF
Chin Med J (Engl); 2006 Jan; 119(2):103-9. PubMed ID: 16454991
[TBL] [Abstract][Full Text] [Related]
11. [Genotype and phenotype of gastrointestinal symptoms analysis in children with cystic fibrosis].
Iwańczak F; Smigiel R; Stawarski A; Pawłowicz J; Stembalska A; Mowszet K; Sasiadek M
Pol Merkur Lekarski; 2005 Feb; 18(104):205-9. PubMed ID: 17877132
[TBL] [Abstract][Full Text] [Related]
12. Cystic fibrosis and congenital pancreatic insufficiency.
Alaswad B; Rose VM
J Pediatr Gastroenterol Nutr; 1999 Jul; 29(1):108. PubMed ID: 10400120
[No Abstract] [Full Text] [Related]
13. V232D mutation in patients with cystic fibrosis: Not so rare, not so mild.
Fernández-Lorenzo AE; Moreno-Álvarez A; Colon-Mejeras C; Barros-Angueira F; Solar-Boga A; Sirvent-Gómez J; Couce ML; Leis R
Medicine (Baltimore); 2018 Jul; 97(28):e11397. PubMed ID: 29995784
[TBL] [Abstract][Full Text] [Related]
14. Type of CFTR mutation determines risk of pancreatitis in patients with cystic fibrosis.
Ooi CY; Dorfman R; Cipolli M; Gonska T; Castellani C; Keenan K; Freedman SD; Zielenski J; Berthiaume Y; Corey M; Schibli S; Tullis E; Durie PR
Gastroenterology; 2011 Jan; 140(1):153-61. PubMed ID: 20923678
[TBL] [Abstract][Full Text] [Related]
15. Misdiagnosis of cystic fibrosis based on transient pancreatic insufficiency and elevated sweat chloride.
Bagheri-Behrouzi A; Steiß JO; Zimmer KP; Nährlich L
Klin Padiatr; 2015 Mar; 227(2):96-7. PubMed ID: 25751685
[No Abstract] [Full Text] [Related]
16. [Molecular diagnosis of two Chinese cystic fibrosis children and literature review].
Xu BP; Wang H; Zhao YH; Liu J; Yao Y; Feng XL; Shen KL
Zhonghua Er Ke Za Zhi; 2016 May; 54(5):344-8. PubMed ID: 27143075
[TBL] [Abstract][Full Text] [Related]
17. Clinical Phenotypes and Genotypic Spectrum of Cystic Fibrosis in Chinese Children.
Shen Y; Liu J; Zhong L; Mogayzel PJ; Zeitlin PL; Sosnay PR; Zhao S
J Pediatr; 2016 Apr; 171():269-76.e1. PubMed ID: 26826884
[TBL] [Abstract][Full Text] [Related]
18. Elevated Levels of Toxic Bile Acids in Serum of Cystic Fibrosis Patients with
Tabori H; Schneider J; Lüth S; Zagoya C; Barucha A; Lehmann T; Kauf E; Barth A; Mainz JG
Int J Mol Sci; 2022 Oct; 23(20):. PubMed ID: 36293293
[TBL] [Abstract][Full Text] [Related]
19. Splice mutation 1811+1.6kbA>G causes severe cystic fibrosis with pancreatic insufficiency: report of 11 compound heterozygous and two homozygous patients.
Reboul MP; Bieth E; Fayon M; Biteau N; Barbier R; Dromer C; Desgeorges M; Claustres M; Bremont F; Lacombe D; Iron A
J Med Genet; 2002 Nov; 39(11):e73. PubMed ID: 12414835
[No Abstract] [Full Text] [Related]
20. Cystic fibrosis in Korean children:a case report identified by a quantitative pilocarpine iontophoresis sweat test and genetic analysis.
Ahn KM; Park HY; Lee JH; Lee MG; Kim JH; Kang IJ; Lee SI
J Korean Med Sci; 2005 Feb; 20(1):153-7. PubMed ID: 15716623
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
