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Medicine, ISSN 0025-7974, 12/2018, Volume 97, Issue 51, p. e13729
Previous studies have shown that hyperuricemia is an independent risk factor for cardiovascular disease. The aim of the study was to examine the association... 
MORTALITY | NEUTROPHILS | ATHEROSCLEROSIS RISK | AMERICAN | hyperuricemia | WOMEN | MEDICINE, GENERAL & INTERNAL | INFLAMMATION | MEN | LEUKOCYTE COUNT | coronary heart disease | white blood cell count | HYPERTENSION | Hyperuricemia | Risk assessment | Analysis | Aged | Research | Leukocytes | Coronary heart disease | Health aspects | Risk factors
Journal Article
Thrombosis Research, ISSN 0049-3848, 2019, Volume 183, pp. 36 - 44
AbstractIntroductionSarcopenia is attracting increasing attention due to its harmful impacts on health. Chronic inflammation is proposed to be a major cause of... 
Hematology, Oncology, and Palliative Medicine | Sarcopenia | Platelet | Chronic inflammation | White blood cell | MORTALITY | PREDICTOR | INTERLEUKIN-6 | INSULIN-RESISTANCE | INFLAMMATION | CARDIOVASCULAR-DISEASE | LEUKOCYTE COUNT | PERIPHERAL VASCULAR DISEASE | HEALTH | POSTMENOPAUSAL WOMEN | HEMATOLOGY | AGE
Journal Article
CLINICS, ISSN 1807-5932, 2019, Volume 74, p. e775
Journal Article
PLoS ONE, ISSN 1932-6203, 08/2016, Volume 11, Issue 8, pp. e0161539 - e0161539
In this study we sought to identify genetic factors associated with the presenting white blood cell (WBC) count in B-precursor acute lymphoblastic leukemia... 
RISK | CHANNELS | EXPRESSION | CHILDHOOD | MULTIDISCIPLINARY SCIENCES | Carrier Proteins - physiology | Receptors, Interleukin-1 Type I - physiology | Oligonucleotide Array Sequence Analysis | Humans | Child, Preschool | ERG1 Potassium Channel - physiology | Male | Guanine Nucleotide Exchange Factors | Precursor B-Cell Lymphoblastic Leukemia-Lymphoma - genetics | Precursor B-Cell Lymphoblastic Leukemia-Lymphoma - immunology | Carrier Proteins - genetics | Adaptor Proteins, Signal Transducing - physiology | Protein Interaction Maps - genetics | Genetic Markers - genetics | Adaptor Proteins, Signal Transducing - genetics | Receptors, Interleukin-1 Type I - genetics | ERG1 Potassium Channel - genetics | Female | Leukocyte Count | Nuclear Proteins - physiology | Nuclear Proteins - genetics | Child | Real-Time Polymerase Chain Reaction | Gene Expression Regulation, Neoplastic - genetics | Genetic aspects | Acute lymphocytic leukemia | Research | Gene expression | Blood cell count | Analysis | Cell culture | Pediatrics | Target recognition | Leukemia | Genes | Estrogen | Oncology | Biology | Statistical methods | Blood | Cell adhesion & migration | Immunology | Precursors | Interleukin 1 | Bone marrow | Genetic factors | Statistical analysis | Acute lymphatic leukemia | Hematology | Principal components analysis | Runx1 protein | Breast cancer | Lymphatic leukemia | Patients | White blood cells | Medicine | Lymphocytes B | Medical prognosis | Hormone replacement therapy | Potassium | Index Medicus
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