Congenital Amegakaryocytic Thrombocytopenia Type II Presenting with Multiple Central Nervous System Anomalies-Reference-Cited by-同舟云学术

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Congenital Amegakaryocytic Thrombocytopenia Type II Presenting with Multiple Central Nervous System Anomalies

Published:2016-02-08 Issue:02 Volume:47 Page:128-131
ISSN:0174-304X
Container-title:Neuropediatrics
language:en
Short-container-title:Neuropediatrics

Author:

Versluys Anne¹,Stokman Marijn²,van der Crabben Saskia²,Nij Bijvank Sebastiaan³,van Wezel-Meijler Gerda⁴,Eshuis-Peters Ellis⁵

Affiliation:

1. Department of Pediatric Hematology, University Medical Center Utrecht, Wilhelmina Children's Hospital, Utrecht, The Netherlands

2. Department of Medical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands

3. Department of Obstetrics and Gynaecology, Isala, Zwolle, The Netherlands

4. Department of Neonatology, Isala, Zwolle, The Netherlands

5. Department of Neonatology, University Medical Center Utrecht, Wilhelmina Children's Hospital, Utrecht, The Netherlands

Publisher

Georg Thieme Verlag KG

Subject

Clinical Neurology,General Medicine,Pediatrics, Perinatology, and Child Health

Link

http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0036-1571800.pdf

Cited by 8 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. Congenital amegakaryocytic thrombocytopenia presenting with a new thrombopoietin receptor (MPL) pathogenic variant: An instructive neonatal case;Journal of Paediatrics and Child Health;2022-08-16

2. COL4A1/COL4A2 and inherited platelet disorder gene variants in fetuses showing intracranial hemorrhage;Prenatal Diagnosis;2022-02-20

3. Risk and Management of Intracerebral Hemorrhage in Patients with Bleeding Disorders;Seminars in Thrombosis and Hemostasis;2022-01-06

4. Congenital amegakaryocytic thrombocytopenia – Not a single disease;Best Practice & Research Clinical Haematology;2021-06

5. Pure Red Cell Aplasia (PRCA) and Cerebellar Hypoplasia as Atypical Features of Polyglandular Autoimmune Syndrome Type I (APS-1): Two Sisters With the Same AIRE Mutation but Different Phenotypes;Frontiers in Pediatrics;2019-02-26

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