9 results on '"Santoro, Lucio"'
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2. Selected items from the Charcot-Marie-Tooth (CMT) Neuropathy Score and secondary clinical outcome measures serve as sensitive clinical markers of disease severity in CMT1A patients
3. Influence of comorbidities on the phenotype of patients affected by Charcot–Marie–Tooth neuropathy type 1A
4. Centronuclear myopathy related to dynamin 2 mutations: Clinical, morphological, muscle imaging and genetic features of an Italian cohort
5. GDAP1 mutations in Italian axonal Charcot–Marie–Tooth patients: Phenotypic features and clinical course
6. Are novel outcome measures for Charcot–Marie–Tooth disease sensitive to change? The 6-minute walk test and StepWatch™ Activity Monitor in a 12-month longitudinal study
7. Familial aggregation of white matter lesions in myotonic dystrophy type 1
8. Two new mutations in the myophosphorylase gene in Italian patients with McArdle's disease
9. Brain MRI features of congenital- and adult-form myotonic dystrophy type 1: case-control study
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