Hypochondroplasia and temporal lobe epilepsy – A series of 4 cases-Reference-Cited by-同舟云学术

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Hypochondroplasia and temporal lobe epilepsy – A series of 4 cases

Published:2022-01 Issue: Volume:126 Page:108479
ISSN:1525-5050
Container-title:Epilepsy & Behavior
language:en
Short-container-title:Epilepsy & Behavior

Author:

Ahmadi Mehdi,Herting Arne,Mueffelmann Birgitt,Woermann Friedrich G.,Abou Jamra Rami,Bien Christian G.,Polster Tilman,Brandt Christian

Publisher

Elsevier BV

Subject

Behavioral Neuroscience,Neurology (clinical),Neurology

Reference20 articles.

1. Clinical and genetic heterogeneity of hypochondroplasia;Rousseau;J Med Genet,1996

2. Hypochondroplasia: molecular analysis of the fibroblast growth factor receptor 3 gene;Bellus;Ann N Y Acad Sci,1996

3. Medial temporal lobe dysgenesis in hypochondroplasia;Kannu;Am J Med Genet.,2005

4. FGFR3 mutations and medial temporal lobe dysgenesis;Kannu;J Child Neurol.,2007

5. Neuroimagining and neurological findings in patients with hypochondroplasia and FGFR3 mutation;Linnankivi;Am J Med Genet.,2012

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Chronic traumatic encephalopathy-neuropathologic change in a routine neuropathology service: 7-year follow-up;Journal of Neuropathology & Experimental Neurology;2023-10-16

2. Molecular Basis for Hypochondroplasia in Japan;Endocrines;2022-07-22

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