Zobrazeno 1 - 10
of 89
pro vyhledávání: '"Dung, Vu Chi"'
Autor:
Ng, Sze May, Malene, IV, Nilar, Myint, Rassavong, Khaysy, Dung Vu, Chi, Hui Sieng Tan, Florence, Yazid Jalaludin, Muhammad, Toomey, Charles, Lek, Ngee
Publikováno v:
In Diabetes Research and Clinical Practice May 2022 187
Autor:
Linh Thuy Dinh, Van Khanh Tran, Long Hoang Luong, Phuong Thi Le, Anh Duy Nguyen, Bang Suong Thi Nguyen, Dung Vu Chi, Thinh Huy Tran, The-Hung Bui, Thanh Van Ta, Duc Hinh Nguyen
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 58, Iss 5, Pp 645-649 (2019)
Objective: Duchenne Muscular Dystrophy is an X-linked recessive disorder characterized by progressive muscular degeneration, patients often develop cardiac failure in the later stage and death occurs before 20 years of age. For a disease with poor po
Externí odkaz:
https://doaj.org/article/a690e57365354762a32c01b962b03abe
Autor:
Dominique P. Germain, Sergey Moiseev, Fernando Suárez‐Obando, Faisal Al Ismaili, Huda Al Khawaja, Gheona Altarescu, Fellype C. Barreto, Farid Haddoum, Fatemeh Hadipour, Irina Maksimova, Mirelle Kramis, Sheela Nampoothiri, Khanh Ngoc Nguyen, Dau‐Ming Niu, Juan Politei, Long‐Sun Ro, Dung Vu Chi, Nan Chen, Sergey Kutsev
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 5, Pp n/a-n/a (2021)
Abstract Background Family genetic testing of patients newly diagnosed with a rare genetic disease can improve early diagnosis of family members, allowing patients to receive disease‐specific therapies when available. Fabry disease, an X‐linked l
Externí odkaz:
https://doaj.org/article/7133386bff6342479156e20d5b14da8e
Autor:
Siri Atma W. Greeley, Michel Polak, Pål R. Njølstad, Fabrizio Barbetti, Rachel Williams, Luis Castano, Klemens Raile, Dung Vu Chi, Abdelhadi Habeb, Andrew T. Hattersley, Ethel Codner
Publikováno v:
Pediatric Diabetes. 23:1188-1211
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2cdd229eeb5ac3c581a77e7dc0b33e08
https://doi.org/10.1111/pedi.13426
https://doi.org/10.1111/pedi.13426
Autor:
Kubaski, Francyne, Yabe, Hiromasa, Suzuki, Yasuyuki, Seto, Toshiyuki, Hamazaki, Takashi, Mason, Robert W., Xie, Li, Onsten, Tor Gunnar Hugo, Leistner-Segal, Sandra, Giugliani, Roberto, Dũng, Vũ Chí, Ngoc, Can Thi Bich, Yamaguchi, Seiji, Montaño, Adriana M., Orii, Kenji E., Fukao, Toshiyuki, Shintaku, Haruo, Orii, Tadao, Tomatsu, Shunji *
Publikováno v:
In Biology of Blood and Marrow Transplantation October 2017 23(10):1795-1803
Akademický článek
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Autor:
Tomatsu, Shunji *, Montaño, Adriana M, Dung, Vu Chi, Ohashi, Amiko, Oikawa, Hirotaka, Oguma, Toshihiro, Orii, Tadao, Barrera, Luis, Sly, William S
Publikováno v:
In Molecular Therapy June 2010 18(6):1094-1102
Autor:
Fellype C. Barreto, Nan Chen, Huda Al Khawaja, Faisal Al Ismaili, Dau-Ming Niu, Sergey Moiseev, Gheona Altarescu, Sergey Kutsev, Sheela Nampoothiri, Mirelle Kramis, Long-Sun Ro, Juan Politei, Dominique P. Germain, Farid Haddoum, Fernando Suárez-Obando, Irina Maksimova, Dung Vu Chi, Khanh Ngoc Nguyen, Fatemeh Hadipour
Publikováno v:
Molecular Genetics and Genomic Medicine
Molecular Genetics and Genomic Medicine, Wiley, 2021, 9 (5), pp.e1666. ⟨10.1002/mgg3.1666⟩
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine, Vol 9, Iss 5, Pp n/a-n/a (2021)
Molecular Genetics and Genomic Medicine, Wiley, 2021, 9 (5), pp.e1666. ⟨10.1002/mgg3.1666⟩
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine, Vol 9, Iss 5, Pp n/a-n/a (2021)
Background Family genetic testing of patients newly diagnosed with a rare genetic disease can improve early diagnosis of family members, allowing patients to receive disease‐specific therapies when available. Fabry disease, an X‐linked lysosomal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc3859260d88426bdf394d02f1263bb9
https://hal.archives-ouvertes.fr/hal-03256438/file/mgg3.1666.pdf
https://hal.archives-ouvertes.fr/hal-03256438/file/mgg3.1666.pdf
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Ngoc, Can Thi Bich, Dien, Tran Minh, De Franco, Elisa, Ellard, Sian, Houghton, Jayne A. L., Lan, Nguyen Ngoc, Thao, Bui Phuong, Khanh, Nguyen Ngoc, Flanagan, Sarah E., Craig, Maria E., Dung, Vu Chi
Publikováno v:
Frontiers in Endocrinology; 9/9/2021, Vol. 12, p1-9, 9p