Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Loan, Hsieh"'
Autor:
Satheesh Chonat, Mary Risinger, Haripriya Sakthivel, Omar Niss, Jennifer A. Rothman, Loan Hsieh, Stella T. Chou, Janet L. Kwiatkowski, Eugene Khandros, Matthew F. Gorman, Donald T. Wells, Tamara Maghathe, Neha Dagaonkar, Katie G. Seu, Kejian Zhang, Wenying Zhang, Theodosia A. Kalfa
Publikováno v:
Frontiers in Physiology, Vol 10 (2019)
Externí odkaz:
https://doaj.org/article/840996a63d2c4519a193f1ac68e710b4
Autor:
Satheesh Chonat, Mary Risinger, Haripriya Sakthivel, Omar Niss, Jennifer A. Rothman, Loan Hsieh, Stella T. Chou, Janet L. Kwiatkowski, Eugene Khandros, Matthew F. Gorman, Donald T. Wells, Tamara Maghathe, Neha Dagaonkar, Katie G. Seu, Kejian Zhang, Wenying Zhang, Theodosia A. Kalfa
Publikováno v:
Frontiers in Physiology, Vol 10 (2019)
Hereditary spherocytosis (HS) is the most common red blood cell (RBC) membrane disorder causing hereditary hemolytic anemia. Patients with HS have defects in the genes coding for ankyrin (ANK1), band 3 (SLC4A1), protein 4.2 (EPB42), and α (SPTA1) or
Externí odkaz:
https://doaj.org/article/ad840012f1744b04820b5b66c13c0ebd
Publikováno v:
Journal of Pediatric Hematology/Oncology. 44:421-422
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b76117e23858967c48bf7b391f504e40
https://doi.org/10.1097/mph.0000000000002540
https://doi.org/10.1097/mph.0000000000002540
Publikováno v:
Drug Design, Development and Therapy
Primary immune thrombocytopenia (ITP) is an autoimmune disorder characterized by isolated thrombocytopenia. In approximately one-third of cases, the duration of thrombocytopenia will extend beyond 12 months consistent with a diagnosis of chronic ITP.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::339d76b583e78206c06cf88fc2ebbb11
https://doi.org/10.2147/dddt.s113191
https://doi.org/10.2147/dddt.s113191
Autor:
Melissa Eisen, Kimo C. Stine, James B. Bussel, Ram Kalpatthi, Loan Hsieh, Kun Nie, David J. Gnarra, George R. Buchanan, Richard H. Ho
Publikováno v:
Pediatric Blood & Cancer
Background Treatment of chronic severe pediatric ITP is not well studied. In a phase 1/2 12–16-week study, 15/17 romiplostim-treated patients achieved platelet counts ≥50 × 109/L, and romiplostim treatment was well tolerated. In a subsequent ope
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e35dcbdbf59beeec7fafe56a866e8538
https://doi.org/10.1002/pbc.25136
https://doi.org/10.1002/pbc.25136
Autor:
Doris, Quon, Meera, Chitlur, Madhvi, Rajpurkar, Mindy, Simpson, Sarah, O'Brien, Veronica, Flood, Loan, Hsieh, Suchitra, Acharya, Rebecca, Kruse-Jarres, Suman, Sood, Jennifer, Maahs
Publikováno v:
American journal of hematology. 91
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cd5b2de85747168fdb9f2340f2059b13
https://pubmed.ncbi.nlm.nih.gov/26851875
https://pubmed.ncbi.nlm.nih.gov/26851875
Autor:
Loan Hsieh, Diane J. Nugent
Publikováno v:
Current Opinion in Hematology. 19:380-384
Purpose of review By definition, rare factor deficiencies have a prevalence of less than 200,000 in the US population, or an incidence of less than one in 2000 in Europe. The very small numbers of patients with rare disorders present challenges in di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b02a1882dbb0dbce28b9f9d385ec0f1
https://doi.org/10.1097/moh.0b013e328356edd5
https://doi.org/10.1097/moh.0b013e328356edd5
Autor:
Geetha Puthenveetil, Loan Hsieh, Amit Soni, Colin G. Steward, Ivan I. Kirov, Diane J. Nugent, Steven Neudorf, David Buchbinder
Publikováno v:
Pediatric Transplantation. 17:E20-E24
Buchbinder D, Steward CG, Puthenveetil G, Nugent D, Hsieh L, Kirov I, Neudorf S, Soni A. Successful cord blood transplantation in a patient with malignant infantile osteopetrosis and hemophilia. Abstract: MIOP is a congenital disorder of osteoclast d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b676918a3bdbd93f0d84f545d4ee776d
https://doi.org/10.1111/j.1399-3046.2012.01758.x
https://doi.org/10.1111/j.1399-3046.2012.01758.x
Autor:
Jill Stites, Aaron Sassoon, Loan Hsieh, Diane J. Nugent, Tristen Ness-Jorden, Bassam Younes, Amit Soni, Steven Neudorf, David Buchbinder, Geetha Puthenveetil
Publikováno v:
Pediatric Transplantation. 16:E188-E191
Buchbinder D, Younes B, Sassoon A, Soni A, Hsieh L, Puthenveetil G, Stites J, Ness-Jorden T, Neudorf S, Nugent D. Inflammatory polyps following successful HLA-matched cord blood transplantation in a patient with X-linked lymphoproliferative syndrome.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b98315010db0b6db90ef7780233dacbe
https://doi.org/10.1111/j.1399-3046.2011.01520.x
https://doi.org/10.1111/j.1399-3046.2011.01520.x
Autor:
Loan Hsieh, Mohamad Badawi, Omar Niss, Karen L. Bride, Jill S. Menell, Cynthia J. Rutherford, Mary Risinger, Vandy Black, Katie Giger Seu, Wenying Zhang, Theodosia A. Kalfa, Charles T. Quinn, Renee C. Prins
Publikováno v:
Blood. 132:1040-1040
Hereditary xerocytosis (HX) is a rare autosomal dominant hemolytic anemia caused by mutations in the mechanosensitive cation channel PIEZO1 or, less commonly, in the Ca2+-gated K+ channel KCNN4 (Gardos channel). It is a clinically heterogeneous condi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b7f2f8b4e5020ea0dd6fa449b8b2128d
https://doi.org/10.1182/blood-2018-99-117299
https://doi.org/10.1182/blood-2018-99-117299