Zobrazeno 1 - 10
of 78
pro vyhledávání: '"Kimo C. Stine"'
Autor:
Varsha G. Desai, Taewon Lee, Carrie L. Moland, Kelly Davis, Vikrant Vijay, Kimo C. Stine, James C. Fuscoe, Tao Han, Bounleut Phanavanh, Levan Muskhelishvili
Publikováno v:
Journal of applied toxicology : JATREFERENCES. 42(5)
Subclinical cardiotoxicity at low total cumulative doxorubicin (DOX) doses can manifest into cardiomyopathy in long-term cancer survivors. However, the underlying mechanisms are poorly understood. In male B6C3F1 mice, assessment of cardiac function b
Publikováno v:
Journal of pediatric hematology/oncology. 43(8)
Increasing availability of genomic testing poses new challenges to clinicians, particularly where variant interpretation from commercial sources may be equivocal. The authors report a patient with recurrent rhabdomyosarcoma and subsequent bilateral b
Autor:
Nathan Visweshwar, Jeremy Rupon, Annie Fang, Frank Plonski, Lynne Smith, Adam Giermasz, Steven Arkin, Gregory Di Russo, Kimo C. Stine, Li-Jung Tseng, Andrew D. Leavitt, Didier Rouy, Barbara A. Konkle, Bettina M. Cockroft, Thomas J. Harrington
Publikováno v:
Blood. 136:12-12
Introduction: Hemophilia A is a rare bleeding disorder caused by pathogenic variants in the F8 gene, resulting in insufficient factor VIII (FVIII) activity. Adeno-associated virus (AAV)-mediated gene transfer enables the delivery of a modified functi
Autor:
Alexis A. Thompson, Peter W. Forbes, Kimo C. Stine, Jenny M. Despotovic, Rachael F. Grace, Yves D. Pastore, Cindy E. Neunert, Robert J. Klaassen, Kristin A. Shimano, Kristina M. Haley, Kerri Nottage, Travis Brown, Carolyn M. Bennett, Michele P. Lambert
Publikováno v:
Pediatric Blood & Cancer. 63:1407-1413
Background Data on second-line treatment options for pediatric patients with immune thrombocytopenia (ITP) are limited. Thrombopoietin receptor agonists (TPO-RA) provide a nonimmunosuppressive option for children who require an increased platelet cou
Autor:
David L. Becton, Jaclyn VanderSchilden, Richard W. Nicholas, Kimo C. Stine, Lichu Liu, Robert C. Bunn, Charles K. Lumpkin, Larry J. Suva, Corey O. Montgomery, Robert A. Skinner, James Aronson, Elizabeth C. Wahl, Christopher J. Swearingen
Publikováno v:
Journal of Orthopaedic Research. 34:1716-1724
The majority of Osteosarcoma (OS) patients are treated with a combination of chemotherapy, resection, and limb salvage protocols. These protocols include distraction osteogenesis (DO), which is characterized by direct new bone formation. Cisplatin (C
Autor:
Kimo C. Stine, Ashley Snyder, Gregory Di Russo, Steven Arkin, Adam Giermasz, Thomas J. Harrington, Didier Rouy, Barbara A. Konkle, Andrew D. Leavitt, Nathan Visweshwar, Adrian Woolfson
Publikováno v:
Blood. 134:2060-2060
Introduction: Hemophilia A is a rare blood disorder caused by an F8 variant resulting in insufficient Factor VIII (FVIII) activity. Updated results and follow-up of an ongoing gene therapy study in patients with severe hemophilia A are presented. Met
Autor:
Sara Seepo, Kyle Beckman, Clifford M. Takemoto, Todd Cooper, Johann Hitzler, Philip A. Roehrs, Todd R. Golub, Tiffany Y. Chang, Scott R. Olsen, Tali Mazor, Patrick A. Brown, Robert J. Hayashi, Mara Rosenberg, Reuven J. Schore, Rakesh K. Goyal, Philip M. Monteleone, Emilio Esquivel, Jeffrey A. Toretsky, Elliot Stieglitz, Robert B. Gerbing, Mignon L. Loh, Adam B. Olshen, Gad Getz, Yong Dong Wang, Yongjin Li, Benjamin Carcamo, Laura C. Gelston, Kimo C. Stine, Ghada Abusin, Chip Stewart, Peter D. Emanuel, Todd A. Alonzo, Y. Lucy Liu, Yoav Messinger, Gary V. Dahl, Joseph F. Costello, Kimberly Stegmaier, Christopher Hugge, Donald H. Mahoney, Jing Ma, Eneida R. Nemecek, Sophie Archambeault, Amaro Taylor-Weiner, Ariel Yu, Mark Fluchel, Tanja A. Gruber, Michael Briones
