Zobrazeno 1 - 10
of 45
pro vyhledávání: '"Connie M. Piccone"'
Autor:
Abena Appiah-Kubi, Seethal A Jacob, Matthew M. Heeney, Clark Brown, Susan E. Creary, Christine R Hollenkamp, Emily Riehm Meier, Omar Niss, Connie M. Piccone, Maa-Ohui Quarmyne, Charles T. Quinn, Allison Remiker, Kay L Saving, Min Dong, Patrick T. McGann
Publikováno v:
Blood. 140:5416-5417
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::304204b52abb6d10c0597d5f212752b4
https://doi.org/10.1182/blood-2022-158623
https://doi.org/10.1182/blood-2022-158623
Autor:
Beverly A Schaefer, Jonathan M Flanagan, Ofelia A Alvarez, Stephen C Nelson, Banu Aygun, Kerri A Nottage, Alex George, Carla W Roberts, Connie M Piccone, Thad A Howard, Barry R Davis, Russell E Ware
Publikováno v:
PLoS ONE, Vol 11, Iss 10, p e0164364 (2016)
Discovery and validation of genetic variants that influence disease severity in children with sickle cell anemia (SCA) could lead to early identification of high-risk patients, better screening strategies, and intervention with targeted and preventiv
Externí odkaz:
https://doaj.org/article/f7ba0935a92c4de69929dbb63e87b5f5
Autor:
William T Zempsky, Mary Yanaros, Mohammed Sayeem, Donna Boruchov, Connie M Piccone, Deepa Manwani, Crawford Strunk, Immacolata Tartaglione, Raffaella Colombatti, Sophia Akatue, Bianca Oteng, Ahmed Owda, Rose Bamfo, Samuel Wilson, Angela Rivers, Fatimah Farooq, Rebekah Urbonya, Gifty Dankwah Boatemaa, Sudha Rao, Baba Inusa, Charles Antwi-Boasiako, Catherine Segbefia, Fredericka Sey, Biree Andemariam, Eugenia Vicky Asare, Andrew D Campbell
Objectives Sickle Cell Disease (SCD) is a genetic blood disorder affecting over 1 million people globally. The aim of this analysis is to explore the pain burden of patients with SCD in two countries: the United States and Ghana. Methods The Consorti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58350059a74d1ee6f93c6e9f59bc1a24
http://hdl.handle.net/11591/465294
http://hdl.handle.net/11591/465294
Publikováno v:
Pediatrics in review. 42(Suppl 2)
1. Sneha Butala, MD* 2. Saloni Sheth, MD* 3. Keval Parikh, MD† 4. Connie Piccone, MD‡,§ 1. *Department of Pediatrics, Rainbow Babies and Children’s Hospital, Cleveland, OH 2. †Department of Radiology, University Hospitals Cleveland Medical C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b28e75f4faab266a37fb72a2689c28de
https://pubmed.ncbi.nlm.nih.gov/34470901
https://pubmed.ncbi.nlm.nih.gov/34470901
Autor:
Navneet S. Majhail, Amy S. Nowacki, Rabi Hanna, Alicia M Stallings, Connie M. Piccone, Grace I. Onimoe
Publikováno v:
British Journal of Haematology. 188:976-984
Beginning early in childhood, patients with sickle cell disease [SCD; a group of genetic haemoglobin disorders characterized by the sickle or HbS mutation (HBB E7V)] are at risk of life-threatening and debilitating health events. Despite the high mor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65d45fb8d1c5c2d5ceb6f64a1e7ba101
https://doi.org/10.1111/bjh.16248
https://doi.org/10.1111/bjh.16248
Autor:
Connie M. Piccone, Charles T. Quinn, Lewis L. Hsu, Grace I. Onimoe, Alicia M Stallings, Jasmine Umana, Jillian Wen, Amy S. Nowacki, Navneet S. Majhail, Rabi Hanna
Publikováno v:
Journal of Pediatric Hematology/Oncology. 41:187-193
Beginning early in childhood, patients with sickle cell disease (SCD) are at risk of life-threatening and debilitating health events. Despite the high morbidity and mortality of this disease, hematopoietic cell transplantation (HCT), a curative treat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c9bea6308f9b826c15a0c55d7f065cc
https://doi.org/10.1097/mph.0000000000001433
https://doi.org/10.1097/mph.0000000000001433
Autor:
Allison A. King, Anna M Hood, Kim Smith-Whitley, Steven K Reader, Aimee K. Hildenbrand, Connie M. Piccone, Marsha Treadwell, Francis J. Real, Charles T. Quinn, Lisa M Shook, Jean L. Raphael, Cara Nwankwo, Amy Sobota, Yolanda Johnson, Amber M Yates, Maria T. Britto, Rogelle Hackworth, Susan E Creary, William B. Brinkman, Kay L. Saving, James Peugh, Lori E. Crosby, Heather Strong, Sohail Rana, Alexis A. Thompson, Lynne Neumayr, Melissa Klein, Sherif M. Badawy, Cecelia Calhoun, Constance A. Mara, Emily Riehm Meier, Russell E. Ware
Publikováno v:
JMIR Research Protocols, Vol 10, Iss 5, p e27650 (2021)
