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Autosomal dominant cerebellar ataxia deafness and narcolepsy

Published:1995-12 Issue:1-2 Volume:134 Page:119-129
ISSN:0022-510X
Container-title:Journal of the Neurological Sciences
language:en
Short-container-title:Journal of the Neurological Sciences

Author:

Melberg Atle,Hetta Jerker,Dahl Niklas,Nennesmo Inger,Bengtsson Mats,Wibom Rolf,Grant Crawford,Gustavson Karl Henrik,Lundberg Per Olov

Publisher

Elsevier BV

Subject

Clinical Neurology,Neurology

Reference41 articles.

1. Activities of citrate synthase and NAD+-linked and NADP+-linked isocitrate dehydrogenase in muscle from vertebrates and invertebrates;Alp;Biochem. J.,1976

2. Comparative polysomnographic study of narcolepsy and idiopathic central nervous system hypersomnia;Baker;Sleep,1986

3. Genetic study of the narcoleptic syndrome;Baraitser;J. Med. Genet.,1978

4. Autosomal dominant late onset cerebellar ataxia with myoclonus, peripheral neuropathy and sensorineural deafness: a clinicopathological report;Baraitser;J. Neurol. Neurosurg. Psychiat.,1984

5. Heredofamilial aspects of narcolepsy and hypersomnia;Bruhova;Arch. Suisse Neurol. Neurochir. Psychiat.,1972

Cited by 39 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. First case of autosomal dominant cerebellar ataxia with deafness and narcolepsy (ADCA-DN) with confirmed DMNT1 gene mutation in Spain. Review of the DMNT1 mutation syndromes;Neurological Sciences;2023-10-13

2. Mutations in human DNA methyltransferase DNMT1 induce specific genome-wide epigenomic and transcriptomic changes in neurodevelopment;Human Molecular Genetics;2023-08-16

3. Mitochondrial transport and metabolism of the major methyl donor and versatile cofactor S‐adenosylmethionine, and related diseases: A review ^†;IUBMB Life;2022-06-22

4. The orexin story, sleep and sleep disturbances;Journal of Sleep Research;2022-06-13

5. Cerebellar Ataxia as a Common Clinical Presentation Associated with DNMT1 p.Y511H and a Review of the Literature;Journal of Molecular Neuroscience;2021-01-12

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