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Biophysical Journal, ISSN 0006-3495, 02/2016, Volume 110, Issue 3, pp. 653a - 653a
Journal Article
Lancet, The, ISSN 0140-6736, 2010, Volume 376, Issue 9757, pp. 2018 - 2031
Summary Sickle-cell disease is one of the most common severe monogenic disorders in the world. Haemoglobin polymerisation, leading to erythrocyte rigidity and... 
Internal Medicine | FETAL-HEMOGLOBIN LEVELS | MEDICINE, GENERAL & INTERNAL | HOSPITAL ADMISSIONS | RISK-FACTORS | PULMONARY-HYPERTENSION | ACUTE CHEST SYNDROME | HYDROXYUREA THERAPY | NITRIC-OXIDE | ADHESION MOLECULES | ACUTE VASOOCCLUSIVE CRISIS | PLASMODIUM-FALCIPARUM MALARIA | Haplotypes | Antisickling Agents - therapeutic use | Acute Chest Syndrome - etiology | Acute Chest Syndrome - therapy | Humans | Pain Management | Hypertension, Pulmonary - therapy | Blood Transfusion | Anemia, Sickle Cell - epidemiology | Erythrocytes - pathology | Pain - etiology | Anemia, Sickle Cell - classification | Hemolysis | Severity of Illness Index | Gene Transfer Techniques | Iron Chelating Agents - therapeutic use | Disease Susceptibility | Anemia, Sickle Cell - complications | Africa | Hematopoietic Stem Cell Transplantation | Polymerization | Nervous System Diseases - therapy | Anemia, Sickle Cell - therapy | Heart Diseases - etiology | Mass Screening | Heart Diseases - therapy | Kidney Diseases - therapy | Nervous System Diseases - etiology | Hydroxyurea - therapeutic use | Anemia, Sickle Cell - blood | Anemia, Sickle Cell - diagnosis | Kidney Diseases - etiology | Hypertension, Pulmonary - etiology | Hematopoietic Stem Cells | Care and treatment | Sickle cell anemia | Hemoglobin | Development and progression | Diagnosis | Health aspects | Risk factors | Disease | Rodents | Nitric oxide | Mutation | Gene therapy | Epidemiology | Federal funding
Journal Article
04/2013
Background:Hip disease is a complication of Sickle Cell Disease most commonly occurs during adolescence and early adult life that constitutes from 3.3% to... 
Hip disease- diagnosis-sickle cell anemia- young adult-Kinshasa
Web Resource
Lancet, The, ISSN 0140-6736, 2017, Volume 390, Issue 10091, pp. 311 - 323
Summary Sickle cell disease is a common and life-threatening haematological disorder that affects millions of people worldwide. Abnormal sickle-shaped... 
Internal Medicine | MEDICINE, GENERAL & INTERNAL | RISK-FACTORS | PULMONARY-HYPERTENSION | CLINICAL-TRIAL | SUB-SAHARAN AFRICA | FETAL-HEMOGLOBIN | EARLY-CHILDHOOD MORTALITY | TRANSCRANIAL DOPPLER ULTRASONOGRAPHY | TRANSFUSION-TRANSMITTED INFECTIONS | IRON OVERLOAD | YOUNG-CHILDREN | Hemolysis | Antisickling Agents - therapeutic use | Pregnancy Complications, Hematologic - prevention & control | Stroke - prevention & control | Anemia, Sickle Cell - complications | Humans | Pregnancy | Anemia, Sickle Cell - therapy | Global Burden of Disease | Stem Cell Transplantation - methods | Stroke - etiology | Cerebrovascular Disorders - prevention & control | Point-of-Care Systems | Iron Overload - therapy | Female | Hydroxyurea - therapeutic use | Anemia, Sickle Cell - diagnosis | Chronic Disease | Early Diagnosis | Hemolytic Plaque Technique | Blood Transfusion - methods | Genetic Therapy - methods | Prevention | Transplantation | Diagnostic imaging | Sickle cell anemia | Mortality | Stem cells | Occlusion | Erythrocytes | Iron | Pain | Ischemia | Penicillin | Hemoglobin | Sickle cell disease | Genetic modification | Stroke | Hematology | Anemia | Vessels | Blood vessels | Medical screening | Disease control | Morbidity | Blood flow | Magnetic resonance imaging | Antibiotics | Medical prognosis | Diagnostic systems | Chelating agents | Gene therapy | Risk management
Journal Article
02/2010
Objective: Sickle cell disease (SCD) is a common hereditary disease in Iran. In developed countries, newborn screening programs have been established to ensure... 
Sickle Cell Anemia | Iran | Hemoglobin SC Disease | Sickle Cell Disease | Thalassemia | Children
Web Resource
by Anon
Internal Medicine Journal, ISSN 1444-0903, 05/2015, Volume 45, Issue S3, pp. 10 - 10
Journal Article
Journal Article