Cargando…

Molecular Genetic Characterization of β-Thalassemia and Sickle Cell Syndrome in the Albanian Population

β-Thalassemia (β-thal) is a major public health problem in Albania as it is in many Mediterranean countries. We determined the different β-thal alleles that are present in the Albanian population by using the temporal temperature gradient electrophoresis (TTGE) method because of its high throughput,...

Descripción completa

Detalles Bibliográficos
Autores principales:	Babameto-Laku, A, Mitre, A, Berisha, S, Mokini, V, Roko, D
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Macedonian Science of Sciences and Arts 2011
Materias:	Original Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3776692/ https://www.ncbi.nlm.nih.gov/pubmed/24052702 http://dx.doi.org/10.2478/v10034-011-0017-0

Ejemplares similares

16p Subtelomeric Duplication with Vascular Anomalies: an Albanian Case Report and Literature Review
por: Babameto-Laku, A, et al.
Publicado: (2012)

Genetic Diagnosis of Chromosomal Congenital Anomalies in Albanian Pediatric Patients by Array CGH
por: Babameto-Laku, Anila, et al.
Publicado: (2017)

Self-reported Prevalence and Risk Factors of Non-communicable Diseases in the Albanian Adult Population
por: Kraja, Fatjona, et al.
Publicado: (2016)

Genetic characterization of the Albanian Gaucher disease patient population
por: Cullufi, Paskal, et al.
Publicado: (2020)

Direct-Acting Antiviral Treatment in Albanian Patients With Chronic Hepatitis C and Advanced Liver Fibrosis
por: Cuko, Liri, et al.
Publicado: (2022)

Low serum levels of dehydroepiandrosterone sulfate and testosterone in Albanian female patients with allergic disease
por: Lokaj-Berisha, Violeta, et al.
Publicado: (2021)

High Prevalence of Anti Thyroid Antibodies in an Albanian Cohort of Patients
por: Minxuri, Dorina, et al.
Publicado: (2021)

There Is No Elevation of Immunoglobulin E Levels in Albanian Patients with Autoimmune Thyroid Diseases
por: Latifi-Pupovci, Hatixhe, et al.
Publicado: (2014)

Genetic Correction of Sickle Cell Anemia and β-Thalassemia: Progress and New Perspective
por: Perumbeti, Ajay, et al.
Publicado: (2010)

Echocardiografic abnormalities in patients with sickle cell/β-thalassemia do not depend on the β-thalassemia phenotype
por: Benites, Bruno Deltreggia, et al.
Publicado: (2019)

Clinical, hematologic and molecular variability of sickle cell-β thalassemia in western India
por: Mukherjee, Malay B., et al.
Publicado: (2010)

Corrigendum to “There Is No Elevation of Immunoglobulin E Levels in Albanian Patients with Autoimmune Thyroid Diseases”
por: Latifi-Pupovci, Hatixhe, et al.
Publicado: (2022)

INCIDENCE OF ACUTE PANCREATITIS IN ALBANIAN POPULATION
por: Kurti, Floreta, et al.
Publicado: (2015)

Anesthetic management of a patient with sickle β(+) thalassemia
por: Bharati, Saswata, et al.
Publicado: (2011)

The Albanians : a modern history /
por: Vickers, Miranda

Prevalence and Genetic Analysis of α- and β-Thalassemia and Sickle Cell Anemia in Southwest Iran
por: Nezhad, Forozan H., et al.
Publicado: (2018)

Clinical Utility of Confirmatory Genetic Testing to Differentiate Sickle Cell Trait from Sickle-β(+)-Thalassemia by Newborn Screening
por: Shook, Lisa M., et al.
Publicado: (2020)

Responses of β-thalassemia and compound heterozygote of Sickle/βthalassemia of BCL11A Gene Polymorphism in Pakistani Patients
por: Soomro, Nayab, et al.
Publicado: (2023)

Graves’ Disease in Albanian Children
por: GJIKOPULLI, A., et al.
Publicado: (2014)

Molecular genetics of β-thalassemia: A narrative review
por: Jaing, Tang-Her, et al.
Publicado: (2021)

Molecular characterization of β-thalassemia intermedia in the West Bank, Palestine
por: Faraon, Rashail, et al.
Publicado: (2019)

Therapeutic Hemoglobin Levels after Gene Transfer in β-Thalassemia Mice and in Hematopoietic Cells of β-Thalassemia and Sickle Cells Disease Patients
por: Breda, Laura, et al.
Publicado: (2012)

Albanian Treatment for Ribbentrop's Chauffeur
por: Dumoulin, J. G.
Publicado: (1990)

Pregnancy in Thalassemia and Sickle Cell Disease: The Experience of an Italian Thalassemia Center
por: Sorrentino, Francesco, et al.
Publicado: (2020)

Oral health conditions in an Albanian adolescent population: an epidemiological study
por: Laganà, Giuseppina, et al.
Publicado: (2015)

Sickle cell-β thalassemia with concomitant hemophilia A: a rare presentation
por: Dhiman, Pratibha, et al.
Publicado: (2015)

Targeting the Hematopoietic Stem Cell Niche in β-Thalassemia and Sickle Cell Disease
por: Aprile, Annamaria, et al.
Publicado: (2022)

Side effects of hydroxyurea in patients with Thalassemia major and thalassemia intermedia and sickle cell anemia
por: Ghasemi, A, et al.
Publicado: (2014)

Redox Balance in β-Thalassemia and Sickle Cell Disease: A Love and Hate Relationship
por: Bou-Fakhredin, Rayan, et al.
Publicado: (2022)

Molecular Diagnostics of β-Thalassemia
por: Atanasovska, B, et al.
Publicado: (2012)

Relationship of Cord Blood Immunoglobulin E and Maternal Immunoglobulin E with Birth Order and Maternal History of Allergy in Albanian Mother/Neonate Pairs
por: Latifi-Pupovci, Hatixhe, et al.
Publicado: (2017)

Cytogenetic Study in Children with Down Syndrome Among Kosova Albanian Population Between 2000 and 2010
por: Kolgeci, Selim, et al.
Publicado: (2013)

Pattern and Frequency of Short Stature in Albanian Children
por: GJIKOPULLI, A., et al.
Publicado: (2016)

Nationwide carrier detection and molecular characterization of β-thalassemia and hemoglobin E variants in Bangladeshi population
por: Noor, Farjana Akther, et al.
Publicado: (2020)

Fat Embolism Syndrome in Sickle Cell β-Thalassemia Patient With Osteonecrosis: An Uncommon Presentation in a Young Adult
por: Sangani, Vikram, et al.
Publicado: (2021)

PB2214: SCD POPULATION SURVEY IN ALBANIA, A PROSPECTIVE NON-INTERVENTIONAL MULTI-CENTER STUDY EVALUATING DISEASE AND PATIENTS CHARACTERISTICS OF SICKLE CELL DISEASE IN ALBANIAN SCD POPULATION
por: Cili, A., et al.
Publicado: (2022)

Medical ethnobotany of the Albanian Alps in Kosovo
por: Mustafa, Behxhet, et al.
Publicado: (2012)

Attitude of Albanian psychiatrists towards their patients
por: Dashi, E., et al.
Publicado: (2023)

Evaluation of procalcitonin in patients with sepsis in Albanian adults
por: Puca, E, et al.
Publicado: (2012)

Iron Metabolism in Thalassemia and Sickle Cell Disease.
por: Mariani, Raffaella, et al.
Publicado: (2009)

Cannot write session to /tmp/vufind_sessions/sess_her99mhnufdpj42t1jfvmg6gjq