Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Hamza, Müslümanoğlu"'
Autor:
Ramazan Emre, Serhat Özkan, Kemal Murat Cantürk, Hüseyin Aslan, Muhsin özdemir, Özgür Aldemir, Mehmet Fatih Celayir, Muhammed Hamza Müslümanoğlu
Publikováno v:
Namık Kemal Tıp Dergisi, Vol 3, Iss 3, Pp 98-105 (2015)
AimIn this study, we aimed to investigate the effects of MTHFR C677T and A1298C polymorphisms to homocysteine levels in patients with Parkinson's disease who were treated with levodopa and entekapone.Materials and MethodsPlasma homocysteine (hcy), fo
Externí odkaz:
https://doaj.org/article/7884bad4e2264e018c050b832f0c466a
Autor:
Sevilhan Artan, Muhsin Özdemir, Turgay Şener, Muhammed Hamza Müslümanoğlu, Hüseyin Özden Yurdakul, Beyhan Durak, Oguz Cilingir
Publikováno v:
Journal of the Turkish-German Gynecological Association, Vol 11, Iss 04, Pp 199-203 (2010)
To test whether the Multiplex Ligation-dependent Probe Amplification (MLPA) technique can be used as a screening test for rapid diagnosis of aneuploidies in uncultured amniocentesis.In this prospective blind study, MLPA with chromosomes 13,18,21,X an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13ad0bbb6599adce5ae34434cc1b6f85
https://doi.org/10.5152/jtgga.2010.37
https://doi.org/10.5152/jtgga.2010.37
Autor:
Beyhan Durak, Oguz Cilingir, Muhsin Özdemir, Sevilhan Artan, Mesut Yeşil, M. Hamza Müslümanoğlu, Guney Bademci, Turgay Şener
Publikováno v:
Turkiye Klinikleri Journal of Medical Sciences. 30:1465-1468
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3c14792dbb4ddd88438d9f518dfedf1c
https://doi.org/10.5336/medsci.2009-13334
https://doi.org/10.5336/medsci.2009-13334
Autor:
Derya Uzun, Mehmet Turgut, Ahmet Uludag, Selma Demir, Muhammed Hamza Müslümanoğlu, Emre Tepeli, Kemal Murat Canturk, Engin Atli, Muhsin Özdemir
Publikováno v:
Genetic Testing and Molecular Biomarkers. 13:641-645
Prostate cancer is the most common cause of cancer deaths in men and is a major health problem worldwide. Methylene tetrahydrofolate reductase (MTHFR) plays an important role for folate metabolism and is also an important source for DNA methylation a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5843b17be0ae137da082065a9b79e9ec
https://doi.org/10.1089/gtmb.2009.0046
https://doi.org/10.1089/gtmb.2009.0046
Autor:
Sevilhan Artan, Oguz Cilingir, Muhammed Hamza Müslümanoğlu, Mehmet Turgut, Cavit Can, Yusuf Ozyürek
Publikováno v:
Fertility and Sterility. 84:519-522
To determine the prevalence of Y-chromosome microdeletions among infertile men and to correlate the clinical presentation of the men with specific deletions, microdeletion analysis in 53 infertile men (30 nonobstructive azoospermic, 23 severely oligo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5fdf920abc965643a06ac036d4f8e6eb
https://doi.org/10.1016/j.fertnstert.2005.02.024
https://doi.org/10.1016/j.fertnstert.2005.02.024
Autor:
Oguz Cilingir, Sukru Saygin Demir, Guney Bademci, Sevilhan Artan, Muhammed Hamza Müslümanoğlu, T. Basmaci, S. Urer, N. Saracoglu, I. Sabuncu
Publikováno v:
British Journal of Dermatology. 155:467-469
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3c277ba60a5f20483cbc479837e57d0d
https://doi.org/10.1111/j.1365-2133.2006.07288.x
https://doi.org/10.1111/j.1365-2133.2006.07288.x
Autor:
Ozge Ozalp Yuregir, Cagatay Unsal, Muhammed Hamza Müslümanoğlu, Sevcan Tug Bozdogan, Hakan Erkman, Ahmet Genc, Huseyin Aslan
Publikováno v:
Hemoglobin. 36(3)
Thalassemias are genetically heterogeneous group of disorders with reduced or absent production of globin. β-Thalassemia major can be caused by homozygosity or compound heterozygosity for β-globin gene mutation. Here we report, for the first time i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9571984bde57786e6c3863bd8e58d856
https://pubmed.ncbi.nlm.nih.gov/22385009
https://pubmed.ncbi.nlm.nih.gov/22385009
Autor:
Salih Kavukcu, Judith A. Goodship, M Hamza Müslümanoğlu, John P. Atkinson, Ronny Decorte, Yves Pirson, M. Kathryn Liszewski, Guido Filler, Elizabeth J. Kemp, Anna Richards, Timothy H.J. Goodship, AK Lampe, Leana S. Wen
Membrane cofactor protein (MCP; CD46) is a widely expressed transmembrane complement regulator. Like factor H it inhibits complement activation by regulating C3b deposition on targets. Factor H mutations occur in 10-20% of patients with hemolytic ure
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e3ec2eb1121fb6dacc1885ea694529e
https://avesis.deu.edu.tr/publication/details/09a7b351-4afa-464d-937e-0e7ce55cfb5d/oai
https://avesis.deu.edu.tr/publication/details/09a7b351-4afa-464d-937e-0e7ce55cfb5d/oai
Autor:
Ali, Arslantas, Sevilhan, Artan, Ulkü, Oner, Ramazan, Durmaz, Hamza, Müslümanoğlu, Metin Ant, Atasoy, Nurettin, Başaran, Eşref, Tel
Publikováno v:
Acta neurologica Belgica. 102(2)
Meningiomas are common tumors of the central nervous system. Although most are benign tumors, approximately 10% show a histologic progression to a higher malignancy grade similar to atypical (GII) and anaplastic (GIII) meningiomas. Monosomy 22q12 is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e07577f0a88e90edc3744d5949718f78
https://pubmed.ncbi.nlm.nih.gov/12161900
https://pubmed.ncbi.nlm.nih.gov/12161900
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