Works matching DE "SICKLE cell anemia diagnosis"
Results: 312
KNOWLEDGE, ATTITUDE AND PRACTICE OF PRE-MARITAL GENETIC COUNSELLING AND TESTING OF SICKLE CELL DISEASE AMONG WOMEN IN ZARIA, NIGERIA.
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- West African Journal of Nursing, 2014, v. 25, n. 2, p. 1
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- Article
Knowledge and Awareness of Sickle Cell Trait Among Young African American Adults.
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- Western Journal of Nursing Research, 2017, v. 39, n. 9, p. 1222, doi. 10.1177/0193945916665089
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- Article
Acute Vaso-Occlusive Pain is Temporally Associated with the Onset of Menstruation in Women with Sickle Cell Disease.
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- Journal of Women's Health (15409996), 2019, v. 28, n. 2, p. 162, doi. 10.1089/jwh.2018.7147
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- Article
Developing a Public Health Research Agenda for Women with Blood Disorders.
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- Journal of Women's Health (15409996), 2010, v. 19, n. 7, p. 1231, doi. 10.1089/jwh.2010.2127
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Diagnosis support of sickle cell anemia by classifying red blood cell shape in peripheral blood images.
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- 2020
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- journal article
Factors Associated with Acceptability of Newborn Screening for Sickle Cell Disease in Lubumbashi City, Democratic Republic of the Congo.
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- Global Journal of Medical Pharmaceutical & Biomedical Update, 2022, v. 17, p. 1, doi. 10.25259/GJMPBU_7_2022
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- Article
Dual diagnosis of autosomal dominant polycystic kidney disease and sickle cell disease in a teenage male.
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- Pediatric Nephrology, 2023, v. 38, n. 9, p. 3189, doi. 10.1007/s00467-023-05873-6
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Kidney biopsy findings in children with sickle cell disease: a Midwest Pediatric Nephrology Consortium study.
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- Pediatric Nephrology, 2019, v. 34, n. 8, p. 1435, doi. 10.1007/s00467-019-04237-3
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Evaluating risk factors for chronic kidney disease in pediatric patients with sickle cell anemia.
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- Pediatric Nephrology, 2017, v. 32, n. 9, p. 1565, doi. 10.1007/s00467-017-3658-8
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A child with sickle cell trait and macroscopic hematuria: answer.
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- Pediatric Nephrology, 2009, v. 24, n. 7, p. 1309, doi. 10.1007/s00467-008-0984-x
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- Article
A child with sickle cell trait and macroscopic hematuria: question.
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- Pediatric Nephrology, 2009, v. 24, n. 7, p. 1307, doi. 10.1007/s00467-008-0983-y
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- Article
Interaction of Normal and Sickle Hemoglobins for Sodium Dodecylsulphate and Hydrogen Peroxide at pH 5.0 and 7.2.
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- ISRN Hematology, 2013, p. 1, doi. 10.1155/2013/629640
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Addition of Multimodal Therapy to Standard Management of Steady State Sickle Cell Disease.
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- ISRN Hematology, 2013, p. 1, doi. 10.1155/2013/236374
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Hematological and Genetic Predictors of Daytime Hemoglobin Saturation in Tanzanian Children with and without Sickle Cell Anemia.
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- ISRN Hematology, 2013, p. 1, doi. 10.1155/2013/472909
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- Article
ASSESSMENT OF MICRONUCLEI FREQUENCY IN SICKLED TRIBAL POPULATION (HALBA & GOND) OF DISRICT DURG, CHHATTISGARH, INDIA.
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- International Journal of Pharmacology & Biological Sciences, 2015, v. 9, n. 2, p. 223
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- Article
Psychiatric Disorders and Learning Problems in Children and Adolescents with Sickle Cell Disease.
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- Medical Journal of Bakirkoy, 2012, v. 8, n. 3, p. 95
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- Article
Characteristic Vertebral Imaging in Sickle Cell Disease.
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- Journal of Neurosciences in Rural Practice, 2017, v. 8, n. 2, p. 270, doi. 10.4103/0976-3147.203816
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Implementation and utilization of genetic testing in personalized medicine.
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- Pharmacogenomics & Personalized Medicine, 2014, v. 7, p. 227, doi. 10.2147/PGPM.S48887
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Co-occurrence of sickle cell disease and oculocutaneous albinism in a Congolese patient: a case report.
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- 2021
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- journal article
Variability in Notification of Positive Newborn Screening Results for Sickle Cell Trait Across the United States.
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- Advances in Hematology, 2024, v. 2024, p. 1, doi. 10.1155/ah/3854629
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- Article
Homozygous Sickle Cell Disease after Age of 40: Follow-Up of a Cohort of 209 Patients in Senegal, West Africa.
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- Advances in Hematology, 2024, p. 1, doi. 10.1155/2024/7501577
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- Article
Burden of Sickle Cell Disease in Ghana: The Korle-Bu Experience.
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- Advances in Hematology, 2018, p. 1, doi. 10.1155/2018/6161270
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- Article
Validation of the fine motor subtest of the Bayley‐III with children with sickle cell disease using Rasch analysis.
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- Child: Care, Health & Development, 2020, v. 46, n. 5, p. 576, doi. 10.1111/cch.12795
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The relation between health-related quality of life, treatment adherence and disease severity in a paediatric sickle cell disease sample.
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- Child: Care, Health & Development, 2012, v. 38, n. 2, p. 204, doi. 10.1111/j.1365-2214.2011.01223.x
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Pulmonary hypertension in Nigerian adults with sickle cell anemia.
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- 2017
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- journal article
Enhancing the care of patients with sickle cell disease.
