Wilschanski M - Search Results

1

Nasal potential difference in suspected cystic fibrosis patients with 5T polymorphism.

Aalbers BL, Yaakov Y, Derichs N, Simmonds NJ, De Wachter E, Melotti P, De Boeck K, Leal T, Tümmler B, Wilschanski M, Bronsveld I. Aalbers BL, et al. Among authors: wilschanski m. J Cyst Fibros. 2020 Jul;19(4):627-631. doi: 10.1016/j.jcf.2019.07.001. Epub 2019 Jul 19. J Cyst Fibros. 2020. PMID: 31331863 Free article.

2

Gentamicin-induced correction of CFTR function in patients with cystic fibrosis and CFTR stop mutations.

Wilschanski M, Yahav Y, Yaacov Y, Blau H, Bentur L, Rivlin J, Aviram M, Bdolah-Abram T, Bebok Z, Shushi L, Kerem B, Kerem E. Wilschanski M, et al. N Engl J Med. 2003 Oct 9;349(15):1433-41. doi: 10.1056/NEJMoa022170. N Engl J Med. 2003. PMID: 14534336 Free article. Clinical Trial.

3

Basic protocol for transepithelial nasal potential difference measurements.

Schüler D, Sermet-Gaudelus I, Wilschanski M, Ballmann M, Dechaux M, Edelman A, Hug M, Leal T, Lebacq J, Lebecque P, Lenoir G, Stanke F, Wallemacq P, Tümmler B, Knowles MR. Schüler D, et al. Among authors: wilschanski m. J Cyst Fibros. 2004 Aug;3 Suppl 2:151-5. doi: 10.1016/j.jcf.2004.05.032. J Cyst Fibros. 2004. PMID: 15463949 Free article. Review.

4

Nonsense-mediated mRNA decay affects nonsense transcript levels and governs response of cystic fibrosis patients to gentamicin.

Linde L, Boelz S, Nissim-Rafinia M, Oren YS, Wilschanski M, Yaacov Y, Virgilis D, Neu-Yilik G, Kulozik AE, Kerem E, Kerem B. Linde L, et al. Among authors: wilschanski m. J Clin Invest. 2007 Mar;117(3):683-92. doi: 10.1172/JCI28523. Epub 2007 Feb 8. J Clin Invest. 2007. PMID: 17290305 Free PMC article.

5

Reproducibility of nasal potential difference measurements in cystic fibrosis.

Yaakov Y, Kerem E, Yahav Y, Rivlin J, Blau H, Bentur L, Aviram M, Picard E, Bdolah-Abram T, Wilschanski M. Yaakov Y, et al. Among authors: wilschanski m. Chest. 2007 Oct;132(4):1219-26. doi: 10.1378/chest.06-2975. Epub 2007 Sep 21. Chest. 2007. PMID: 17890478

6

Cystic fibrosis transmembrane conductance regulator ion channel function testing in recurrent acute pancreatitis.

Segal I, Yaakov Y, Adler SN, Blau H, Broide E, Santo M, Yahav Y, Klar A, Lerner A, Aviram M, Ellis I, Mountford R, Shteyer E, Kerem E, Wilschanski M. Segal I, et al. Among authors: wilschanski m. J Clin Gastroenterol. 2008 Aug;42(7):810-4. doi: 10.1097/MCG.0b013e318156617c. J Clin Gastroenterol. 2008. PMID: 18360295

7

Nasal potential difference in non-classic cystic fibrosis-long term follow up.

Jaron R, Yaakov Y, Rivlin J, Blau H, Bentur L, Yahav Y, Kerem E, Bibi H, Picard E, Wilschanski M. Jaron R, et al. Among authors: wilschanski m. Pediatr Pulmonol. 2008 Jun;43(6):545-9. doi: 10.1002/ppul.20807. Pediatr Pulmonol. 2008. PMID: 18433042 Free article.

8

Patterns of gastrointestinal disease associated with mutations of CFTR.

Wilschanski M. Wilschanski M. Curr Gastroenterol Rep. 2008 Jun;10(3):316-23. doi: 10.1007/s11894-008-0062-3. Curr Gastroenterol Rep. 2008. PMID: 18625144 Review.

9

Effectiveness of PTC124 treatment of cystic fibrosis caused by nonsense mutations: a prospective phase II trial.

Kerem E, Hirawat S, Armoni S, Yaakov Y, Shoseyov D, Cohen M, Nissim-Rafinia M, Blau H, Rivlin J, Aviram M, Elfring GL, Northcutt VJ, Miller LL, Kerem B, Wilschanski M. Kerem E, et al. Among authors: wilschanski m. Lancet. 2008 Aug 30;372(9640):719-27. doi: 10.1016/S0140-6736(08)61168-X. Epub 2008 Aug 20. Lancet. 2008. PMID: 18722008 Clinical Trial.

10

Exocrine pancreatic function testing in patients with cystic fibrosis and pancreatic sufficiency: a correlation study.

Weintraub A, Blau H, Mussaffi H, Picard E, Bentur L, Kerem E, Stankiewicz H, Wilschanski M. Weintraub A, et al. Among authors: wilschanski m. J Pediatr Gastroenterol Nutr. 2009 Mar;48(3):306-10. doi: 10.1097/mpg.0b013e318180af4f. J Pediatr Gastroenterol Nutr. 2009. PMID: 19274786

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