Publikováno v:
Nature genetics
Juvenile myelomonocytic leukemia (JMML) is a myeloproliferative neoplasm (MPN) of childhood with a poor prognosis. Mutations in NF1, NRAS, KRAS, PTPN11 and CBL occur in 85% of patients, yet there are currently no risk stratification algorithms capabl
Autor:
Nicolino Ruperto, Antonella Buoncompagni, Bianca Lattanzi, Zane Davidsone, Maka Ioseliani, Jaime de Inocencio, Carmen De Cunto, Jeffrey M. Lipton, Angelo Ravelli, Claudia Saad Magalhães, Sandra Enciso, Thomas A. Griffin, Patrizia Barone, Hasan Tezer, Michael Jeng, Francesca Bovis, Paolo Picco, Sulaiman M. Al-Mayouf, Ageza M Kapovic, Nuray Aktay Ayaz, Jonathan D Akikusa, Erkan Demirkaya, Ingrida Rumba-Rozenfelde, Silvia Magni Manzoni, Olga Vougiouka, B. Bica, Alberto Martini, Randy Q. Cron, Romina Gallizzi, Francesca Minoia, Isabel Bolt, Wafaa Sewairi, Luciana Breda, AnnaCarin Horne, Sergio Davì, Teresa Hennon, G. Horneff, Lehn K. Weaver, Kimo C. Stine
Publikováno v:
The Journal of Rheumatology. 42:994-1001
Objective.To seek insights into the heterogeneity of macrophage activation syndrome (MAS) complicating systemic juvenile idiopathic arthritis (sJIA) through the analysis of a large patient sample collected in a multinational survey.Methods.Internatio
Autor:
Francesca Minoia, Francesca Bovis, Sergio Davì, Antonella Insalaco, Kai Lehmberg, Susan Shenoi, Sheila Weitzman, Graciela Espada, Yi-Jin Gao, Jordi Anton, Toshiyuki Kitoh, Ozgur Kasapcopur, Helga Sanner, Rosa Merino, Itziar Astigarraga, Maria Alessio, Michael Jeng, Vyacheslav Chasnyk, Kim E. Nichols, Zeng Huasong, Caifeng Li, Concetta Micalizzi, Nicolino Ruperto, Alberto Martini, Randy Q. Cron, Angelo Ravelli, AnnaCarin Horne, Mario Abinun, Amita Aggarwal, Jonathan Akikusa, Sulaiman Al-Mayouf, Maria Teresa Apaz, Tadej Avcin, Nuray Aktay Ayaz, Patrizia Barone, Bianca Bica, Isabel Bolt, Luciana Breda, Rolando Cimaz, Fabrizia Corona, Ruben Cuttica, Zane Davidsone, Carmen De Cunto, Jaime De Inocencio, Erkan Demirkaya, Eli M. Eisenstein, Sandra Enciso, Michel Fischbach, Michael Frosch, Romina Gallizzi, Maria Luz Gamir, Thomas Griffin, Alexei Grom, Soad Hashad, Teresa Hennon, Jan-Inge Henter, Gerd Horneff, Adam Huber, Norman Ilowite, Maka Ioseliani, Agneza Marija Kapović, Raju Khubchandani, Isabelle Koné-Paut, Sheila Knupp Feitosa de Oliveira, Bianca Lattanzi, Loredana Lepore, Jeffrey M. Lipton, Silvia Magni-Manzoni, Despoina Maritsi, Deborah McCurdy, Paivi Miettunen, Velma Mulaosmanovic, Susan Nielsen, Seza Ozen, Priyankar Pal, Sampath Prahalad, Donato Rigante, Ingrida Rumba-Rozenfelde, Ricardo Russo, Claudia Saad Magalhães, Wafaa Mohamed Saad Sewairi, Clovis Artur Silva, Valda Stanevicha, Gary Sterba, Kimo C. Stine, Gordana Susic, Flavio Sztajnbok, Syuji Takei, Ralf Trauzeddel, Elena Tsitsami, Erbil Unsal, Yosef Uziel, Olga Vougiouka, Carol A. Wallace, Lehn Weaver, Jennifer E. Weiss, Carine Wouters, Nico Wulffraat, Mabruka Zletni, Maurizio Arico, R. Maarten Egeler, Alexandra H. Filipovich, Helmut Gadner, Shinsaku Imashuku, Gritta Janka, Stephan Ladisch, Ken L. McClain, David Webb
Publikováno v:
JOURNAL OF PEDIATRICS
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu
OBJECTIVE: To develop and validate a diagnostic score that assists in discriminating primary hemophagocytic lymphohistiocytosis (pHLH) from macrophage activation syndrome (MAS) related to systemic juvenile idiopathic arthritis. STUDY DESIGN: The clin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d908099e02f637432862a51326748c61
http://hdl.handle.net/10807/104902
http://hdl.handle.net/10807/104902
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