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Page 1
Classification of CFTR mutation classes.
Stanke F, Tümmler B. Stanke F, et al. Lancet Respir Med. 2016 Aug;4(8):e36. doi: 10.1016/S2213-2600(16)30147-3. Epub 2016 Jul 1. Lancet Respir Med. 2016. PMID: 27377412 No abstract available.
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: stanke f. 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.
Genetic modifiers in cystic fibrosis.
Stanke F, Tümmler B, Becker T. Stanke F, et al. N Engl J Med. 2006 Jan 5;354(1):88-90; author reply 88-90. doi: 10.1056/NEJMc052980. N Engl J Med. 2006. PMID: 16394309 No abstract available.
Ex vivo biochemical analysis of CFTR in human rectal biopsies.
van Barneveld A, Stanke F, Ballmann M, Naim HY, Tümmler B. van Barneveld A, et al. Among authors: stanke f. Biochim Biophys Acta. 2006 Apr;1762(4):393-7. doi: 10.1016/j.bbadis.2006.01.007. Epub 2006 Feb 13. Biochim Biophys Acta. 2006. PMID: 16504487 Free article.
Spontaneous rescue from cystic fibrosis in a mouse model.
Charizopoulou N, Wilke M, Dorsch M, Bot A, Jorna H, Jansen S, Stanke F, Hedrich HJ, de Jonge HR, Tümmler B. Charizopoulou N, et al. Among authors: stanke f. BMC Genet. 2006 Mar 29;7:18. doi: 10.1186/1471-2156-7-18. BMC Genet. 2006. PMID: 16571105 Free PMC article.
Cystic fibrosis disease-specific centiles in 2000 and 2005.
Stanke F, Ballmann M, Tümmler B. Stanke F, et al. Am J Respir Crit Care Med. 2006 May 1;173(9):1047; author reply 1047. doi: 10.1164/ajrccm.173.9.1047. Am J Respir Crit Care Med. 2006. PMID: 16632637 No abstract available.
73 results