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A placebo-controlled crossover trial of creatine in mitochondrial diseases.
Klopstock T, Querner V, Schmidt F, Gekeler F, Walter M, Hartard M, Henning M, Gasser T, Pongratz D, Straube A, Dieterich M, Müller-Felber W. Klopstock T, et al. Among authors: gasser t. Neurology. 2000 Dec 12;55(11):1748-51. doi: 10.1212/wnl.55.11.1748. Neurology. 2000. PMID: 11113239 Clinical Trial.
Age and cause of death in mitochondrial diseases.
Klopstock T, Jaksch M, Gasser T. Klopstock T, et al. Among authors: gasser t. Neurology. 1999 Sep 11;53(4):855-7. doi: 10.1212/wnl.53.4.855. Neurology. 1999. PMID: 10489054
[Molecular diagnosis of hereditary neurologic diseases. Position paper].
Gasser T, Dichgans M, Jurkat-Rott K, Klockgether T, Klopstock T, Kretzschmar H, Lehmann-Horn F, Reichmann H, Rolfs A, Sander T, Stögbauer F. Gasser T, et al. Nervenarzt. 2000 Oct;71(10):774-96. doi: 10.1007/s001150050665. Nervenarzt. 2000. PMID: 11082808 Review. German. No abstract available.
The fragile X tremor ataxia syndrome in the differential diagnosis of multiple system atrophy: data from the EMSA Study Group.
Kamm C, Healy DG, Quinn NP, Wüllner U, Moller JC, Schols L, Geser F, Burk K, Børglum AD, Pellecchia MT, Tolosa E, del Sorbo F, Nilsson C, Bandmann O, Sharma M, Mayer P, Gasteiger M, Haworth A, Ozawa T, Lees AJ, Short J, Giunti P, Holinski-Feder E, Illig T, Wichmann HE, Wenning GK, Wood NW, Gasser T; European Multiple System Atrophy Study Group. Kamm C, et al. Among authors: gasser t. Brain. 2005 Aug;128(Pt 8):1855-60. doi: 10.1093/brain/awh535. Epub 2005 Jun 9. Brain. 2005. PMID: 15947063
Phenotyping of the thoracic-onset variant of amyotrophic lateral sclerosis.
Kandler K, Witzel S, Eder K, Rothenbacher D, Nagel G, Peter RS, Schuster J, Dorst J, Rosenbohm A, Ludolph AC; ALS Registry Study Group. Kandler K, et al. J Neurol Neurosurg Psychiatry. 2022 May;93(5):563-565. doi: 10.1136/jnnp-2021-326712. Epub 2021 Oct 19. J Neurol Neurosurg Psychiatry. 2022. PMID: 34667101 No abstract available.
1,084 results