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Brain : a Journal of Neurology|May 13, 1998
The natural history of degenerative ataxia: a retrospective study in 466 patientsT Klockgether, R Lüdtke, B Kramer, et al.Cerebellum (London, England)|August 19, 2019
Characterization of Cerebellar Atrophy and Resting State Functional Connectivity Patterns in Sporadic Adult-Onset Ataxia of Unknown Etiology (SAOA)Xueyan Jiang, J Faber, I Giordano, et al.Human Molecular Genetics|August 1, 1997
SCA6 is caused by moderate CAG expansion in the alpha1A-voltage-dependent calcium channel geneO Riess, L Schöls, H Bottger, et al.Journal of Neural Transmission (Vienna, Austria : 1996)|October 14, 2004
L-carnitine and creatine in Friedreich's ataxia. A randomized, placebo-controlled crossover trialL Schöls, J Zange, M Abele, et al.Cell Death and Differentiation|April 16, 1999
Extended therapeutic window for caspase inhibition and synergy with MK-801 in the treatment of cerebral histotoxic hypoxiaJ B Schulz, M Weller, R T Matthews, et al.Clinical Autonomic Research : Official Journal of the Clinical Autonomic Research Society|December 30, 1998
Consensus statement on the diagnosis of multiple system atrophy. American Autonomic Society and American Academy of NeurologyS Gilman, P Low, N Quinn, et al.Neurologia (Barcelona, Spain)|December 29, 1999
[Consensus on the diagnosis of multi-system atrophy]S Gilman, P Low, N Quinn, et al.Neurology|February 16, 2006
Methionine metabolism and phenotypic variability in X-linked adrenoleukodystrophyM Linnebank, S Kemp, R J A Wanders, et al.Journal of Biomedical Informatics|October 13, 2010
Designing mobile support for glycemic control in patients with diabetesLynne T Harris, James Tufano, Tung Le, et al.Diabetes Care|October 11, 2013
Nutrition therapy recommendations for the management of adults with diabetesAlison B Evert, Jackie L Boucher, Marjorie Cypress, et al.Pageof 22