Auer-Grumbach M - Search Results

1

Autosomal dominant inherited neuropathies with prominent sensory loss and mutilations: a review.

Auer-Grumbach M, De Jonghe P, Verhoeven K, Timmerman V, Wagner K, Hartung HP, Nicholson GA. Auer-Grumbach M, et al. Arch Neurol. 2003 Mar;60(3):329-34. doi: 10.1001/archneur.60.3.329. Arch Neurol. 2003. PMID: 12633143 Review.

2

[Charcot-Marie-Tooth syndrome. Clinico-genetic correlation in an affected family].

Auer-Grumbach M, Wagner K, Strasser-Fuchs S, Millner M, Fazekas F. Auer-Grumbach M, et al. Nervenarzt. 1996 Feb;67(2):155-9. Nervenarzt. 1996. PMID: 8851297 German.

3

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. J Neurol Sci. 1998 Jan 21;154(1):72-5. doi: 10.1016/s0022-510x(97)00218-9. J Neurol Sci. 1998. PMID: 9543325

4

Troyer syndrome: a combination of central brain abnormality and motor neuron disease?

Auer-Grumbach M, Fazekas F, Radner H, Irmler A, Strasser-Fuchs S, Hartung HP. Auer-Grumbach M, et al. J Neurol. 1999 Jul;246(7):556-61. doi: 10.1007/s004150050403. J Neurol. 1999. PMID: 10463356

5

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. Ann N Y Acad Sci. 1999 Sep 14;883:469-71. Ann N Y Acad Sci. 1999. PMID: 10586276 No abstract available.

6

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. Neurology. 2000 Jan 11;54(1):45-52. doi: 10.1212/wnl.54.1.45. Neurology. 2000. PMID: 10636124

7

[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. Nervenarzt. 1999 Dec;70(12):1052-61. doi: 10.1007/s001150050539. Nervenarzt. 1999. PMID: 10637810 Review. German.

8

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. Brain. 2000 Aug;123 ( Pt 8):1612-23. doi: 10.1093/brain/123.8.1612. Brain. 2000. PMID: 10908191

9

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. 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

10

Comparison of second lumbrical and interosseus latencies with standard measures of median nerve function across the carpal tunnel: a prospective study of 450 hands.

Löscher WN, Auer-Grumbach M, Trinka E, Ladurner G, Hartung HP. Löscher WN, et al. J Neurol. 2000 Jul;247(7):530-4. doi: 10.1007/s004150070152. J Neurol. 2000. PMID: 10993495

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