Prognostic Challenges of SCN1A Genetic Mutations: Report on Two Children with Mild Features-Reference-Cited by-同舟云学术

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Prognostic Challenges of SCN1A Genetic Mutations: Report on Two Children with Mild Features

Published:2016-04-28 Issue:02 Volume:14 Page:082-088
ISSN:1304-2580
Container-title:Journal of Pediatric Neurology
language:en
Short-container-title:J Pediatr Neurol

Author:

Falsaperla Raffaele¹,Ruggieri Martino²,Corsello Giovanni³,Pavone Piero¹,Praticò Andrea²

Affiliation:

1. University-Hospital “Policlinico-Vittorio Emanuele,” University of Catania, Catania, Italy

2. Department of Clinical and Experimental Medicine, University of Catania, Catania, Italy

3. Department of Sciences for Health Promotion and Mother and Child Care, Pediatric Unit, University of Palermo, Palermo, Italy

Publisher

Georg Thieme Verlag KG

Subject

Clinical Neurology,Pediatrics, Perinatology, and Child Health

Link

http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0036-1583274.pdf

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2. Lissencephaly, Pachygyrias, Band Heterotopias, RELN Pathway, and ARX Mutations (Incomplete Neuron Migration);Journal of Pediatric Neurology;2024-05-11

3. Focal Cortical Dysplasia: Diagnosis, Classification, and Treatment Options;Journal of Pediatric Neurology;2024-04

4. Malformations of the Cerebral Commissures;Journal of Pediatric Neurology;2024-04

5. SLC2A1 and Its Related Epileptic Phenotypes;Journal of Pediatric Neurology;2021-06-01

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