Temporal lobe malformations, focal epilepsy, and FGFR3 mutations: a non-causal association?-Reference-Cited by-同舟云学术

Temporal lobe malformations, focal epilepsy, and FGFR3 mutations: a non-causal association?

Published:2021-01-03 Issue:5 Volume:42 Page:2063-2067
ISSN:1590-1874
Container-title:Neurological Sciences
language:en
Short-container-title:Neurol Sci

Author:

Bernardo Pia^ORCID,Budetta Mauro,Aliberti Ferdinando,Carpentieri Maria Luisa,De Brasi Daniele,Sorrentino Livio,Russo Carmela,D’amico Alessandra,Cinalli Giuseppe,Santoro Claudia,Coppola Antonietta

Publisher

Springer Science and Business Media LLC

Subject

Psychiatry and Mental health,Neurology (clinical),Dermatology,General Medicine

Link

https://link.springer.com/content/pdf/10.1007/s10072-020-04923-3.pdf

Reference10 articles.

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2. Kannu P, Hayes IM, Mandelstam S, Donnan L, Savarirayan R (2005) Medial temporal lobe dysgenesis in hypochondroplasia. Am J Med Genet A 138:389–391

3. Kannu P, Aftimos S (2007) FGFR3 mutations and medial temporal lobe dysgenesis. J Child Neurol 22:211–213

4. Grosso S, Farnetani MA, Berardi R, Bartalini G, Carpentieri M, Galluzzi P, Mostardini R, Morgese G, Balestri P (2003) Medial temporal lobe dysgenesis in Muenke syndrome and hypochondroplasia. Am J Med Genet A 120A(1):88–91

5. Linnankivi T, Mäkitie O, Valanne L, Toiviainen-Salo S (2012) Neuroimaging and neurological findings in patients with hypochondroplasia and FGFR3 N540K mutation. Am J Med Genet A 158A:3119–3125

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