Walter MC - Search Results

1

A founder mutation in Anoctamin 5 is a major cause of limb-girdle muscular dystrophy.

Hicks D, Sarkozy A, Muelas N, Köehler K, Huebner A, Hudson G, Chinnery PF, Barresi R, Eagle M, Polvikoski T, Bailey G, Miller J, Radunovic A, Hughes PJ, Roberts R, Krause S, Walter MC, Laval SH, Straub V, Lochmüller H, Bushby K. Hicks D, et al. Among authors: walter mc. Brain. 2011 Jan;134(Pt 1):171-182. doi: 10.1093/brain/awq294. Brain. 2011. PMID: 21186264 Free PMC article.

2

High-dose immunoglobulin therapy in sporadic inclusion body myositis: a double-blind, placebo-controlled study.

Walter MC, Lochmüller H, Toepfer M, Schlotter B, Reilich P, Schröder M, Müller-Felber W, Pongratz D. Walter MC, et al. J Neurol. 2000 Jan;247(1):22-8. doi: 10.1007/s004150050005. J Neurol. 2000. PMID: 10701893 Clinical Trial.

3

Creatine monohydrate in muscular dystrophies: A double-blind, placebo-controlled clinical study.

Walter MC, Lochmüller H, Reilich P, Klopstock T, Huber R, Hartard M, Hennig M, Pongratz D, Müller-Felber W. Walter MC, et al. Neurology. 2000 May 9;54(9):1848-50. doi: 10.1212/wnl.54.9.1848. Neurology. 2000. PMID: 10802796 Clinical Trial.

4

Novel approaches to treat muscular dystrophies.

Walter MC, Lochmüller H. Walter MC, et al. Expert Opin Investig Drugs. 2001 Apr;10(4):695-707. doi: 10.1517/13543784.10.4.695. Expert Opin Investig Drugs. 2001. PMID: 11281819 Review.

5

Prion codon 129 homozygosity and sporadic inclusion body myositis.

Lampe J, Gossrau G, Reichmann H, Walter MC, Mendel B, Lochmüller H. Lampe J, et al. Among authors: walter mc. Neurology. 2001 Jul 24;57(2):368. doi: 10.1212/wnl.57.2.368. Neurology. 2001. PMID: 11468340 No abstract available.

6

Genetic identity of Marinesco-Sjögren/myoglobinuria and CCFDN syndromes.

Merlini L, Gooding R, Lochmüller H, Müller-Felber W, Walter MC, Angelicheva D, Talim B, Hallmayer J, Kalaydjieva L. Merlini L, et al. Among authors: walter mc. Neurology. 2002 Jan 22;58(2):231-6. doi: 10.1212/wnl.58.2.231. Neurology. 2002. PMID: 11805249

7

Creatine monohydrate in myotonic dystrophy: a double-blind, placebo-controlled clinical study.

Walter MC, Reilich P, Lochmüller H, Kohnen R, Schlotter B, Hautmann H, Dunkl E, Pongratz D, Müller-Felber W. Walter MC, et al. J Neurol. 2002 Dec;249(12):1717-22. doi: 10.1007/s00415-002-0923-x. J Neurol. 2002. PMID: 12529796 Clinical Trial.

8

Gentamicin fails to increase dystrophin expression in dystrophin-deficient muscle.

Dunant P, Walter MC, Karpati G, Lochmüller H. Dunant P, et al. Among authors: walter mc. Muscle Nerve. 2003 May;27(5):624-7. doi: 10.1002/mus.10341. Muscle Nerve. 2003. PMID: 12707984

9

Successful treatment of muscle sarcoidosis with thalidomide.

Walter MC, Lochmüller H, Schlotter-Weigel B, Meindl T, Müller-Felber W. Walter MC, et al. Acta Myol. 2003 May;22(1):22-5. Acta Myol. 2003. PMID: 12966701

10

A synonymous codon change in the LMNA gene alters mRNA splicing and causes limb girdle muscular dystrophy type 1B.

Todorova A, Halliger-Keller B, Walter MC, Dabauvalle MC, Lochmüller H, Müller CR. Todorova A, et al. Among authors: walter mc. J Med Genet. 2003 Oct;40(10):e115. doi: 10.1136/jmg.40.10.e115. J Med Genet. 2003. PMID: 14569138 Free PMC article. No abstract available.

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