Search Pediatric aspects. Adolescence and neurological diseasesAnálisis de situación de las remisiones a SIFCO en la CV.Vaccination calendar in other countries.CdL facial phenotypes.Newborn screening for SMA.Palliative care.Endocrinopathies and neurogenetic disorders.Mitochondrial diseases.Diseases peroxisomal.Enfermedades prevenibles mediante la vacunación.Rare diseases in the school.Equipment-specific intervention in childhood and adolescence (EIIA)Estados y sistemas de salud.Nutritional strategies in PCIInternet secure for kids.Cardiomyopathies in neuromuscular diseases.Nirsevimab en neurología pediátrica.Pediatric dentistry in special patients.Orphan AnesthesiaPaciente crónico complejo. Clinical method. When to suspect a genetic disease?Family history.Red flags of neurodevelopment (red flags).Bibliography essential for the consultation of pediatric neurology.Clonus ankle.Deformities of the skull.Development of the drawing.Sleep development.Motor development.Normal development of the game.Socio-emotional development.Corrected age and prematurity.Elements of morphology.Scale of strength MRC.Scales of infant development.Exploration dismorfológica.Exploration neurocutaneous.Neurological examination of more than 3 years:Neurological examination of the child.Exploration neurooftalmológica pediatric Neurological diseases. When do you suspect an error congenital metabolism?ARX gene.Ataxia congénita no progresiva.Base de datos SCNx.Beyond The Pediatric Epilepsy Program.Bilirrubin induced neurological dysfunction (spectrum disorders, encephalopathy by bilirubin).BIS.CDG roadmap.CdL facial phenotypes.Child Muscle WeaknessCytomegalovirus congenital.Classification of epilepsies of the ILAE Task Force.Coenzyme Q10 (Decorenone).Comparador de farmacocinética de fármacos estimulantes para el TDAH.Newborn screening for SMA.Crisis benign-associated gastroenteritis.Febrile seizures. Infographics.Criteria for the diagnosis of cerebral palsy child.Diagnostic criteria of ASD.Criteria to be attributed causally to the cerebral palsy at an event perinatal. Complementary explorations. When to suspect a genetic disease?Family history.ARX gene.Base de datos SCNx.Beyond The Pediatric Epilepsy Program.Karyotype in the era of the aCGH:CdL facial phenotypes.How to understand a report of sequencing.ConsanguinityNewborn screening for SMA.Criterios de patogenicidad de la ACMG.Criteria of realization of aCGH.Cromatinopatías.Chromosomes in the ring.Decipher Genome BrowserGross deletions intragenic (exon-level deletions).Distonías genéticas con tratamiento «curativo».Double trouble. Several genetic diseases in the same individual.Transmissible epilepsy and development.Genetic diseases in minoritary populations. Administrative procedures.What do you need college to a report neuropediátrico?What you need to the pediatric neurologist a school report?Ayudas técnicas.Scholarships and grants MEyFPEncodings diagnostic.Informed consent for exchange of information.Dependence.Disability.Education based on the evidence.The children with academic problems.The children with conduct problems.Guide for teachers on child neurology.Report neuropediátrico.Internet secure for kids.Drugs and school.PATI (personal Assistant).Procedure for referral to a CSUR and SIFCOProcedure for the application of 2nd medical opinionProcedure for the application of free choice of doctor.Recursos del área de sagunto. Treatments.Early CareCoenzyme Q10 (Decorenone).Deformidades esqueléticas en parálisis cerebral.Corrected age and prematurity.Clinical TrialsStrategy of Acquired Brain InjuryAntiepileptic drugs.Master formulaSlt health.Orphan drugsNeurorehabilitación en PCI. Evidencia científica.Orphan AnesthesiaPCI: Treatments with scientific evidence.Protocolo de osteoporosis:Pseudotherapies.Recursos del área de sagunto.Therapeutic resources and non-drug for children with t. neurodevelopmental disorders.Network of associations of Camp de Morvedre.Technologies aumentativas and alternative communication.Compassionate use, medication, foreign and drug use out-of-specification (out-of-the technical data sheet). Entries recently published Mecanismos en AED.Comparador de farmacocinética de fármacos estimulantes para el TDAH.Evidencia científica en tratamientos para el TDAH.Parálisis cerebral infantil y RM normal.Recursos del área de sagunto.KCNx databases.Protocolo de osteoporosis:Pobreza y discapacidad.Riesgo en paises destino de viaje.Estados y sistemas de salud.Enfermedades prevenibles mediante la vacunación.Síntomas que incrementan la probabilidad de diagnóstico en NGS (yield).Tareas para explorar trastornos del movimiento.Wicked spikes.ARX gene.CdL facial phenotypes.Distrofias musculares congénitas.Estadios del síndrome de Rett.M-wave, H-wave, F-wave.Diagrama de Reiber
