Literature DB >> 26422091

X-linked moyamoya syndrome associated with severe haemophilia A.

M Lavin1,2, P V Jenkins1,2, C Keenan2, B White1,2, D R Betts3, J S O'Donnell1,2, N M O'Connell1,2.   

Abstract

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Year:  2015        PMID： 26422091     DOI： 10.1111/hae.12806

Source DB:  PubMed          Journal:  Haemophilia        ISSN： 1351-8216            Impact factor:   4.287


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  4 in total

1.  Probable Moyamoya Syndrome in Association with Hemophilia A in an Infant.

Authors:  Arushi Gahlot Saini; Jyotindra Narayan Goswami; Renu Suthar; Naveen Sankhyan; Sameer Vyas; Pratibha Singhi
Journal:  Indian J Pediatr       Date:  2016-09-15       Impact factor: 1.967

2.  Severe Hemophilia A and Moyamoya Syndrome in a 19-Year-Old Boy Caused by Xq28 Microdeletion.

Authors:  Evangelia Tzeravini; Stamatia Samara; Anna Kouramba; Georgios Vakrinos; Athina Efthimiou; Maria Tzetis; Theodoros Androutsakos
Journal:  Case Rep Neurol       Date:  2022-05-30

3.  Deletion of FUNDC2 and CMC4 on Chromosome Xq28 Is Sufficient to Cause Hypergonadotropic Hypogonadism in Men.

Authors:  Xinxian Deng; He Fang; Asha Pathak; Angela M Zou; Whitney Neufeld-Kaiser; Emily A Malouf; Richard A Failor; Fuki M Hisama; Yajuan J Liu
Journal:  Front Genet       Date:  2020-09-22       Impact factor: 4.599

Review 4.  Western Moyamoya Phenotype: A Scoping Review.

Authors:  Raphael Miller; Santiago R Unda; Ryan Holland; David J Altschul
Journal:  Cureus       Date:  2021-11-22
  4 in total

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