Wagner K - Search Results

1

Proximal Charcot-Marie-Tooth syndrome with duplication on chromosome 17p11.2.

Auer-Grumbach M, Wagner K, Payer F, Hartung HP. Auer-Grumbach M, et al. Among authors: wagner k. Ann N Y Acad Sci. 1999 Sep 14;883:469-71. Ann N Y Acad Sci. 1999. PMID: 10586276 No abstract available.

2

Proximal Charcot-Marie-Tooth Syndrome with Duplication on Chromosome 17p11.2.

Auer-Grumbach M, Wagner K, Payer F, Hartung HP. Auer-Grumbach M, et al. Among authors: wagner k. Ann N Y Acad Sci. 1999 Oct;883(1):469-471. doi: 10.1111/j.1749-6632.1999.tb08613.x. Ann N Y Acad Sci. 1999. PMID: 29086978 No abstract available.

3

[Hereditary motor-sensory neuropathies (Charcot-Marie-Tooth syndrome) and related neuropathies. Current classification and genotype-phenotype correlation].

Auer-Grumbach M, Wagner K, Fazekas F, Löscher WN, Strasser-Fuchs S, Hartung HP. Auer-Grumbach M, et al. Among authors: wagner k. Nervenarzt. 1999 Dec;70(12):1052-61. doi: 10.1007/s001150050539. Nervenarzt. 1999. PMID: 10637810 Review. German.

4

Clinical predominance of proximal upper limb weakness in CMT1A syndrome.

Auer-Grumbach M, Wagner K, Strasser-Fuchs S, Löscher WN, Fazekas F, Millner M, Hartung HP. Auer-Grumbach M, et al. Among authors: wagner k. Muscle Nerve. 2000 Aug;23(8):1243-9. doi: 10.1002/1097-4598(200008)23:8<1243::aid-mus13>3.0.co;2-z. Muscle Nerve. 2000. PMID: 10918262

5

Late onset Charcot-Marie-Tooth 2 syndrome caused by two novel mutations in the MPZ gene.

Auer-Grumbach M, Strasser-Fuchs S, Robl T, Windpassinger C, Wagner K. Auer-Grumbach M, et al. Among authors: wagner k. Neurology. 2003 Nov 25;61(10):1435-7. doi: 10.1212/01.wnl.0000094197.46109.75. Neurology. 2003. PMID: 14638973

6

Roussy-Lévy syndrome is a phenotypic variant of Charcot-Marie-Tooth syndrome IA associated with a duplication on chromosome 17p11.2.

Auer-Grumbach M, Strasser-Fuchs S, Wagner K, Körner E, Fazekas F. Auer-Grumbach M, et al. Among authors: wagner k. J Neurol Sci. 1998 Jan 21;154(1):72-5. doi: 10.1016/s0022-510x(97)00218-9. J Neurol Sci. 1998. PMID: 9543325

7

Refinement of the Silver syndrome locus on chromosome 11q12-q14 in four families and exclusion of eight candidate genes.

Windpassinger C, Wagner K, Petek E, Fischer R, Auer-Grumbach M. Windpassinger C, et al. Among authors: wagner k. Hum Genet. 2003 Dec;114(1):99-109. doi: 10.1007/s00439-003-1021-6. Epub 2003 Sep 16. Hum Genet. 2003. PMID: 13680364

8

Phenotypes of the N88S Berardinelli-Seip congenital lipodystrophy 2 mutation.

Auer-Grumbach M, Schlotter-Weigel B, Lochmüller H, Strobl-Wildemann G, Auer-Grumbach P, Fischer R, Offenbacher H, Zwick EB, Robl T, Hartl G, Hartung HP, Wagner K, Windpassinger C; Austrian Peripheral Neuropathy Study Group. Auer-Grumbach M, et al. Among authors: wagner k. Ann Neurol. 2005 Mar;57(3):415-24. doi: 10.1002/ana.20410. Ann Neurol. 2005. PMID: 15732094

9

Ulcero-mutilating neuropathy in an Austrian kinship without linkage to hereditary motor and sensory neuropathy IIB and hereditary sensory neuropathy I loci.

Auer-Grumbach M, Wagner K, Timmerman V, De Jonghe P, Hartung HP. Auer-Grumbach M, et al. Among authors: wagner k. Neurology. 2000 Jan 11;54(1):45-52. doi: 10.1212/wnl.54.1.45. Neurology. 2000. PMID: 10636124

10

Phenotypic and genotypic heterogeneity in hereditary motor neuronopathy type V: a clinical, electrophysiological and genetic study.

Auer-Grumbach M, Löscher WN, Wagner K, Petek E, Körner E, Offenbacher H, Hartung HP. Auer-Grumbach M, et al. Among authors: wagner k. Brain. 2000 Aug;123 ( Pt 8):1612-23. doi: 10.1093/brain/123.8.1612. Brain. 2000. PMID: 10908191

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