Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Yaman Saglam"'
Autor:
Yaman Saglam, Michaela Kendall, Timothy Barrett, Murat Doğan, Kristien Boelaert, Hakan Cangul, Eamonn R. Maher
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology
Objective: Congenital hypothyroidism (CH) is the most common neonatal endocrine disorder and mutations in the TPO gene have been reported to cause CH. Our aim in this study was to determine the genetic basis of CH in two affected individuals co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d942bbb87fa379045c8b0f6a35f08be
https://doi.org/10.4274/jcrpe.1404
https://doi.org/10.4274/jcrpe.1404
Publikováno v:
Fertility and Sterility. 112:e240
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9be0f0b490d639111693be438c258746
https://doi.org/10.1016/j.fertnstert.2019.07.1372
https://doi.org/10.1016/j.fertnstert.2019.07.1372
Autor:
Ibrahim Yaman Saglam, Ebru Demiralay, Esra Sağlam, Göksel Şener, Ahmet Ozer Sehirli, Emine Nur Ozdamar
Publikováno v:
Burns. 39:897-904
WOS: 000321602800010
PubMed ID: 23137627
Objective: To investigate the role of endogenous neuronal nitric oxide synthase (nNOS) on brain injury after burn and the effects of the captopril. Methods: Wistar albino rats (200-250 g) were expose
PubMed ID: 23137627
Objective: To investigate the role of endogenous neuronal nitric oxide synthase (nNOS) on brain injury after burn and the effects of the captopril. Methods: Wistar albino rats (200-250 g) were expose
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f85716a9e999f211081d32d2fbd07a2
https://doi.org/10.1016/j.burns.2012.10.008
https://doi.org/10.1016/j.burns.2012.10.008
Publikováno v:
Surgical Science. :111-115
Purpose: K-ras mutations were reported to be in 40% - 60% of patients with sporadic colorectal cancers (CRCs). HER-2/neu oncogene that is important in breast carcinoma was reported in CRCs in several studies. The aims of our study are to determine; t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0516c99e0d6b8d6d4a8a8383d508384d
https://doi.org/10.4236/ss.2012.33022
https://doi.org/10.4236/ss.2012.33022
Autor:
Feyza Darendeliler, Hakan Cangul, Eamonn R. Maher, Michaela Kendall, Kristien Boelaert, Yaman Saglam, Banu Kucukemre, Timothy Barrett
Publikováno v:
Endocrine research. 40(3)
Absract Purpose: Mutations in the TPO gene have been reported to cause congenital hypothyroidism (CH), and our aim in this study was to determine the genetic basis of congenital hypothyroidism in two affected children coming from a consanguineous fam
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::811babc17371f58f26ed2fd62e81387b
https://pubmed.ncbi.nlm.nih.gov/25328990
https://pubmed.ncbi.nlm.nih.gov/25328990
Autor:
Murat Doğan, Kristien Boelaert, Hakan Cangul, Michaela Kendall, Eamonn R. Maher, Yaman Saglam, Timothy Barrett
Mutations in the thyroglobulin (TG) gene have been reported to cause congenital hypothyroidism (CH) and we have been investigating the genetic architecture of CH in a large cohort of consanguineous/multi-case families. Our aim in this study was to de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d9a9ad9b9e522f01a08c99e4bc5ab69
https://avesis.yyu.edu.tr/publication/details/c0db530c-5477-4ff9-a902-fa79e642a2be/oai
https://avesis.yyu.edu.tr/publication/details/c0db530c-5477-4ff9-a902-fa79e642a2be/oai
Autor:
Erdal Eren, Durmuş Doğan, Halil Saglam, Ömer Tarım, Yaman Saglam, Michaela Kendall, Timothy Barrett, Hakan Cangul, Eamonn R. Maher
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism. 27
Congenital hypothyroidism (CH) is the most common neonatal endocrine disorder and 2% of cases have familial origin. Our aim in this study was to determine the genetic alterations in two siblings with CH coming from a consanguineous family. Because CH
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b0180e4969f2e3480cfe134ab2cd7e4
https://doi.org/10.1515/jpem-2014-0048
https://doi.org/10.1515/jpem-2014-0048
Autor:
Michaela Kendall, Zehra Aycan, Veysel Nijat Baş, Hakan Cangul, Eamonn R. Maher, Yaman Saglam, Timothy Barrett
Publikováno v:
Journal of pediatric endocrinologymetabolism : JPEM. 27(11-12)
Congenital hypothyroidism (CH), one of the most important preventable causes of mental retardation, is a clinical condition characterized by thyroid hormone deficiency in newborns. CH is most often caused by defects in thyroid development leading to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5dd252f81985ab1329d5a98097e8755
https://pubmed.ncbi.nlm.nih.gov/24945425
https://pubmed.ncbi.nlm.nih.gov/24945425
Autor:
Zehra Aycan, Yaman Saglam, Timothy Barrett, Veysel Nijat Baş, Hakan Cangul, Eamonn R. Maher, Michaela Kendall
Publikováno v:
Journal of pediatric endocrinologymetabolism : JPEM. 27(3-4)
Mutations in DUOX2 have been reported to cause congenital hypothyroidism (CH), and our aim in this study was to determine the genetic basis of CH in two affected individuals coming from a consanguineous family. Because CH is usually inherited in auto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b0cbca4ee8a783a37986fab2a56adde
https://pubmed.ncbi.nlm.nih.gov/24127536
https://pubmed.ncbi.nlm.nih.gov/24127536
Autor:
Esra Sağlam, Emine Nur Ozdamar, Ibrahim Yaman Saglam, Ebru Demiralay, Göksel Şener, Ahmet Ozer Sehirli
WOS: 000321477200012
PubMed ID: 23756977
AIM:The purpose of this study was to determine the possible protective effects of captopril treatment against apoptosis in the brain induced by burn injury. MATERIAL and METHODS: Under ether anaesthe
PubMed ID: 23756977
AIM:The purpose of this study was to determine the possible protective effects of captopril treatment against apoptosis in the brain induced by burn injury. MATERIAL and METHODS: Under ether anaesthe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d62f40b6208b6263016ce305e9af66a4
https://hdl.handle.net/20.500.12415/1881
https://hdl.handle.net/20.500.12415/1881