Zobrazeno 1 - 10 of 66 pro vyhledávání: '"Düzcan, F."'
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2
Fatal Pulmonary Embolism Due to Inherited Thrombophilia Factors in a Child With Wolfram Syndrome
Autor: Küçüktaşçi K, Semiz S, Balci YI, Özsari T, Gürses D, Önem G, Saçar M, Düzcan F, Yüksel D, Semiz E
Wolfram syndrome-1 is a rare and severe autosomal recessive neurodegenerative disease characterized by diabetes mellitus (DM), optic atrophy, diabetes insipidus, and deafness. Poorly controlled type 1 DM increases the risk for thrombosis. However, co
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3566::71892b7e9bc76aae570542a580b0d6f0
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3
A Newborn with Congenital Mixed Phenotype Acute Leukemia After In Vitro Fertilization
Autor: Ergin H, Özdemir ÖM, Karaca A, Türk NŞ, Düzcan F, Ergin Ş, Kazancı E, Vergin C, Erbay A
Congenital leukemia is a rare disease. The majority of cases of this disease are acute myelogenous leukemia (AML). Congenital acute lymphoblastic leukemia (ALL) is rare and most often is of B cell lineage. Rarely, some cases have been designated biph
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3566::813ffb8f9fd35bc8d54038caffb5fe43
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4
A Newborn with Congenital Mixed Phenotype Acute Leukemia After In Vitro Fertilization
Autor: Ergin, Hacer., Özdemir, Özmert Muhamet Ali, Karaca, A., Türk, Nilay Şen, Düzcan, F., Ergin, Ş., Kazanci, E., Vergin, C., Erbay, A.
Congenital leukemia is a rare disease. The majority of cases of this disease are acute myelogenous leukemia (AML). Congenital acute lymphoblastic leukemia (ALL) is rare and most often is of B cell lineage. Rarely, some cases have been designated biph
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3566::30cf8be329200f12b98de0c6a2d3244e
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/10072
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5
Expression of ERCC1 and its clinicopathological correlations in non-small cell lung cancer
Autor: Tepeli E, Caner V, Büyükpınarbaşılı N, Çetin GO, Düzcan F, Elmas L, Bağcı G
Excision Repair Cross-Complementing Group 1 (ERCC1) is an important DNA repair gene, playing critical role in nucleotide excision repair pathway and having a significant influence on genomic instability. Some studies support that ERCC1 might be a pot
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3566::6bc1c2285feefac9506a212d79b6ffed
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6
Determination of apoptosis, proliferation status and O6-methylguanine DNA methyltransferase methylation profiles in different immunophenotypic profiles of diffuse large B-cell lymphoma
Autor: Şen Türk N, Özsan N, Caner V, Karagenç N, Düzcan F, Düzcan E, Hekimgil M
OBJECTIVE: Our aim was to investigate the expression of apoptosis-associated proteins (bcl-2, bcl-xl, bax, bak, bid), apoptotic index (AI) and proliferation index (PI) in germinal center B-cell-like immunophenotypic profile (GCB) and non-GCB of diffu
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3566::3660e50907b96d4e5fbbd12e0d5451cb
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8
Ovarian agenesis and MURCS association
Autor: Yildirim, B., Semerci, C.N., Yaǧci, B., Duman, K., Düzcan, F.
The MURCS (MUllerian duct aplasia, Renal aplasia, Cervicothoracic Somite dysplasia) association is a rare and sporadic disease. The etiology is unknown. We present a patient with short stature, absence of uterus, tubes, left ovary, left renal agenesi
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::8ebd3cf9cb8092a7ed4caeb02a1de544
https://hdl.handle.net/11499/4515
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