Lochmüller H - Search Results

1

Global FKRP Registry: observations in more than 300 patients with Limb Girdle Muscular Dystrophy R9.

Murphy LB, Schreiber-Katz O, Rafferty K, Robertson A, Topf A, Willis TA, Heidemann M, Thiele S, Bindoff L, Laurent JP, Lochmüller H, Mathews K, Mitchell C, Stevenson JH, Vissing J, Woods L, Walter MC, Straub V. Murphy LB, et al. Among authors: lochmuller h. Ann Clin Transl Neurol. 2020 May;7(5):757-766. doi: 10.1002/acn3.51042. Epub 2020 Apr 28. Ann Clin Transl Neurol. 2020. PMID: 32342672 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. Among authors: lochmuller h. 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. Among authors: lochmuller h. 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. Among authors: lochmuller h. 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: lochmuller h. 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: lochmuller h. 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. Among authors: lochmuller h. 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: lochmuller h. 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. Among authors: lochmuller h. 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: lochmuller h. 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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