Kress W - Search Results

1

Thirty-seven CAG repeats in the androgen receptor gene in two healthy individuals.

Kuhlenbäumer G, Kress W, Ringelstein EB, Stögbauer F. Kuhlenbäumer G, et al. Among authors: kress w. J Neurol. 2001 Jan;248(1):23-6. doi: 10.1007/s004150170265. J Neurol. 2001. PMID: 11266016

2

[X-chromosomal recessive spinobulbar muscular atrophy (Kennedy type). Description of a family, clinical aspects, molecular genetics, differential diagnosis and therapy].

Kuhlenbäumer G, Bocchicchio M, Kress W, Young P, Oberwittler C, Stögbauer F. Kuhlenbäumer G, et al. Among authors: kress w. Nervenarzt. 1998 Aug;69(8):660-5. doi: 10.1007/s001150050325. Nervenarzt. 1998. PMID: 9757416 Review. German.

3

The metabolic and endocrine characteristics in spinal and bulbar muscular atrophy.

Rosenbohm A, Hirsch S, Volk AE, Grehl T, Grosskreutz J, Hanisch F, Herrmann A, Kollewe K, Kress W, Meyer T, Petri S, Prudlo J, Wessig C, Müller HP, Dreyhaupt J, Weishaupt J, Kubisch C, Kassubek J, Weydt P, Ludolph AC. Rosenbohm A, et al. Among authors: kress w. J Neurol. 2018 May;265(5):1026-1036. doi: 10.1007/s00415-018-8790-2. Epub 2018 Feb 20. J Neurol. 2018. PMID: 29464380

4

Homozygosity for CCTG mutation in myotonic dystrophy type 2.

Schoser BG, Kress W, Walter MC, Halliger-Keller B, Lochmüller H, Ricker K. Schoser BG, et al. Among authors: kress w. Brain. 2004 Aug;127(Pt 8):1868-77. doi: 10.1093/brain/awh210. Epub 2004 Jul 1. Brain. 2004. PMID: 15231584

5

The use of monoclonal antibodies in diagnostic tests for Becker and Duchenne muscular dystrophy.

Gold R, Kress W, Reichmann H, Müller CR. Gold R, et al. Among authors: kress w. J Neurol. 1993 Jan;240(1):21-4. doi: 10.1007/BF00838441. J Neurol. 1993. PMID: 8423459

6

Phenotype variability and histopathological findings in centronuclear myopathy due to DNM2 mutations.

Hanisch F, Müller T, Dietz A, Bitoun M, Kress W, Weis J, Stoltenburg G, Zierz S. Hanisch F, et al. Among authors: kress w. J Neurol. 2011 Jun;258(6):1085-90. doi: 10.1007/s00415-010-5889-5. Epub 2011 Jan 9. J Neurol. 2011. PMID: 21221624

7

A 400-kb tandem duplication within the dystrophin gene leads to severe Becker muscular dystrophy.

Gold R, Kress W, Bettecken T, Reichmann H, Müller CR. Gold R, et al. Among authors: kress w. J Neurol. 1994 Mar;241(5):331-4. doi: 10.1007/BF00868442. J Neurol. 1994. PMID: 8006687

8

Proximal myotonic myopathy: evidence for anticipation in families with linkage to chromosome 3q.

Schneider C, Ziegler A, Ricker K, Grimm T, Kress W, Reimers CD, Meinck H, Reiners K, Toyka KV. Schneider C, et al. Among authors: kress w. Neurology. 2000 Aug 8;55(3):383-8. doi: 10.1212/wnl.55.3.383. Neurology. 2000. PMID: 10932272

9

A sporadic case of rippling muscle disease caused by a de novo caveolin-3 mutation.

Vorgerd M, Ricker K, Ziemssen F, Kress W, Goebel HH, Nix WA, Kubisch C, Schoser BG, Mortier W. Vorgerd M, et al. Among authors: kress w. Neurology. 2001 Dec 26;57(12):2273-7. doi: 10.1212/wnl.57.12.2273. Neurology. 2001. PMID: 11756609

10

A paucisymptomatic neuromuscular disease mimicking type III 5q-SMA with complex rearrangements in the SMN gene.

Lohkamp LN, von Au K, Goebel HH, Kress W, Grieben U, Drossel K, Garbes L, Wirth B, Heppner FL, Stenzel W. Lohkamp LN, et al. Among authors: kress w. J Child Neurol. 2014 Feb;29(2):254-9. doi: 10.1177/0883073813511858. Epub 2013 Dec 11. J Child Neurol. 2014. PMID: 24334346

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