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1دورية أكاديمية
المؤلفون: Runge, Ava, Brazel, Danielle, Pakbaz, Zahra
المصدر: Journal of Community Hospital Internal Medicine Perspectives. 11(5)
مصطلحات موضوعية: Biomedical and Clinical Sciences, Cardiovascular Medicine and Haematology, Stroke, Hematology, Rare Diseases, Clinical Research, Pain Research, Sickle Cell Disease, 2.1 Biological and endogenous factors, Aetiology, Blood, Sickle cell disease, sickle cell beta-plus thalassemia, compound heterozygous, stroke
وصف الملف: application/pdf
URL الوصول: https://escholarship.org/uc/item/2qw7m2c4
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2دورية أكاديمية
المؤلفون: Ava Runge, Danielle Brazel, Zahra Pakbaz
المصدر: Journal of Community Hospital Internal Medicine Perspectives, Vol 11, Iss 5, Pp 713-718 (2021)
مصطلحات موضوعية: sickle cell disease, sickle cell beta-plus thalassemia, compound heterozygous, stroke, Internal medicine, RC31-1245
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2000-9666
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المؤلفون: Zahra Pakbaz, Danielle Brazel, Ava Runge
المصدر: Journal of Community Hospital Internal Medicine Perspectives, Vol 11, Iss 5, Pp 713-718 (2021)
Journal of community hospital internal medicine perspectives, vol 11, iss 5
Journal of Community Hospital Internal Medicine Perspectives
article-version (VoR) Version of Recordمصطلحات موضوعية: Pediatrics, medicine.medical_specialty, Cell, Case Report, Disease, Compound heterozygosity, Rare Diseases, Clinical Research, hemic and lymphatic diseases, Internal Medicine, 2.1 Biological and endogenous factors, Medicine, Aetiology, Stroke, compound heterozygous, Sickle Cell Disease, Sickle cell trait, business.industry, Pain Research, Hematology, Emergency department, medicine.disease, stroke, RC31-1245, sickle cell beta-plus thalassemia, Pathophysiology, Blood, medicine.anatomical_structure, Etiology, sickle cell disease, business
وصف الملف: application/pdf
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4دورية أكاديمية
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5
المؤلفون: Nathan Price, Sarah M. Desoky, Neha Bhasin
مصطلحات موضوعية: Male, Pediatrics, medicine.medical_specialty, medicine.medical_treatment, Thalassemia, Exchange transfusion, Anemia, Sickle Cell, Disease, Gastroenterology, hemic and lymphatic diseases, Internal medicine, medicine, Humans, Hydroxyurea, Mild form, Mild disease, Acute pain, Pelvis, Sickle Beta Plus Thalassemia, business.industry, beta-Thalassemia, Osteonecrosis, Hematology, medicine.disease, medicine.anatomical_structure, Oncology, Child, Preschool, Pediatrics, Perinatology and Child Health, Hemoglobin, business
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38ddb164b00c68c540076ba5d5f55811
https://doi.org/10.22541/au.159569149.93205812 -
6
المؤلفون: Notarangelo, L. D., Agostini, A., Casale, M., Samperi, P., Arcioni, F., Gorello, P., Perrotta, S., Masera, N., Barone, A., Bertoni, E., Bonetti, E., Burnelli, R., Casini, T., Del, Vecchio, Filippini, G. C., Giona, B., Giordano, F., Gorio, P., Marchina, C., Nardi, E., Petrone, M., Colombatti, A., Sainati, R., Russo, L. r., Email Author View Correspondence (jump link), G.
المساهمون: Notarangelo, L. D., Agostini, A., Casale, M., Samperi, P., Arcioni, F., Gorello, P., Perrotta, S., Masera, N., Barone, A., Bertoni, E., Bonetti, E., Burnelli, R., Casini, T., Del Vecchio, G. C., Filippini, B., Giona, F., Giordano, P., Gorio, C., Marchina, E., Nardi, M., Petrone, Angelo, Colombatti, R., Sainati, L., Russo, G.
المصدر: European journal of haematologyREFERENCES. 104(3)
مصطلحات موضوعية: Male, Thalassemia, Hemoglobin, Sickle, HbS/β+ thalassemia, Italy, Sickle cell disease, children, genotype, phenotype, Avascular necrosis, Disease, beta-Globins, Gastroenterology, Sickle, 0302 clinical medicine, Genotype, Public Health Surveillance, Child, Stroke, Anemia, Hematology, General Medicine, Middle Aged, Sickle Cell, Phenotype, 030220 oncology & carcinogenesis, Child, Preschool, Cohort, Female, HbS, beta plus thalassemia, Adult, medicine.medical_specialty, Adolescent, Anemia, Sickle Cell, Sepsis, 03 medical and health sciences, Young Adult, Internal medicine, medicine, Humans, Hemoglobin, Preschool, Alleles, Genetic Association Studies, Infant, Retrospective Studies, beta-Thalassemia, business.industry, Retrospective cohort study, medicine.disease, business, 030215 immunology
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7كتاب إلكتروني
المساهمون: Goldstein, Sam, editorAff480, Naglieri, Jack A., editorAff481
المصدر: Encyclopedia of Child Behavior and Development. :1362-1362
Degree: Ph.D.
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8
المؤلفون: Lalit Mohan Bhardwaj, Bhattacharyya PC, Swapnav Borthakur
المصدر: International Journal of Medical Research and Health Sciences, Vol 6, Iss 7, Pp 40-41 (2017)
مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, lcsh:R5-920, Sickle beta plus thalassemia, hemic and lymphatic diseases, lcsh:R, lcsh:Medicine, lcsh:Medicine (General), Haemoglobinopathies, Acute pancreatitis
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doajarticles::381fc7e84a8ac45ee1b036d272b29419
http://www.ijmrhs.com/medical-research/sickle-beta -plus -thalassemia -presenting-as-acute-pancreatitis--a-case-report.pdf -
9دورية أكاديمية
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10
المؤلفون: P. Levy, Robin Johnson, A. Koranda, R. Bellvue, A.P. Kraus, R. Entsuah, Zanet Flournoy-Gill, Mabel Koshy
المصدر: Blood. 74:1403-1408
مصطلحات موضوعية: medicine.medical_specialty, Sickle Beta Plus Thalassemia, business.industry, Thalassemia, Incidence (epidemiology), Immunology, Cell Biology, Hematology, medicine.disease, Biochemistry, Sickle cell anemia, Surgery, Hemoglobinopathy, Internal medicine, hemic and lymphatic diseases, Fetal hemoglobin, medicine, Hemoglobin F, Hemoglobinemia, business
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32b3bf6dc9549580845db630871fd73c
https://doi.org/10.1182/blood.v74.4.1403.bloodjournal7441403
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