Association of Serum Triglyceride-to-High-density Lipoprotein Cholesterol Ratio with Insulin Resistance and Non-alcoholic Fatty Liver Disease in Children and Adolescents

Autor: Ala Üstyol, Funda Kökali, Nilgün Selçuk Duru, Murat Elevli

Publikováno v: Haseki Tıp Bülteni, Vol 55, Iss 4, Pp 286-291 (2017)

Aim: Insulin resistance (IR) is considered the main contributor to non-alcoholic fatty liver disease (NAFLD). Triglyceride (TG)-to-high-density lipoprotein cholesterol (HDL-C) ratio (TG/HDL-C) has been recommended as a surrogate index of IR. However,

Externí odkaz: https://doaj.org/article/affce9472ac84fc7b2db80675504a77f

Personality and Psychiatric Disorders among Employees of New York City Workplaces Affected by the 9/11 Attacks on the World Trade Center

Autor: C. Robert Cloninger, Maria E. Reynolds, Rachel E. Zettl, Carol S. North, Josh M. Raitt, Ala Üstyol

Publikováno v: Psychiatry

OBJECTIVE. Personality is associated with psychopathology after disasters, but its association with the portion of postdisaster psychopathology that is incident remains unclear. It is also unclear whether any particular attributes of personality are

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15a3074c985fae80e5f855d37c17496b
https://pubmed.ncbi.nlm.nih.gov/34780318

Association of Serum Triglyceride-to-High-density Lipoprotein Cholesterol Ratio with Insulin Resistance and Non-alcoholic Fatty Liver Disease in Children and Adolescents

Autor: Nilgün Selçuk Duru, Ala Üstyol, Funda Kokali, Murat Elevli

Publikováno v: Haseki Tıp Bülteni, Vol 55, Iss 4, Pp 286-291 (2017)

Aim: Insulin resistance (IR) is considered the main contributor to non-alcoholic fatty liver disease (NAFLD). Triglyceride (TG)-to-high-density lipoprotein cholesterol (HDL-C) ratio (TG/HDL-C) has been recommended as a surrogate index of IR. However,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f11fe77268bdd2c25e0314141c7aedc0
http://www.hasekidergisi.com/archives/archive-detail/article-preview/association-of-serum-triglyceride-to-high-density-/16604

Incidence of Type 1 Diabetes in Children Aged Below 18 Years during 2013-2015 in Northwest Turkey

Autor: Tulay Guran, Ilknur Arslanoglu, Ala Üstyol, Sukran Poyrazoglu, Derya Karaman Aksakal, Songül Karadeniz, Nurcan Cebeci, Olcay Evliyaoğlu, Halim Issever, Nihal Memioglu, Ahmet Uçar, Serap Semiz, Firdevs Bas, Didem Bezen, Feyza Darendeliler, Erdal Adal, Gül Yeşiltepe Mutlu, Hasan Önal, Saygin Abali, Abdurrahman Akgun, Serpil Bas, Nese Akcan, Sevil Sarikaya, Gulcan Seymen Karabulut, Ayla Güven, Ömer Tarım, Elif Sagsak, Melek Yildiz, Esra Deniz Papatya Cakir, Havva Nur Peltek, Bahar Ozcabi, Teoman Akcay, Aysegul Yuksel, Şükrü Hatun, Zeynep Atay, Hüseyin Anıl Korkmaz, Mehmet Azizoğlu, Oya Ercan, Pinar Isguven, Aydilek Dağdeviren, Abdullah Bereket, Filiz Tutunculer, Erdal Eren, Semih Bolu, Serap Turan, Tolga Özgen, Filiz Mine Çizmecioğlu, Emine Dilek, Yaşar Cesur, Heves Kırmızıbekmez, Metin Yildiz, Zehra Yavas Abali, Rüveyde Bundak, Cigdem Binay, Fatma Dursun

Publikováno v: Journal of Clinical Research in Pediatric Endocrinology

ABALI, SAYGIN/0000-0001-6552-2801; Turan, Serap/0000-0002-5172-5402; Hatun, Sukru/0000-0003-1633-9570; Akgun, Abdurrahman/0000-0002-2917-2469; yesiltepe mutlu, gul/0000-0003-3919-7763; Ozgen, Ilker Tolga/0000-0001-6592-9652 WOS: 000451667000006 PubMe

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65aab0f3d06236cbc7acf777c68a0d8b
https://hdl.handle.net/11443/2827

A novel CYP17A1 deletion causes a functional knockout of the steroid enzyme 17-hydroxylase and 17,20-lyase in a Turkish family and illustrates the precise role of the CYP17A1 gene

Autor: Christa E. Flück, Ala Üstyol, Núria Camats, Mehmet Emre Atabek, Bernhard Dick

Publikováno v: Clinical Case Reports
Camats Tarruella, Núria; Üstyol, Ala; Atabek, Mehmet Emre; Dick, Bernhard; Flück, Christa Emma (2015). A novel CYP17A1 deletion causes a functional knockout of the steroid enzyme 17-hydroxylase and 17,20-lyase in a Turkish family and illustrates the precise role of the CYP17A1 gene. Clinical case reports, 3(10), pp. 793-797. Wiley 10.1002/ccr3.343

Key Clinical Message A novel homozygous long-range deletion of the CYP17A1 gene abolished protein expression and caused the severest form of 17-hydroxylase deficiency in one kindred of a Turkish family. The affected subjects presented with 46,XY sex

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2f1fb3101f9fe5b0f3c241f437f0c21
http://europepmc.org/articles/PMC4614641