A hereditary moyamoya syndrome with multisystemic manifestations-Reference-Cited by-同舟云学术

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A hereditary moyamoya syndrome with multisystemic manifestations

Published:2010-07-19 Issue:3 Volume:75 Page:259-264
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Herve D.,Touraine P.,Verloes A.,Miskinyte S.,Krivosic V.,Logeart D.,Alili N.,Laredo J. D.,Gaudric A.,Houdart E.,Metzger J. P.,Tournier-Lasserve E.,Woimant F.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 40 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. Optical genome mapping with genome sequencing identifies subtelomeric Xq28 deletion and inserted 7p22.3 duplication in a male with multisystem developmental disorder;American Journal of Medical Genetics Part A;2024-07-16

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3. Other Monogenetic Stroke Disorders;Stroke Genetics;2024

4. An Endocrine Perspective of Juvenile Moyamoya Syndrome/Disease;Medical Journal of Babylon;2023-01

5. Hypogonadism in Males With Genetic Neurodevelopmental Syndromes;The Journal of Clinical Endocrinology & Metabolism;2022-08-01

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