User profiles for Gulden Diniz

g diniz

Izmir Democracy University
Verified email at idu.edu.tr
Cited by 1415

White sponge nevus: clinical suspicion and diagnosis

M Songu, H Adibelli, G Diniz - Pediatric dermatology, 2012 - Wiley Online Library
White sponge nevus is a rare, autosomal‐dominant disorder that affects the noncornified
stratified squamous epithelia. Clinically, the presence of white, spongy plaques mostly in the …

Effects of resveratrol on incisional wound healing in rats

I Yaman, H Derici, C Kara, E Kamer, G Diniz, R Ortac… - Surgery today, 2013 - Springer
Purpose The objective of this study was to investigate the effect of resveratrol on the healing
process after midline laparotomy in rats. Methods The study was performed on adult female …

A novel TRAPPC11 mutation in two Turkish families associated with cerebral atrophy, global retardation, scoliosis, achalasia and alacrima

…, D Landgraf, E Utine, F Hazan, G Diniz… - Journal of Medical …, 2017 - jmg.bmj.com
Background Triple A syndrome (MIM #231550) is associated with mutations in the AAAS
gene. However, about 30% of patients with triple A syndrome symptoms but an unresolved …

[HTML][HTML] Tissue expression of neutrophil gelatinase-associated lipocalin and kidney injury molecule-1 in breast cancers

G Diniz, AG Pulular, DS Kahraman… - European Journal of …, 2022 - ncbi.nlm.nih.gov
Objective: Breast cancer is the most common cancer among women worldwide. Neutrophil
gelatinase-associated lipocalin (NGAL) has important roles in immunity, cell proliferation, and …

Impact of next‐generation sequencing panels in the evaluation of limb‐girdle muscular dystrophies

…, B Kiliç, F Sertpoyraz, G Diniz… - Annals of Human …, 2019 - Wiley Online Library
Introduction Limb‐girdle muscular dystrophy (LGMD) is the fourth most common muscular
dystrophy, with progressive proximal muscle weakness. However, a large number of …

[HTML][HTML] Childhood onset limb-girdle muscular dystrophies in the Aegean part of Turkey

ULU Yİş, G Di̇ni̇z, F Hazan… - Acta …, 2018 - ncbi.nlm.nih.gov
The aim of this study is to analyze the epidemiology of the clinical and genetic features of
childhood-onset limb-girdle muscular dystrophies (LGMD) in the Aegean part of Turkey. In total …

Effect of sildenafil on wound healing: an experimental study

H Derici, E Kamer, HR Ünalp, G Diniz… - … archives of surgery, 2010 - Springer
Purpose We aimed to investigate the effect of sildenafil on the healing process of abdominal
wall wound in rats. Materials and methods The study was performed with adult female Wistar…

[HTML][HTML] SURF1 related Leigh syndrome: Clinical and molecular findings of 16 patients from Turkey

…, O Adebali, A Durmaz, A Bircan, G Diniz… - Molecular Genetics and …, 2020 - Elsevier
Introduction Pathogenic variants in SURF1, a nuclear-encoded gene encoding a mitochondrial
chaperone involved in COX assembly, are one of the most common causes of Leigh …

Expression of stromal caveolin-1 may be a predictor for aggressive behaviour of breast cancer

N Eliyatkin, S Aktas, G Diniz, HH Ozgur, ZY Ekin… - Pathology & Oncology …, 2018 - Springer
Caveolin-1 (Cav-1) is well known as a principal scaffolding protein of caveolae which are
specialized plasma membrane structures. The role of Cav-1 in tumorigenesis of breast cancers …

GNE myopathy in Turkish sisters with a novel homozygous mutation

G Diniz, Y Secil, S Ceylaner… - Case Reports in …, 2016 - Wiley Online Library
Background. Hereditary inclusion body myopathy is caused by biallelic defects in the GNE
gene located on chromosome 9p13. It generally affects adults older than 20 years of age. …