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Pediatric Blood & Cancer
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March 14, 2008
Health-related quality of life in sickle cell disease
Julie A Panepinto
Hematology. American Society of Hematology. Education Program
|
December 13, 2012
Health-related quality of life in patients with hemoglobinopathies
Julie A Panepinto
Blood Advances
|
July 27, 2019
Clinical meaning of PROMIS pain domains for children with sickle cell disease
Ashima Singh, Julie A Panepinto
Pediatric Blood & Cancer
|
April 24, 2012
Health-related quality of life in sickle cell disease: past, present, and future
Julie A Panepinto, Melanie Bonner
Microcirculation (New York, N.Y. : 1994)
|
July 29, 2004
Pathophysiology of stroke in sickle cell disease
Cheryl A Hillery, Julie A Panepinto
Pediatric Blood & Cancer
|
August 30, 2020
Cognitive functioning, patient health communication, and worry mediate pain predictive effects on health-related quality of life in youth with sickle cell disease
James W Varni, Julie A Panepinto
Current Pharmaceutical Design
|
October 31, 2015
Pharmacotherapy of Sickle Cell Disease in Children
Kathleen A Neville, Julie A Panepinto
Journal of Pediatric Hematology/Oncology
|
February 25, 2016
Clinical Interpretation of Quantitative Sensory Testing as a Measure of Pain Sensitivity in Patients With Sickle Cell Disease
Amanda M Brandow, Julie A Panepinto
Hematology. American Society of Hematology. Education Program
|
December 13, 2012
What is the evidence that hydroxyurea improves health-related quality of life in patients with sickle cell disease?
Deepika S Darbari, Julie A Panepinto
Blood Advances
|
May 25, 2018
Identification of patients with hemoglobin SS/Sβ<sup>0</sup> thalassemia disease and pain crises within electronic health records
Ashima Singh, Javier Mora, Julie A Panepinto
Page
of 10
Search research articles
Search
Showing results (1-10 of 92) with videos related to
Sort By:
Page
of 10
Pediatric Blood & Cancer
|
March 14, 2008
Health-related quality of life in sickle cell disease
Julie A Panepinto
Hematology. American Society of Hematology. Education Program
|
December 13, 2012
Health-related quality of life in patients with hemoglobinopathies
Julie A Panepinto
Blood Advances
|
July 27, 2019
Clinical meaning of PROMIS pain domains for children with sickle cell disease
Ashima Singh, Julie A Panepinto
Pediatric Blood & Cancer
|
April 24, 2012
Health-related quality of life in sickle cell disease: past, present, and future
Julie A Panepinto, Melanie Bonner
Microcirculation (New York, N.Y. : 1994)
|
July 29, 2004
Pathophysiology of stroke in sickle cell disease
Cheryl A Hillery, Julie A Panepinto
Pediatric Blood & Cancer
|
August 30, 2020
Cognitive functioning, patient health communication, and worry mediate pain predictive effects on health-related quality of life in youth with sickle cell disease
James W Varni, Julie A Panepinto
Current Pharmaceutical Design
|
October 31, 2015
Pharmacotherapy of Sickle Cell Disease in Children
Kathleen A Neville, Julie A Panepinto
Journal of Pediatric Hematology/Oncology
|
February 25, 2016
Clinical Interpretation of Quantitative Sensory Testing as a Measure of Pain Sensitivity in Patients With Sickle Cell Disease
Amanda M Brandow, Julie A Panepinto
Hematology. American Society of Hematology. Education Program
|
December 13, 2012
What is the evidence that hydroxyurea improves health-related quality of life in patients with sickle cell disease?
Deepika S Darbari, Julie A Panepinto
Blood Advances
|
May 25, 2018
Identification of patients with hemoglobin SS/Sβ<sup>0</sup> thalassemia disease and pain crises within electronic health records
Ashima Singh, Javier Mora, Julie A Panepinto
Page
of 10