A familial case of diffuse periventricular nodular heterotopia identified prenatally: Filamin A defect as the probable cause-Reference-Cited by-同舟云学术

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A familial case of diffuse periventricular nodular heterotopia identified prenatally: Filamin A defect as the probable cause

Published:2024-11 Issue:11 Volume:19 Page:5393-5398
ISSN:1930-0433
Container-title:Radiology Case Reports
language:en
Short-container-title:Radiology Case Reports

Author:

Neves Mariana Tomásio,Borges André Luís^ORCID,Martins Guilherme^ORCID,Sá Graça,Loureiro Teresa,Moldovan Oana^ORCID

Publisher

Elsevier BV

Reference14 articles.

1. Gray matter heterotopia;Barkovich;Neurology,2000

2. The epilepsy phenome/genome project;Collaborative;Clin Trials,2013

3. Periventricular heterotopia: phenotypic heterogeneity and correlation with Filamin A mutations;Parrini;Brain,2006

4. Gray matter volumes and cognitive ability in the epileptogenic brain malformation of periventricular nodular heterotopia;Walker;Epilepsy Behavior,2009

5. X-linked hereditary periventricular nodular heterotopia;Angulo-Maldonado;Neurologia (Engl Ed),2022

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