Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Isil Ozer"'
Autor:
Isil Ozer
Publikováno v:
Clinical Medicine Insights: Case Reports. 15:117954762210932
Kwashiorkor is a serious nutritional disease. The 7-month-old male patient presented with severe metabolic acidosis and elevated liver enzymes. His condition was similar to fatty acid oxidation defect. He was taken to the hospital on the previous day
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4cde9a8a3dbafe2a25b0c03e25665004
https://doi.org/10.1177/11795476221093287
https://doi.org/10.1177/11795476221093287
Autor:
Sezen Soyer-Uzun, Isil Ozer
Publikováno v:
Ceramics International. 41:10192-10198
X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM) and compressive strength measurements were performed to fully characterize metakaolin-based geopolymers with molar Si/Al ratios of 1.12, 1.77
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d707a45fc039cece308cce3041a8b15f
https://doi.org/10.1016/j.ceramint.2015.04.125
https://doi.org/10.1016/j.ceramint.2015.04.125
Autor:
Ayse Kilic, Emin Ünüvar, Müjgan Sidal, Isil Ozer, Murat Sütçü, Nelgin Gerenli, Ozlem Durmaz, Fatma Oguz, Muhammet Serdar Cantez, Gülden Gökçay
Publikováno v:
Tuberculin Skin Test in Children. 11:32-35
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a1a1cb4b530303681dde304c52b1091
https://doi.org/10.5222/j.child.2011.032
https://doi.org/10.5222/j.child.2011.032
Autor:
Mübeccel Demirkol, Yoshiko Aoyama, Teodor Podskarbi, Tetsu Ebara, Minoru Okubo, Isil Ozer, Yoon S. Shin, Toshio Murase, Gülden Gökçay
Publikováno v:
Journal of Human Genetics. 54:681-686
Glycogen storage disease type III (GSD III) is an autosomal recessive disorder caused by deficiency in the glycogen debranching enzyme (gene symbol: AGL) with two enzyme activities: transferase and glucosidase. A missense mutation causing isolated gl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b468bc1a6c0b6363b9af74d2bee474f3
https://doi.org/10.1038/jhg.2009.100
https://doi.org/10.1038/jhg.2009.100
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::04d6db7def664705110baee34943ff22
https://doi.org/10.1530/endoabs.35.p796
https://doi.org/10.1530/endoabs.35.p796
Autor:
Mehmet Mujdat Uysal, T. Baykal, Zehra Kılınclı, Gülden Gökçay, Isil Ozer, Mübeccel Demirkol
Publikováno v:
Journal of Nutritional Disorders & Therapy.
Vitamin C is the cofactor in biosynthesis of collagen, catecholamines and iron metabolism. The clinical features of scurvy may resemble metabolic disorders and hamper early diagnosis. A 2-year, 5-months old male child was admitted to hospital with co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::db29e1a356b184158eb3fe7e727c874f
https://doi.org/10.4172/2161-0509.1000113
https://doi.org/10.4172/2161-0509.1000113
Autor:
Beat Thöny, Clifford C. Ellingson, T. Baykal, Steven F. Dobrowolski, Trent Miller, Clinton Ellingson, Caroline Heintz, Mübeccel Demirkol, Isil Ozer, Nenad Blau, Gülden Gökçay
Publikováno v:
Molecular genetics and metabolism. 102(2)
Background The prevalence of phenylalanine hydroxylase (PAH)-deficient phenylketonuria (PKU) in Turkey is high (1 in 6500 births), but data concerning the genotype distribution and impact of the genotype on tetrahydrobiopterin (BH 4 ) therapy are sca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4c8a6356947a09d16480f91ce5f5809
https://pubmed.ncbi.nlm.nih.gov/21147011
https://pubmed.ncbi.nlm.nih.gov/21147011
Autor:
Stefanie Sander, Johannes Sander, Michael Peter, Anibh M. Das, Michael Terhardt, Nils Janzen, Mübeccel Demirkol, Isil Ozer, Gülden Gökçay
Publikováno v:
Clinica chimica acta; international journal of clinical chemistry. 412(1-2)
Background Quantification of nitisinone, 2-(nitro-4-trifluoromethylbenzoyl)1,3-cyclohexanedione (NTBC) has been repeatedly described. Nevertheless monitoring of NTBC has not yet become part of routine therapy surveillance in tyrosinaemia type I (OMIM
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a20959b14a7f1775d242118d026f95a
https://pubmed.ncbi.nlm.nih.gov/20883679
https://pubmed.ncbi.nlm.nih.gov/20883679
Autor:
Yoriko Endo, Yoshiko Aoyama, Minoru Okubo, Gülden Gökçay, Teodor Podskarbi, Yoon S. Shin, Toshio Murase, Tetsu Ebara, Mübeccel Demirkol, Isil Ozer
Publikováno v:
Pediatrics international : official journal of the Japan Pediatric Society. 52(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::226add04e56c809af001dc5c2dba061e
https://pubmed.ncbi.nlm.nih.gov/20158661
https://pubmed.ncbi.nlm.nih.gov/20158661
Autor:
Işil Özer
Publikováno v:
Clinical Medicine Insights: Case Reports, Vol 14 (2021)
Cat-scratch disease can be transmitted from cats and dogs in winter. It is usually self-limited and caused by Bartonella henselae . It may cause serious symptoms, including neurological findings, especially in immune-deficient patients. A female pati
Externí odkaz:
https://doaj.org/article/c89d587e9a7148668938421f015055e9