Zobrazeno 1 - 10 of 13 pro vyhledávání: '"Durmuş Doğan"'
1
Retrospective Evaluation of Diagnosis and Treatment of Patients with Type 1 Diabetes Mellitus
Autor: Durmuş Doğan, Zeynep Karaca Aydoğan, Fatih Battal
Publikováno v: Volume: 5, Issue: 2 111-117
Türkiye Diyabet ve Obezite Dergisi
Amaç: Çanakkale ili ve çevresindeki Tip 1 Diyabetes Mellitus (DM) tanılı olguların demografik özelliklerinin, klinik ve laboratuvar bulgularının, başvuru anında diyabetik ketoasidoz (DKA) durumlarının ve aldıkları tedavilerin değerlen
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c4f6170261e513df05f8346fdc9ee037
https://dergipark.org.tr/tr/pub/tudod/issue/64671/884914
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2
Novel
Autor: Durmuş Doğan, Esra Eren, Fatma Turkan Mutlu, Gokce Yıldız, Aysegul Yilmaz, Songul Gokay, Pembe Soylu Ustkoyuncu
Publikováno v: Journal of Clinical Research in Pediatric Endocrinology
JCRPE, Vol 12, Iss 2, Pp 223-224 (2020)
JCRPE, Vol 12, Iss 4, Pp 427-431 (2020)
Abetalipoproteinaemia (ABL) is an autosomal recessive disorder characterized by very low plasma concentrations of total cholesterol and triglyceride (TG). It results from mutations in the gene encoding microsomal TG transfer protein (MTTP). A nine-mo
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0edecf85906d4cd00b6b7f255523706e
https://pubmed.ncbi.nlm.nih.gov/31914726
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4
Akademický článek
Research trends on the gut microbiota in endocrine metabolism: a thematic and bibliometric analysis
Autor: Durmus Doğan, Taylan Çelik
Publikováno v: Frontiers in Cellular and Infection Microbiology, Vol 14 (2024)
BackgroundGut microbiota studies in the field of endocrinology metabolism have attracted increasing attention in recent years. To comprehensively assess the evolving landscape of this research field, we conducted a thorough bibliometric analysis of g
Externí odkaz: https://doaj.org/article/f1550d0b0e20495091801d4918f8f170
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5
Akademický článek
Genetic influence on urinary vitamin D binding protein excretion and serum levels: a focus on rs4588 C>A polymorphism in the GC gene
Autor: Durmus Doğan, Eda Gül Özcan, Dilek Ülker Çakır, Fatma Sılan
Publikováno v: Frontiers in Endocrinology, Vol 14 (2023)
IntroductionVitamin D binding protein (VDBP) plays a crucial role in vitamin D transport and metabolism. The rs4588-A polymorphism of the GC gene, encoding VDBP, has been associated with altered serum VDBP and 25-hydroxyvitamin D (25OHD) levels. Howe
Externí odkaz: https://doaj.org/article/c1d3bd95258744f2bf63ed7a08cdf48f
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6
Mutational analysis of PHEX, FGF23 and CLCN5 in patients with hypophosphataemic rickets
Autor: Suna Hancili, Yufei Shi, Essa Y. Baitei, Ayla Güven, Durmuş Doğan, Walaa E Kattan, Yılmaz Kor, Minjing Zou, Brian F. Meyer, Roua A. Al-Rijjal, Anwar F Al-Enezi, Huda A BinEssa, Ömer Tarım, Namik Kaya
SummaryContext Hypophosphataemic rickets (HR) is a group of rare hereditary renal phosphate wasting disorders caused by mutations in PHEX, FGF23, DMP1, ENPP1, CLCN5 or SLC34A3. Objective To investigate underlying genetic defects in patients with hypo
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce8f9a24a7eded464b640e5355c93009
http://hdl.handle.net/11452/29306
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7
Anthropometric findings from birth to adulthood and their relation with karyotpye distribution in Turkish girls with Turner syndrome
Autor: Nesibe Akyürek, Esra Deniz Çakır, Deniz Özalp Kızılay, Ayşenur Ökten, Fatih Gurbuz, Halil Saglam, Ayşehan Akıncı, Erkan Sari, Hatice Dilek Can, Bumin Dündar, Oya Ercan, Hakan Doneray, Bayram Özhan, Murat Doğan, Saygin Abali, Filiz Mine Çizmecioğlu, Firdevs Bas, Cigdem Binay, Gönül Çatlı, Veysel Nijat Baş, Huseyin Demirbilek, Hamdi Cihan Emeksiz, Samim Özen, Davut Gül, Feyza Darendeliler, Zerrin Orbak, Olcay Evliyaoğlu, Derya Tepe, Şükran Darcan, Mehmet Emre Atabek, Mehmet Keskin, Tsolga Unuvar, Cengizhan Açıkel, Ömer Tarım, Kezban Bulan, Ahmet Anık, Kursat Fidanci, Hasan Önal, Betül Ersoy, Mehmet Nuri Ozbek, Fatma Demirel, Nurullah Çelik, Ali Ataş, Erdal Adal, Semih Bolu, Enver Simsek, Beray Selver Eklioğlu, Korcan Demir, Yaşar Şen, Nesibe Andiran, Ayhan Abaci, Erdal Eren, Abdullah Bereket, Muammer Buyukinan, Peyami Cinaz, Bilgin Yüksel, Behzat Özkan, Serap Turan, Tolga Özgen, Serpil Bas, Şükrü Hatun, Ali Kemal Topaloglu, Ozgur Pirgon, Banu Kucukemre Aydin, Sultan Kaba, Gülay Karagüzel, Ediz Yeşilkaya, Leyla Akin, Rüveyde Bundak, Durmuş Doğan, Cengiz Kara, Adem Polat, Damla Gökşen
