Zobrazeno 1 - 10
of 379
pro vyhledávání: '"van TA, To"'
Autor:
Vu Viet Ha Vuong, Phuoc-Dung Nguyen, Nha Nguyen Thi, Phuong Le Thi, Dang Thi Minh Nguyet, Manh Ha Nguyen, Hai Anh Tran, Nhat-Minh Dang-Tran, The-Hung Bui, Thinh Huy Tran, Thanh Van Ta, Van-Khanh Tran
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 63, Iss 3, Pp 375-380 (2024)
Objectives: α-thalassemia is an autosomal recessive monogenic blood disorder, affecting up to 5% of the world's population. The occurrence rate of the disease in Vietnam varies up to up to 51.5%, with high rate of mutation carriers, of couples consi
Externí odkaz:
https://doaj.org/article/97b2709f55004b258e4dd79714c5b636
Autor:
Oanh L. Meyer, Sarah Tomaszewski Farias, Rachel A. Whitmer, Alka M. Kanaya, Danielle Harvey, Ladson Hinton, Quyen Q. Tiet, Quyen Vuong, Brandon Gavett, Van Ta Park
Publikováno v:
Alzheimer’s & Dementia: Translational Research & Clinical Interventions, Vol 10, Iss 3, Pp n/a-n/a (2024)
Abstract Introduction There is a dearth of research on cognitive aging and dementia in Asian Americans, particularly in Vietnamese Americans, the fourth largest Asian subgroup in the United States. Methods The Vietnamese Insights into Cognitive Aging
Externí odkaz:
https://doaj.org/article/a148e9a9b4b54fa58a864971b9270ace
Autor:
Van Khanh Tran, My Ha Cao, Thi Thanh Hai Nguyen, Phuong Thi Le, Hai Anh Tran, Dung Chi Vu, Ha Thu Nguyen, Mai Thi Phương Nguyen, The-Hung Bui, Thanh Binh Nguyen, Thanh Van Ta, Thinh Huy Tran
Publikováno v:
Frontiers in Pediatrics, Vol 12 (2024)
BackgroundPathogenic variants in the IGHMBP2 gene are associated with two distinct autosomal recessive neuromuscular disorders: spinal muscular atrophy with respiratory distress type 1 (SMARD1; OMIM #604320) and Charcot–Marie–Tooth type 2S (CMT2S
Externí odkaz:
https://doaj.org/article/34e601b1ab524311b5ad6983acea6d57
Autor:
Hung Manh Pham, Duy Phuong Dang, Thanh Dat Ta, Thi Phuong Le, Dinh Phong Phan, Hoai An Trinh, Tuan Viet Tran, Thi Lan Anh Luong, Ha Minh Nguyen, The‐Hung Bui, Thinh Huy Tran, Thanh Van Ta, Van‐Khanh Tran
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 11, Iss 12, Pp n/a-n/a (2023)
Abstract Background Brugada syndrome (BrS) is a rare genetic disease that causes sudden cardiac death (SCD) and arrhythmia. SCN5A pathogenic variants (about 30% of diagnosed patients) are responsible for BrS. Aims Lack of knowledge regarding molecula
Externí odkaz:
https://doaj.org/article/0f0b031ef8d4428c9c6d5ec81044eadf
Autor:
Dao Nguyen Ha Linh, Nguyen Van Huy, Phuoc‐Dung Nguyen, Phuong Le Thi, Hoang Anh Tuan, Trong Van Nguyen, Thu Ha Tran, Hai Anh Tran, Thanh Dat Ta, Tuan L. A. Pham, The‐Hung Bui, Thinh Huy Tran, Thanh Van Ta, Van‐Khanh Tran
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 11, Iss 11, Pp n/a-n/a (2023)
Abstract Background Retinoblastoma (RB), an intraocular malignancy commonly diagnosed in children, is mostly caused by inactivating mutations of both alleles of the RB1 gene. Early genetic screening for RB1 gene mutations would greatly improve treatm
Externí odkaz:
https://doaj.org/article/6aa8a8dd1de147cc936ffd732b2f07dd
Autor:
Do, Van-Ta, Chun, Doo-Man
Publikováno v:
In Colloids and Surfaces A: Physicochemical and Engineering Aspects 20 August 2023 671
Autor:
Thi Minh Phuong Bui, Van Khanh Tran, Thi Thanh Hai Nguyen, Thi Phuong Le, Thi Mai Nguyen, Hai Anh Tran, Vu Dung Luu, Manh Ha Nguyen, The-Hung Bui, Thanh Van Ta, Thinh Huy Tran
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 61, Iss 6, Pp 1009-1014 (2022)
Objective: Hemophilia A (HA) is an X-linked recessive bleeding disease caused by a deficiency or dysfunction of blood coagulation factor VIII (FVIII). Available treatment to replenish the missing factor may not reach a good outcome for all patients b
Externí odkaz:
https://doaj.org/article/d37e2a63a61e4e1da8201b46278843f0
Autor:
Tiffany W Chow, Hyun-Sik Yang, Haeok Lee, Hoehun Ha, Sejung Yim, Veronica Lee, Eunju Hong, Van Ta Park, Li-San Wang, Gyungah Jun, Yun-Beom Choi
Publikováno v:
BMJ Open, Vol 13, Iss 8 (2023)
Objective This study aims to show the usefulness of incorporating a community-based geographical information system (GIS) in recruiting research participants for the Asian Cohort for Alzheimer’s Disease (ACAD) study for using the subgroup of Korean
Externí odkaz:
https://doaj.org/article/930495fa9e224154ae8827c119d43562
Autor:
Van Khanh Tran, Ngoc-Lan Nguyen, Lan Ngoc Thi Tran, Phuong Thi Le, Anh Hai Tran, Tuan L. A. Pham, Nguyen Thi Kim Lien, Nguyen Thi Xuan, Le Tat Thanh, Thanh Van Ta, Thinh Huy Tran, Huy-Hoang Nguyen
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Background: Merosin-deficient congenital muscular dystrophy type 1A (MDC1A), also known as laminin-α2 chain-deficient congenital muscular dystrophy (LAMA2-MD), is an autosomal recessive disease caused by biallelic variants in the LAMA2 gene. In MDC1
Externí odkaz:
https://doaj.org/article/00fc6956be4d4d9eaf9b0684d9146f12
Autor:
Bui, Thi Minh Phuong, Tran, Van Khanh, Nguyen, Thi Thanh Hai, Le, Thi Phuong, Nguyen, Thi Mai, Tran, Hai Anh, Luu, Vu Dung, Nguyen, Manh Ha, Bui, The-Hung, Van Ta, Thanh, Tran, Thinh Huy
Publikováno v:
In Taiwanese Journal of Obstetrics & Gynecology November 2022 61(6):1009-1014