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11. A recessive ataxia diagnosis algorithm for the next generation sequencing era. Issue 6 (21st November 2017)

13. Delayed‐onset Friedreich's ataxia revisited. Issue 1 (21st September 2015)

14. Putative founder effect of Arg338* AP4M1 (SPG50) variant causing severe intellectual disability, epilepsy and spastic paraplegia: Report of three families. Issue 3 (2nd December 2022)

16. Progression of Nigrostriatal Denervation in Cerebellar Multiple System Atrophy: A Prospective Study. (8th February 2022)

17. A step toward essential tremor gene discovery: identification of extreme phenotype and screening of HTRA2 and ANO3. Issue 1 (December 2016)