Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Alpaslan, Tuzcu"'
Publikováno v:
Diabetes & Metabolic Syndrome: Clinical Research & Reviews. 2:253-258
Summary Aim Obesity is a major risk factor for insulin resistance, type 2 diabetes, heart disease, and many other chronic diseases. The factors regulating cytokine production seem to have a role on the determination of adipocyte volume. We aimed to i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::41e0833ca905a671678bee1082ac1bbd
https://doi.org/10.1016/j.dsx.2008.07.001
https://doi.org/10.1016/j.dsx.2008.07.001
Autor:
Yung Seng Lee, Alpaslan Tuzcu, Mithat Bahceci, Stephen O'Rahilly, Deniz Gokalp, Anne White, Robert L. Oliver, I. Sadaf Farooqi, John W.M. Creemers, Julia M. Keogh, Stefan Herber
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 93:4494-4499
Context: Mutations in the proopiomelanocortin (POMC) gene that impair the synthesis or structure of POMC-derived peptides predispose to human obesity. Objective: Our objective was to identify and characterize novel mutations in the POMC gene found in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3beb9eb2588c30c1ee44a7ccedbab302
https://doi.org/10.1210/jc.2008-0954
https://doi.org/10.1210/jc.2008-0954
Autor:
Aziz Karabulut, Yasin Aksu, Kenan Iltumur, Alpaslan Tuzcu, İsmail Hamdi Kara, Abdurrahman Kaplan, Nizamettin Toprak
Publikováno v:
International Heart Journal. 46:761-770
Hyperinsulinemia is related to coronary artery disease (CAD), as an indication of decreased insulin sensitivity. Although there are many studies showing the relation between fasting insulin levels and insulin resistance, there are fewer studies on po
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3770c2f3f850c54acd58432eed219dba
https://doi.org/10.1536/ihj.46.761
https://doi.org/10.1536/ihj.46.761
Publikováno v:
Dicle Medical Journal, Vol 31, Iss 4, Pp 34-37 (2004)
Russel Silver Syndrome (RSS) is a very rare syndrome with phenotypicchanges and its etiology has not explained yet. In 1953 and 1954, a specialgroup of Intrauterin Growth Reterdation, childiren with short staturealong a small triangular face, low-set
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::018f22bf9037aba30cbdded7055e9e0c
http://4181.indexcopernicus.com/fulltxt.php?ICID=887961
http://4181.indexcopernicus.com/fulltxt.php?ICID=887961
Autor:
Alpaslan Tuzcu, Ayse Dicle Turhanoglu, Mithat Bahçeci, Hatice Öztürkmen Akay, Zülfü Karabulut
Publikováno v:
Dicle Medical Journal, Vol 31, Iss 2, Pp 68-72 (2004)
Coexistence of acromegaly and anklosing spondylitis had been rarelyreported. Only two case reports were described coexistence of two diseasesin literature. These two diseases have some similar clinical andradiographic features. Calcaneal epin formati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::e23f2fdc583ac90e4c004c49f1227e2d
http://4181.indexcopernicus.com/fulltxt.php?ICID=887927
http://4181.indexcopernicus.com/fulltxt.php?ICID=887927
Publikováno v:
Dicle Medical Journal, Vol 31, Iss 3, Pp 62-65 (2004)
A 42-year-old male was hospitalized in Department of Endocrinologyfor evaluation of persistent hypertriglyceridemia and hypercholestrolemia.He was normal on physical examination except having multiple xanthomasin elbow, knee and ankle. ApoE genotypin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::b915228a918739c0fde8653e32c1aded
http://4181.indexcopernicus.com/fulltxt.php?ICID=887950
http://4181.indexcopernicus.com/fulltxt.php?ICID=887950
Autor:
Deniz Gökalp, Alpaslan Tuzcu, Mithat Bahçeci, Müzeyyen Yıldırım, Sedat Akdeniz, Selver Özekinci, Zuhat Urakçı, Şenay Arıkan
Publikováno v:
Turkish Journal of Endocrinology and Metabolism, Vol 13, Iss 3, Pp 60-62 (2009)
Lipoid proteinosis (LP) is a rare disorder inherited as an autosomal recessive trait. LP is characterized by deposition of hyaline-like material in the skin, mucous membranes, and other tissues. LP has been mapped to chromosome 1q21, the locus for th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::95da65effd362414c7ca95554229db24
http://www.turkjem.org/eng/yazilar.asp?yaziid=612&sayiid=
http://www.turkjem.org/eng/yazilar.asp?yaziid=612&sayiid=
Publikováno v:
Turkish Journal of Endocrinology and Metabolism, Vol 12, Iss 2, Pp 60-62 (2008)
Turkish Journal of Endocrinology and Metabolism, Vol 12, Iss 2, Pp 42-45 (2008)
Turkish Journal of Endocrinology and Metabolism, Vol 12, Iss 2, Pp 42-45 (2008)
This report describes the delayed presentation of right-side Morgagni hernia in a 15-year-old girl with Turner syndrome. It is commonly associated with a number of systemic malformations and abnormalities. Morgagni hernia is a rare type of congenital
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::13a88aa6dc093d5414f4b57455ed9130
http://www.turkjem.org/eng/yazilar.asp?yaziid=563&sayiid=53
http://www.turkjem.org/eng/yazilar.asp?yaziid=563&sayiid=53
Publikováno v:
Journal of endocrinological investigation.
Ahead of Print article withdrawn by publisher.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bb3c3692aed1236e77175e8be06f8ad6
https://pubmed.ncbi.nlm.nih.gov/19474527
https://pubmed.ncbi.nlm.nih.gov/19474527
Publikováno v:
Kulak burun bogaz ihtisas dergisi : KBB = Journal of ear, nose, and throat. 17(4)
Mucormycosis is a rare, saprophytic, invasive, and fulminant fungal disease. It occurs in immunocompromised patients such as those with diabetes mellitus or blood dyscrasia, or in patients under immunosuppressive therapy. A 17-year-old female patient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::92533497681375431fa4d7e9fe2c75d9
https://pubmed.ncbi.nlm.nih.gov/18187976
https://pubmed.ncbi.nlm.nih.gov/18187976