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Updated: Jun 27, 2025

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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Moyamoya syndrome in a patient with D-2-hydroxyglutaric aciduria type II: a rare association

Tobias Kühnl1, Elke Januschek2, Sana Klinikum Offenbach2

  • 1Department of Neurosurgery, Offenbach, Hessen, Germany. tobias.kuehnl@sana.de.

Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|April 26, 2024
PubMed
Abstract

Keywords:
D-2-Hydroxyglutaric aciduria type IIEDAMSMoyamoya syndrome

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