Klopstock T - Search Results

1

Recessive dystonia-ataxia syndrome in a Turkish family caused by a COX20 (FAM36A) mutation.

Doss S, Lohmann K, Seibler P, Arns B, Klopstock T, Zühlke C, Freimann K, Winkler S, Lohnau T, Drungowski M, Nürnberg P, Wiegers K, Lohmann E, Naz S, Kasten M, Bohner G, Ramirez A, Endres M, Klein C. Doss S, et al. Among authors: klopstock t. J Neurol. 2014 Jan;261(1):207-12. doi: 10.1007/s00415-013-7177-7. Epub 2013 Nov 8. J Neurol. 2014. PMID: 24202787

2

Multiple symmetric lipomatosis: abnormalities in complex IV and multiple deletions in mitochondrial DNA.

Klopstock T, Naumann M, Schalke B, Bischof F, Seibel P, Kottlors M, Eckert P, Reiners K, Toyka KV, Reichmann H. Klopstock T, et al. Neurology. 1994 May;44(5):862-6. doi: 10.1212/wnl.44.5.862. Neurology. 1994. PMID: 8190288

3

Mitochondrial DNA in migraine with aura.

Klopstock T, May A, Seibel P, Papagiannuli E, Diener HC, Reichmann H. Klopstock T, et al. Neurology. 1996 Jun;46(6):1735-8. doi: 10.1212/wnl.46.6.1735. Neurology. 1996. PMID: 8649580

4

Aggressive confusional state as a clinical manifestation of status epilepticus in MELAS.

Feddersen B, Bender A, Arnold S, Klopstock T, Noachtar S. Feddersen B, et al. Among authors: klopstock t. Neurology. 2003 Oct 28;61(8):1149-50. doi: 10.1212/01.wnl.0000092497.53706.1b. Neurology. 2003. PMID: 14581687 No abstract available.

5

Genotypic and phenotypic spectrum of PANK2 mutations in patients with neurodegeneration with brain iron accumulation.

Hartig MB, Hörtnagel K, Garavaglia B, Zorzi G, Kmiec T, Klopstock T, Rostasy K, Svetel M, Kostic VS, Schuelke M, Botz E, Weindl A, Novakovic I, Nardocci N, Prokisch H, Meitinger T. Hartig MB, et al. Among authors: klopstock t. Ann Neurol. 2006 Feb;59(2):248-56. doi: 10.1002/ana.20771. Ann Neurol. 2006. PMID: 16437574

6

Creatine supplementation in Parkinson disease: a placebo-controlled randomized pilot trial.

Bender A, Koch W, Elstner M, Schombacher Y, Bender J, Moeschl M, Gekeler F, Müller-Myhsok B, Gasser T, Tatsch K, Klopstock T. Bender A, et al. Among authors: klopstock t. Neurology. 2006 Oct 10;67(7):1262-4. doi: 10.1212/01.wnl.0000238518.34389.12. Neurology. 2006. PMID: 17030762 Clinical Trial.

7

SPG10 is a rare cause of spastic paraplegia in European families.

Schüle R, Kremer BP, Kassubek J, Auer-Grumbach M, Kostic V, Klopstock T, Klimpe S, Otto S, Boesch S, van de Warrenburg BP, Schöls L. Schüle R, et al. Among authors: klopstock t. J Neurol Neurosurg Psychiatry. 2008 May;79(5):584-7. doi: 10.1136/jnnp.2007.137596. Epub 2008 Feb 1. J Neurol Neurosurg Psychiatry. 2008. PMID: 18245137 Free article.

8

Clinical and molecular characterisation of a Parkinson family with a novel PINK1 mutation.

Prestel J, Gempel K, Hauser TK, Schweitzer K, Prokisch H, Ahting U, Freudenstein D, Bueltmann E, Naegele T, Berg D, Klopstock T, Gasser T. Prestel J, et al. Among authors: klopstock t. J Neurol. 2008 May;255(5):643-8. doi: 10.1007/s00415-008-0763-4. Epub 2008 Feb 21. J Neurol. 2008. PMID: 18286320

9

Dopaminergic midbrain neurons are the prime target for mitochondrial DNA deletions.

Bender A, Schwarzkopf RM, McMillan A, Krishnan KJ, Rieder G, Neumann M, Elstner M, Turnbull DM, Klopstock T. Bender A, et al. Among authors: klopstock t. J Neurol. 2008 Aug;255(8):1231-5. doi: 10.1007/s00415-008-0892-9. Epub 2008 Jul 11. J Neurol. 2008. PMID: 18604467

10

Heteroplasmic mutation in the anticodon-stem of mitochondrial tRNA(Val) causing MNGIE-like gastrointestinal dysmotility and cachexia.

Horváth R, Bender A, Abicht A, Holinski-Feder E, Czermin B, Trips T, Schneiderat P, Lochmüller H, Klopstock T. Horváth R, et al. Among authors: klopstock t. J Neurol. 2009 May;256(5):810-5. doi: 10.1007/s00415-009-5023-8. Epub 2009 Mar 1. J Neurol. 2009. PMID: 19252805

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