Lochmüller H - Search Results

1

What's in the serum of seronegative MG and LEMS?: MuSK et al.

Abicht A, Lochmüller H. Abicht A, et al. Among authors: lochmuller h. Neurology. 2002 Dec 10;59(11):1672-3. doi: 10.1212/01.wnl.0000041026.90947.79. Neurology. 2002. PMID: 12473750 No abstract available.

2

Congenital myasthenic syndromes: clinical and genetic analysis of 18 patients.

Abicht A, Müller-Felber W, Fischer P, Jakob I, Kürz L, Rudel R, Mortier W, Pongratz D, Lochmüller H. Abicht A, et al. Among authors: lochmuller h. Eur J Med Res. 1997 Dec 31;2(12):515-22. Eur J Med Res. 1997. PMID: 9498929

3

Localization of transforming growth factor beta in association with neuromuscular junctions in adult human muscle.

Toepfer M, Fischer P, Abicht A, Lochmüller H, Pongratz D, Müller-Felber W. Toepfer M, et al. Among authors: lochmuller h. Cell Mol Neurobiol. 1999 Apr;19(2):297-300. doi: 10.1023/a:1006989530148. Cell Mol Neurobiol. 1999. PMID: 10081612

4

Myotonic ADR-MDX mutant mice show less severe muscular dystrophy than MDX mice.

Krämer R, Lochmüller H, Abicht A, Rüdel R, Brinkmeier H. Krämer R, et al. Among authors: lochmuller h. Neuromuscul Disord. 1998 Dec;8(8):542-50. doi: 10.1016/s0960-8966(98)00078-9. Neuromuscul Disord. 1998. PMID: 10093060

5

A common mutation (epsilon1267delG) in congenital myasthenic patients of Gypsy ethnic origin.

Abicht A, Stucka R, Karcagi V, Herczegfalvi A, Horváth R, Mortier W, Schara U, Ramaekers V, Jost W, Brunner J, Janssen G, Seidel U, Schlotter B, Müller-Felber W, Pongratz D, Rüdel R, Lochmüller H. Abicht A, et al. Among authors: lochmuller h. Neurology. 1999 Oct 22;53(7):1564-9. doi: 10.1212/wnl.53.7.1564. Neurology. 1999. PMID: 10534268

6

Leber's hereditary optic neuropathy presenting as multiple sclerosis-like disease of the CNS.

Horváth R, Abicht A, Shoubridge EA, Karcagi V, Rózsa C, Komoly S, Lochmüller H. Horváth R, et al. Among authors: lochmuller h. J Neurol. 2000 Jan;247(1):65-7. doi: 10.1007/s004150050015. J Neurol. 2000. PMID: 10701903 Review. No abstract available.

7

A modified alignment of human and rodent 5' untranslated sequences of the acetylcholine receptor epsilon subunit gene reveals additional regions of high homology.

Stucka R, Abicht A, Song IH, Bönsch D, Deufel T, Lochmüller H. Stucka R, et al. Among authors: lochmuller h. Neuromuscul Disord. 2000 Mar;10(3):213-4. doi: 10.1016/s0960-8966(99)00112-1. Neuromuscul Disord. 2000. PMID: 10841620 No abstract available.

8

Technology evaluation: CRIB (CNTF delivery) CytoTherapeutics Inc.

Abicht A, Lochmüller H. Abicht A, et al. Among authors: lochmuller h. Curr Opin Mol Ther. 1999 Oct;1(5):645-50. Curr Opin Mol Ther. 1999. PMID: 11249671 Review.

9

Technology evaluation: edrecolomab, Centocor Inc.

Abicht A, Lochmüller H. Abicht A, et al. Among authors: lochmuller h. Curr Opin Mol Ther. 2000 Oct;2(5):593-600. Curr Opin Mol Ther. 2000. PMID: 11249762 Review.

10

Deactivation and desensitization of mouse embryonic- and adult-type nicotinic receptor channel currents.

Jahn K, Mohammadi B, Krampfl K, Abicht A, Lochmüller H, Bufler J. Jahn K, et al. Among authors: lochmuller h. Neurosci Lett. 2001 Jul 13;307(2):89-92. doi: 10.1016/s0304-3940(01)01929-2. Neurosci Lett. 2001. PMID: 11427307

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