ABALI, SAYGIN/0000-0001-6552-2801; Gurbuz, Fatih/0000-0003-2160-9838; Hatun, Sukru/0000-0003-1633-9570; Abaci, Ayhan/0000-0002-1812-0321; Turan, Serap/0000-0002-5172-5402; Buyukinan, Muammer/0000-0002-2937-823X; yuksel, bilgin/0000-0003-4378-3255; Oz
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c9122d0e2396d42fcb6cd0da59a93d21
https://hdl.handle.net/20.500.12712/13420
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8
Growth curves for Turkish Girls with Turner Syndrome: Results of the Turkish Turner Syndrome Study Group
Autor: Durmuş Doğan, Sultan Kaba, Bayram Özhan, Huseyin Demirbilek, Cigdem Binay, Ayşehan Akıncı, Davut Gül, Halil Saglam, Bumin Dündar, Oya Ercan, Fatih Gurbuz, Gülay Karagüzel, Esra Deniz Çakır, Erdal Eren, Olcay Evliyaoğlu, Serpil Bas, Firdevs Bas, Tolga Ünüvar, Nesibe Andiran, Mehmet Nuri Ozbek, Muammer Buyukinan, Beray Selver Eklioğlu, Fatma Demirel, Cengiz Kara, Feyza Darendeliler, Ayhan Abaci, Kezban Bulan, Cengizhan Açıkel, Şükrü Hatun, Erdal Adal, Ömer Tarım, Bilgin Yüksel, Peyami Cinaz, Nurullah Çelik, Nesibe Akyürek, Mehmet Keskin, Saygin Abali, Korcan Demir, Damla Gökşen, Deniz Özalp Kızılay, Ahmet Anık, Ayşenur Ökten, Ozgur Pirgon, Şükran Darcan, Betül Ersoy, Celal Sağlam, M. Mümtaz Mazıcıoğlu, Filiz Mine Çizmecioğlu, Abdullah Bereket, Yaşar Şen, Hakan Doneray, Semih Bolu, Murat Doğan, Gönül Çatlı, Veysel Nijat Baş, Erkan Sari, Behzat Özkan, Rüveyde Bundak, Hatice Dilek Can, Hasan Önal, Ali Ataş, Adem Polat, Derya Tepe, Enver Simsek, Tolga Özgen, Ali Kemal Topaloglu, Serap Turan, Banu Kucukemre Aydin, Ediz Yeşilkaya, Leyla Akin, Hamdi Cihan Emeksiz, Zerrin Orbak, Samim Özen, Mehmet Emre Atabek
Publikováno v: Journal of Clinical Research in Pediatric Endocrinology
WOS: 000360842500004
PubMed: 26831551
Objective: Children with Turner syndrome (TS) have a specific growth pattern that is quite different from that of healthy children. Many countries have population-specific growth charts for TS. Consider
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ec2e025ced20531619eec7bb849d470
http://hdl.handle.net/20.500.12645/25231
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9
Turner Syndrome and Associated Problems in Turkish Children: A Multicenter Study
Autor: Ahmet Anık, Hakan Doneray, Ayşehan Akıncı, Kursat Fidanci, Olcay Evliyaoğlu, Davut Gül, Ali Ataş, Serpil Bas, Betül Ersoy, Derya Tepe, Erdal Eren, Cigdem Binay, Mehmet Nuri Ozbek, Carolyn Bondy, Hasan Önal, Tolga Ünüvar, Beray Selver Eklioğlu, Şükran Darcan, Erdal Adal, Feyza Darendeliler, Gönül Çatlı, Semih Bolu, Bayram Özhan, Nesibe Andiran, Ayşenur Ökten, Fatma Demirel, Yaşar Şen, Huseyin Demirbilek, Şükrü Hatun, Enver Simsek, Mehmet Keskin, Behzat Özkan, Sultan Kaba, Adem Polat, Kezban Bulan, Muammer Buyukinan, Halil Saglam, Hatice Dilek Can, Bumin Dündar, Oya Ercan, Damla Gökşen, Nurullah Çelik, Deniz Özalp Kızılay, Abdullah Bereket, Ömer Tarım, Cengiz Kara, Erkan Sari, Ayhan Abaci, Gülay Karagüzel, Peyami Cinaz, Filiz Mine Çizmecioğlu, Cengizhan Açıkel, Bilgin Yüksel, Ozgur Pirgon, Fatih Gurbuz, Nesibe Akyürek, Durmuş Doğan, Saygin Abali, Banu Kucukemre Aydin, Korcan Demir, Ediz Yeşilkaya, Leyla Akin, Serap Turan, Tolga Özgen, Esra Deniz Çakır, Murat Doğan, Veysel Nijat Baş, Ali Kemal Topaloglu, Firdevs Bas, Sukran Poyrazoglu, Hamdi Cihan Emeksiz, Zerrin Orbak, Samim Özen, Mehmet Emre Atabek
Publikováno v: Journal of Clinical Research in Pediatric Endocrinology
WOS: 000351307200005
PubMed ID: 25800473
Objective: Turner syndrome (TS) is a chromosomal disorder caused by complete or partial X chromosome monosomy that manifests various clinical features depending on the karyotype and on the genetic ba
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a13949772b0ba3c11c6a6543db8ed61b
https://hdl.handle.net/20.500.12684/5285
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10
An essential splice site mutation (c.317+1G>A) in the TSHR gene leads to severe thyroid dysgenesis
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
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