Zobrazeno 1 - 10
of 82
pro vyhledávání: '"Sunitha Vege"'
Autor:
Ruth H. Walker, Mariana Barreto, James R. Bateman, M. Leonor Bustamante, Graham Chiu, Scott Feitell, Beat M. Frey, Patricio Guerra, Sofia Guerrero, Hans H. Jung, Fernando Maldonado, Eduardo Meyer, Marcelo Miranda, Emelie McFarland, Patricia Oates, Gorka Ochoa, Karin Olsson, Martin Paucar, Jonatan Alvarez Proschle, Esther M. Sammler, Monica Troncoso, Rachel Wu-Wallace, Leo Young, Sunitha Vege, Connie M. Westhoff, Adrian Danek
Publikováno v:
Frontiers in Neuroscience, Vol 18 (2024)
XK disease is a very rare, multi-system disease, which can present with a wide spectrum of symptoms. This disorder can also be identified pre-symptomatically with the incidental detection of serological abnormalities when typing erythrocytes in perip
Externí odkaz:
https://doaj.org/article/6593764dccbd407cabe77da3d2d6c3c6
Autor:
William J. Lane, Judith Aeschlimann, Sunitha Vege, Christine Lomas-Francis, Anna Burgos, Helen H. Mah, Justin B. L. Halls, Peter Baeck, Peter C. Ligthart, Barbera Veldhuisen, Ripal J. Shah, Sanmukh R. Joshi, Connie M. Westhoff
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-11 (2021)
Abstract Emm is a high incidence red cell antigen with eight previously reported Emm− probands. Anti-Emm appears to be naturally occurring yet responsible for a clinically significant acute hemolytic transfusion reaction. Previous work suggests tha
Externí odkaz:
https://doaj.org/article/74df5f183e1f4e48a09153f5df5dff55
Autor:
Ripal J Shah, Snehal B Senjaliya, V Harimoorthy, Anna Burgos, Sunitha Vege, Christine Lomas-Francis, Connie M Westhoff, Sanmukh Ratilal Joshi
Publikováno v:
Asian Journal of Transfusion Science, Vol 15, Iss 2, Pp 223-225 (2021)
A transfusion recipient lacking a high-incidence antigen (HIA) and has corresponding alloantibody pose a problem in providing compatible blood unit. We encountered a patient with an antibody to an HIA that required identification to assess if compati
Externí odkaz:
https://doaj.org/article/9373db1e07124ca3a70a60d2a6febe03
Autor:
Stella T. Chou, Jonathan M. Flanagan, Sunitha Vege, Naomi L.C. Luban, R. Clark Brown, Russell E. Ware, Connie M. Westhoff
Publikováno v:
Blood Advances, Vol 1, Iss 18, Pp 1414-1422 (2017)
Abstract: RH genes are highly polymorphic and encode the most complex of the 35 human blood group systems. This genetic diversity contributes to Rh alloimmunization in patients with sickle cell anemia (SCA) and is not avoided by serologic Rh-matched
Externí odkaz:
https://doaj.org/article/f015d3504c7143288d2f205f62b428dc
Autor:
Abigail Joseph, Cody J. Murray, Natasha D. Novikov, Randall W. Velliquette, Sunitha Vege, Justin B.L. Halls, Helen H. Mah, Jamie L. Dellagatta, Edward Comeau, Maria Aguad, Richard M. Kaufman, Martin L. Olsson, Indira Guleria, Sean R. Stowell, Edgar L. Milford, Annika K. Hult, Melissa Y. Yeung, Connie M. Westhoff, Cathi L. Murphey, William J. Lane
Publikováno v:
American Journal of Transplantation. 23:512-519
Autor:
Aline Floch, Christine Lomas‐Francis, Sunitha Vege, Steven Brennan, Gayane Shakarian, Alexandre G. de Brevern, Connie M. Westhoff
Publikováno v:
Transfusion. 63:798-807
Autor:
Nancy L. Van Buren, Barbara Gillen, Christine Lomas‐Francis, Anna Burgos, Daniel Pease, Maria Beaver, Adam Imbryk, Julia Dugger, Alexandra Fugate, Eric Hebel, Michelle Lodermeier, Sunitha Vege, Connie M. Westhoff
Publikováno v:
Transfusion. 62:1917-1922
Autor:
Kaoru Takasaki, David F. Friedman, Stacey Uter, Sunitha Vege, Connie M. Westhoff, Stella T. Chou
Publikováno v:
British Journal of Haematology.
Autor:
Sunitha Vege, Aline Floch, Anna Burgos, Toufik Tahiri, Julie Kirkegaard, Megan Dupont, Gorka Ochoa‐Garay, Christine Lomas‐Francis, Connie M. Westhoff
Publikováno v:
Transfusion. 63
Autor:
Zhe Zhang, Hyun Hyung An, Sunitha Vege, Taishan Hu, Shiping Zhang, Timothy Mosbruger, Pushkala Jayaraman, Dimitri Monos, Connie M. Westhoff, Stella T. Chou
Publikováno v:
Am J Hum Genet
Next-generation sequencing (NGS) technologies have transformed medical genetics. However, short-read lengths pose a limitation on identification of structural variants, sequencing repetitive regions, phasing of distant nucleotide changes, and disting