Výsledky vyhledávání - "Adam NAJAFLI"

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

DIAGNOSTIC APPLICATION AND CLINICAL SIGNIFICANCE OF FCM WELLS SCORING SYSTEM IN MYELODYSPLASTIC SYNDROMES

Autor: Reyhan Aliyeva, Agarza Aghayev, Adam Najafli, Reyhan Tagizade, Azer Kerimov

Publikováno v: Hematology, Transfusion and Cell Therapy, Vol 43, Iss , Pp S26- (2021)

Objective: Myelodysplastic syndromes (MDS) are group of clonal diseases of the hematopoietic system characterized by ineffective hematopoiesis, dysmyelopoiesis, a high frequency karyotype abnormalities and the risk of transformation into acute leukem

Externí odkaz: https://doaj.org/article/cc6e7a3d9e1a48228ab9feac447ebd8a

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DIAGNOSTIC APPLICATION AND CLINICAL SIGNIFICANCE OF FCM WELLS SCORING SYSTEM IN MYELODYSPLASTIC SYNDROMES

Autor: Adam Najafli, Agarza Aghayev, Reyhan Aliyeva, Azer Kerimov, Reyhan Tagizade

Publikováno v: Hematology, Transfusion and Cell Therapy, Vol 43, Iss, Pp S26-(2021)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eca4d78a77725eb623ff142c30d1a420
http://www.sciencedirect.com/science/article/pii/S2531137921011421

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Akademický článek

PROKR2 Mutations in Patients with Short Stature Who Have Isolated Growth Hormone Deficiency and Multiple Pituitary Hormone Deficiency

Autor: Aslı Derya Kardelen, Adam Najaflı, Firdevs Baş, Birsen Karaman, Güven Toksoy, Şükran Poyrazoğlu, Şahin Avcı, Umut Altunoğlu, Zehra Yavaş Abalı, Ayşe Pınar Öztürk, Esin Karakılıç Özturan, Seher Başaran, Feyza Darendeliler, Z. Oya Uyguner

Publikováno v: JCRPE, Vol 15, Iss 4, Pp 338-347 (2023)

INTRODUCTION: Recent reports have indicated the role of the prokineticin receptor 2 gene (PROKR2) in the etiology of pituitary hormone deficiencies, suggesting a potential role for the PROK2 pathway in pituitary development, in addition to its role i

Externí odkaz: https://doaj.org/article/18a4807ddfcf44a1a51a2d2bcc230afd

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