Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Linda G. Shaffer"'
Autor:
Sandeep K. Rajan, Linda G. Shaffer, Timothy L. McCavit, Miguel A. Escobar, Novinyo S. Amega, Mark Holguin
Publikováno v:
Haemophilia. 27
Autor:
Omar Niss, Robert B. Lorsbach, Mikaela Berger, Satheesh Chonat, Morgan McLemore, David Buchbinder, Timothy McCavit, Linda G. Shaffer, Jessica Simpson, Jeffrey H. Schwartz, Jessica Meznarich, Myesa Emberesh, Katie G. Seu, Wenying Zhang, Theodosia A. Kalfa, Ammar Husami, Theodosia Kalfa, Robert Lorsbach, Carolyn Lutzko, Adam Nelson, Charles Quinn, Clarissa Johnson, Jennifer A. Rothman, Sweta Gupta, Mara Nuñez Toscano, Melissa Forouhar, Vinod K. Gidvani-Diaz, James B. Ball, Gavin D. Roach, KayeLyn Wagner, Sam Milanovich, James Boyer, Jane Chawla, Christine Moore Smith, Adrienne Lee, Vlad C. Radulescu, Yasmina L. Abajas, A. Kim Ritchey, Hunter R. Underhill, Yaddanapudi Ravindranath, Niketa C. Shah
Publikováno v:
Blood Cells Mol Dis
Congenital dyserythropoietic anemias (CDAs) are characterized by ineffective erythropoiesis and distinctive erythroblast abnormalities; the diagnosis is often missed or delayed due to significant phenotypic heterogeneity. We established the CDA Regis
Autor:
Linda G. Shaffer, M. John Hicks, Kenneth L. McClain, Stephen J. Simko, Timothy L. McCavit, Don W. Coulter, Timothy P. Garrington, Carl E. Allen, Huy D. Tran, Francisco Rivera-Ortegón, Linda C. Stork, Colin Moore, Lynda K. Beaupin, Esperanza C. Welsh, Mrinalini Bilgi, Lucie M. Turcotte, Jeremy Jones
Publikováno v:
Pediatric Blood & Cancer. 61:479-487
Background Existing therapies for recurrent or refractory histiocytoses, including Langerhans cell histiocytosis (LCH), juvenile xanthogranuloma (JXG), and Rosai-Dorfman disease (RDD), have limited effectiveness. We report our experience with using c
Autor:
Mazen Y Arar, Nancy A. Turner, Jun Teruya, Joel L. Moake, Shiu Ki Hui, Linda G. Shaffer, Ewa Elenberg, Mini Michael, Richard J.H. Smith
Publikováno v:
Clinical Kidney Journal
A 3-month-old male infant developed an extremely severe episode of atypical hemolytic uremic syndrome (aHUS) associated with partial deficiencies of full-length complement factor H (FH; ∼15% of infant normal) and a disintegrin and metalloproteinase
Autor:
Barbara A. Konkle, Joseph Addiego, Benjamin Deulbesonic, George R. Buchanan, Brad Lewis, Linda G. Shaffer, Alton L. Lightsey, Ari J. Cohen, W. Keith Hoots, James L. Harper, John Bouhasin, Thomas H. Howard, Donald Mahoney, Gilbert C. White, Parvin Saidi, Carol K. Kasper, D. C. Talbert, Eric Larsen, David Lilligrap, Jack Lazerson, Martin J. Inwood, Bruce Ritchie, Elizabeth Kurczynski, Margaret Heisel, James Harper, J. Paul Scott, Robert L. Janco, Peter A. Kouides, Frederick Rickles, Alan Cohen, Anne Thomas, Indira Warrier, Prad Phatak, John D. Bouhasin, Cathy Rosenfield, S. R. Seitcher, David Green, Deborah L Brown, J. Heinreich Joist, Bridget Freeman, Mark Mancino, Edward H. Romond, Felicia Little, Leticia Valdez, Eric J. Werner, Patricia McCusker, Robert Bona, W. Paul Bowman, Louis Geeraerts, J. Teitel, Donna DiMichele, Catherine S. Manno, Jerry S. Powell, Bruce M. Ewenstein, Michael D. Tarantino, Dennis Gastineau, Richard Edwards, Thomas C. Abshire, Craig M. Kessler, Rachelle Nuss, Judy Wilimas, Gerald Gilchrist, Cindy Lessinger, Roshini Kulkarni, Jeannne M. Lusher, Margaret V. Ragni, Alberao Pappo, Sarah Hawk, Georges E. Rivard, Man Chiu Poon
Publikováno v:
Haemophilia. 7:235-241
The optimal treatment of patients with von Willebrand's disease (vWD) remains to be defined. Moreover, it has not been firmly established which, if any, commonly measured parameters of von Willebrand factor (vWF) protein in the plasma are useful in g
Publikováno v:
Current opinion in oncology. 10(4)
In this past year, a large number of reports have described cytogenetic and biologic studies of sarcomas. The cytogenetic studies provide further evidence that a growing number of sarcomas seem to be defined by consistent chromosomal abnormalities th
Autor:
Linda G. Shaffer
Publikováno v:
Annals of Internal Medicine. 128:325
Autor:
Linda G. Shaffer, Martin D. Phillips
Publikováno v:
Annals of Internal Medicine. 127:206
Acquired autoantibodies to factor VIII in patients without hemophilia are rare, but they cause severe illness and death if not eradicated.To examine daily therapy with oral cyclophosphamide and prednisone for acquired hemophilia.Case series.Academic