R147W in PROC Gene Is a Risk Factor of Thromboembolism in Thai Children-Reference-Cited by-同舟云学术

R147W in PROC Gene Is a Risk Factor of Thromboembolism in Thai Children

Published:2017-05-17 Issue:2 Volume:24 Page:263-267
ISSN:1076-0296
Container-title:Clinical and Applied Thrombosis/Hemostasis
language:en
Short-container-title:Clin Appl Thromb Hemost

Author:

Sirachainan Nongnuch¹,Chuansumrit Ampaiwan¹,Sasanakul Werasak¹,Yudhasompop Najwa¹²,Mahaklan Lalita¹,Vaewpanich Jarin¹,Charoenkwan Pimlak³,Kanjanapongkul Somjai⁴,Visudtibhan Anannit¹,Wongwerawattanakoon Pakawan⁵

Affiliation:

1. Faculty of Medicine, Department of Pediatrics, Ramathibodi Hospital, Mahidol University, Bangkok, Thailand

2. Department of Pediatrics, Hatyai Hospital, Hatyai, Songkhla, Thailand

3. Faculty of Medicine, Department of Pediatrics, Chiang Mai University, Chiang Mai, Thailand

4. Department of Pediatrics, Queen Sirikit National Institute of Child Health, Bangkok, Thailand

5. Faculty of Medicine, Division of Pediatric Nursing, Nursing Department, Ramathibodi Hospital, Bangkok, Thailand

Funder

Thailand Research Fund

Publisher

SAGE Publications

Subject

Hematology,General Medicine

Link

http://journals.sagepub.com/doi/pdf/10.1177/1076029617709085

Reference18 articles.

1. VENOUS THROMBOEMBOLISM IN THAI CHILDREN

2. Protein S and protein C gene mutations in Japanese deep vein thrombosis patients

3. Risk factors of venous thromboembolism in Thai patients

4. Prothrombotic Risk Factors in Children with Spontaneous Venous Thrombosis and Their Asymptomatic Parents

5. Identification of mutations in 15 Hungarian families with hereditary protein C deficiency

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1. Analysis of PROC mutations and clinical features in 22 unrelated families with inherited protein C deficiency;Annals of Hematology;2023-11-10

2. Evaluation of prothrombotic risk of two PROC hotspot mutations (Arg189Trp and Lys193del) in Chinese population: a retrospective study;Thrombosis Journal;2023-10-03

3. Case report: Severe nonketotic hyperglycinemia in a neonate without apparent seizures but concomitant cleft palate and cerebral sinovenous thrombosis;Frontiers in Pediatrics;2023-08-08

4. Identification of Alpha Thalassemia, RNF 213 p.R4810K and PROC p.R189W among Children with Moyamoya Disease/Syndrome;Mediterranean Journal of Hematology and Infectious Diseases;2022-06-29

5. Racial differences in protein S Tokushima and two protein C variants as genetic risk factors for venous thromboembolism;Research and Practice in Thrombosis and Haemostasis;2020-10-20