Nguyen Thi Van Anh - Vietnam Natl Hosp Pediat, Allergy Immunol & Rheumatol Dept, 18-879 La Thanh Str, Hanoi, Vietnam

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论文共 14 篇作者统计合作学者相似作者

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Human germline heterozygous gain-of-function STAT6 variants cause severe allergic disease

Mehul Sharma,Daniel Leung,Mana Momenilandi, Lauren C W Jones,Lucia Pacillo,Alyssa E James,Jill R Murrell,Selket Delafontaine,Jesmeen Maimaris,Maryam Vaseghi-Shanjani,Kate L Del Bel,Henry Y Lu,

J Exp Med（2023）

引用17浏览0WOS引用

Human germline heterozygous gain-of-functionSTAT6variants cause severe allergic disease

Mehul Sharma,Daniel Leung,Mana Momenilandi, Lauren C.W. Jones,Lucia Pacillo,Alyssa E. James,Jill R. Murrell,Selket Delafontaine,Jesmeen Maimaris,Maryam Vaseghi-Shanjani,Kate L. Del Bel,Henry Y. Lu,

Journal of Experimental Medicine（2023）

引用15浏览0引用

The first successful bone marrow transplantation in Vietnam for a young Vietnamese boy with chronic granulomatous disease: a case report

Binh Nguyen-Thanh, Le Nguyen-Ngoc-Quynh, Ha Dang-Thi, Chi Le-Quynh,Anh Nguyen-Thi-Van, Huyen Thuc-Thanh, Duong Dang-Anh, Pamela P. Lee, Tung Cao-Viet, Dien Tran-Minh

Frontiers in Immunology（2023）

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Transition practice for primary immunodeficiency diseases in Southeast Asia: a regional survey

Chee Mun Chan,Amir Hamzah Abdul Latiff,Lokman Mohd Noh,Intan Hakimah Ismail,Intan Juliana Abd Hamid,Woei Kang Liew,Youjia Zhong,Narissara Suratannon,Rapisa Nantanee,Fatima Johanna Santos-Ocampo, Mary Anne R Castor, Le Nguyen-Ngoc-Quynh,

Frontiers in immunology (2023): 1209315

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Targeted Gene Sanger Sequencing Should Remain the First-Tier Genetic Test for Children Suspected to Have the Five Common X-Linked Inborn Errors of Immunity

Koon-Wing Chan,Chung-Yin Wong,Daniel Leung,Xingtian Yang,Susanna F S Fok,Priscilla H S Mak,Lei Yao,Wen Ma,Huawei Mao,Xiaodong Zhao,Weiling Liang,Surjit Singh,

FRONTIERS IN IMMUNOLOGY（2022）

引用2浏览0WOS引用

Novel mutations in unrelated Vietnamese patients with chronic granulomatous disease

Nguyen Thanh Binh,Nguyen Thi Kim Lien,Nguyen Thi Van Anh,Nguyen Thi Phuong Mai, Nguyen Thi Viet Ha, Dang Thuy Ha,Nguyen Van Tung,Nguyen Huy Hoang

Clinica Chimica Acta（2022）

引用1浏览0WOS引用

Identification of the causative mutation in the ITGB2 gene in a LAD1 patient by whole exome sequencing

Nguyen Thi Kim Lien,Nguyen Thi Van Anh,Nguyen Van Tung, Duong Anh Linh,Nguyen Thi Phuong Mai,Nguyen Huy Hoang

Tạp chí công nghê sinh họcno. 2 (2022): 213-218

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De novo mutations of \(\textit{ ELANE}\) gene in three Vietnamese patients with severe congenital neutropenia

Duong Anh Linh,Nguyen Thi Van Anh,Nguyen Van Tung,Nguyen Huy Hoang, Ngo Diem Ngoc,Nguyen Thi Phuong Mai, Ngo Manh Tien,Nguyen Thi Kim Lien

Academia Journal of Biologyno. 3 (2022): 77-85

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First CD3/CD45RA depleted haploidentical transplant for severe combined immunodeficiency disease with Rotavirus gastroenteritis in Vietnam

Nguyen Thanh Binh, Dang Anh Duong, Bui Ngoc Lan,Nguyen Thi Van Anh, Tran Quynh Huong, Le Thi Minh Huong, Cao Viet Tung,Tran Minh Dien, Nguyen Ngoc Quynh Le

Tạp chí Nghiên cứu Y họcno. 6 (2022): 52-60

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Whole-exome sequencing as a diagnostic tool for ipex syndrome

Duong Anh Linh,Nguyen Thi Kim Lien,Nguyen Van Tung,Nguyen Thi Van Anh,Nguyen Thi Phuong Mai, Ngo Manh Tien, Tran Thi My Hanh,Nguyen Huy Hoang

Academia Journal of Biololyno. 1 (2022): 53-60

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