Vorgerd M - Search Results

1

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

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

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

4

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

5

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

6

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

7

[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.

8

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

9

Reduced intracortical facilitation in patients with cerebellar degeneration.

Liepert J, Wessel K, Schwenkreis P, Trillenberg P, Otto V, Vorgerd M, Malin JP, Tegenthoff M. Liepert J, et al. Among authors: vorgerd m. Acta Neurol Scand. 1998 Nov;98(5):318-23. doi: 10.1111/j.1600-0404.1998.tb01741.x. Acta Neurol Scand. 1998. PMID: 9858101

10

Phenotypic variability in rippling muscle disease.

Vorgerd M, Bolz H, Patzold T, Kubisch C, Malin JP, Mortier W. Vorgerd M, et al. Neurology. 1999 Apr 22;52(7):1453-9. doi: 10.1212/wnl.52.7.1453. Neurology. 1999. PMID: 10227634

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

204 results

Search Page

Filters