A case report of a Chinese patient with 22q11.2 deletion accompanied with EOPD, severe dystonia and hypocalcemia-Reference-Cited by-同舟云学术

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A case report of a Chinese patient with 22q11.2 deletion accompanied with EOPD, severe dystonia and hypocalcemia

Published:2019 Issue: Volume:1 Page:72-73
ISSN:2590-1125
Container-title:Clinical Parkinsonism & Related Disorders
language:en
Short-container-title:Clinical Parkinsonism & Related Disorders

Author:

Hu Zheng-Xiang,Lu Xiao-Dong,Lou Dan-Ning,Zhou Meng-Lu,Zhu Qian-Ru,Luo Shan-Shan,Chen Mei-Yuan

Funder

Medical and Health Science and Technology Foundation of Zhejiang Province

Publisher

Elsevier BV

Subject

General Medicine

Reference5 articles.

1. Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association data;Mok;Lancet Neurol.,2016

2. Allele-specific quantification of structural variations in cancer genomes;Li;Cell Systems,2016

3. A rare case of idiopathic hypoparathyroidism with varied neurological manifestations;Abe;Intern. Med.,1996

4. Association between Early-Onset Parkinson Disease and 22q11.2 deletion syndrome: identification of a novel genetic form of Parkinson Disease and its clinical implications;Butcher;JAMA Neurol.,2013

5. Large 3-Mb deletions at 22q11.2 locus in Parkinson's disease and schizophrenia;Foo;Mov. Disord.,2016

Cited by 2 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. Updated clinical practice recommendations for managing adults with 22q11.2 deletion syndrome;Genetics in Medicine;2023-03

2. Levodopa/benserazide;Reactions Weekly;2020-02

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