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Blood Cells, Molecules & Diseases
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September 27, 2016
Genotype-phenotype correlations in hereditary elliptocytosis and hereditary pyropoikilocytosis
Omar Niss, Satheesh Chonat, Neha Dagaonkar, et al.
American Journal of Hematology
|
May 21, 2019
Robust clinical and laboratory response to hydroxyurea using pharmacokinetically guided dosing for young children with sickle cell anemia
Patrick T McGann, Omar Niss, Min Dong, et al.
Scientific Reports
|
February 6, 2020
Left atrial dysfunction in sickle cell anemia is associated with diffuse myocardial fibrosis, increased right ventricular pressure and reduced exercise capacity
Tarek Alsaied, Omar Niss, Justin T Tretter, et al.
Scientific Reports
|
March 14, 2020
Author Correction: Left atrial dysfunction in sickle cell anemia is associated with diffuse myocardial fibrosis, increased right ventricular pressure and reduced exercise capacity
Tarek Alsaied, Omar Niss, Justin T Tretter, et al.
Cardiology in the Young
|
April 7, 2020
Lymphopenia in adults after the Fontan operation: prevalence and associations
Tarek Alsaied, Mathias Possner, Nicole Brown, et al.
British Journal of Haematology
|
July 6, 2021
Early initiation of hydroxyurea (hydroxycarbamide) using individualised, pharmacokinetics-guided dosing can produce sustained and nearly pancellular expression of fetal haemoglobin in children with sickle cell anaemia
Charles T Quinn, Omar Niss, Min Dong, et al.
Blood Cells, Molecules & Diseases
|
January 5, 2021
Congenital dyserythropoietic anemia type I: First report from the Congenital Dyserythropoietic Anemia Registry of North America (CDAR)
Omar Niss, Robert B Lorsbach, Mikaela Berger, et al.
Health Care Transitions
|
June 1, 2026
Community health worker support to adolescents and young adults with sickle cell disease: A multi-method analysis on transition-related support
Jayanne Forrest, Claudio Galea, Caren Steinway, et al.
JAMA Network Open
|
November 17, 2025
Community Health Worker and Mobile Health Interventions for Quality of Life Among Young Adults With Sickle Cell Disease: A Randomized Clinical Trial
Sophia Jan, Caren Steinway, Tanisha Belton, et al.
Frontiers in Physiology
|
July 24, 2019
The Spectrum of <i>SPTA1</i>-Associated Hereditary Spherocytosis
Satheesh Chonat, Mary Risinger, Haripriya Sakthivel, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 39) with videos related to
Sort By:
Page
of 4
Blood Cells, Molecules & Diseases
|
September 27, 2016
Genotype-phenotype correlations in hereditary elliptocytosis and hereditary pyropoikilocytosis
Omar Niss, Satheesh Chonat, Neha Dagaonkar, et al.
American Journal of Hematology
|
May 21, 2019
Robust clinical and laboratory response to hydroxyurea using pharmacokinetically guided dosing for young children with sickle cell anemia
Patrick T McGann, Omar Niss, Min Dong, et al.
Scientific Reports
|
February 6, 2020
Left atrial dysfunction in sickle cell anemia is associated with diffuse myocardial fibrosis, increased right ventricular pressure and reduced exercise capacity
Tarek Alsaied, Omar Niss, Justin T Tretter, et al.
Scientific Reports
|
March 14, 2020
Author Correction: Left atrial dysfunction in sickle cell anemia is associated with diffuse myocardial fibrosis, increased right ventricular pressure and reduced exercise capacity
Tarek Alsaied, Omar Niss, Justin T Tretter, et al.
Cardiology in the Young
|
April 7, 2020
Lymphopenia in adults after the Fontan operation: prevalence and associations
Tarek Alsaied, Mathias Possner, Nicole Brown, et al.
British Journal of Haematology
|
July 6, 2021
Early initiation of hydroxyurea (hydroxycarbamide) using individualised, pharmacokinetics-guided dosing can produce sustained and nearly pancellular expression of fetal haemoglobin in children with sickle cell anaemia
Charles T Quinn, Omar Niss, Min Dong, et al.
Blood Cells, Molecules & Diseases
|
January 5, 2021
Congenital dyserythropoietic anemia type I: First report from the Congenital Dyserythropoietic Anemia Registry of North America (CDAR)
Omar Niss, Robert B Lorsbach, Mikaela Berger, et al.
Health Care Transitions
|
June 1, 2026
Community health worker support to adolescents and young adults with sickle cell disease: A multi-method analysis on transition-related support
Jayanne Forrest, Claudio Galea, Caren Steinway, et al.
JAMA Network Open
|
November 17, 2025
Community Health Worker and Mobile Health Interventions for Quality of Life Among Young Adults With Sickle Cell Disease: A Randomized Clinical Trial
Sophia Jan, Caren Steinway, Tanisha Belton, et al.
Frontiers in Physiology
|
July 24, 2019
The Spectrum of <i>SPTA1</i>-Associated Hereditary Spherocytosis
Satheesh Chonat, Mary Risinger, Haripriya Sakthivel, et al.
Page
of 4