Vorgerd M - Search Results

1

Isolated loss of gamma-sarcoglycan: diagnostic implications in autosomal recessive limb-girdle muscular dystrophies.

Vorgerd M, Gencik M, Mortier J, Epplen JT, Malin JP, Mortier W. Vorgerd M, et al. Muscle Nerve. 2001 Mar;24(3):421-4. doi: 10.1002/1097-4598(200103)24:3<421::aid-mus1016>3.0.co;2-r. Muscle Nerve. 2001. PMID: 11353430

2

A missense point mutation (Ser515Phe) in the adrenoleukodystrophy gene in a family with adrenomyeloneuropathy: a clinical, biochemical, and genetic study.

Vorgerd M, Fuchs S, Tegenthoff M, Malin JP. Vorgerd M, et al. J Neurol Neurosurg Psychiatry. 1995 Feb;58(2):229-31. doi: 10.1136/jnnp.58.2.229. J Neurol Neurosurg Psychiatry. 1995. PMID: 7876858 Free PMC article.

3

Enhancement of inhibitory mechanisms in the motor cortex of patients with cerebellar degeneration: a study with transcranial magnetic brain stimulation.

Wessel K, Tegenthoff M, Vorgerd M, Otto V, Nitschke MF, Malin JP. Wessel K, et al. Among authors: vorgerd m. Electroencephalogr Clin Neurophysiol. 1996 Aug;101(4):273-80. doi: 10.1016/0924-980x(96)95531-9. Electroencephalogr Clin Neurophysiol. 1996. PMID: 8761036

4

Postexcitatory inhibition after transcranial magnetic single and double brain stimulation in Huntington's disease.

Tegenthoff M, Vorgerd M, Juskowiak F, Roos V, Malin JP. Tegenthoff M, et al. Among authors: vorgerd m. Electroencephalogr Clin Neurophysiol. 1996 Aug;101(4):298-303. doi: 10.1016/0924-980x(96)94645-7. Electroencephalogr Clin Neurophysiol. 1996. PMID: 8761039

5

Spinal MRI in progressive myeloneuropathy associated with vitamin E deficiency.

Vorgerd M, Tegenthoff M, Kühne D, Malin JP. Vorgerd M, et al. Neuroradiology. 1996 May;38 Suppl 1:S111-3. doi: 10.1007/BF02278134. Neuroradiology. 1996. PMID: 8811695

6

Muscle phosphofructokinase deficiency in two generations.

Vorgerd M, Karitzky J, Ristow M, Van Schaftingen E, Tegenthoff M, Jerusalem F, Malin JP. Vorgerd M, et al. J Neurol Sci. 1996 Sep 15;141(1-2):95-9. doi: 10.1016/0022-510x(96)00131-1. J Neurol Sci. 1996. PMID: 8880699

7

Spinocerebellar ataxia type 2. Genotype and phenotype in German kindreds.

Schöls L, Gispert S, Vorgerd M, Menezes Vieira-Saecker AM, Blanke P, Auburger G, Amoiridis G, Meves S, Epplen JT, Przuntek H, Pulst SM, Riess O. Schöls L, et al. Among authors: vorgerd m. Arch Neurol. 1997 Sep;54(9):1073-80. doi: 10.1001/archneur.1997.00550210011007. Arch Neurol. 1997. PMID: 9311350

8

Mutation analysis in myophosphorylase deficiency (McArdle's disease).

Vorgerd M, Kubisch C, Burwinkel B, Reichmann H, Mortier W, Tettenborn B, Pongratz D, Lindemuth R, Tegenthoff M, Malin JP, Kilimann MW. Vorgerd M, et al. Ann Neurol. 1998 Mar;43(3):326-31. doi: 10.1002/ana.410430310. Ann Neurol. 1998. PMID: 9506549

9

[Adrenoleukodystrophy and adrenomyeloneuropathy. Clinical biochemical and molecular genetic findings].

Vorgerd M, Benkmann HG, Tegenthoff M, Gal A, Malin JP. Vorgerd M, et al. Nervenarzt. 1998 Feb;69(2):174-9. doi: 10.1007/s001150050257. Nervenarzt. 1998. PMID: 9551465 German.

10

Impaired aerobic glycolysis in muscle phosphofructokinase deficiency results in biphasic post-exercise phosphocreatine recovery in 31P magnetic resonance spectroscopy.

Grehl T, Müller K, Vorgerd M, Tegenthoff M, Malin JP, Zange J. Grehl T, et al. Among authors: vorgerd m. Neuromuscul Disord. 1998 Oct;8(7):480-8. doi: 10.1016/s0960-8966(98)00066-2. Neuromuscul Disord. 1998. PMID: 9829278

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