Moyamoya disease in two patients with Noonan-like syndrome with loose anagen hair

Author:

Lo Fu-Sung1,Wang Chao-Jan2,Wong Mun-Ching2,Lee Ni-Chung3

Affiliation:

1. Division of Pediatric Endocrinology and Genetics; Department of Pediatrics; Chang-Gung Memorial Hospital and Chang Gung University College of Medicine; Taoyuan Taiwan

2. Department of Medical Imaging and Intervention; Chang-Gung Memorial Hospital and Chang Gung University College of Medicine; Taoyuan Taiwan

3. Department of Pediatrics and Medical Genetics; National Taiwan University Hospital; Taipei Taiwan

Funder

Chang Gung Memorial Hospital

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Cited by 19 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. Central nervous system involvement in individuals with RASopathies;American Journal of Medical Genetics Part C: Seminars in Medical Genetics;2022-12

2. The role of USP7 in the Shoc2-ERK1/2 signaling axis and Noonan-like syndrome with loose anagen hair;Journal of Cell Science;2021-11-01

3. Cutaneous manifestations in Moyamoya angiopathy: A review;European Journal of Neurology;2021-03

4. Pediatric Neurovascular Conditions;Pediatric Vascular Neurosurgery;2021

5. Moyamoya syndrome in a child with Legius syndrome: Introducing a cerebral vasculopathy to the SPRED1 phenotype?;American Journal of Medical Genetics Part A;2020-10-20

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