Showing results (101-110 of 284) with videos related to

Sort By:
Pageof 29
Italian Journal of Neurological Sciences|December 1, 1992
Biopsy diagnosis of a case of adult onset orthochromatic leukodystrophy. Clinical and brain biopsy findingsL Calandriello, C Matteucci, E Bertini, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|May 24, 2011
Evidence of different spinal pathways for the warmth evoked potentialsM Valeriani, C Pazzaglia, D Ferraro, et al.
Epilepsy & Behavior : E&B|March 21, 2020
Improvement of quality of life in adolescents with epilepsy after an empowerment and sailing experienceS Cappelletti, I Tondo, N Pietrafusa, et al.
Neurology|June 25, 2003
Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancyR Nabbout, E Gennaro, B Dalla Bernardina, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 22, 2000
Familial spastic paraplegia, axonal sensory-motor polyneuropathy and bulbar amyotrophy with facial dysmorphia: new cases of Troyer-like syndromeE Bertini, M Sabatelli, M Di Capua, et al.
American Journal of Medical Genetics|July 1, 1989
Distal infantile spinal muscular atrophy associated with paralysis of the diaphragm: a variant of infantile spinal muscular atrophyE Bertini, J L Gadisseux, G Palmieri, et al.
Neurology|August 18, 2010
Protocadherin 19 mutations in girls with infantile-onset epilepsyC Marini, D Mei, L Parmeggiani, et al.
Annali Di Igiene : Medicina Preventiva E Di Comunita|October 26, 2021
Diagnostic and therapeutic pathway for pain in a Continuing Care setting: a survey at an Italian Continuing Care ServiceA Piroli, C Leuter, L Fusco, et al.
SAGE Open Medicine|May 26, 2017
Clinical outcomes for the obese hospital inpatient: An observational studyK L Fusco, H C Robertson, H Galindo, et al.
Biochemical and Biophysical Research Communications|May 8, 1998
A novel insertion mutation (A169i) in the CLN1 gene is associated with infantile neuronal ceroid lipofuscinosis in an Italian patientF M Santorelli, E Bertini, V Petruzzella, et al.
Pageof 29