28 results on '"Soto-Insuga, Víctor"'
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2. Anatomo-Electro-Clinical Phenotypes in Children With Epilepsy and DYNC1H1 Mutations
3. Smell and Taste Dysfunction in Pediatric Patients With SARS-CoV-2 Infection
4. Fanconi Syndrome Secondary to Sodium Valproate Therapy: Experience and Literature Review
5. Efficacy of Brivaracetam in children with epilepsy
6. Utility of the transcranial doppler in the evaluation and follow-up of children with Sturge-Weber Syndrome
7. Associations of paediatric demyelinating and encephalitic syndromes with myelin oligodendrocyte glycoprotein antibodies: a multicentre observational study
8. Developmental outcome of electroencephalographic findings in SYNGAP1 encephalopathy
9. L-serine treatment in patients with GRIN-related encephalopathy: A phase 2A, non-randomized study
10. Frequency, symptoms, risk factors, and outcomes of autoimmune encephalitis after herpes simplex encephalitis: a prospective observational study and retrospective analysis
11. Do children with attention deficit and hyperactivity disorder (ADHD) have a different gait pattern? Relationship between idiopathic toe-walking and ADHD
12. ¿Caminan de manera diferente los niños con trastorno por déficit de atención hiperactividad (TDAH)? Relación entre marcha de puntillas idiopática y TDAH
13. Relationship Between Epileptic Activity and Developmental Outcome in KCNQ2-Related Epilepsy
14. Relationship Between Epileptic Activity and Developmental Outcome in KCNQ2-Related Epilepsy
15. Insomnia in children and adolescents. A consensus document
16. Insomnio en niños y adolescentes. Documento de consenso
17. Paradigmatic De Novo GRIN1 Variants Recapitulate Pathophysiological Mechanisms Underlying GRIN1-Related Disorder Clinical Spectrum
18. Sodium channel blockers for the treatment of epilepsy in CDKL5 deficiency disorder: Findings from a multicenter cohort
19. Critical Illness Myopathy in a Child with SARS-CoV-2 Infection
20. Disease-associated GRIN protein truncating variants trigger NMDA receptor loss-of-function
21. Glut1 deficiency is a rare but treatable cause of childhood absence epilepsy with atypical features
22. Disease-associated GRIN protein truncating variants trigger NMDA receptor loss-of-function
23. Associations of paediatric demyelinating and encephalitic syndromes with myelin oligodendrocyte glycoprotein antibodies: a multicentre observational study
24. Análisis de utilidad del estudio genético en las epilepsias percibido por familiares y personal médico
25. Frequency, symptoms, risk factors, and outcomes of autoimmune encephalitis after herpes simplex encephalitis: a prospective observational study and retrospective analysis
26. ¿Caminan de manera diferente los niños con trastorno por déficit de atención hiperactividad (TDAH)? Relación entre marcha de puntillas idiopática y TDAH
27. Disease-associated GRIN protein truncating variants trigger NMDA receptor loss-of-function.
28. [Analysis of a series of cases with an initial diagnosis of acute disseminated encephalomyelitis over the period 2000-2010].
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