Autori: Pasquariello R

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KLHL40-Related Myopathy: A Systematic Review and Insight into a Follow-up Biomarker via a New Case Report.

Congenital Myopathy as a Phenotypic Expression of CACNA1S Gene Mutation: Case Report and Systematic Review of the Literature.

Complex neurodevelopmental disorder in a preterm child with unilateral cerebellar hemorrhage

Structural brain damage and visual disorders in children with cerebral palsy due to periventricular leukomalacia

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