Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Sue Geraghty"'
Autor:
Sue Geraghty, Greig Blamey, David L. Cooper, Hossam Saad, Susan Cutter, Cathy Buranahirun, Andrea Buzzi, Renchi Yang
Publikováno v:
Patient Related Outcome Measures. 10:243-255
Background Sexual health plays a primary role in quality of life (QoL) for many people, including those with hemophilia; however, there is little information available about sexual relationships and satisfaction in patients with hemophilia. Methods T
Autor:
W. K. Hoots, Roshni Kulkarni, Joan Cox Gill, J. M. Soucie, Rodney J Presley, Bruce L. Evatt, Prasad Mathew, Diane J. Nugent, Sue Geraghty, Amy D. Shapiro, Jeanne M. Lusher, Marilyn J. Manco-Johnson, Donna DiMichele, Thomas C. Abshire, Marion A. Koerper
Aim To describe the prevalence and complications in babies ≤2 years with haemophilia. Methods We used a standardized collection tool to obtain consented data on eligible babies aged ≤2 years with haemophilia enrolled in the Centers for Disease Co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f9f5ea7445aa0af845e3da57c1cff62
https://europepmc.org/articles/PMC5354941/
https://europepmc.org/articles/PMC5354941/
Autor:
Prasad Mathew, Rodney J Presley, J. M. Soucie, Donna DiMichele, Thomas C. Abshire, Marilyn J. Manco-Johnson, Sue Geraghty, Rohit N. Kulkarni, Diane J. Nugent, Bruce L. Evatt, Joan Cox Gill, Marion A. Koerper, Jeanne M. Lusher, A. Shapiro, Keith Hoots, Robert L. Janco
Publikováno v:
Haemophilia. 15:1281-1290
Lack of detailed natural history and outcomes data for neonates and toddlers with haemophilia hampers the provision of optimal management of the disorder. We report an analysis of prospective data collected from 580 neonates and toddlers aged 0-2 yea
Autor:
Marilyn J. Manco-Johnson, George R. Buchanan, Victor S. Blanchette, Bruce M. Ewenstein, R. Stuart, Leonard A. Valentino, Janna M. Journeycake, Michael D. Tarantino, Amy D. Shapiro, R. J. Navickis, Jennifer Maahs, K. L. Miller, W. K. Hoots, T. Dunham, Georges-Etienne Rivard, Sue Geraghty
Publikováno v:
Haemophilia. 10:629-648
Venous access is essential for delivery of haemophilia factor concentrate. Wherever possible, peripheral veins remain the route of choice, and the use of central venous access devices (CVADs) should be limited to cases of clear need in patients with
Autor:
Angela Lambing, Mary G. Hudson, Deanna Mitchell, Angela Tackney, Michael Recht, Erica Johnson, Ray L. Watts, Adam Cuker, JeanMarie M. Zoland, Karen Gutting, Cherys Zimmerman, Ellen White, Glenda Eckert, Gita Massey, Elizabeth Sandon-Kleiboer, Steve Hopewell, Trish Underland, Leslie Witkoff, Angie Riedel, Susan Karp, Cheryl Brower, Kathy McGinty, Charles Sexauer, Glenn Heggie, Joanne Porter, Mark T. Reding, Susumu Inoue, Vivek R. Sharma, Ashley T. Brummel, Marion Koerper, Sarah May, Jonathan M. Ducore, John S. Rogers, Claudia Lupia, C. Wang, Sue Geraghty, Eric H. Kraut, Neiha Dhar, Eric J. Werner, Bertil Glader, Margaret Bosch, Bryce A. Kerlin, Jodi Haar, Roberto Torres, Hassan M. Yaish, Mia Frank, Jay Charles, Jeanne M. Lusher, Dominique Joseph, Philip Kuriakose, Paula L. Bockenstedt, JoAnn A. Ruff, Mary Catherine Noa, Amy E. Lovejoy, Anaadriana Zakarija, Ilene Goldberg, Donna DiMichele, Anne T. Neff, Miriam Granat, Edwin N. Forman, Robin