Wehnert MS - Search Results

1

NDUFA-1 is not a nuclear modifier gene in Leber hereditary optic neuropathy.

Yu-Wai-Man P, Brown DT, Wehnert MS, Zeviani M, Carrara F, Turnbull DM, Chinnery PF. Yu-Wai-Man P, et al. Among authors: wehnert ms. Neurology. 2002 Jun 25;58(12):1861-2. doi: 10.1212/wnl.58.12.1861. Neurology. 2002. PMID: 12084895 No abstract available.

2

Sequence variations in the NDUFA1 gene encoding a subunit of complex I of the respiratory chain.

Wittig I, Augstein P, Brown GK, Fujii T, Rötig A, Rustin P, Munnich A, Seibel P, Thorburn D, Wissinger B, Tamboom K, Metspalu A, Lamantea E, Zeviani M, Wehnert MS. Wittig I, et al. Among authors: wehnert ms. J Inherit Metab Dis. 2001 Feb;24(1):15-27. doi: 10.1023/a:1005638218246. J Inherit Metab Dis. 2001. PMID: 11286378

3

What message does the nuclear envelope hold?

Lochmüller H, Wehnert M. Lochmüller H, et al. Neurology. 2007 May 29;68(22):1879-80. doi: 10.1212/01.wnl.0000267408.99536.de. Neurology. 2007. PMID: 17536042 No abstract available.

4

The nuclear muscular dystrophies.

Wehnert MS, Bonne G. Wehnert MS, et al. Semin Pediatr Neurol. 2002 Jun;9(2):100-7. doi: 10.1053/spen.2002.33806. Semin Pediatr Neurol. 2002. PMID: 12138994 Review.

5

Further evidence supporting linkage of hereditary neuralgic amyotrophy to chromosome 17q.

Wehnert M, Timmerman V, Spoelders P, Meuleman J, Nelis E, Van Broeckhoven C. Wehnert M, et al. Neurology. 1997 Jun;48(6):1719-21. doi: 10.1212/wnl.48.6.1719. Neurology. 1997. PMID: 9191796

6

Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C gene.

Bonne G, Mercuri E, Muchir A, Urtizberea A, Bécane HM, Recan D, Merlini L, Wehnert M, Boor R, Reuner U, Vorgerd M, Wicklein EM, Eymard B, Duboc D, Penisson-Besnier I, Cuisset JM, Ferrer X, Desguerre I, Lacombe D, Bushby K, Pollitt C, Toniolo D, Fardeau M, Schwartz K, Muntoni F. Bonne G, et al. Ann Neurol. 2000 Aug;48(2):170-80. Ann Neurol. 2000. PMID: 10939567

7

Genomic organization of the human complex I 13-kDa subunit gene NDUFA5.

Tensing K, Pata I, Wittig I, Wehnert M, Metspalu A. Tensing K, et al. Cytogenet Cell Genet. 1999;84(1-2):125-7. doi: 10.1159/000015237. Cytogenet Cell Genet. 1999. PMID: 10343126

8

Characterization of three new deletions at the 5' end of the HPRT structural gene.

Wehnert M, Herrmann FH. Wehnert M, et al. J Inherit Metab Dis. 1990;13(2):178-83. doi: 10.1007/BF01799683. J Inherit Metab Dis. 1990. PMID: 2116548

9

Direct molecular genetic diagnosis and heterozygote identification in X-linked Emery-Dreifuss muscular dystrophy by heteroduplex analysis.

Wulff K, Ebener U, Wehnert CS, Ward PA, Reuner U, Hiebsch W, Herrmann FH, Wehnert M. Wulff K, et al. Dis Markers. 1997 Apr;13(2):77-86. Dis Markers. 1997. PMID: 9160182

10

Six novel mutations in the emerin gene causing X-linked Emery-Dreifuss muscular dystrophy.

Wulff K, Parrish JE, Herrmann FH, Wehnert M. Wulff K, et al. Hum Mutat. 1997;9(6):526-30. doi: 10.1002/(SICI)1098-1004(1997)9:6<526::AID-HUMU5>3.0.CO;2-#. Hum Mutat. 1997. PMID: 9195226

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