Results 201 to 210 of about 10,746,438 (360)

Acute Care Use Among People With Sickle Cell Disease, Sickle Cell Data Collection Program, 8 US States, 2018. [PDF]

Public Health Rep
Parks P, Miller JI, Cromartie Jones S, Attell BK, Brousseau DC, Clyde CL, Cooper WO, Dasgupta M, Desai J, Hardesty BM, Kayle M, Latta K, Mukhopadhyay A, Plaxco AP, Reeves SL, Singh A, Snyder AB, Valle J, Zhou M, Sontag MK.   +19 more
europepmc   +1 more source

Tocilizumab provides a potential therapeutic option for the management of hyperhaemolysis syndrome in sickle cell disease: A case series and brief narrative overview of the literature

Transfusion Medicine, EarlyView.
Abstract Background and Objectives Hyperhaemolysis syndrome is a life‐threatening complication of transfusion, potentially triggered by macrophage activation, with limited treatment options. Tocilizumab, an anti‐IL6 monoclonal antibody, has mechanistic rationale for use and has been shown to be effective in a small number of cases.
S. Wolf, B. Singh, A. Zaidi, P. Greaves, F. Oyesanya, S. Bennett, B. Kaya, F. Barroso, P. Telfer   +8 more
wiley   +1 more source

Biological parenthood rates among men with sickle cell disease. [PDF]

Blood Adv
Young AN, Hayford SR, Chandrasena SS, Conroy S, Karkare TP, Kroner BL, King A, Cronin RM, Badolato L, Nahata L, Creary SE.   +10 more
europepmc   +1 more source

Characterisation of RHD and RHCE variations in blood donors from Jazan Province, Southwestern Saudi Arabia

Transfusion Medicine, EarlyView.
Abstract Background and Objectives Rh is among the most important and highly polymorphic blood group systems due to the proximity of the RHD and RHCE genes, which encode numerous highly immunogenic antigens. However, in areas of Saudi Arabia with a high prevalence of hemoglobinopathy, the molecular characteristics of RHD and RHCE variations are lacking.
Maymoon M. Madkhali, Mayisah Khormy, Abdullah A. Meshi, Bandar Kameli, Khaled Ghazwani, Ohoud Sufyani, Salha Hakami, Yahya Khawaji, Abdullah A. Mobarki, Khaled Essawi, Waleed Hakami, Yara Alyahyawi, Aymen M. Madkhali, Gasim Dobie, Hassan A. Hamali   +14 more
wiley   +1 more source

Abdominal pain in adult sickle cell disease patients: a nigerian experience.

, 2011
Titilola S. Akingbola, B Kolude, Ehimen Aneni, Ayokunnu Raji, Kapona Iwara, Y A Aken'Ova, Olaitan Soyannwo   +6 more
openalex   +1 more source

The Relation between Glutathione S Transferase (GSTM1, GSTP1 and GSTT1) Polymorphisms and Clinical Diversity of Sickle Cell Disease among Pediatric Sudanese Patients

, 2021
Naif Taleb Ali, Ozaz Yagoup Mohammed Ahmed, Fayad O. Mohammed, Huda Mohammed Haroun   +3 more
openalex   +2 more sources

Development and validation of a pediatric transfusion medicine education assessment tool

Transfusion, EarlyView.
Abstract Background Pediatric transfusion medicine presents unique challenges due to differences in pediatric physiology and pathology compared to adults. Research shows that pediatric healthcare professionals have knowledge gaps in transfusion medicine, contributing to suboptimal practice.
Ines Zuna, Yulia Lin, Richard Haspel, Catharine M. Walsh, Jeffrey N. Bone, Casey Kapitany, Lani Lieberman, Teresa Skelton   +7 more
wiley   +1 more source

Enrollment patterns among medicaid beneficiaries with sickle cell disease: Multistate findings from the sickle cell data collection program. [PDF]

PLoS One
Singh A, Dasgupta M, Peng HK, Zhou M, Clyde C, Attell BK, Valle J, Reeves SL, Huebner J, Snyder AB.   +9 more
europepmc   +1 more source

Presumptive Treatment with Sulfadoxine- Pyrimethamine Versus Weekly Chloroquine for Malaria Prophylaxis in Children Attending the Sickle Cell Clinic, Mulago Hospital, Uganda: A Randomized Controlled Trial [PDF]

, 2008
Victoria Nakibuuka
openalex   +1 more source

Comparison of Serum Electrolytes between Sickle Cell and Control Group: A Meta-Analysis

, 2023
Abhishek Bansal
openalex   +2 more sources