[Contribution to the study of heredo-familial dystrophic syndrome; case of the association of Charcot-Marie type of amyotrophia with Friedreich's disease].
D005621:Friedreich Ataxia; D006801:Humans; D009133:Muscular Atrophy; D009134:Muscular Atrophy, Spinal; D009207:Myoclonus / Q000503:physiopathology*; D013132:Spinocerebellar Degenerations
PARAMYOCLONUS MULTIPLEX; PROGRESSIVE MUSCULAR ATROPHY
Contributo allo studio delle sindromi distrofiche eredo-familiari; su un caso di associazione dell'amiotrofia tipo Charcot-Marie con il morbo di Friedreich.