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92. Safety and efficacy of riluzole in spinocerebellar ataxia type 2 in France (ATRIL): a multicentre, randomised, double-blind, placebo-controlled trial. Issue 3 (March 2022)

93. SCA13 causes dominantly inherited non-progressive myoclonus ataxia. (May 2017)

94. Short-interval observational data to inform clinical trial design in Huntington's disease. Issue 12 (10th February 2015)

95. Spinocerebellar ataxia type 11 (SCA11) is an uncommon cause of dominant ataxia among French and German kindreds. Issue 11 (28th July 2010)

96. Standardized Assessment of Hereditary Ataxia Patients in Clinical Studies. Issue 3 (11th February 2016)

97. Structural and functional brain network correlates of depressive symptoms in premanifest Huntington's disease. Issue 6 (15th March 2017)

98. Survival and severity in dominant cerebellar ataxias. (7th January 2015)

99. Survival in patients with spinocerebellar ataxia types 1, 2, 3, and 6 (EUROSCA): a longitudinal cohort study. Issue 4 (April 2018)