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The Lancet (British edition), 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
Journal of the American College of Cardiology, ISSN 0735-1097, 2009, Volume 54, Issue 1, pp. S43 - S54
The aim of a clinical classification of pulmonary hypertension (PH) is to group together different manifestations of disease sharing similarities in... 
Cardiovascular | Internal Medicine | clinical classification | pulmonary arterial hypertension | pulmonary hypertension | VENOOCCLUSIVE-DISEASE | CHRONIC HEART-FAILURE | CARDIAC & CARDIOVASCULAR SYSTEMS | HEREDITARY HEMORRHAGIC TELANGIECTASIA | CONNECTIVE-TISSUE-DISEASE | SYSTEMIC-SCLEROSIS | INTERSTITIAL LUNG-DISEASE | GLYCOGEN-STORAGE-DISEASE | ARTERIAL-HYPERTENSION | SICKLE-CELL-DISEASE | OF-THE-LITERATURE | Hypertension, Pulmonary - classification | Prognosis | Comorbidity | Humans | Calcium Channel Blockers - therapeutic use | Antihypertensive Agents - administration & dosage | Anticoagulants - therapeutic use | Treatment Outcome | Hypertension, Pulmonary - epidemiology | Evidence-Based Medicine | Scleroderma, Systemic - epidemiology | Randomized Controlled Trials as Topic | Algorithms | Hypertension, Pulmonary - drug therapy | Endothelin Receptor Antagonists | Epoprostenol - administration & dosage | Hypertension | Medical colleges | Micropollutants | Sickle cell anemia | Architecture | Respiratory agents | Congenital heart disease | HIV (Viruses) | Peptide hormones | Coronary heart disease | Gene mutations | Bone morphogenetic proteins | Kidney diseases | Cardiology | Health aspects | Personal video recorders | Anemia | Pulmonary hypertension | Genetic counseling | Surgery | Classification | Clinical trials | Cardiovascular disease | Mutation | Family medical history | Drug therapy | Defects
Journal Article