Výsledky vyhledávání - "Valeh HUSEYNOV"

Akademický článek

Treatment of Mantle Cell Lymphoma in Transplant Non-Eligible Patients

Autor: Valeh Huseynov

Publikováno v: Hematology, Transfusion and Cell Therapy, Vol 44, Iss , Pp S2-S3 (2022)

MCL is a rare but usually aggressive non-Hodgkin lymphoma that most commonly affects the elder population. It is now recognized as a heterogeneous disease with variable biologic and clinical behavior. MCL is considered incurable with current therapie

Externí odkaz: https://doaj.org/article/ec9e6ac530a44015b0bd8d54fb219201

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Akademický článek

Ghosal hematodiaphyseal dysplasia (GHDD) diagnosis and treatment: case report

Autor: Gular MAMMADOVA, Samira HASANOVA, Konul BAGHIROVA, Avesta ALLAHVERDIYEVA, Narmin EYVAZOVA, Adam NAJAFLI, Kamala MAMMADOVA, Afag NASIBOVA, Valeh HUSEYNOV

Publikováno v: Hematology, Transfusion and Cell Therapy, Vol 44, Iss , Pp S22-S23 (2022)

Objective: Ghosal hematodiaphyseal dysplasia syndrome (GHDD) is a rare authosomal ressesive disorder characterized by increased bone density and regenerative corticosteroid-sensitive anemia.We describe GHDD in an 11-year old Azerbaijani boy with refr

Externí odkaz: https://doaj.org/article/ff90ba443129438abd3e25ee2c3aad5e

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Akademický článek

RARE UNSTABLE ALPHA GLOBIN VARIANT HB TAYBE (HBA1:C.118_120DELACC) WITH HBA2 POLY A MUTATIONS, CAUSES TO HEMOLYTIC ANEMIA IN TWO CASES FROM AZERBAIJAN

Autor: AghaRza Aghayev, Khuraman Jafarova, Afsana Mammadova, Zenfira Mirzeyeva, Valeh Huseynov

Publikováno v: Hematology, Transfusion and Cell Therapy, Vol 44, Iss , Pp S40-S41 (2022)

Objective: Sequence variants are usually silent and rarer in α-globin, some may lead to an unstable protein with hemolytic or thalassemic phenotype. The most common HBA variant is ConstantSpring which is leading to an unstable elongated protein chai

Externí odkaz: https://doaj.org/article/13bee7411a78413ab1e216282b3328d2

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Akademický článek

HBH DISEASE AND SYSTEMIC LUPUS ERYTHEMATOSUS

Autor: Valeh Huseynov, Afag Nasibova, Sevinj Nabiyeva

Publikováno v: Hematology, Transfusion and Cell Therapy, Vol 44, Iss , Pp S41- (2022)

Objective: The association between thalassemia and systemic lupus erythematosus (SLE) is very rare. There are many articles in the literature showing that patients diagnosed with SLE with Beta-Thalassemia have a more severe hemolytic picture. The com

Externí odkaz: https://doaj.org/article/dc7638cb7b344739839a6848b59c6d5d

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Akademický článek

GRISCELLI SYNDROME TYPE 2 –CLINICAL APPROACH AND CASE REPORT

Autor: Konul Baghirova, Gular Mammadova, Avesta Allahverdiyeva, Narmin Eyvazova, Narmin Verdiyeva, Agarza Agayev, Samira Hasanova, Valeh Huseynov

Publikováno v: Hematology, Transfusion and Cell Therapy, Vol 44, Iss , Pp S39- (2022)

Objective: Griscelli syndrome type 2 is rare authosomal ressesive disorder caused by a defect in the RAB27A gene, which affects a melanosome-anchoring complex in melanocytes, affecting release of cytolytic granules from T and NK cells. Children with

Externí odkaz: https://doaj.org/article/fd266475424a4533b3eabaf99ef1f0f7

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MOLECULAR BASIS OF HEMOGLOBINOPATHIES IN AZERBAIJAN

Autor: Agharza Aghayev, Valeh Huseynov, Ramin Bayramli, Oya Uyguner Z.

Introduction: Thalassemias are defined by the absence or decrease of globin chain(s), which may lead imbalances of globin chains, ineffective erythropoiesis, hemolysis, and eventually to a variable degree of anemia. With the estimated carrier frequen

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c8cfd85fcae894b3048bec630957691

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