Tümmler B - Search Results

1

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: tummler b. 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.

2

Cystic-fibrosis-like disease unrelated to the cystic fibrosis transmembrane conductance regulator.

Mekus F, Ballmann M, Bronsveld I, Dörk T, Bijman J, Tümmler B, Veeze HJ. Mekus F, et al. Among authors: tummler b. Hum Genet. 1998 May;102(5):582-6. doi: 10.1007/s004390050744. Hum Genet. 1998. PMID: 9654209

3

Clinical presentation of exclusive cystic fibrosis lung disease.

Bronsveld I, Bijman J, Mekus F, Ballmann M, Veeze HJ, Tümmler B. Bronsveld I, et al. Among authors: tummler b. Thorax. 1999 Mar;54(3):278-81. doi: 10.1136/thx.54.3.278. Thorax. 1999. PMID: 10325907 Free PMC article.

4

Residual chloride secretion in intestinal tissue of deltaF508 homozygous twins and siblings with cystic fibrosis. The European CF Twin and Sibling Study Consortium.

Bronsveld I, Mekus F, Bijman J, Ballmann M, Greipel J, Hundrieser J, Halley DJ, Laabs U, Busche R, De Jonge HR, Tümmler B, Veeze HJ. Bronsveld I, et al. Among authors: tummler b. Gastroenterology. 2000 Jul;119(1):32-40. doi: 10.1053/gast.2000.8524. Gastroenterology. 2000. PMID: 10889152

5

Categories of deltaF508 homozygous cystic fibrosis twin and sibling pairs with distinct phenotypic characteristics.

Mekus F, Ballmann M, Bronsveld I, Bijman J, Veeze H, Tümmler B. Mekus F, et al. Among authors: tummler b. Twin Res. 2000 Dec;3(4):277-93. doi: 10.1375/136905200320565256. Twin Res. 2000. PMID: 11463149

6

Chloride conductance and genetic background modulate the cystic fibrosis phenotype of Delta F508 homozygous twins and siblings.

Bronsveld I, Mekus F, Bijman J, Ballmann M, de Jonge HR, Laabs U, Halley DJ, Ellemunter H, Mastella G, Thomas S, Veeze HJ, Tümmler B. Bronsveld I, et al. Among authors: tummler b. J Clin Invest. 2001 Dec;108(11):1705-15. doi: 10.1172/JCI12108. J Clin Invest. 2001. PMID: 11733566 Free PMC article.

7

Cystic fibrosis transmembrane conductance regulator (CFTR)-mediated residual chloride secretion does not protect against early chronic Pseudomonas aeruginosa infection in F508del homozygous cystic fibrosis patients.

Derichs N, Mekus F, Bronsveld I, Bijman J, Veeze HJ, von der Hardt H, Tummler B, Ballmann M. Derichs N, et al. Among authors: tummler b. Pediatr Res. 2004 Jan;55(1):69-75. doi: 10.1203/01.PDR.0000100758.66805.CE. Epub 2003 Nov 6. Pediatr Res. 2004. PMID: 14605249

8

Instability of the insertional mutation in CftrTgH(neoim)Hgu cystic fibrosis mouse model.

Charizopoulou N, Jansen S, Dorsch M, Stanke F, Dorin JR, Hedrich HJ, Tümmler B. Charizopoulou N, et al. Among authors: tummler b. BMC Genet. 2004 Apr 21;5:6. doi: 10.1186/1471-2156-5-6. BMC Genet. 2004. PMID: 15102331 Free PMC article.

9

Intestinal current measurements to diagnose cystic fibrosis.

Hug MJ, Tümmler B. Hug MJ, et al. Among authors: tummler b. J Cyst Fibros. 2004 Aug;3 Suppl 2:157-8. doi: 10.1016/j.jcf.2004.05.033. J Cyst Fibros. 2004. PMID: 15463950 Free article. Review.

10

Ex vivo CF diagnosis by intestinal current measurements (ICM) in small aperture, circulating Ussing chambers.

De Jonge HR, Ballmann M, Veeze H, Bronsveld I, Stanke F, Tümmler B, Sinaasappel M. De Jonge HR, et al. Among authors: tummler b. J Cyst Fibros. 2004 Aug;3 Suppl 2:159-63. doi: 10.1016/j.jcf.2004.05.034. J Cyst Fibros. 2004. PMID: 15463951 Free article. Review.

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