Abstracts (HTML) List of Authors

Baumstarck, K.

Characteristics of Polyhandicapped Patients. About a 875 Patients Cohort

Bernardi, G.

Acute Flaccid Myelitis: An Emerging Disease with Several Challenges. A Retrospective Study of an Italian Cohort.

Betrouni, N.

An Automated EEG Grading System for the Early Neonatal Brain Injury Severity Prediction Postperinatal Asphyxia

Billette, T.

Congenital Immobility and Stiffness Due to ATAD1 Biallelic Mutations: Report of Two Novel Unrelated Patients

Boespflug-Tanguy, O.

A Novel Hypomyelinating Leukodystrophy Caused by Loss of the Sphingolipid Desaturase DEGS1 with Potential Therapy
Natural History in Leukodystrophies Related to POLR3A and POLR3B Mutations: A Multicentric Survey of 21 Pediatric Cases

Bouilleret, V.

Biallelic PDE2A Mutations: A New Cause of Intellectual Disability with Paroxysmal Dyskinesia and/or Epilepsy

Boussaid, K.

Natural History in Leukodystrophies Related to POLR3A and POLR3B Mutations: A Multicentric Survey of 21 Pediatric Cases

Bova, S.

Acute Flaccid Myelitis: An Emerging Disease with Several Challenges. A Retrospective Study of an Italian Cohort.

Briola, F. La

New Strategies to Assess Neuropsychiatric Involvement and Improve the Outcome in Children and Adolescents with NF1 and TSC

Brisse, C.

Characteristics of Polyhandicapped Patients. About a 875 Patients Cohort

Brunetti, S.

Primary and Secondary Stereotypies in Children: A Pilot Standardized Protocol and Video Analysis

Bunod, R.

Congenital Immobility and Stiffness Due to ATAD1 Biallelic Mutations: Report of Two Novel Unrelated Patients

Burglen, L.

Expanding the Spectrum of Poretti-Boltshauser Syndrome: 10 New Patients with LAMA1 Mutations