Zobrazeno 1 - 10 of 13 pro vyhledávání: '"Dilek Aktaş"'
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Akademický článek
Gorlin Syndrome in Eleven Patients
Autor: Gülen Eda Utine, Yasemin Alanay, Dilek Aktaş, Koray Boduroğlu, Mehmet Alikaşifoğlu, Ergül Tunçbilek
Publikováno v: Journal of Pediatric Research, Vol 4, Iss 2, Pp 63-67 (2017)
Aim: Gorlin syndrome is an autosomal dominant disorder characterized by cutaneous basal cell carcinomas, odontogenic keratocysts and skeletal anomalies. Predisposition to certain types of cancers is among the main features of the disease. Chromosome
Externí odkaz: https://doaj.org/article/3d949a63ce1549af89babbf3e9d713a7
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5
An Important Problem After Colorectal Cancer Surgery: Fecal Incontinence
Autor: Sema Koçaşli, Dilek Aktaş
Publikováno v: Ordu Üniversitesi Hemşirelik Çalışmaları Dergisi. 3:36-43
Son yıllarda kolorektal kanser tanısı konan hasta sayısının artması ile birlikte kolorektal cerrahi oranı da giderek artmaktadır. Kanser tedavisine bağlı olarak ortaya çıkan bağırsak disfonksiyonu bireylerin defekasyon sorunları ile k
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::9a057e424b71793547ac1cdebdb60f02
https://doi.org/10.38108/ouhcd.712645
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6
Effectiveness of training in increasing awareness about managing pressure injuries in emergency departments
Autor: Gülay Yazıcı, Dilek Aktaş, Hülya Bulut, Nilüfer Muslubaş, Sevil Güler Demir, Zehra Göçmen Baykara, Ahmet Demircan
Emergency room conditions and the characteristics of the patients followed up pose a risk for pressure injury.This study was conducted as a pilot study to assess the effectiveness of a training program in increasing the awareness of healthcare profes
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e48aeb53ac1f5cc8438674c78c50f44a
https://avesis.gazi.edu.tr/publication/details/3094c5ef-ba3e-465f-9fa2-869aa9ec1981/oai
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7
Ameliyathanede Çalışan Hemşirelerin Cerrahiye Bağlı Basınç Yaralanmalarına İlişkin Bilgi Düzeyi
Autor: Sema Koçaşli, Dilek Aktaş
Publikováno v: Volume: 7, Issue: 2 173-179
Celal Bayar Üniversitesi Sağlık Bilimleri Enstitüsü Dergisi
Amaç: Bu çalışma ameliyathanede çalışan hemşirelerin intraoperatif dönemde basınç yaralanmaları risk faktörlerine ve önleme yöntemlerine ilişkin bilgi düzeylerini belirlemek amacıyla yapıldı. Yöntem: Çalışma Ankara’da yer al
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f542dc508042027a4b4d6d57929bef6f
https://dergipark.org.tr/tr/pub/cbusbed/issue/55485/654433
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8
Function in unaffected arms of children with obstetric brachial plexus palsy
Autor: Dilek Aktaş, Beyhan Eren, Evrim Karadag-Saygi, Ozge Kenis-Coskun
Publikováno v: European Journal of Paediatric Neurology. 22:610-614
Objective The objective is to compare the fine and gross motor function of unaffected arms of children with obstetric brachial plexus palsy (OBBP) with typically developing children's dominant upper extremities. Methods Fifty-three patients with OBBP
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::090d66a86553b57dec48882aa0af3a7d
https://doi.org/10.1016/j.ejpn.2018.03.005
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9
Jervell and Lange-Nielsen syndrome with homozygous missense mutation of the KCNQ1 gene
Autor: Esra, Kılıç, İlker, Ertuğrul, Sema, Özer, Mehmet, Alikaşifoğlu, Dilek, Aktaş, Koray, Boduroğlu, Gülen Eda, Ütine
Publikováno v: The Turkish journal of pediatrics. 56(5)
Jervell and Lange-Nielsen syndrome (JLNS) is an autosomal recessive cardioauditory ion channel disorder characterized by congenital bilateral sensorineural deafness and long QT interval. JLNS is a ventricular repolarization abnormality and is caused
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::9e2345b26cedd0e0d3317660d6004b06
https://pubmed.ncbi.nlm.nih.gov/26022593
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10
A rare case of 2q37 microdeletion with Albright hereditary osteodystrophy-like phenotype
Autor: Pelin Ozlem, Simşek-Kiper, Gülen Eda, Utine, Yasemin, Alanay, Dilek, Aktaş, Mehmet, Alikaşifoğlu, Koray, Boduroğlu
Publikováno v: The Turkish journal of pediatrics. 53(5)
Chromosome 2q37 microdeletion syndrome is a rare disorder characterized by mild-moderate psychomotor and growth retardation, autistic-like behavior, Albright hereditary osteodystrophy-like metacarpal/metatarsal shortening, and facial characteristics.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::aed18bb042006ddf815656b718302cfa
https://pubmed.ncbi.nlm.nih.gov/22272459
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