Barbara Scelsa
0000-0003-3984-0077
3 papers found
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Pathogenic Variants in STXBP1 and in Genes for GABAa Receptor Subunities Cause Atypical Rett/Rett-like Phenotypes
Mild phenotype in Molybdenum cofactor deficiency: A new patient and review of the literature
Neurodevelopmental outcome at 2 years in twin-twin transfusion syndrome survivors randomized for the Solomon trial
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