Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Hamayun Imran"'
Publikováno v:
Haematologica, Vol 93, Iss 10 (2008)
Externí odkaz:
https://doaj.org/article/af6d5c31b40e4ad1908c56c77abef1e1
Autor:
Soheil Meshinchi, Lane Miller, Stephanie Massaro, Robin Williams, Elizabeth Krieger, Melinda Pauly, Catherine Nelson, Deepa Bhojwani, Rebecca Johnson, Terzah M. Horton, Hamayun Imran, Wen-I Chang, Philip Neff, Matthew Kutny, Raul C. Ribeiro, Felipe Bautista, Terri Guinipero, Kate Murray, Alex Butte, Arturo Molina
Publikováno v:
Blood. 140:159-161
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fc21bda2852168c68a44974de44df675
https://doi.org/10.1182/blood-2022-162842
https://doi.org/10.1182/blood-2022-162842
Autor:
Anna L. Hoppmann, Chen Dai, Marla Daves, Hamayun Imran, Kimberly Whelan, Kelly Kenzik, Smita Bhatia
Publikováno v:
Cancer epidemiology, biomarkersprevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.
Background: One-fifth of U.S. counties are designated persistent child poverty counties (≥20% of children in poverty since 1980). The association between a persistent child poverty environment and mortality in children with cancer is unknown. Metho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38cb60a31c492a71e3fb0b6e651d1221
https://pubmed.ncbi.nlm.nih.gov/36129811
https://pubmed.ncbi.nlm.nih.gov/36129811
Autor:
Kasey Andrews, Soheil Meshinchi, Preethi Marri, Abdul H. Siddiqui, Jacek Polski, Arturo Molina, Joseph Chewning, Lisa Eidenschink Brodersen, Chad A. Hudson, Hamayun Imran
Publikováno v:
Blood. 140:11757-11758
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d34068aba11f3a1af3444b1f82ee077c
https://doi.org/10.1182/blood-2022-164629
https://doi.org/10.1182/blood-2022-164629
Publikováno v:
Journal of pediatric hematology/oncology. 42(7)
The management of ovarian immature teratoma (IT) presents several challenges. It occurs both in children and adults and therefore is managed by pediatric oncologists as well as adult and gynecologic oncologists. Treatment approach; however, varies si
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6735be2b2b4d6881eafc77b0238d43c
https://pubmed.ncbi.nlm.nih.gov/31205224
https://pubmed.ncbi.nlm.nih.gov/31205224
Autor:
Janet L. Kwiatkowski, Lori Luchtman-Jones, Linda B. Piller, Jennifer A. Rothman, Abdullah Kutlar, R. Clark Brown, Theodosia A. Kalfa, Carla W. Roberts, William H. Schultz, Nicole A. Mortier, Robert J. Adams, Alexis A. Thompson, William Owen, Beng Fuh, Margaret T. Lee, Jamie L. Coleman, Judy Luden, Alex George, Donna R. Roberts, John C. Wood, Kerri Nottage, Ofelia A. Alvarez, Sharada A. Sarnaik, Melanie J. Bonner, Susan E. Stuber, Lee Hilliard, Hamayun Imran, Stephen C. Nelson, Sherron M. Jackson, Sara L. Pressel, Banu Aygun, Matthew M. Heeney, Melissa Rhodes, Connie M. Piccone, Naomi L.C. Luban, Zora R. Rogers, Scott T. Miller, Peng Wei, Kathleen J. Helton, Cynthia Gauger, Isaac Odame, Barry R. Davis, Russell E. Ware, Alan R. Cohen, Niren Patel
Publikováno v:
Lancet (London, England)
Summary Background For children with sickle cell anaemia and high transcranial doppler (TCD) flow velocities, regular blood transfusions can effectively prevent primary stroke, but must be continued indefinitely. The efficacy of hydroxycarbamide (hyd
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::70c7e5d79309566d8761ac8cd85c3945
https://doi.org/10.1016/s0140-6736(15)01041-7
