Yılmaz Akbaş

ORCID: 0000-0003-3919-4685
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Research Areas
  • Epilepsy research and treatment
  • Hemoglobinopathies and Related Disorders
  • Pharmacological Effects and Toxicity Studies
  • Nutrition and Health in Aging
  • Iron Metabolism and Disorders
  • Folate and B Vitamins Research
  • Migraine and Headache Studies
  • Family and Disability Support Research
  • Clinical Nutrition and Gastroenterology
  • Osteomyelitis and Bone Disorders Research
  • Genetic Neurodegenerative Diseases
  • Neonatal and fetal brain pathology
  • Bacterial Infections and Vaccines
  • Traumatic Brain Injury and Neurovascular Disturbances
  • Cerebral Venous Sinus Thrombosis
  • Electrolyte and hormonal disorders
  • Metabolism and Genetic Disorders
  • Bone and Joint Diseases
  • RNA modifications and cancer
  • Neurological Complications and Syndromes
  • Autoimmune Neurological Disorders and Treatments
  • Pregnancy-related medical research
  • Intestinal Malrotation and Obstruction Disorders
  • Cystic Fibrosis Research Advances
  • Cardiovascular Syncope and Autonomic Disorders

Istanbul Aydın University
2024

Mustafa Kemal University
2021-2024

Pediatrics and Genetics
2021

Selçuk Üniversitesi Tıp Fakültesi Hastanesi
2021

Gazi University
2016-2020

State Hospital
2020

Rize Devlet Hastanesi
2019

Dokuz Eylül University
2001

Abstract Background It is known that chronic condition also affects siblings without illness. Healthy of children with a and aged 9–14 years healthy sibling illness their parents were included in the study. Aim The aim our study was to examine internet‐game addiction, physical activity, quality life sleep compare them peers sibling. Methods Computer game evaluated respectively by Game Addiction Scale for Children, Child Physical Activity Questionnaire, Children's Sleep Disorder Quality Life...

10.1111/cch.13228 article EN Child Care Health and Development 2024-01-01

Metabolic changes in head and neck carcinogenesis are often non-specifically correlated with carcinomas. The study of metabolic disorders can improve the understanding tumourigenesis at cellular level. This was designed to evaluate role serum homocysteine, folate, vitamin B(12) levels pathogenesis laryngeal squamous cell cancer (LSCC) by measuring 60 consecutive untreated patients LSCC controls (30 smokers 30 non-smokers). Compared smoker non-smoker control groups, significantly lower were...

10.1177/147323001003800619 article EN Journal of International Medical Research 2010-12-01

Migraine, as a chronic neurovascular disease, is known to be risk factor for retinal and optic nerve head damage. Herein, we aimed evaluate the disc microvasculature in pediatric migraine (PM) patients using optical coherence tomography angiography (OCTA).Forty-six eyes of 23 with PM without aura (PM group) 46 age- sex-matched healthy subjects (control were included this cross-sectional prospective study. Demographic features ophthalmological examination including OCTA measurements...

10.1097/wno.0000000000001697 article EN Journal of Neuro-Ophthalmology 2022-08-02

Deficiency of vitamin B12, with an essential role in cellular metabolism, is commonly observed Turkey (Koc A et al., Eur J Nutr 2006; 45: 291–297). The most common cause B12 deficiency insufficient intake the diet. Due to strict vegan diets or pernicious anemia, it among breastfed infants mothers low levels. Mothers are generally asymptomatic. affected continue have healthy development for first 6 months due available hepatic stocks, but if continues irritability, nutritional problems,...

10.1055/a-0981-6355 article EN Klinische Pädiatrie 2019-08-13

Purpose We aimed to explore the utility and additional clinical contribution of brain fluorodeoxyglucose (FDG) PET imaging for assessment children with possible autoimmune encephalitis in comparison MRI. Materials methods conducted a retrospective analysis six pediatric patients (all seronegative) between 2014 2019 initial diagnosis who had FDG PET/CT or PET/MRI MRI during diagnostic period. Diagnosis was based on consensus criteria defined by Graus et al . Brain images were visually...

10.1097/mnm.0000000000001222 article EN Nuclear Medicine Communications 2020-05-25

Objective: Candida species are the most common infectious agents among pathogens responsible for nosocomial fungal infections. Transmissions in intensive care units account a significant proportion of mortality and morbidity associated with candida The present study evaluates prevalence, type, treatment approach, underlying risk factors, outcomes infections patients treated pediatric unit Türkiye dense population children who have fled war Syria. Methods: was conducted 14-bed tertiary city...

10.59213/tp.2023.37450 article EN Trends in Pediatrics 2023-03-15

Introduction/Purpose Recent studies point to an important role for the cerebellum in nonmotor functions, primarily including higher cognitive functions and affect. However, available evidence on cerebellar contribution social faculties are currently sparse exact of cognition is yet be elucidated. The present study aimed investigate impairments a group patients who suffered from isolated stroke. We hypothesized that earlier stages their stroke with posterior lesions would more affected domain...

10.1161/svin.04.suppl_1.143 article EN cc-by-nc-nd Stroke Vascular and Interventional Neurology 2024-11-01

We present two pediatric cases of levetiracetam overdose.The first case was a 3-year-old girl who was, by her family, accidentally given at 115 mg/kg/day for one-month duration.The second case, 3-month-old used 300 dose about one month.We didn't observe remarkable severe side effects in our patients.

10.12996/gmj.2017.39 article EN cc-by Gazi Medical Journal 2017-03-28

Background: Congenital afibrinogenemia is characterized by the absence of fibrinogen. fibrinogen disorders result from several mutations in FGA , FGB or FGG . Their epidemiology not well known. Observation: The present study reports on 2 children with congenital afibrinogenemia. first child, a male who now 9 years old, was diagnosed after spontaneous intracranial bleeding at age 3 years. second child 2-year-old female cousin patient, coagulation tests were carried out due to frequent...

10.1097/mph.0000000000001658 article EN Journal of Pediatric Hematology/Oncology 2019-11-12

Abstract Background Peroxisomal biogenesis disorders (PBDs) include a miscellaneous group of diseases which cause serious multisystem disease. Mutations 13 different PEX genes lead to PBDs including Zellweger syndrome (ZS). Different types mutations PEX1 and PEX10 are correlated with broad-range phenotypes PBDs. Case presentation Patient 1 is 4-month-old boy who was affected by myoclonic seizures, poor oral feeding since birth. The patient hypotonic had hepatosplenomegaly. 2 2-month-old...

10.1515/jpem-2019-0194 article EN Journal of Pediatric Endocrinology and Metabolism 2020-02-17

Introduction:Although nutrition is very effective on mortality in critically ill children, patients cannot be fed adequately.There no suitable biomarker for enteral monitoring and management.The aim of this study; To investigate the usability nefsatin-1 nutritional management children. Methods:In January-September 2019 period, 35 children who were hospitalized tertiary pediatric intensive care unit without any signs inflammation included study.Nesfatin-1, vitamin D level, prealbumin, albumin...

10.4274/cayd.galenos.2022.07830 article EN cc-by-nc Turkish Journal of Pediatric Emergency and Intensive Care Medicine 2023-03-09
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