Pontocerebellar hypoplasia type 2: a neuropathological update-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Pontocerebellar hypoplasia type 2: a neuropathological update

Published:2007-07-20 Issue:4 Volume:114 Page:373-386
ISSN:0001-6322
Container-title:Acta Neuropathologica
language:en
Short-container-title:Acta Neuropathol

Author:

Barth Peter G.,Aronica Eleonora,de Vries Linda,Nikkels Peter G. J.,Scheper Wiep,Hoozemans Jeroen J.,Poll-The Bwe - Tien,Troost Dirk

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Clinical Neurology,Pathology and Forensic Medicine

Link

https://link.springer.com/content/pdf/10.1007/s00401-007-0263-0.pdf

Reference46 articles.

1. Aalfs CM, van den Berg H, Barth PG, Hennekam RCM (1995) The Høyeraal-Hreidarsson syndrome: the fourth case of a separate entity with prenatal growth retardation, progressive pancytopenia and cerebellar hypoplasia. Eur J Pediatr 154:304–308

2. Aronica E, van Kempen AA, van der Heide M, Poll-The BT, van Slooten HJ, Troost D, Rozemuller-Kwakkel JM (2005) Congenital disorder of glycosylation type Ia: a clinicopathological report of a newborn infant with cerebellar pathology. Acta Neuropathol (Berl) 109:433–442

3. Albrecht S, Schneider MC, Belmont J, Armstrong DL (1993) Fatal infantile encephalopathy with olivopontocerebellar hypoplasia and micrencephaly. Acta Neuropathol 85:394–399

4. Arts WFM, Hofstee Y, Drejer GF, Beverstock GC, Oosterwijk JC (1995) Cerebellar and brainstem hypoplasia in a child with a partial monosomy for the short arm of chromosome 5 and partial trisomy for the short arm of chromosome 10. Neuropediatrics 26:41–44

5. Barth PG, Vrensen GFJM, Uylings HBM, Oorthuys JWE, Stam FC (1990) Inherited syndrome of microcephaly, dyskinesia and pontocerebellar hypoplasia: a systemic atrophy with early onset. J Neurol Sci 97:25–42

Cited by 68 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. Pontocerebellar hypoplasia caused by the TSEN54 mutation: clinical and electroencephalographic characteristics based on 3 cases;Russian Journal of Child Neurology;2024-07-18

2. Human organoid model of pontocerebellar hypoplasia 2a recapitulates brain region-specific size differences;Disease Models & Mechanisms;2024-07-01

3. Prenatal diagnosis of pontocerebellar hypoplasia with postnatal follow‐up;Prenatal Diagnosis;2024-01

4. The PARN, TOE1, and USB1 RNA deadenylases and their roles in non-coding RNA regulation;Journal of Biological Chemistry;2023-09

5. Development and Developmental Disorders of the Human Cerebellum;Clinical Neuroembryology;2023

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号京ICP备18003416号-3