Gunay Aliyeva
Overview
Explore the profile of Gunay Aliyeva including associated specialties, affiliations and a list of published articles.
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Articles
12
Citations
63
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Recent Articles
1.
Mammadova T, Asadov C, Alimirzoyeva Z, Abdulalimov E, Aliyeva G
Hemoglobin
. 2024 Nov;
48(5):353-356.
PMID: 39523367
Hereditary hemoglobinopathies, particularly β-thalassemia, are highly prevalent in Azerbaijan, posing a significant public health challenge. In response, the Azerbaijani government implemented a national prevention program that includes mandatory premarital screening...
2.
Hasanova A, Asadov C, Karimova N, Shirinova A, Aliyeva G, Alimirzoyeva Z
Pathol Oncol Res
. 2024 Jan;
29:1611518.
PMID: 38188610
BCR-ABL1 kinase domain (KD) mutations can lead to resistance to first- and second-generation tyrosine kinase inhibitors (TKIs) in chronic myeloid leukemia (CML). Here, we present the first report of the...
3.
Novruzov F, Mehdi E, Orucova N, Aliyeva G, Valla F, Mammadzada H, et al.
Eur J Nucl Med Mol Imaging
. 2023 Sep;
51(2):609-610.
PMID: 37752270
No abstract available.
4.
Aliyev A, Aliyeva I, Giammarile F, Talibova N, Aliyeva G, Novruzov F
Endocrinol Diabetes Metab
. 2022 Sep;
5(6):e373.
PMID: 36149057
Introduction: Ultrasound-guided fine needle aspiration biopsy (FNAB) is currently widely used for the initial screening of patients with thyroid nodules enabling prevention of unnecessary surgery. The purpose of this study...
5.
Aliyeva G, Asadov C, Mammadova T, Gafarova S, Guliyeva Y, Abdulalimov E
Ann Hum Genet
. 2019 Nov;
84(3):249-258.
PMID: 31755088
With the carrier rate of 4%-8.6%, β-thalassemia is one of the most prevalent hereditary disorders in Azerbaijan. Taking into consideration the high frequency of β-thalassemia as well as the occurrences...
6.
Bayramov B, Aliyeva G, Asadov C, Mammadova T, Karimova N, Eynullazadeh K, et al.
Hemoglobin
. 2019 Sep;
43(4-5):280-282.
PMID: 31476942
We identified a novel mutation of β-thalassemia (β-thal) in a heterozygous carrier from Azerbaijan. Phenotypical data and molecular mechanisms of codon 2 (-T) (: c.9delT) was relevant to β-thal. Additionally,...
7.
Aliyeva G, Asadov C, Mammadova T, Musayev S, Abdulalimov E, Gafarova S, et al.
Hemoglobin
. 2018 Nov;
42(4):276-277.
PMID: 30422720
Codon 14 (+T) (HBB: c.44_45insT) is a very rare β-thalassemia (β-thal) mutation previously reported in three β-thal major (β-TM) patients of Azerbaijani origin. None of the previous reports described the...
8.
Aliyeva G, Asadov C, Mammadova T, Gafarova S, Abdulalimov E
Clin Chem Lab Med
. 2018 Aug;
57(2):165-174.
PMID: 30138112
Thalassemia is one of the most common hereditary disorders of the developing world, and it is associated with severe anemia and transfusion dependence. The global health burden of thalassemia has...
9.
Aliyeva G, Abdulalimov E, Asadov C, Mammadova T, Gafarova S, Guliyeva Y
Hemoglobin
. 2018 Jun;
45(6):347-348.
PMID: 29893155
The -92 (C>T) (: c.-142C>T) is a silent β-thalassemia (β-thal) mutation previously described in combination with several β mutations and expressed as β-thal intermedia (β-TI). Heterozygous individuals are known to...
10.
Asadov C, Alimirzoeva Z, Mammadova T, Aliyeva G, Gafarova S, Mammadov J
Int J Hematol
. 2018 Jan;
108(1):5-21.
PMID: 29380178
β-Thalassemia intermedia is a clinical condition of intermediate gravity between β-thalassemia minor, the asymptomatic carrier, and β-thalassemia major, the transfusion-dependent severe anemia. It is characterized by a significant clinical polymorphism,...