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- Nursing Standard, 2019, v. 34, n. 10, p. 29, doi. 10.7748/ns.2019.e11348
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A Traveler to Holland With a Benign Killer: A Case Report of a Sickle Cell Trait Male with Splenic Infarction.
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- Egyptian Journal of Hospital Medicine, 2018, v. 71, n. 3, p. 2664, doi. 10.12816/0045827
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- Article
Nouveautés dans le traitement de la drépanocytose chez l'enfant.
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- Médecine Thérapeutique: Pédiatrie, 2017, v. 20, n. 4, p. 281, doi. 10.1684/mtp.2018.0657
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Données actuelles du dépistage néonatal de la drépanocytose en France ; autres anomalies de l'hémoglobine dépistées et éléments de prise en charge.
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- Médecine Thérapeutique: Pédiatrie, 2017, v. 20, n. 4, p. 233, doi. 10.1684/mtp.2018.0653
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Multicenter Evaluation of HemoTypeSC as a Point-of-Care Sickle Cell Disease Rapid Diagnostic Test for Newborns and Adults Across India.
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- 2020
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- journal article
Emerging point-of-care technologies for sickle cell disease screening and monitoring.
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- Expert Review of Medical Devices, 2016, v. 13, n. 12, p. 1073, doi. 10.1080/17434440.2016.1254038
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- Article
Evolving locally appropriate models of care for Indian sickle cell disease.
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- Indian Journal of Medical Research, 2016, v. 143, n. 4, p. 405, doi. 10.4103/0971-5916.184282
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Sickle cell disease in India: A perspective.
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- 2016
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- Opinion
The Platelet Count and its Implications in Sickle Cell Disease Patients Admitted for Intensive Care.
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- Indian Journal of Critical Care Medicine, 2018, v. 22, n. 8, p. 585, doi. 10.4103/ijccm.IJCCM_49_18
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‘Talk to Me. There’s Two of Us’: Fathers and Sickle Cell Screening.
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- Sociology, 2016, v. 50, n. 1, p. 178, doi. 10.1177/0038038514560261
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Bone marrow edema syndromes of the hip: MRI features in different hip disorders.
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- Clinical Rheumatology, 2008, v. 27, n. 4, p. 475, doi. 10.1007/s10067-007-0731-x
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BEHIND THE CURVE.
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- Community Practitioner, 2021, v. 94, n. 3, p. 28
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Successful outcome of three patients with sickle-cell disease and fat embolism syndrome treated with intensive exchange transfusion.
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- Clinical Case Reports, 2017, v. 5, n. 1, p. 39, doi. 10.1002/ccr3.727
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PREVALENCE AND FACTORS THAT AFFECT TRANSITION FROM PAEDIATRIC TO ADULT SERVICES AMONG ADOLESCENTS WITH SICKLE CELL DISEASE AT A LEVEL IV HEALTH FACILITY IN WESTERN KENYA.
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- East African Medical Journal, 2022, v. 99, n. 12, p. 5472
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- Article
PREVALENCE OF PLASMODIUM SPECIES AND ASSOCIATED DEMOGRAPHIC AND RISK FACTORS IN CANCER, SICKLE CELL AND FEBRILE PATIENTS ATTENDING A TERTIARY HOSPITALS IN ZARIA-NIGERIA.
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- East African Medical Journal, 2021, v. 98, n. 6, p. 3848
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Exercise-Induced Abnormal Increase of Systolic Pulmonary Artery Pressure in Adult Patients With Sickle Cell Anemia: An Exercise Stress Echocardiography Study.
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- Echocardiography, 2016, v. 33, n. 12, p. 1880, doi. 10.1111/echo.12853
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Sickle cell anaemia: epidemiology and cost of illness.
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- 2002
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- journal article
Acid Elution (Kleihauer-Betke) Test in a Patient with Homozygous Sickle Cell Disease and Elevated Hemoglobin-F Levels.
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- Balkan Medical Journal, 2023, v. 40, n. 5, p. 373, doi. 10.4274/balkanmedj.galenos.2023.2023-5-109
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- Article
Neonatal Screening for Sickle Cell Disease in Southwest Iran.
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- Iranian Journal of Pediatric Hematology & Oncology, 2018, v. 8, n. 2, p. 105
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- Article
Invasive Pulmonary Aspergillosis in a Haematopoietic Stem Cell Transplant Recipient with Sickle Cell Disease: a Successful Treatment.
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- Mediterranean Journal of Hematology & Infectious Diseases, 2015, v. 7, p. 11, doi. 10.4084/MJHID.2015.006
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Age at Diagnosis of Sickle Cell Anaemia in Lagos, Nigeria.
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- Mediterranean Journal of Hematology & Infectious Diseases, 2013, v. 5, n. 1, p. 1, doi. 10.4084/MJHID.2013.001
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Predictors of Abnormal Bone Mass Density in Adult Patients with Homozygous Sickle-Cell Disease.
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- Clinical Medicine Insights: Endocrinology & Diabetes, 2015, n. 8, p. 35, doi. 10.4137/CMED.S24501
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Clinical features at diagnosis of sickle cell disease prior to universal newborn screening in Alberta.
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- Paediatrics & Child Health (1205-7088), 2022, v. 27, n. 8, p. 464, doi. 10.1093/pch/pxac070
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Beyond Berets: The Black Panthers as Health Activists.
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- 2016
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- Publication type:
- Editorial
FROM THE CENTERS FOR DISEASE CONTROL AND PREVENTION.
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- JAMA: Journal of the American Medical Association, 2000, v. 284, n. 11, p. 1373
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- Article