Crossref Citations
This article has been cited by the following publications. This list is generated based on data provided by
Crossref.
Bertrand, M.J.
Bouchard, R.
Gauthier, G.L.
Bouchard, J.P.
and
Barbeau, A.
1982.
Quantitative Metabolic Profiling ofα-Keto Acids in Friedreich’s Ataxia.
Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques,
Vol. 9,
Issue. 2,
p.
231.
Barbeau, André
1982.
Friedreich’s Disease 1982: Etiologic Hypotheses A personal analysis.
Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques,
Vol. 9,
Issue. 2,
p.
243.
Barbeau, A.
Plasse, L.
Cloutier, T.
Paris, S.
and
Roy, M.
1984.
Lysosomal enzymes in ataxia: discovery of two new cases of late onset hexosaminidase A and B deficiency (adult sandhoff disease) in French Canadians.
Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques,
Vol. 11,
Issue. S4,
p.
601.
Bundey, Sarah
1985.
Genetics and Neurology.
p.
223.
Sorbi, Sandro
Tonini, Stefano
Giannini, Emiliana
Piacentini, Silvia
Marini, Paolo
and
Amaducci, Luigi
1986.
Abnormal platelet glutamate dehydrogenase activity and activation in dominant and nondominant olivopontocerebellar atrophy.
Annals of Neurology,
Vol. 19,
Issue. 3,
p.
239.
Cedarbaum, Jesse M.
and
Blass, John P.
1986.
Mitochondrial dysfunction and spinocerebellar degenerations.
Neurochemical Pathology,
Vol. 4,
Issue. 1,
p.
43.
Sorbi, S.
Piacentini, S.
Fani, C.
Tonini, S.
Marini, P.
and
Amaducci, L.
1989.
Abnormalities of mitochondrial enzymes in hereditary ataxias.
Acta Neurologica Scandinavica,
Vol. 80,
Issue. 2,
p.
103.
Gonçalves, A.
Oliveira, C.
Ferro, M.A.
Dinis, M.
and
Cunha, L.
1993.
Glutamate Dehydrogenase Deficiency in Machado-Joseph Disease.
Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques,
Vol. 20,
Issue. 2,
p.
147.
Campuzano, V.
Montermini, L.
Lutz, Y.
Cova, L.
Hindelang, C.
Jiralerspong, S.
Trottier, Y.
Kish, S. J.
Faucheux, B.
Trouillas, P.
Authier, F. J.
Durr, A.
Mandel, J.-L.
Vescovi, A.
Pandolfo, M.
and
Koenig, M.
1997.
Frataxin is Reduced in Friedreich Ataxia Patients and is Associated with Mitochondrial Membranes.
Human Molecular Genetics,
Vol. 6,
Issue. 11,
p.
1771.
Kaakkola, S.
Marnela, K.-M.
Oja, S. S.
Icén, A.
and
Palo, J.
2009.
Leukocyte glutamate dehydrogenase and CSF amino acids in late onset ataxias.
Acta Neurologica Scandinavica,
Vol. 82,
Issue. 4,
p.
225.
Kaakkola, S.
Marnela, K.-M.
Oja, S. S.
Icén, A.
and
Palo, J.
2009.
Leukocyte glutamate dehydrogenase and CSF amino acids in late onset ataxias.
Acta Neurologica Scandinavica,
Vol. 82,
Issue. 5,
p.
292.