Abstracts (HTML) List of Authors

Martin, A. De Saint

Early-Onset Epileptic Encephalopathy Related to Germline PIGA Mutations: A Series of Four Patients

Masnada, S.

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

Mendell, J.R.

AVXS-101 Phase 1 Gene-Replacement Therapy (GRT) Clinical Trial in Spinal Muscular Atrophy Type 1 (SMA1): 24-Month Event-Free Survival and Achievement of Developmental Milestones

Menier, M.

Early Diagnosis and Speed to Effect in Spinal Muscular Atrophy Type 1 (SMA-1)

Micheletti, S.

Environmental Adaptation and Early Visual Training to Promote Neurodevelopment in Infants with Visual Impairment: A Pilot Study

Mignot, C.

Biallelic PDE2A Mutations: A New Cause of Intellectual Disability with Paroxysmal Dyskinesia and/or Epilepsy
Congenital Immobility and Stiffness Due to ATAD1 Biallelic Mutations: Report of Two Novel Unrelated Patients

Milleret-Pignot, C.

Epilepsy and EEG Patterns in Children Diagnosed with Hyperinsulinism. Report of Two Cases Presented as Atypical Generalized Epilepsy and Review of EEGS of 15 Supplementary Cases.

Moal, L.

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

Molinaro, A.

Environmental Adaptation and Early Visual Training to Promote Neurodevelopment in Infants with Visual Impairment: A Pilot Study

Muschol, N.

Design, Baseline Characteristics, and 2-Year Follow-up from The MPS IIIA Natural History Study Used as Control Group in Gene Therapy Trial