A critical appraisal and clinical application of Charache S, Terrin ML, Moore RD, et al. Effect of hydroxyurea on the frequency of painful crises in sickle cell anemia. N Engl J Med 1995;(332):1317-1322 doi: 10.1056/nejm19950518332200
AIMS AND OBJECTIVES: The aim of this study was to analyze the demographic, clinical and laboratory ...
We conducted the first nation-wide cohort study of sickle cell disease (SCD) in Italy, a Southern Eu...
Although hemoglobin SC (HbSC) disease is usually considered less severe than sickle cell anemia (SCA...
The purpose of this evidence based practice literature review is to research the long term effects o...
The purpose of this evidence based practice literature review is to research the long term effects o...
Recurrent acute sickle cell painful crises are the hallmark of sickle cell anemia. These events may ...
Abstract Background Vaso–occlusive crises (VOCs) are acute and common painful complication of sickle...
Background: The Multicenter Study of Hydroxyurea (HU) in Sickle Cell Anemia (MSH) previously showed ...
Abstract Background The Multicenter Study of Hydroxyurea (HU) in Sickle Cell Anemia (MSH) previously...
Sickle cell is a hereditary disease affecting more than 100,000 people in the United States alone th...
A critical appraisal and clinical application of van Beers EJ, van Tuijn CF, Nieuwkerk PT, Friederic...
Clinical experience with hydroxyurea for patients with sickle cell disease (SCD) has been accumulati...
Background: Sickle cell disease (SCD) an inheritable disorder of haemoglobin structure resulting fro...
Jeffrey D Lebensburger, Rakeshkumar J Patel, Prasannalaxmi Palabindela, Christina J Bemrich-Stolz, T...
AbstractObjectiveThe objective of this study is to demonstrate the effects of hydroxyurea in childre...
AIMS AND OBJECTIVES: The aim of this study was to analyze the demographic, clinical and laboratory ...
We conducted the first nation-wide cohort study of sickle cell disease (SCD) in Italy, a Southern Eu...
Although hemoglobin SC (HbSC) disease is usually considered less severe than sickle cell anemia (SCA...
The purpose of this evidence based practice literature review is to research the long term effects o...
The purpose of this evidence based practice literature review is to research the long term effects o...
Recurrent acute sickle cell painful crises are the hallmark of sickle cell anemia. These events may ...
Abstract Background Vaso–occlusive crises (VOCs) are acute and common painful complication of sickle...
Background: The Multicenter Study of Hydroxyurea (HU) in Sickle Cell Anemia (MSH) previously showed ...
Abstract Background The Multicenter Study of Hydroxyurea (HU) in Sickle Cell Anemia (MSH) previously...
Sickle cell is a hereditary disease affecting more than 100,000 people in the United States alone th...
A critical appraisal and clinical application of van Beers EJ, van Tuijn CF, Nieuwkerk PT, Friederic...
Clinical experience with hydroxyurea for patients with sickle cell disease (SCD) has been accumulati...
Background: Sickle cell disease (SCD) an inheritable disorder of haemoglobin structure resulting fro...
Jeffrey D Lebensburger, Rakeshkumar J Patel, Prasannalaxmi Palabindela, Christina J Bemrich-Stolz, T...
AbstractObjectiveThe objective of this study is to demonstrate the effects of hydroxyurea in childre...
AIMS AND OBJECTIVES: The aim of this study was to analyze the demographic, clinical and laboratory ...
We conducted the first nation-wide cohort study of sickle cell disease (SCD) in Italy, a Southern Eu...
Although hemoglobin SC (HbSC) disease is usually considered less severe than sickle cell anemia (SCA...
DOI
Add to ORKG