Malin JP - Search Results

1

Spinal MRI in progressive myeloneuropathy associated with vitamin E deficiency.

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

2

[So-called whiplash injury of the cervical spine. Comments from the neurological viewpoint].

Tegenthoff M, Malin JP. Tegenthoff M, et al. Among authors: malin jp. Dtsch Med Wochenschr. 1991 Jun 28;116(26):1030-4. doi: 10.1055/s-2008-1063713. Dtsch Med Wochenschr. 1991. PMID: 2060471 Review. German. No abstract available.

3

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. Among authors: malin jp. 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.

4

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: malin jp. Electroencephalogr Clin Neurophysiol. 1996 Aug;101(4):273-80. doi: 10.1016/0924-980x(96)95531-9. Electroencephalogr Clin Neurophysiol. 1996. PMID: 8761036

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. Among authors: malin jp. 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

The glutamate antagonist riluzole suppresses intracortical facilitation.

Liepert J, Schwenkreis P, Tegenthoff M, Malin JP. Liepert J, et al. Among authors: malin jp. J Neural Transm (Vienna). 1997;104(11-12):1207-14. doi: 10.1007/BF01294721. J Neural Transm (Vienna). 1997. PMID: 9503266 Clinical Trial.

7

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. Among authors: malin jp. Ann Neurol. 1998 Mar;43(3):326-31. doi: 10.1002/ana.410430310. Ann Neurol. 1998. PMID: 9506549

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: malin jp. Neuromuscul Disord. 1998 Oct;8(7):480-8. doi: 10.1016/s0960-8966(98)00066-2. Neuromuscul Disord. 1998. PMID: 9829278

9

[Adult polyglucosan antibody disease. Case report with predominant involvement of the central and peripheral nervous system and branching enzyme defect in leukocytes].

Sindern E, Patzold T, Vorgerd M, Shin YS, Podskarbi T, Schröder JM, Malin JP. Sindern E, et al. Among authors: malin jp. Nervenarzt. 1999 Aug;70(8):745-9. doi: 10.1007/s001150050505. Nervenarzt. 1999. PMID: 10483576 German.

10

Assessment of postexcitatory inhibition in patients with focal dystonia.

Schwenkreis P, Vorgerd M, Malin JP, Tegenthoff M. Schwenkreis P, et al. Among authors: malin jp. Acta Neurol Scand. 1999 Oct;100(4):260-4. doi: 10.1111/j.1600-0404.1999.tb00391.x. Acta Neurol Scand. 1999. PMID: 10510687

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

133 results

Search Page

Filters