Výsledky vyhledávání - "Ozlem, Engiz"

The relation between increased carotid intima‐media thickness with fibrin monomers in obese children

Autor: Betül Şimşek, Esra Yazarli, Ozlem Engiz, Yıldız Dallar, Rukiye Ünsal Saç, Bulent Alioglu

Publikováno v: International Journal of Clinical Practice. 75

Objective: This study aimed to investigate the association between carotid intima-media changes that play a part in the atherosclerotic process in childhood obesity and fibrin monomers as an important indicator of fibrin plaque. Methods: This is a cr

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e4f563d75ad7faa30b0595c3beeabc00
https://doi.org/10.1111/ijcp.14199

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Prevalence of Obesity and Associated Risk Factors Among Adolescents in Ankara, Turkey

Autor: Sırma Ercan, Yıldız Dallar, Serdar Önen, Ozlem Engiz

Publikováno v: Journal of Clinical Research in Pediatric Endocrinology

Objective: The purpose of this study was to investigate the prevalence of and the risk factors associated with obesity among adolescents in Ankara, Turkey. Methods: The study was conducted in 26 schools in Ankara during the time period from September

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::552e5317fd43891d3bc9e20d82b02695
http://europepmc.org/articles/PMC3537287

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Bilateral periventricular nodular heterotopia, severe learning disability, and epilepsy in a male patient with 46,XY,der(19)t(X;19) (q11.1-11.2;p13.3)

Autor: Thomas Liehr, Ozlem Engiz, Serap Saygi, Dilek Aktas, Kristin Mrasek, Sevim Balci, Aysun Ünal, Madelaine Gross

Publikováno v: Developmental Medicine & Child Neurology. 49:219-224

Periventricular nodular heterotopia (PNH) is a rare neuronal migration disorder in which immature neurons fail to undergo a directed migration from the ventricular and subventricular zones to the cerebral cortex. Classic PNH occurs predominantly in f

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::315752a3d4bb8e48ed2e4bb27afeb4cd
https://doi.org/10.1111/j.1469-8749.2007.00219.x

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Cytokines as a Common Components of Two Different Disorders: Metabolic Syndrome and Hemophagocytic Lymphohystiositosis

Autor: Gönül Öcal, Mehmet Ertem, Ozlem Engiz, Funda Erkasar Citak, Merih Berberoğlu, Zeynep Şıklar, Pelin Bilir, Zümrüt Uysal

Publikováno v: Experimental and Clinical Endocrinology & Diabetes. 117:57-59

Increased cytokines secretion occurs in several different disorders. Hemophagocytic lymphohystiositosis (HLH) and metabolic syndrome (MS) are consist two of them. Hemophagocytic lymphohystiositosis results from uncontrolled macrophage activation and

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::774a410eee94800dc7b23d1175530dc2
https://doi.org/10.1055/s-2008-1076717

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Infantile malignant osteopetrosis: a rare cause of neonatal hypocalcemia

Autor: Bulent Alioglu, Yıldız Dallar Bilge, İnci Arikan, Semra Kara, Ozlem Engiz, Denizhan Bagrul, Georgia Lahr

Publikováno v: Journal of pediatric endocrinologymetabolism : JPEM. 25(11-12)

Infantile malignant osteopetrosis (IMO; OMIM 259700) is a rare inherited bone disease characterized by reduced or dysregulated activity of osteoclasts, resulting in generalized osteosclerosis. The disease usually presents within the first few months

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d41517e7adbeeb81a6708437e5658495
https://pubmed.ncbi.nlm.nih.gov/23329773

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Is basal serum 17-OH progesterone a reliable parameter to predict nonclassical congenital adrenal hyperplasia in premature adrenarche?

Autor: E Nazli, Gönç, Z Alev, Ozön, Ayfer, Alikaşifoğlu, Ozlem, Engiz, Burcu, Bulum, Nurgün, Kandemir

Publikováno v: The Turkish journal of pediatrics. 53(3)

To determine the critical features for the diagnosis of nonclassical 21 hydroxylase deficiency (NC210HD) without performing adrenocorticotropic hormone (ACTH) test, we studied 186 cases with premature adrenarche. Clinical and laboratory features as w

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::40d099aa83c42f7e35125c7f506f6063
https://pubmed.ncbi.nlm.nih.gov/21980808

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Two pediatric patients with Von Hippel-Lindau disease type 2b: from patient to screening, from screening to patient

Autor: Huseyin Demirbilek, Ayfer Alikasifoglu, Ozlem Engiz, Hartmut P.H. Neumann, Nazli Gonc, Nurgun Kandemir, Alev Ozon

Publikováno v: Journal of Pediatric Endocrinology and Metabolism. 24

Von Hippel-Lindau (VHL) disease is an autosomal dominantly inherited tumor susceptibility disease characterized by the development of hemangioblastomas of the brain, spinal cord and retina; pheochromocytomas and renal cell carcinoma. The disease is c

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e38819aa8cf60901e63bc96ab0a8ce40
https://doi.org/10.1515/jpem.2011.118

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Growth hormone deficiency due to traumatic brain injury in a patient with X-linked congenital adrenal hypoplasia

Autor: Ozlem, Engiz, Alev, Ozön, Felix, Riepe, Ayfer, Alikaşifoğlu, Nazli, Gönç, Nurgün, Kandemir

Publikováno v: The Turkish journal of pediatrics. 52(3)

X-linked adrenal hypoplasia congenita (AHC) is characterized by primary adrenal insufficiency and is frequently associated with hypogonadotropic hypogonadism (HH). The production of other pituitary hormones (adrenocorticotropic hormone [ACTH], growth

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::16eb3caa7a52ee6e32afe0bd5e274ce8
https://pubmed.ncbi.nlm.nih.gov/20718192

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