Kress W - Search Results

1

Novel fukutin mutations in limb-girdle muscular dystrophy type 2M with childhood onset.

Smogavec M, Zschüntzsch J, Kress W, Mohr J, Hellen P, Zoll B, Pauli S, Schmidt J. Smogavec M, et al. Among authors: kress w. Neurol Genet. 2017 Jul 10;3(4):e167. doi: 10.1212/NXG.0000000000000167. eCollection 2017 Aug. Neurol Genet. 2017. PMID: 28785732 Free PMC article. No abstract available.

2

Estimate of severe autosomal recessive limb-girdle muscular dystrophy (LGMD2C, LGMD2D) among sporadic muscular dystrophy males: a study of 415 familes.

Stec I, Kress W, Meng G, Müller B, Müller CR, Grimm T. Stec I, et al. Among authors: kress w. J Med Genet. 1995 Dec;32(12):930-3. doi: 10.1136/jmg.32.12.930. J Med Genet. 1995. PMID: 8825917 Free PMC article.

3

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

4

Assessing the influence of age and gender on the phenotype of myotonic dystrophy type 2.

Montagnese F, Mondello S, Wenninger S, Kress W, Schoser B. Montagnese F, et al. Among authors: kress w. J Neurol. 2017 Dec;264(12):2472-2480. doi: 10.1007/s00415-017-8653-2. Epub 2017 Oct 30. J Neurol. 2017. PMID: 29086017

5

Aprataxin mutations are a rare cause of early onset ataxia in Germany.

Habeck M, Zühlke C, Bentele KH, Unkelbach S, Kress W, Bürk K, Schwinger E, Hellenbroich Y. Habeck M, et al. Among authors: kress w. J Neurol. 2004 May;251(5):591-4. doi: 10.1007/s00415-004-0374-7. J Neurol. 2004. PMID: 15164193

6

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

7

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

8

Leg Muscle Involvement in Facioscapulohumeral Muscular Dystrophy: Comparison between Facioscapulohumeral Muscular Dystrophy Types 1 and 2.

Mair D, Huegens-Penzel M, Kress W, Roth C, Ferbert A. Mair D, et al. Among authors: kress w. Eur Neurol. 2017;77(1-2):32-39. doi: 10.1159/000452763. Epub 2016 Nov 18. Eur Neurol. 2017. PMID: 27855411

9

Brugada-like cardiac disease in myotonic dystrophy type 2: report of two unrelated patients.

Rudnik-Schöneborn S, Schaupp M, Lindner A, Kress W, Schulze-Bahr E, Zumhagen S, Elbracht M, Zerres K. Rudnik-Schöneborn S, et al. Among authors: kress w. Eur J Neurol. 2011 Jan;18(1):191-4. doi: 10.1111/j.1468-1331.2010.03077.x. Eur J Neurol. 2011. PMID: 20491895

10

Myotonic dystrophy type 2: molecular, diagnostic and clinical spectrum.

Day JW, Ricker K, Jacobsen JF, Rasmussen LJ, Dick KA, Kress W, Schneider C, Koch MC, Beilman GJ, Harrison AR, Dalton JC, Ranum LP. Day JW, et al. Among authors: kress w. Neurology. 2003 Feb 25;60(4):657-64. doi: 10.1212/01.wnl.0000054481.84978.f9. Neurology. 2003. PMID: 12601109

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