Abicht A - Search Results

1

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: abicht a. Neurosci Lett. 2001 Jul 13;307(2):89-92. doi: 10.1016/s0304-3940(01)01929-2. Neurosci Lett. 2001. PMID: 11427307

2

Guideline for the management of myasthenic syndromes.

Wiendl H, Abicht A, Chan A, Della Marina A, Hagenacker T, Hekmat K, Hoffmann S, Hoffmann HS, Jander S, Keller C, Marx A, Melms A, Melzer N, Müller-Felber W, Pawlitzki M, Rückert JC, Schneider-Gold C, Schoser B, Schreiner B, Schroeter M, Schubert B, Sieb JP, Zimprich F, Meisel A. Wiendl H, et al. Among authors: abicht a. Ther Adv Neurol Disord. 2023 Dec 26;16:17562864231213240. doi: 10.1177/17562864231213240. eCollection 2023. Ther Adv Neurol Disord. 2023. PMID: 38152089 Free PMC article. Review.

3

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. Eur J Med Res. 1997 Dec 31;2(12):515-22. Eur J Med Res. 1997. PMID: 9498929

4

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: abicht a. Cell Mol Neurobiol. 1999 Apr;19(2):297-300. doi: 10.1023/a:1006989530148. Cell Mol Neurobiol. 1999. PMID: 10081612

5

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: abicht a. Neuromuscul Disord. 1998 Dec;8(8):542-50. doi: 10.1016/s0960-8966(98)00078-9. Neuromuscul Disord. 1998. PMID: 10093060

6

Technology evaluation: CRIB (CNTF delivery) CytoTherapeutics Inc.

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

7

Technology evaluation: edrecolomab, Centocor Inc.

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

8

A newly identified chromosomal microdeletion and an N-box mutation of the AChR epsilon gene cause a congenital myasthenic syndrome.

Abicht A, Stucka R, Schmidt C, Briguet A, Höpfner S, Song IH, Pongratz D, Müller-Felber W, Ruegg MA, Lochmüller H. Abicht A, et al. Brain. 2002 May;125(Pt 5):1005-13. doi: 10.1093/brain/awf095. Brain. 2002. PMID: 11960891

9

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

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

10

Congenital myasthenic syndrome due to a novel missense mutation in the gene encoding choline acetyltransferase.

Schmidt C, Abicht A, Krampfl K, Voss W, Stucka R, Mildner G, Petrova S, Schara U, Mortier W, Bufler J, Huebner A, Lochmüller H. Schmidt C, et al. Among authors: abicht a. Neuromuscul Disord. 2003 Mar;13(3):245-51. doi: 10.1016/s0960-8966(02)00273-0. Neuromuscul Disord. 2003. PMID: 12609506

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