Résultats de la recherche

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Movement disorders in mitochondrial diseases.
Pathophysiogical and therapeutic progress in Friedreich ataxia
The autosomal recessive cerebellar ataxias
Adult centronuclear myopathies: A hospital-based study
SPG15: a cause of juvenile atypical levodopa responsive parkinsonism
Bedtime-related jerks in the upper limbs associated with restless arms syndrome.
Genes for spinocerebellar ataxia with blindness and deafness (SCABD/SCAR3, MIM# 271250 and SCABD2)
Anti-Hu-associated brainstem encephalitis with ganglioneuroblastoma in a young adult
Blood Cell Palmitoleate-Palmitate Ratio Is an Independent Prognostic Factor for Amyotrophic Lateral Sclerosis.
Next generation sequencing for molecular diagnosis of neuromuscular diseases

Islandora displays