Lam J, Dohil MA, Eichenfield LF, et al. SCALP syndrome: sebaceous nevus syndrome, CNS malformations, aplasia cutis congenita, limbal dermoid, and pigmented nevus (giant congenital melanocytic nevus) with neurocutaneous melanosis: a ...
Merks JH, de Vries LS, Zhou XP, et al. PTEN hamartoma tumour syndrome: variability of an entity. J Med Genet. 2003;40:e111. Nie K, Molnár Z, Szele FG. Proliferation but not migration is associated with blood vessels during development ...
Dodd KJ, Foley S. Partial bodyweightsupported treadmill training can improve walking in children with cerebral palsy: a clinical controlled trial. Dev Med Child Neurol. 2007;49:101–105. ... Fowler EG, Kolebe THA, Damiano DL, et al.
recognition by these diagnostic instruments also had major consequences on the current broadening of autism criteria. SDIs helped to make the diagnosis of autism possible in individuals scoring in the normal range of measured ...
The practice of pediatric neurology demands a high level of responsibility at multiple levels.
The preoperative study of patients who are candidates for epilepsy surgery often classifies their epileptic foci as “lesional” or “non-lesional” based upon evidence from neuroimaging.
The “neurofibromatoses” are a set of distinct genetic disorders that have in common the occurrence of tumors of the nerve sheath.
Epileptic encephalopathy with continuous spike-waves during slow-wave sleep (CSWS) is a spectrum of epileptic conditions best defined by the association of cognitive or behavioral impairment acquired during childhood and not related to ...
Epilepsy has protean manifestations and may be diagnosed when two unprovoked seizures have occurred.
This chapter reviews the principal genes that program neural crest development and also are documented, implicated, or suspected in the pathogenesis of neurocutaneous syndromes.
Sturge−Weber syndrome (SWS) is a rare sporadic neurocutaneous syndrome defined by the association of a facial capillary malformation in the ophthalmic distribution of the trigeminal nerve, with ipsilateral vascular glaucoma and vascular ...
Le Coz P. Les enjeux internationaux de la bioéthique et le sommet mondial de Paris de 2008. In: Convergences et divergences en débats. Paris: La documentation française; 2009;1117–1132. Annuaire Français des Relations Internationales ...
Idiopathic focal epilepsies Federico Vigevano, Nicola Specchio, Natalio Fejerman ... Epilepsies Partielles Graves Pharmacorésistantes de l'enfant: Stratégies Diagnostiques et Traitements Chirurgicaux. Montrouge: John Libbey Eurotext; ...
Idiopathic generalized epilepsies (IGEs) may start in infancy, childhood, or adolescence, but some have an onset in adulthood.
A good understanding of the long-term outcome of epileptic disorders that have begun in infancy or childhood allows the practitioner to choose the best medical management and to adjust it throughout the life of the patient.
Whereas there is no specific neurosurgical technique in pediatric epilepsy, the frequency of each type of surgery is very different from epilepsy surgery applied in adults, and reflects the underlying etiologies, which are much more diverse ...
The spectrum of focal epileptogenic lesions and their clinical manifestations in children differ substantially from those seen in adults.
Developmental dyslexia (DD) is a specific and persistent disability affecting the acquisition of written language.
This is the case for the Landau–Kleffner syndrome, which generally appears during speech development and affects language.
Memory disorders are a frequent consequence of a variety of childhood neurological conditions.