Genetic analysis of a family presenting with coexisting cerebral cavernous malformations and polycystic kidney disease-Reference-Cited by-同舟云学术

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Genetic analysis of a family presenting with coexisting cerebral cavernous malformations and polycystic kidney disease

Published:2022-11 Issue:11 Volume:121 Page:2331-2337
ISSN:0929-6646
Container-title:Journal of the Formosan Medical Association
language:en
Short-container-title:Journal of the Formosan Medical Association

Author:

Hsieh Pei-Feng^ORCID,Liu Shih-Yao,Chen Chih-Hao^ORCID,Chen Pei-Lung,Tang Sung-Chun^ORCID,Jeng Jiann-Shing

Publisher

Elsevier BV

Subject

General Medicine

Reference25 articles.

1. Mutation analysis of ccm 1, ccm 2 and ccm 3 genes in a cohort of Italian patients with cerebral cavernous malformation;D'Angelo;Brain Pathol,2011

2. Synopsis of guidelines for the clinical management of cerebral cavernous malformations: consensus recommendations based on systematic literature review by the angioma alliance scientific advisory board clinical experts panel;Akers;Neurosurgery,2017

3. Mutations within the programmed cell death 10 gene cause cerebral cavernous malformations;Bergametti;Am J Hum Genet,2005

4. Polycystic kidney disease;Bergmann;Nat Rev Dis Prim,2018

5. Genetic complexity of autosomal dominant polycystic kidney and liver diseases;Cornec-Le Gall;J Am Soc Nephrol,2018

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