Convulsion and cerebellar ataxia associated with maternally inherited diabetes and deafness: a case report
Author:
Affiliation:
1. Department of Neurology Toho University Ohashi Medical Center Tokyo Japan
Publisher
Wiley
Subject
General Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ccr3.309
Reference17 articles.
1. Mutation in mitochondrial tRNALeu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness
2. Clinical features, diagnosis and management of maternally inherited diabetes and deafness (MIDD) associated with the 3243A>G mitochondrial point mutation
3. Maternally Inherited Diabetes and Deafness: A Multicenter Study
4. A Mother and a Child with Maternally Inherited Diabetes and Deafness (MIDD) Showing Atrophy of the Cerebrum, Cerebellum and Brainstem on Magnetic Resonance Imaging (MRI)
5. Brain anomalies in maternally inherited diabetes and deafness syndrome
Cited by 3 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. Mitochondrial Ataxias: Molecular Classification and Clinical Heterogeneity;Neurology International;2022-04-02
2. NEUROLOGINĖ PATOLOGIJA SERGANT 2 TIPO CUKRINIU DIABETU;Medicinos teorija ir praktika;2017-01-10
3. Maternally Inherited Diabetes and Deafness is Phenotypically and Genotypically Heterogeneous;Journal of Neuro-Ophthalmology;2016-09
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