Valeria Capra
0000-0002-3097-0388
7 papers found
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Early Developmental Intervention and Enriched Environment in CDKL5 Developmental and Epileptic Encephalopathy
International Consensus Statement on the Radiological Evaluation of Dysraphic Malformations of the Spine and Spinal Cord
Elucidating the clinical and molecular spectrum of SMARCC2-associated NDD in a cohort of 65 affected individuals
Natural history of familial cerebral cavernous malformation syndrome in children: a multicenter cohort study
L1CAM variants cause two distinct imaging phenotypes on fetal MRI
Epileptic encephalopathy caused by ARV1 deficiency: Refinement of the genotype–phenotype spectrum and functional impact on GPI ‐anchored proteins
CNNM2 homozygous mutations cause severe refractory hypomagnesemia, epileptic encephalopathy and brain malformations
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