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Journal of Neurosurgery
|
September 2, 2008
Examination of the management of traumatic brain injury in the developing and developed world: focus on resource utilization, protocols, and practices that alter outcome
Odette A Harris, Carl A Bruce, Marvin Reid, et al.
Pain Research & Management
|
November 3, 2025
Cannabis Use Patterns Among Adults Living With Chronic Pain Before and During the COVID Pandemic: Insights From the COVID-19 Cannabis Health Study
Amrit Baral, Denise C Vidot, Bria-Necole A Diggs, et al.
American Journal of Hematology
|
February 23, 2026
Artificial Intelligence-Based Analysis of Central Nervous System Vasculopathy in Pediatric Sickle Cell Anemia
Meredith E Fay, Raghav Tandon, Teresa Latham, et al.
British Journal of Haematology
|
February 18, 2011
Improvements in haemolysis and indicators of erythrocyte survival do not correlate with acute vaso-occlusive crises in patients with sickle cell disease: a phase III randomized, placebo-controlled, double-blind study of the Gardos channel blocker senicapoc (ICA-17043)
Kenneth I Ataga, Marvin Reid, Samir K Ballas, et al.
Haematologica
|
July 14, 2011
Frequency of pain crises in sickle cell anemia and its relationship with the sympatho-vagal balance, blood viscosity and inflammation
Danitza Nebor, Andre Bowers, Marie-Dominique Hardy-Dessources, et al.
American Journal of Hematology
|
August 14, 2012
A phase 1/2 trial of HQK-1001, an oral fetal globin inducer, in sickle cell disease
Abdullah Kutlar, Kenneth Ataga, Marvin Reid, et al.
BMC Hematology
|
August 28, 2014
Vitamin D levels are low in adult patients with sickle cell disease in Jamaica and West Africa
Bamidele O Tayo, Titilola S Akingbola, Babatunde L Salako, et al.
British Journal of Haematology
|
March 6, 2018
Transcranial Doppler velocity among Jamaican children with sickle cell anaemia: determining the significance of haematological values and nutrition
Angela E Rankine-Mullings, Nadine Morrison-Levy, Deanne Soares, et al.
Clinical Hemorheology and Microcirculation
|
March 31, 2012
Relationship between acute chest syndrome and the sympatho-vagal balance in adults with hemoglobin SS disease; a case control study
Jennifer M Knight-Madden, Philippe Connes, Andre Bowers, et al.
Human Molecular Genetics
|
January 31, 2025
A replication study of novel fetal hemoglobin-associated genetic variants in sickle cell disease-only cohorts
Yann Ilboudo, Nicolas Brosseau, Ken Sin Lo, et al.
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Search research articles
Search
Showing results (61-70 of 74) with videos related to
Sort By:
Page
of 8
Journal of Neurosurgery
|
September 2, 2008
Examination of the management of traumatic brain injury in the developing and developed world: focus on resource utilization, protocols, and practices that alter outcome
Odette A Harris, Carl A Bruce, Marvin Reid, et al.
Pain Research & Management
|
November 3, 2025
Cannabis Use Patterns Among Adults Living With Chronic Pain Before and During the COVID Pandemic: Insights From the COVID-19 Cannabis Health Study
Amrit Baral, Denise C Vidot, Bria-Necole A Diggs, et al.
American Journal of Hematology
|
February 23, 2026
Artificial Intelligence-Based Analysis of Central Nervous System Vasculopathy in Pediatric Sickle Cell Anemia
Meredith E Fay, Raghav Tandon, Teresa Latham, et al.
British Journal of Haematology
|
February 18, 2011
Improvements in haemolysis and indicators of erythrocyte survival do not correlate with acute vaso-occlusive crises in patients with sickle cell disease: a phase III randomized, placebo-controlled, double-blind study of the Gardos channel blocker senicapoc (ICA-17043)
Kenneth I Ataga, Marvin Reid, Samir K Ballas, et al.
Haematologica
|
July 14, 2011
Frequency of pain crises in sickle cell anemia and its relationship with the sympatho-vagal balance, blood viscosity and inflammation
Danitza Nebor, Andre Bowers, Marie-Dominique Hardy-Dessources, et al.
American Journal of Hematology
|
August 14, 2012
A phase 1/2 trial of HQK-1001, an oral fetal globin inducer, in sickle cell disease
Abdullah Kutlar, Kenneth Ataga, Marvin Reid, et al.
BMC Hematology
|
August 28, 2014
Vitamin D levels are low in adult patients with sickle cell disease in Jamaica and West Africa
Bamidele O Tayo, Titilola S Akingbola, Babatunde L Salako, et al.
British Journal of Haematology
|
March 6, 2018
Transcranial Doppler velocity among Jamaican children with sickle cell anaemia: determining the significance of haematological values and nutrition
Angela E Rankine-Mullings, Nadine Morrison-Levy, Deanne Soares, et al.
Clinical Hemorheology and Microcirculation
|
March 31, 2012
Relationship between acute chest syndrome and the sympatho-vagal balance in adults with hemoglobin SS disease; a case control study
Jennifer M Knight-Madden, Philippe Connes, Andre Bowers, et al.
Human Molecular Genetics
|
January 31, 2025
A replication study of novel fetal hemoglobin-associated genetic variants in sickle cell disease-only cohorts
Yann Ilboudo, Nicolas Brosseau, Ken Sin Lo, et al.
Page
of 8