Marilena Vecchi

Consensus Statement of the Movement Disorder Society on Tremor

Cell type-selective secretome profiling in vivo

DisGeNET: a comprehensive platform integrating information on human disease-associated genes and variants

Sphingolipids and their metabolism in physiology and disease

Juvenile idiopathic arthritis

Imaging characteristics of hemophagocytic lymphohistiocytosis

A spectrum of neuroradiological findings in children with haemophagocytic lymphohistiocytosis

Familial and Acquired Hemophagocytic Lymphohistiocytosis

Frequency and spectrum of central nervous system involvement in 193 children with haemophagocytic lymphohistiocytosis

Genetic mutations associated with status epilepticus

Identification of an elaborate complex mediating postsynaptic inhibition

Chromone: A Valid Scaffold in Medicinal Chemistry

Impairment of ceramide synthesis causes a novel progressive myoclonus epilepsy

Structural characterization of the cyclin-dependent protein kinase family

Hematological Problems in Pediatric Intensive Care

Electroclinical diagnosis of Angelman syndrome: a study of 7 cases

No Evidence of a Major Locus for Benign Familial Infantile Convulsions on Chromosome 19q12‐q13.1

Acute encephalopathy as a primary manifestation of haemophagocytic lymphohistiocytosis

The CDKL5 disorder is an independent clinical entity associated with early-onset encephalopathy

14q12 duplication including FOXG1: Is there a common age-dependent epileptic phenotype?

Acute encephalopathy as a primary manifestation of haemophagocytic lymphohistiocytosis