Neumann T - Search Results

1

Characterization of a novel 21-kb deletion, CFTRdele2,3(21 kb), in the CFTR gene: a cystic fibrosis mutation of Slavic origin common in Central and East Europe.

Dörk T, Macek M Jr, Mekus F, Tümmler B, Tzountzouris J, Casals T, Krebsová A, Koudová M, Sakmaryová I, Macek M Sr, Vávrová V, Zemková D, Ginter E, Petrova NV, Ivaschenko T, Baranov V, Witt M, Pogorzelski A, Bal J, Zékanowsky C, Wagner K, Stuhrmann M, Bauer I, Seydewitz HH, Neumann T, Jakubiczka S. Dörk T, et al. Among authors: neumann t. Hum Genet. 2000 Mar;106(3):259-68. doi: 10.1007/s004390000246. Hum Genet. 2000. PMID: 10798353

2

Cystic fibrosis with three mutations in the cystic fibrosis transmembrane conductance regulator gene.

Dörk T, Wulbrand U, Richter T, Neumann T, Wolfes H, Wulf B, Maass G, Tümmler B. Dörk T, et al. Among authors: neumann t. Hum Genet. 1991 Aug;87(4):441-6. doi: 10.1007/BF00197165. Hum Genet. 1991. PMID: 1715308

3

Exon 9 of the CFTR gene: splice site haplotypes and cystic fibrosis mutations.

Dörk T, Fislage R, Neumann T, Wulf B, Tümmler B. Dörk T, et al. Among authors: neumann t. Hum Genet. 1994 Jan;93(1):67-73. doi: 10.1007/BF00218916. Hum Genet. 1994. PMID: 7505767

4

Detection of more than 50 different CFTR mutations in a large group of German cystic fibrosis patients.

Dörk T, Mekus F, Schmidt K, Bosshammer J, Fislage R, Heuer T, Dziadek V, Neumann T, Kälin N, Wulbrand U, et al. Dörk T, et al. Among authors: neumann t. Hum Genet. 1994 Nov;94(5):533-42. doi: 10.1007/BF00211022. Hum Genet. 1994. PMID: 7525450

5

Intra- and extragenic marker haplotypes of CFTR mutations in cystic fibrosis families.

Dörk T, Neumann T, Wulbrand U, Wulf B, Kälin N, Maass G, Krawczak M, Guillermit H, Ferec C, Horn G, et al. Dörk T, et al. Among authors: neumann t. Hum Genet. 1992 Feb;88(4):417-25. doi: 10.1007/BF00215676. Hum Genet. 1992. PMID: 1371263

6

Genetic determinants of airways' colonisation with Pseudomonas aeruginosa in cystic fibrosis.

Kubesch P, Dörk T, Wulbrand U, Kälin N, Neumann T, Wulf B, Geerlings H, Weissbrodt H, von der Hardt H, Tümmler B. Kubesch P, et al. Among authors: neumann t. Lancet. 1993 Jan 23;341(8839):189-93. doi: 10.1016/0140-6736(93)90062-l. Lancet. 1993. PMID: 7678316

7

Cystic fibrosis: the impact of analytical technology for genotype-phenotype studies.

Tümmler B, Dörk T, Kubesch P, Fislage R, Kälin N, Neumann T, Wulbrand U, Wulf B, Steinkamp G, von der Hardt H. Tümmler B, et al. Among authors: neumann t. Clin Chim Acta. 1993 Jul 30;217(1):23-8. doi: 10.1016/0009-8981(93)90234-u. Clin Chim Acta. 1993. PMID: 8222279 Review.

8

Olfactory receptor-gene clusters, genomic-inversion polymorphisms, and common chromosome rearrangements.

Giglio S, Broman KW, Matsumoto N, Calvari V, Gimelli G, Neumann T, Ohashi H, Voullaire L, Larizza D, Giorda R, Weber JL, Ledbetter DH, Zuffardi O. Giglio S, et al. Among authors: neumann t. Am J Hum Genet. 2001 Apr;68(4):874-83. doi: 10.1086/319506. Epub 2001 Feb 26. Am J Hum Genet. 2001. PMID: 11231899 Free PMC article.

9

Allelic heterogeneity in the COH1 gene explains clinical variability in Cohen syndrome.

Hennies HC, Rauch A, Seifert W, Schumi C, Moser E, Al-Taji E, Tariverdian G, Chrzanowska KH, Krajewska-Walasek M, Rajab A, Giugliani R, Neumann TE, Eckl KM, Karbasiyan M, Reis A, Horn D. Hennies HC, et al. Am J Hum Genet. 2004 Jul;75(1):138-45. doi: 10.1086/422219. Epub 2004 May 20. Am J Hum Genet. 2004. PMID: 15154116 Free PMC article.

10

Multiple giant cell lesions in patients with Noonan syndrome and cardio-facio-cutaneous syndrome.

Neumann TE, Allanson J, Kavamura I, Kerr B, Neri G, Noonan J, Cordeddu V, Gibson K, Tzschach A, Krüger G, Hoeltzenbein M, Goecke TO, Kehl HG, Albrecht B, Luczak K, Sasiadek MM, Musante L, Laurie R, Peters H, Tartaglia M, Zenker M, Kalscheuer V. Neumann TE, et al. Eur J Hum Genet. 2009 Apr;17(4):420-5. doi: 10.1038/ejhg.2008.188. Epub 2008 Oct 15. Eur J Hum Genet. 2009. PMID: 18854871 Free PMC article.

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