Cargando…

Non-S Sickling Hemoglobin Variants: Historical, Genetic, Diagnostic, and Clinical Perspectives

Apart from hemoglobin-S (HbS), there are other Hb variants (non-S sickling Hb variants) that cause sickle cell disease. However, the profiles of these non-S sickling Hb variants have neither been collated nor harmonized. A literature search revealed 14 non-S sickling Hb variants (HbC-Harlem, HbC-Zig...

Descripción completa

Detalles Bibliográficos
Autores principales:	Ahmed, Sagir G., Ibrahim, Umma A.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	OMJ 2021
Materias:	Review Articles
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8170066/ https://www.ncbi.nlm.nih.gov/pubmed/34113458 http://dx.doi.org/10.5001/omj.2021.102

Ejemplares similares

Pharmacological Induction of Fetal Hemoglobin in β-Thalassemia and Sickle Cell Disease: An Updated Perspective
por: Bou-Fakhredin, Rayan, et al.
Publicado: (2022)

Hematological, Biochemical Properties, and Clinical Correlates of Hemoglobin S Variant Disorder: A New Insight Into Sickle Cell Trait
por: Khaled, Safaa A.A., et al.
Publicado: (2022)

Identifying genetic variants and pathways associated with extreme levels of fetal hemoglobin in sickle cell disease in Tanzania
por: Nkya, Siana, et al.
Publicado: (2020)

An “acquired” hemoglobin J variant in a sickle cell disease patient
por: Swedan, Nawwar, et al.
Publicado: (2008)

Human hemoglobin G-Makassar variant masquerading as sickle cell anemia
por: Mohamad, Ahmad Sabry, et al.
Publicado: (2018)

THE STATE OF HEMOGLOBIN IN SICKLED ERYTHROCYTES
por: Stetson, Chandler A.
Publicado: (1966)

Perspectives and challenges to discovering hemoglobin-inducing agents in Sickle Cell Disease
por: Pavan, Aline Renata, et al.
Publicado: (2022)

Hematological parameters in sick cell anemia patients with and without priapism
por: Ahmed, Sagir G., et al.
Publicado: (2006)

Clinical and Laboratory Features of Hemoglobin La Desirade Variant in Association with Sickle Cell and Alpha Thalassemia Genes
por: Alkindi, S., et al.
Publicado: (2021)

Prevalence of Sickle Cell Trait and Rare Hemoglobin Variants in the Metropolitan Washington DC Area
por: Niu, Xiaomei, et al.
Publicado: (2020)

Sickle Cell Disease and Fetal Hemoglobin
por: Rivera, Alicia
Publicado: (2018)

GELS OF NORMAL AND SICKLED HEMOGLOBIN : COMPARATIVE STUDY
por: White, James G., et al.
Publicado: (1970)

Genetic reversal of the globin switch concurrently modulates both fetal and sickle hemoglobin and reduces red cell sickling
por: De Souza, Daniel C., et al.
Publicado: (2023)

The Role of Infection in the Pathogenesis of Vaso-Occlusive Crisis in Patients with Sickle Cell Disease.
por: Ahmed, Sagir G.
Publicado: (2011)

Candidate Sequence Variants and Fetal Hemoglobin in Children with Sickle Cell Disease Treated with Hydroxyurea
por: Green, Nancy S., et al.
Publicado: (2013)

Incidence of Sickle Cell Disease and Other Hemoglobin Variants in 10,095 Lebanese Neonates
por: Khoriaty, Evelyne, et al.
Publicado: (2014)

Sickle Cell Disease in Children and Adolescents: A Review of the Historical, Clinical, and Public Health Perspective of Sub-Saharan Africa and Beyond
por: Egesa, Walufu Ivan, et al.
Publicado: (2022)

Fetal hemoglobin reactivation and cell engineering in the treatment of sickle cell anemia
por: Eridani, Sandro, et al.
Publicado: (2011)

Fetal Hemoglobin in Sickle Hemoglobinopathies: High HbF Genotypes and Phenotypes
por: Steinberg, Martin H.
Publicado: (2020)

Natural Remedies for the Treatment of Beta-Thalassemia and Sickle Cell Anemia—Current Status and Perspectives in Fetal Hemoglobin Reactivation
por: Ng, Noel Yat Hey, et al.
Publicado: (2014)

CRISPR-Cas9 to induce fetal hemoglobin for the treatment of sickle cell disease
por: Demirci, Selami, et al.
Publicado: (2021)

Comparative study of sickle cell anemia and hemoglobin SC disease: clinical characterization, laboratory biomarkers and genetic profiles
por: Aleluia, Milena Magalhães, et al.
Publicado: (2017)

Teleultrasound: Historical Perspective and Clinical Application
por: Ferreira, Adilson Cunha, et al.
Publicado: (2015)

Genetics in Atopic Dermatitis: Historical Perspective and Future Prospects
por: BROWN, Sara J., et al.
Publicado: (2020)

Role of Extracellular Hemoglobin in Thrombosis and Vascular Occlusion in Patients with Sickle Cell Anemia
por: Zhou, Zhou, et al.
Publicado: (2011)

Fetal hemoglobin and hemolysis markers in sickle cell anemia()
por: Colella, Marina Pereira, et al.
Publicado: (2015)

Rapid and inefficient kinetics of sickle hemoglobin fiber growth
por: Castle, Brian T., et al.
Publicado: (2019)

Hemoglobin level and macular thinning in sickle cell disease
por: Hussnain, S Amal, et al.
Publicado: (2019)

Genetic modifiers of fetal hemoglobin affect the course of sickle cell disease in patients treated with hydroxyurea
por: Allard, Pierre, et al.
Publicado: (2021)

Hematological and Genetic Predictors of Daytime Hemoglobin Saturation in Tanzanian Children with and without Sickle Cell Anemia
por: Cox, Sharon E., et al.
Publicado: (2013)

Pericardial tamponade, a diagnostic chameleon: from the historical perspectives to contemporary management
por: Kaemmerer, Ann-Sophie, et al.
Publicado: (2023)

Perspectives on genetics: anecdotal, historical, and critical commentaries, 1987–1998
por: Cain, Joe
Publicado: (2002)

The Future of Influenza Vaccines: A Historical and Clinical Perspective
por: Bouvier, Nicole M.
Publicado: (2018)

Hemoglobin-Based Blood Substitutes and the Treatment of Sickle Cell Disease: More Harm than Help?
por: Alayash, Abdu I.
Publicado: (2017)

Clinical Implications of the Association of Fetal Hemoglobin with Peripheral Oxygen Saturation in Sickle Cell Disease
por: Abdulmalik, Osheiza, et al.
Publicado: (2017)

Vivisection in historical perspective
por: Tansey, E. M.
Publicado: (1988)

THE PHYSICAL STATE OF HEMOGLOBIN IN SICKLE-CELL ANEMIA ERYTHROCYTES IN VIVO
por: Döbler, Johanna, et al.
Publicado: (1968)

Sickle Retinopathy in a Person with Hemoglobin S/New York Disease
por: Calder, Donovan, et al.
Publicado: (2012)

The Sickle Effect: The Silent Titan Affecting Glycated Hemoglobin Reliability
por: Gordon, Domonick K, et al.
Publicado: (2020)

Fetal hemoglobin rescues ineffective erythropoiesis in sickle cell disease
por: El Hoss, Sara, et al.
Publicado: (2020)

Cannot write session to /tmp/vufind_sessions/sess_eliq9a3184f2sk8vto6nt56n72