Lochmüller H - Search Results

1

Methionine homozygosity at prion gene codon 129 may predispose to sporadic inclusion-body myositis.

Lampe J, Kitzler H, Walter MC, Lochmüller H, Reichmann H. Lampe J, et al. Among authors: lochmuller h. Lancet. 1999 Feb 6;353(9151):465-6. doi: 10.1016/S0140-6736(98)05208-8. Lancet. 1999. PMID: 9989722 No abstract available.

2

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.

3

Analysis of HLA class I and II alleles in sporadic inclusion-body myositis.

Lampe JB, Gossrau G, Kempe A, Füssel M, Schwurack K, Schröder R, Krause S, Kohnen R, Walter MC, Reichmann H, Lochmüller H. Lampe JB, et al. Among authors: lochmuller h. J Neurol. 2003 Nov;250(11):1313-7. doi: 10.1007/s00415-003-0204-3. J Neurol. 2003. PMID: 14648147

4

[New insights in pathogenesis and therapy of sporadic inclusion body myositis (s-IBM)].

Walter MC, Lochmüller H, Schlotter B, Reilich P, Müller-Felber W, Pongratz D. Walter MC, et al. Among authors: lochmuller h. Nervenarzt. 2001 Feb;72(2):117-21. doi: 10.1007/s001150050723. Nervenarzt. 2001. PMID: 11256145 Review. German.

5

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.

6

A novel homozygous missense mutation in the GNE gene of a patient with quadriceps-sparing hereditary inclusion body myopathy associated with muscle inflammation.

Krause S, Schlotter-Weigel B, Walter MC, Najmabadi H, Wiendl H, Müller-Höcker J, Müller-Felber W, Pongratz D, Lochmüller H. Krause S, et al. Among authors: lochmuller h. Neuromuscul Disord. 2003 Dec;13(10):830-4. doi: 10.1016/s0960-8966(03)00140-8. Neuromuscul Disord. 2003. PMID: 14678807

7

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.

8

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.

9

Eosinophilic myositis as presenting symptom in gamma-sarcoglycanopathy.

Baumeister SK, Todorovic S, Milić-Rasić V, Dekomien G, Lochmüller H, Walter MC. Baumeister SK, et al. Among authors: lochmuller h. Neuromuscul Disord. 2009 Feb;19(2):167-71. doi: 10.1016/j.nmd.2008.11.010. Epub 2009 Jan 23. Neuromuscul Disord. 2009. PMID: 19167890

10

Brain imaging and neuropsychology in late-onset dementia due to a novel mutation (R93C) of valosin-containing protein.

Krause S, Göhringer T, Walter MC, Schoser BG, Reilich P, Linn J, Pöpperl GE, Frölich L, Hentschel F, Lochmüller H, Danek A. Krause S, et al. Among authors: lochmuller h. Clin Neuropathol. 2007 Sep-Oct;26(5):232-40. doi: 10.5414/npp26232. Clin Neuropathol. 2007. PMID: 17907600

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