Tegenthoff M - Search Results

1

Robustness and stability of volume-based tractography in a multicenter setting.

Forsting J, Rehmann R, Rohm M, Güttsches AK, Froeling M, Kan HE, Tegenthoff M, Vorgerd M, Schlaffke L. Forsting J, et al. Among authors: tegenthoff m. NMR Biomed. 2022 Jul;35(7):e4707. doi: 10.1002/nbm.4707. Epub 2022 Feb 18. NMR Biomed. 2022. PMID: 35102637

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. Among authors: tegenthoff m. 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: tegenthoff 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. 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. Among authors: tegenthoff m. 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. Among authors: tegenthoff m. 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

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: tegenthoff m. Ann Neurol. 1998 Mar;43(3):326-31. doi: 10.1002/ana.410430310. Ann Neurol. 1998. PMID: 9506549

8

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

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

9

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

10

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: tegenthoff 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

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