Schwartz, Alice Cohen, Margaret V. Ragni, Brian M. Wicklund, Michael F. Guerrera, Joan Cox Gill, Nadia P. Ewing, Ulrike M. Reiss, Kimo C. Stine, Sue Kovats-Bell, Robin Grant, Tom Coyle, Felicia Kiplinger, Thomas C. Abshire, Desiree Medeiros, Franklin Desposito, Katie Kralovetz, William D. Haire, Paulette Drozdowicz, Michael D. Tarantino, Rosemary P. Holmberg, Angela Stewart, Peter A. Kouides, Jennifer Green, Amy D. Shapiro, Karen Panckeri, Jim Casella, Guy Young, Sylvia Webber, Lee Meadows, Sandy Hibner, Katherine Farrow, Ara Metjian, Cecilia V. Schmidt, Laura Schulz, Robert Mignacca, S. M. Peterson, Sandy Harris, Parvin Saidi, W. Keith Hoots, Hernan Sabio, Diana Mathis, Kenneth D. Herbst, Cathy Glass, Jorge DiPaola, Patricia Fleming, Lisa Palumbo, Richard Lipton, Kristen Jaworski, Valerie Gonzalez, Valerie Crenshaw, Kim Stewart, Craig M. Kessler, Dee Ann Omatsu, Wahid Hanna, Patricia Amerson, Alexis A. Thompson, Afshin Ameri, Helena M. Jacobs, James French, Anne Chambers, Marjorie A. Boyd, George R. Buchanan, Steven W. Pipe, Anita Smith, Jubelirer Sj, Karen Granger, K. A. Schmidt, Suman L. Sood, Becki Berkowitz, Cindy A. Leissinger, Rajiv K. Pruthi, Patricia Ashby, Susan Curoe, Brenda Nielsen, Amy L. Dunn, Mike Lammer, Donna Arden, Carol Diamond, Chris Guelcher, Frances Patterson, Arthur R. Thompson, M. E. Nolte, G. Allen, Alan C. Homans, Marilyn J. Manco-Johnson, Ralph A. Gruppo, Glen Roy, Vlad C. Radulescu, Elizabeth Hanlon, Lynn Menza, Sarah Alexander, J. M. Soucie, Nigel S. Key, Debbie Nelson, Lisa Pullens, Jennifer La Franco, Barbara A. Konkle, Jean Marandola, Jonathan Bernstein, Muriel Herr, Corinthian Bryant
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 15(4)
Type 3 von Willebrand disease (VWD) is a rare bleeding disorder with markedly decreased or absent von Willebrand factor (VWF) protein, accompanied by a parallel decrease in VWF function and factor VIII (FVIII) activity. The goal of this study was to
We used data collected as part of the Universal Data Collection (UDC) surveillance project in haemophilia treatment centers (HTC) to study the incidence, risk factors and impact of septic arthritis among males with haemophilia. Patients participating
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f03d7e18ce1fb61c9713236aa3a1d0e
https://europepmc.org/articles/PMC3951979/
https://europepmc.org/articles/PMC3951979/
Autor:
Heather Huszti, Ann D. Forsberg, Julie Hambleton, Thomas C. Abshire, Angela Forsyth, J. Michael Soucie, Keith Hoots, Sue Geraghty, Robert L. Janco, Bruce L. Evatt, Gilbert C. White, Christy Cianfrini, Margaret Wagner, Randall Curtis, Roshni Kulkarni
Publikováno v:
Blood. 103(7)
Chronic joint disease from repeated bleeding into joints is a serious complication of hemophilia. To measure the extent of and to identify risk factors for deviations from normal in joint range of motion (ROM), we used cross-sectional data collected
Autor:
Ruth Ann Kirschman, Robert Chen, Seligman Paul, Stabler Sally, Justin Call, Sue Geraghty, Brenda Riske
Publikováno v:
Blood. 110:3968-3968
Orthotopic liver transplantation (OLT) is an effective treatment for both hepatitis C associated cirrhosis, hepatocellular carcinoma, and hemophilia A. Factor VIII activity usually increases into the normal range. Only a few patients with hemophilia