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Julie A Panepinto

Showing results (1-10 of 92) with videos related to

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Pediatric Blood & Cancer|March 14, 2008
Health-related quality of life in sickle cell diseaseJulie A Panepinto
Hematology. American Society of Hematology. Education Program|December 13, 2012
Health-related quality of life in patients with hemoglobinopathiesJulie A Panepinto
Blood Advances|July 27, 2019
Clinical meaning of PROMIS pain domains for children with sickle cell diseaseAshima Singh, Julie A Panepinto
Pediatric Blood & Cancer|April 24, 2012
Health-related quality of life in sickle cell disease: past, present, and futureJulie A Panepinto, Melanie Bonner
Microcirculation (New York, N.Y. : 1994)|July 29, 2004
Pathophysiology of stroke in sickle cell diseaseCheryl 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 diseaseJames W Varni, Julie A Panepinto
Current Pharmaceutical Design|October 31, 2015
Pharmacotherapy of Sickle Cell Disease in ChildrenKathleen 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 DiseaseAmanda 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 recordsAshima Singh, Javier Mora, Julie A Panepinto
Pageof 10

Showing results (1-10 of 92) with videos related to

Sort By:
Pageof 10
Pediatric Blood & Cancer|March 14, 2008
Health-related quality of life in sickle cell diseaseJulie A Panepinto
Hematology. American Society of Hematology. Education Program|December 13, 2012
Health-related quality of life in patients with hemoglobinopathiesJulie A Panepinto
Blood Advances|July 27, 2019
Clinical meaning of PROMIS pain domains for children with sickle cell diseaseAshima Singh, Julie A Panepinto
Pediatric Blood & Cancer|April 24, 2012
Health-related quality of life in sickle cell disease: past, present, and futureJulie A Panepinto, Melanie Bonner
Microcirculation (New York, N.Y. : 1994)|July 29, 2004
Pathophysiology of stroke in sickle cell diseaseCheryl 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 diseaseJames W Varni, Julie A Panepinto
Current Pharmaceutical Design|October 31, 2015
Pharmacotherapy of Sickle Cell Disease in ChildrenKathleen 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 DiseaseAmanda 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 recordsAshima Singh, Javier Mora, Julie A Panepinto
Pageof 10