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Archives of Disease in Childhood, ISSN 0003-9888, 07/2018, Volume 103, Issue 7, pp. 648 - 653
Journal Article
Journal Article
MEDITERRANEAN JOURNAL OF HEMATOLOGY AND INFECTIOUS DISEASES, ISSN 2035-3006, 07/2019, Volume 11, Issue 1, p. e2019040
Sickle cell disease (SCD) is the most common inherited hemoglobinopathy and is associated with increased risk of complications and early mortality. Nowadays,... 
Pregnancy | WOMEN | INFECTIOUS DISEASES | MANAGEMENT | HYDROXYUREA | GROWTH | Sickle Cell Disease | OUTCOMES | ANEMIA | HEMATOLOGY | PRENATAL-DIAGNOSIS | Developing Countries | Anemia
Journal Article
MEDITERRANEAN JOURNAL OF HEMATOLOGY AND INFECTIOUS DISEASES, ISSN 2035-3006, 07/2019, Volume 11, Issue 1, p. e2019040
Sickle cell disease (SCD) is the most common inherited hemoglobinopathy and is associated with increased risk of complications and early mortality. Nowadays,... 
Pregnancy | WOMEN | INFECTIOUS DISEASES | MANAGEMENT | HYDROXYUREA | GROWTH | Sickle Cell Disease | OUTCOMES | ANEMIA | HEMATOLOGY | PRENATAL-DIAGNOSIS
Journal Article
Southern Medical Journal, ISSN 0038-4348, 09/2016, Volume 109, Issue 9, pp. 554 - 556
Journal Article
PLoS ONE, ISSN 1932-6203, 10/2016, Volume 11, Issue 10, p. e0164364
Discovery and validation of genetic variants that influence disease severity in children with sickle cell anemia (SCA) could lead to early identification of... 
MICROALBUMINURIA | MULTIDISCIPLINARY SCIENCES | HYDROXYUREA TREATMENT | SALUSIN-ALPHA | RISK | ADVERSE OUTCOMES | RENAL-DISEASE | DEFICIENT MICE | APOL1 | NEPHROPATHY | CHRONIC TRANSFUSION | Albuminuria - complications | Neutrophils - cytology | Lipoproteins, HDL - genetics | Prospective Studies | Humans | Male | Anemia, Sickle Cell - drug therapy | Genetic Variation | Albuminuria - diagnosis | Apolipoproteins - genetics | Female | Leukocyte Count | Child | Leukocytes - cytology | Glomerular Filtration Rate | Anemia, Sickle Cell - complications | Risk Factors | Receptors, Cell Surface - metabolism | Genotype | Transcription Factors - genetics | Sequence Analysis, DNA | Homeodomain Proteins - genetics | Phenotype | Adolescent | Apolipoprotein L1 | Duffy Blood-Group System - metabolism | Hydroxyurea - therapeutic use | Polymorphism, Single Nucleotide | Anemia, Sickle Cell - diagnosis | Duffy Blood-Group System - genetics | Anemia, Sickle Cell - genetics | Receptors, Cell Surface - genetics | Pediatrics | Care and treatment | Sickle cell anemia | Diabetic nephropathies | African Americans | Sickle cell anemia in children | Hydroxyurea | Risk factors | Genetic polymorphisms | Diseases | Preventive health services | Genetic markers | Genetic aspects | Children | Medicine, Preventive | Blood cell count | Therapy | Clinical trials | Gene polymorphism | Blood | Gene sequencing | Duffy antigen | Rodents | Sickle cell disease | Medical research | Stroke | Filtration | Risk groups | Anemia | Mortality | Diabetes mellitus | Health risks | Risk analysis | Gene expression | Glomerular filtration rate | White blood cells | Studies | CD163 antigen | Genetic variance | Biomarkers | Polymorphism | Kidney transplantation
Journal Article
Best Practice & Research: Clinical Obstetrics & Gynaecology, ISSN 1521-6934, 2011, Volume 26, Issue 1, pp. 25 - 36
Journal Article
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, ISSN 1077-4114, 11/2019, Volume 41, Issue 8, pp. 579 - 585
Journal Article