Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Margaret Heisel Kurth"'
Autor:
Michael Recht, Alexis A. Thompson, Robert J. Klaassen, Michele P. Lambert, Leslie A. Kalish, Courtney D. Thornburg, Ellis J. Neufeld, Margaret Heisel Kurth, Michael Jeng, A. Kim Ritchey, George R. Buchanan, Michelle Neier, Rachael F. Grace, Kimo C. Stine, Carolyn M. Bennett, Diane J. Nugent, Victor Blanchette, Manjusha Kumar
Publikováno v:
Pediatric Blood & Cancer. 58:221-225
Abstract 3681 Background: Pediatric Immune Thrombocytopenia (ITP) has an incidence of 4–6/100,000 with 1/3 of cases becoming chronic. Treatment choice is arbitrary, because few studies are powered to identify predictors of therapy response. Increas
Autor:
P. M. Mannucci, Nadia P. Ewing, Srini V. Kaveri, Edward D. Gomperts, Diane J. Nugent, Margaret Heisel Kurth, Craig M. Kessler
Publikováno v:
Haemophilia. 17:e235-e238
Publikováno v:
Journal of Pediatric Hematology/Oncology. 30:81-84
In newborns with hemophilia, intracranial hemorrhage (ICH) is a potentially life-threatening event and in those who survive, there is a risk of long-term neurologic sequelae. A single-center retrospective chart review was performed to look at the uti
Autor:
Elena Santagostino, J. Bozzo, Víctor Jiménez-Yuste, Johannes Oldenburg, Margaret Heisel Kurth, Savita Rangarajan
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 22(1)
Publikováno v:
Pediatric Blood & Cancer. 51:418-420
Cutaneovisceral angiomatosis with thrombocytopenia (CAT) syndrome is a rare vascular disorder of the skin and gastrointestinal tract for which there is no standard treatment. We present a case in which a child with CAT syndrome was treated with bevac
Autor:
Paul M. Fernhoff, Margaret Heisel-Kurth, Laurie D. Smith, Eric Crombez, Nicola Longo, Rebecca Mardach, William J. Rhead, Deborah Elstein, Christine M. Eng, Joel Charrow, P Giraldo, Paul Harmatz, Gregory A. Grabowski, Gregory M. Pastores, David Zahrieh, Ari Zimran, Anna Tylki-Szymańska, Juan Ruiz, Derralynn Hughes
Publikováno v:
American journal of hematology, vol 88, iss 3
Velaglucerase alfa is a glucocerebrosidase produced by gene activation technology in a human fibroblast cell line (HT-1080), and is indicated as an enzyme replacement therapy (ERT) for the treatment of Gaucher disease type 1 (GD1). This multicenter,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc6e24c26f83d8ddb68f4547a82376f0
https://escholarship.org/uc/item/01w7m0cb
https://escholarship.org/uc/item/01w7m0cb
Publikováno v:
The Laryngoscope. 120(12)
Objectives/Hypothesis: To understand Glanzmann's thrombasthenia and provide insight to the management of epistaxis in children with this disease. Study Design: Retrospective chart review. Methods: All children diagnosed with Glanzmann's thrombastheni
Publikováno v:
Journal of pediatric gastroenterology and nutrition. 42(2)
Publikováno v:
Journal of Pediatric Gastroenterology & Nutrition. 44:389-390
Autor:
Margaret Heisel Kurth, A. Kim Ritchey, Robert J. Klaassen, Victor S. Blanchette, Carolyn M. Bennett, George R. Buchanan, Leslie A. Kalish, Michele P. Lambert, Diane J. Nugent, Michael Recht, Kimo C. Stine, Alexis A. Thompson, Michael Jeng, Courtney D. Thornburg, Ellis J. Neufeld, Manjusha Kumar, Rachael F. Grace, Michelle Neier
Publikováno v:
Blood. 116:2509-2509
Abstract 2509 Background: Chronic pediatric immune thrombocytopenia (ITP) has an incidence of 1–2/100,000. Due to its low incidence, large studies in pediatric chronic ITP are difficult. This registry includes patients from 16 sites in the US and C