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1. Quick, Effective Screening Tasks Identify Children With Medical Conditions or Disabilities Needing Physical Literacy Support.

3. Developmental epileptic encephalopathy in DLG4-related synaptopathy

4. Quick, Effective Screening Tasks Identify Children With Medical Conditions or Disabilities Needing Physical Literacy Support

5. A multi-centre, tolerability study of a cannabidiol-enriched Cannabis Herbal Extract for chronic headaches in adolescents: The CAN-CHA protocol.

6. SÍNDROME DE ANGELMAN: ABORDAJE ACTUAL Y EL FUTURO DE LAS TERAPIAS.

7. Understanding the physical literacy development of 8‐ to 12‐year‐old children living with chronic medical conditions: A comprehensive, mixed methods inquiry.

8. Developmental epileptic encephalopathy in DLG4‐related synaptopathy

9. A Multi-Centre, Tolerability Study of a Cannabidiol-enriched Cannabis Herbal Extract for Chronic Headaches in Adolescents: the CAN-CHA Protocol

11. O20: The natural history of Angelman syndrome: Sixteen years and 450 individuals later…*

14. Intracranial Calcifications and Ocular Abnormalities in a Child with Neurodevelopmental Delay

15. A De Novo Missense Variant in TUBG2 in a Child with Global Developmental Delay, Microcephaly, Refractory Epilepsy and Perisylvian Polymicrogyria.

17. Potential Benefit of Add-on Δ9-Tetrahydrocannabinol in Pediatric Drug-Resistant Epilepsy: A Case Series

19. Characterization of physical literacy in children with chronic medical conditions compared with healthy controls: a cross-sectional study

27. teenager with ocular signs after tongue injury.

28. Potential Benefit of Add-on Δ9-Tetrahydrocannabinol in Pediatric Drug-Resistant Epilepsy: A Case Series

29. The impact of electronic consultation on a Canadian tertiary care pediatric specialty referral system: A prospective single-center observational study

31. Neonatal encephalopathy: Case definition & guidelines for data collection, analysis, and presentation of maternal immunisation safety data

32. Congenital microcephaly: Case definition & guidelines for data collection, analysis, and presentation of safety data after maternal immunisation

41. Matchmaking facilitates the diagnosis of an autosomal-recessive mitochondrial disease caused by biallelic mutation of the tRNA isopentenyltransferase ( TRIT1) gene.

49. Broad spectrum of neuropsychiatric phenotypes associated with white matter disease in PTENhamartoma tumor syndrome

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