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A case of amyotrophic lateral sclerosis with a very slow progression over 44 years.
Grohme K, Maravic MV, Gasser T, Borasio GD. Grohme K, et al. Neuromuscul Disord. 2001 May;11(4):414-6. doi: 10.1016/s0960-8966(00)00217-0. Neuromuscul Disord. 2001. PMID: 11369195
Meta-analysis of vascular endothelial growth factor variations in amyotrophic lateral sclerosis: increased susceptibility in male carriers of the -2578AA genotype.
Lambrechts D, Poesen K, Fernández-Santiago R, Al-Chalabi A, Del Bo R, Van Vught PW, Khan S, Marklund SL, Brockington A, van Marion I, Anneser J, Shaw C, Ludolph AC, Leigh NP, Comi GP, Gasser T, Shaw PJ, Morrison KE, Andersen PM, Van den Berg LH, Thijs V, Siddique T, Robberecht W, Carmeliet P. Lambrechts D, et al. J Med Genet. 2009 Dec;46(12):840-6. doi: 10.1136/jmg.2008.058222. Epub 2008 Apr 15. J Med Genet. 2009. PMID: 18413368
A novel SOD1 mutation in an Austrian family with amyotrophic lateral sclerosis.
Bereznai B, Winkler A, Borasio GD, Gasser T. Bereznai B, et al. Neuromuscul Disord. 1997 Mar;7(2):113-6. doi: 10.1016/s0960-8966(96)00419-1. Neuromuscul Disord. 1997. PMID: 9131652
Sequencing studies showed a previously undescribed T to A missense mutation at position 8 in exon 1 of the SOD1 gene. This mutation results in the elimination of an Eco57I restriction site. ...
Sequencing studies showed a previously undescribed T to A missense mutation at position 8 in exon 1 of the SOD1 gene. This mutation r …
Inherited myoclonus-dystonia syndrome.
Gasser T. Gasser T. Adv Neurol. 1998;78:325-34. Adv Neurol. 1998. PMID: 9750929 Review. No abstract available.
GAG deletion in the DYT1 gene in early limb-onset idiopathic torsion dystonia in Germany.
Kamm C, Castelon-Konkiewitz E, Naumann M, Heinen F, Brack M, Nebe A, Ceballos-Baumann A, Gasser T. Kamm C, et al. Mov Disord. 1999 Jul;14(4):681-3. doi: 10.1002/1531-8257(199907)14:4<681::aid-mds1020>;2-m. Mov Disord. 1999. PMID: 10435508
The phenotypic spectrum of CADASIL: clinical findings in 102 cases.
Dichgans M, Mayer M, Uttner I, Brüning R, Müller-Höcker J, Rungger G, Ebke M, Klockgether T, Gasser T. Dichgans M, et al. Ann Neurol. 1998 Nov;44(5):731-9. doi: 10.1002/ana.410440506. Ann Neurol. 1998. PMID: 9818928
Genetic linkage studies in autosomal dominantly inherited L-DOPA responsive parkinsonism. Evaluation of candidate genes.
Gasser T, Wszolek Z, Supala A, Trofatter J, Ozelius L, Uitti RJ, Pfeiffer RF, Gusella J, Calne D, Breakefield XO. Gasser T, et al. Adv Neurol. 1996;69:87-95. Adv Neurol. 1996. PMID: 8615189 Clinical Trial. No abstract available.
[Typical anticipation in type 7 spinocerebellar ataxia].
Jäger M, von Rosen F, Fesl G, Gasser T. Jäger M, et al. Nervenarzt. 2000 Oct;71(10):835-8. doi: 10.1007/s001150050672. Nervenarzt. 2000. PMID: 11082815 German.
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