Wehnert MS - Search Results

1

Severe clinical expression in X-linked Emery-Dreifuss muscular dystrophy.

Hoeltzenbein M, Karow T, Zeller JA, Warzok R, Wulff K, Zschiesche M, Herrmann FH, Grosse-Heitmeyer W, Wehnert MS. Hoeltzenbein M, et al. Among authors: wehnert ms. Neuromuscul Disord. 1999 May;9(3):166-70. doi: 10.1016/s0960-8966(98)00120-5. Neuromuscul Disord. 1999. PMID: 10382910

2

Early onset of cardiomyopathy in two brothers with X-linked Emery-Dreifuss muscular dystrophy.

Talkop UA, Talvik I, Sõnajalg M, Sibul H, Kolk A, Piirsoo A, Warzok R, Wulff K, Wehnert MS, Talvik T. Talkop UA, et al. Among authors: wehnert ms. Neuromuscul Disord. 2002 Nov;12(9):878-81. doi: 10.1016/s0960-8966(02)00134-7. Neuromuscul Disord. 2002. PMID: 12398842 Clinical Trial.

3

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

4

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

5

Evidence supporting tight linkage of X-linked Emery-Dreifuss muscular dystrophy to the factor VIII:C gene.

Wehnert M, Machill G, Grimm T, Janka M, Camman R, Schröder W, Herrmann FH. Wehnert M, et al. Hum Hered. 1991;41(6):364-9. doi: 10.1159/000154028. Hum Hered. 1991. PMID: 1686773

6

Deletion screening and prenatal diagnosis of Duchenne muscular dystrophy using cDNA probes Cf 23a and Cf 56a.

Herrmann FH, Wulff K, Schütz M, Wehnert M. Herrmann FH, et al. Eur J Pediatr. 1990 Jan;149(4):263-5. doi: 10.1007/BF02106289. Eur J Pediatr. 1990. PMID: 1968008

7

Deletion screening in patients with Duchenne muscular dystrophy.

Wulff K, Herrmann FH, Wapenaar MC, Wehnert M. Wulff K, et al. J Neurol. 1989 Dec;236(8):470-3. doi: 10.1007/BF00328509. J Neurol. 1989. PMID: 2614492

8

Abnormal proliferation and spontaneous differentiation of myoblasts from a symptomatic female carrier of X-linked Emery-Dreifuss muscular dystrophy.

Meinke P, Schneiderat P, Srsen V, Korfali N, Lê Thành P, Cowan GJ, Cavanagh DR, Wehnert M, Schirmer EC, Walter MC. Meinke P, et al. Neuromuscul Disord. 2015 Feb;25(2):127-36. doi: 10.1016/j.nmd.2014.09.012. Epub 2014 Oct 6. Neuromuscul Disord. 2015. PMID: 25454731 Free PMC article.

9

Immunohistochemistry on a panel of Emery-Dreifuss muscular dystrophy samples reveals nuclear envelope proteins as inconsistent markers for pathology.

Le Thanh P, Meinke P, Korfali N, Srsen V, Robson MI, Wehnert M, Schoser B, Sewry CA, Schirmer EC. Le Thanh P, et al. Neuromuscul Disord. 2017 Apr;27(4):338-351. doi: 10.1016/j.nmd.2016.12.003. Epub 2016 Dec 21. Neuromuscul Disord. 2017. PMID: 28214269 Free PMC article.

10

Mutations of the iduronate-2-sulfatase (IDS) gene in patients with Hunter syndrome (mucopolysaccharidosis II).

Schröder W, Wulff K, Wehnert M, Seidlitz G, Herrmann FH. Schröder W, et al. Hum Mutat. 1994;4(2):128-31. doi: 10.1002/humu.1380040206. Hum Mutat. 1994. PMID: 7981716

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