JMIR Research Protocols
Hood, A M, Strong, H, Nwankwo, C, Johnson, Y, Peugh, J, Mara, C A, Shook, L M, Brinkman, W B, Real, F J, Klein, M D, Hackworth, R, Badawy, S M, Thompson, A A, Raphael, J L, Yates, A M, Smith-Whitley, K, King, A A, Calhoun, C, Creary, S E, Piccone, C M, Hildenbrand, A K, Reader, S K, Neumayr, L, Meier, E R, Sobota, A E, Rana, S, Britto, M, Saving, K L, Treadwell, M, Quinn, C T, Ware, R E & Crosby, L E 2021, ' Engaging Caregivers and Providers of Children With Sickle Cell Anemia in Shared Decision Making for Hydroxyurea : Protocol for a Multicenter Randomized Controlled Trial ', JMIR research protocols, vol. 10, no. 5, e27650 . https://doi.org/10.2196/27650
JMIR Research Protocols
Hood, A M, Strong, H, Nwankwo, C, Johnson, Y, Peugh, J, Mara, C A, Shook, L M, Brinkman, W B, Real, F J, Klein, M D, Hackworth, R, Badawy, S M, Thompson, A A, Raphael, J L, Yates, A M, Smith-Whitley, K, King, A A, Calhoun, C, Creary, S E, Piccone, C M, Hildenbrand, A K, Reader, S K, Neumayr, L, Meier, E R, Sobota, A E, Rana, S, Britto, M, Saving, K L, Treadwell, M, Quinn, C T, Ware, R E & Crosby, L E 2021, ' Engaging Caregivers and Providers of Children With Sickle Cell Anemia in Shared Decision Making for Hydroxyurea : Protocol for a Multicenter Randomized Controlled Trial ', JMIR research protocols, vol. 10, no. 5, e27650 . https://doi.org/10.2196/27650
Background Sickle cell anemia (SCA) is a genetic blood disorder that puts children at a risk of serious medical complications, early morbidity and mortality, and high health care utilization. Until recently, hydroxyurea was the only disease-modifying
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f8a387c60b735640f7092556fa43b1c0
https://www.researchprotocols.org/2021/5/e27650
https://www.researchprotocols.org/2021/5/e27650
Autor:
Yuncheng Man, Utku Goreke, Sanjay P Ahuja, Russell W. Valentine, Connie M. Piccone, Yuning Huang, Amma Owusu-Ansah, Umut A. Gurkan, Ran An, Erdem Kucukal, Zoe Sekyonda, Jane A. Little
Publikováno v:
Lab Chip
Anemia, characterized by low blood hemoglobin level, affects about 25% of the world's population with the heaviest burden borne by women and children. Anemia leads to impaired cognitive development in children, as well as high morbidity and early mor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16aa45cadb8754609422be56588c9275
https://pubmed.ncbi.nlm.nih.gov/33881041
https://pubmed.ncbi.nlm.nih.gov/33881041
Autor:
Anna M Hood, Heather Strong, Cara Nwankwo, Yolanda Johnson, James Peugh, Constance A Mara, Lisa M Shook, William B Brinkman, Francis J Real, Melissa D Klein, Rogelle Hackworth, Sherif M Badawy, Alexis A Thompson, Jean L Raphael, Amber M Yates, Kim Smith-Whitley, Allison A King, Cecelia Calhoun, Susan E Creary, Connie M Piccone, Aimee K Hildenbrand, Steven K Reader, Lynne Neumayr, Emily R Meier, Amy E Sobota, Sohail Rana, Maria Britto, Kay L Saving, Marsha Treadwell, Charles T Quinn, Russell E Ware, Lori E Crosby
BACKGROUND Sickle cell anemia (SCA) is a genetic blood disorder that puts children at a risk of serious medical complications, early morbidity and mortality, and high health care utilization. Until recently, hydroxyurea was the only disease-modifying
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a584f8f48b0e173db2375c45e3d8948b
https://doi.org/10.2196/preprints.27650
https://doi.org/10.2196/preprints.27650
Autor:
Charles Antwi-Boasiako, Eugenia Vicky Asare, Donna Boruchov, Connie M. Piccone, Fatimah Farooq, Laura Sainati, Silverio Perrotta, Biree Andemariam, William T. Zempsky, Raffaella Colombatti, Immacolata Tartaglione, Rebekah Urbonya, Catherine I. Segbefia, Andrew D. Campbell, Deepa Manwani, Fredericka Sey, Gifty Dankwah Boatemaa, Sudha Rao, Crawford John Strunk, Baba Inusa, Angela Rivers
Publikováno v:
J Racial Ethn Health Disparities
Millions are affected by Sickle Cell Disease (SCD) worldwide with the greatest burden in sub-Saharan Africa. While its origin lies historically within the malaria belt, ongoing changes in migration patterns have shifted the burden of disease resultin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d124b5bf5dd138c01b556aad10638b01
http://hdl.handle.net/11591/430151
http://hdl.handle.net/11591/430151