Zobrazeno 1 - 10
of 97
pro vyhledávání: '"Alev, Hasanoglu"'
Publikováno v:
Balıkesir Medical Journal. 3:102-116
Giris: Obezitenin tek basina ateroskleroz icin bir risk faktoru oldugu bilinmektedir. Obezite ve ateroskleroz iliskisi ile ilgili bilinen baslica faktorler dislipidemi, insulin rezistansi ve insulin duyarliligini artirici bir adipositokin olan adipon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8ac43f69a23ef66d4c5da22ca7726b11
https://doi.org/10.33716/bmedj.567409
https://doi.org/10.33716/bmedj.567409
Autor:
Sevcan A. Bakkaloglu, Burcu Topçu, Tuba Atalay, Aynur Küçükçongar, İlyas Okur, Yusuf Oner, Mustafa Cemri, Çiğdem Seher Kasapkara, Alev Hasanoglu, Serhat Koca, Buket Dalgic, Leyla Tümer, Yasemin Erten, Fatih Süheyl Ezgü, Suna Özhan Oktar, Bahattin Çiftçi, Gürsel Biberoğlu
Publikováno v:
Gene. 687:280-288
Fabry disease results from deficiency of the lysosomal enzyme alpha-galactosidase A. The families of 11 index cases were screened by enzyme and molecular assays. Further clinical and laboratory investigations were carried out in all cases. Including
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a8b1ed7cc62e46e02d714bd11fa3ba6
https://doi.org/10.1016/j.gene.2018.11.054
https://doi.org/10.1016/j.gene.2018.11.054
Publikováno v:
Journal of Pediatric Research, Vol 5, Iss 1, Pp 47-50 (2018)
Inborn errors of metabolism comprise a broad range of genetic diseases of which most are inherited in an autosomal recessive manner. Although being rare, there is a significant increase in their rate especially in countries where consanguineous marri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7bc005a93966e6c91878150453348e12
https://doi.org/10.4274/jpr.55477
https://doi.org/10.4274/jpr.55477
Autor:
İlyas Okur, Alev Hasanoglu, Aynur Küçükçongar Yavaş, Arzu Aral, Leyla Tümer, Tuba F. Eminoglu
Publikováno v:
Journal of Pediatric Research, Vol 4, Iss 1, Pp 1-5 (2017)
Aim: Coronary heart disease is one of the most common causes of death around the world. The pathological process of coronary heart disease like atherosclerosis starts in childhood. During this period thrombosis constitutes a high-risk factor. In this
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a9eff7a671ea628e3ffae7d4ae6b9e0
http://jpedres.org/article_14785/Association-Between-Soluble-Cd40-Ligand-And-Hypercholesterolemia-In-Children-And-Adolescents
http://jpedres.org/article_14785/Association-Between-Soluble-Cd40-Ligand-And-Hypercholesterolemia-In-Children-And-Adolescents
Autor:
Ertan Sal, Ülker Koçak, Idil Yenicesu, Fatih Süheyl Ezgü, Türkiz Gürsel, İlyas Okur, Zühre Kaya, Leyla Tümer, Alev Hasanoglu
Publikováno v:
Journal of pediatric hematology/oncology. 40(5)
Inherited metabolic diseases are pathologic conditions that generally develop as a result of impairment of the production or breakdown of protein, carbohydrate, and fatty acids. Early determination of hematological findings has a positive effect on t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46819f2a6a2613485e4b112566c84e50
https://pubmed.ncbi.nlm.nih.gov/29746437
https://pubmed.ncbi.nlm.nih.gov/29746437
Publikováno v:
Clinical Nutrition. 33:509-512
Vitamin A deficiency (VAD) is one of the most widespread vitamin deficiencies. Vitamin A is essential for children in order to ensure a healthy life span and sustain the normal growth and development. Aim of this study is to examine vitamin A status,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2655a69d2fe076279834931ab6793899
https://doi.org/10.1016/j.clnu.2013.07.008
https://doi.org/10.1016/j.clnu.2013.07.008
Autor:
Robert J. Desnick, Yoruk Divanoglu, Sitkiye Bahceci, Murat Polat, Fatih Süheyl Ezgü, Alev Hasanoglu
Publikováno v:
Genetic Testing and Molecular Biomarkers. 18:3-7
For inborn errors of metabolism, high resolution melting analysis (HRMA) is a rapid, efficient, simple, and inexpensive method for mutation/rare variant screening. HRMA is a recent molecular technique for genotyping single-nucleotide polymorphisms wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99f887843bdc321a39de4d87f99fa3bc
https://doi.org/10.1089/gtmb.2013.0371
https://doi.org/10.1089/gtmb.2013.0371
Publikováno v:
European Journal of Clinical Nutrition. 68:101-105
Glycogen storage disease type I (GSD I) is an autosomal recessive metabolic disorder caused by defects in the glucose-6-phosphatase complex. Deficient activity in the glucose-6-phosphatase-α catalytic unit characterizes GSD Ia and defects in the glu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af2e13877200929e995fb22b5eedce7a
https://doi.org/10.1038/ejcn.2013.186
https://doi.org/10.1038/ejcn.2013.186
Autor:
İlyas Okur, Leyla Tümer, Yasemin Erten, Muzeyyen Isitman, Fatma Tuba Eminoğlu, Alev Hasanoglu, Gürsel Biberoğlu, Fatih Süheyl Ezgü
Publikováno v:
Gene. 527:42-47
Background Chronic renal failure (CRF) is a serious complication of Fabry disease (FD). The aims of the present study were to determine the prevalence of unrecognized FD in Turkish hemodialysis population and to investigate the molecular background.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dbd90fd6f33074f762226d9f17b94389
https://doi.org/10.1016/j.gene.2013.05.050
https://doi.org/10.1016/j.gene.2013.05.050
Publikováno v:
Pediatrics International. 55:428-433
Background The aim of this study was to investigate the quality of life (QoL) of a group of patients with inherited metabolic diseases (IMD) who were treated with restrictive diet. Method A total of 68 patients (35 boys, 51.5%; 33 girls, 48.5%) with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::29c7d418e778d174e5f5d5086cbf7669
https://doi.org/10.1111/ped.12089
https://doi.org/10.1111/ped.12089