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You searched for: Author/Creator Comi, Giacomo P.

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1. A Novel Homozygous VPS11 Variant May Cause Generalized Dystonia. Issue 4 (2nd February 2021)

2. Ataluren treatment of patients with nonsense mutation dystrophinopathy. Issue 4 (October 2014)

3. Characterization of patients with Becker muscular dystrophy by histology, magnetic resonance imaging, function, and strength assessments. Issue 3 (30th December 2021)

4. Congenital Myasthenic Syndrome Due to Choline Acetyltransferase Mutations in Infants: Clinical Suspicion and Comprehensive Electrophysiological Assessment Are Important for Early Diagnosis. (March 2014)

6. Dystonia‐ataxia syndrome with permanent torsional nystagmus caused by ECHS1 deficiency. Issue 5 (24th April 2020)

7. Genetic modifiers of respiratory function in Duchenne muscular dystrophy. Issue 5 (28th April 2020)

8. Histologic muscular history in steroid-treated and untreated patients with Duchenne dystrophy. (24th November 2015)

10. Intravenous thrombolysis + endovascular thrombectomy versus thrombolysis alone in large vessel occlusion mild stroke: a propensity score matched analysis. (24th February 2023)