https://doi.org/10.1016/s0140-6736(15)01041-7
Autor:
Margaret T. Lee, Zora R. Rogers, Theodosia A. Kalfa, Russell E. Ware, Banu Aygun, Kathryn L. Hassell, Courtney D. Thornburg, Janet L. Kwiatkowski, William Owen, Carla W. Roberts, Hamayun Imran, Mary G. Smith, Lee Hilliard, Alexis A. Thompson, Barry R. Davis, R. Clark Brown, Lori Luchtman-Jones, Sara L. Pressel, Cynthia Gauger, Connie M. Piccone, Ofelia A. Alvarez, Jennifer A. Rothman, Stephen C. Nelson
Publikováno v:
American Journal of Hematology. 91:238-242
Although hemoglobin SC (HbSC) disease is usually considered less severe than sickle cell anemia (SCA), which includes HbSS and HbS/β(0) -thalassemia genotypes, many patients with HbSC experience severe disease complications, including vaso-occlusive
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::586155c29994a8aaa917e7a11d382155
https://doi.org/10.1002/ajh.24255
https://doi.org/10.1002/ajh.24255
Autor:
Connie M. Piccone, Zora R. Rogers, John C. Wood, William Owen, Hamayun Imran, Beng Fuh, Carla W. Roberts, William H. Schultz, Sherron M. Jackson, Beatrice E. Gee, Sharada A. Sarnaik, Russell E. Ware, Theodosia A. Kalfa, Lori Luchtman-Jones, Ofelia A. Alvarez, Alex George, Kerri Nottage, Jennifer Webb, Elizabeth Yang, Jane S. Hankins, R. Clark Brown, Sharon A. Singh, Isaac Odame, Barry R. Davis, Lee Hilliard, Kim Smith Whitley, Melissa Rhodes, Cynthia Gauger, Scott T. Miller, Alan R. Cohen, Janet L. Kwiatkowski, Sara L. Pressel, Alexis A. Thompson, Matthew M. Heeney, Jennifer A. Rothman, Margaret T. Lee, Banu Aygun, Brigitta U. Mueller, Stephen C. Nelson
Publikováno v:
British Journal of Haematology. 172:122-130
Transcranial Doppler (TCD) With Transfusions Changing to Hydroxyurea (TWiTCH) trial is a randomized, open-label comparison of hydroxycarbamide (also termed hydroxyurea) versus continued chronic transfusion therapy for primary stroke prevention in pat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd92b8c6025ff6bcfbe78df8e4d8328f
https://doi.org/10.1111/bjh.13791
https://doi.org/10.1111/bjh.13791
Publikováno v:
Blood. 132:3665-3665
Introduction The incidence of invasive pneumococcal infections in patients with sickle cell disease (SCD) decreased after introduction of penicillin prophylaxis and pneumococcal conjugate vaccine (PCV). However, the decrease in pneumococcal infection
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::30196ccb7e4e5f0000e431d14b36411a
https://doi.org/10.1182/blood-2018-99-111362
https://doi.org/10.1182/blood-2018-99-111362
Autor:
Lori, Luchtman-Jones, Sara, Pressel, Lee, Hilliard, R Clark, Brown, Mary G, Smith, Alexis A, Thompson, Margaret T, Lee, Jennifer, Rothman, Zora R, Rogers, William, Owen, Hamayun, Imran, Courtney, Thornburg, Janet L, Kwiatkowski, Banu, Aygun, Stephen, Nelson, Carla, Roberts, Cynthia, Gauger, Connie, Piccone, Theodosia, Kalfa, Ofelia, Alvarez, Kathryn, Hassell, Barry R, Davis, Russell E, Ware
Publikováno v:
American journal of hematology. 91(2)
Although hemoglobin SC (HbSC) disease is usually considered less severe than sickle cell anemia (SCA), which includes HbSS and HbS/β(0) -thalassemia genotypes, many patients with HbSC experience severe disease complications, including vaso-occlusive
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f676d74c5a9460f4dc765ad37a14a9dc
https://pubmed.ncbi.nlm.nih.gov/26615793
https://pubmed.ncbi.nlm.nih.gov/26615793