Ayten Eraydın

ORCID: 0000-0002-6131-0390
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About
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Research Areas
  • Thyroid Disorders and Treatments
  • Pituitary Gland Disorders and Treatments
  • Thyroid Cancer Diagnosis and Treatment
  • Inflammatory Biomarkers in Disease Prognosis
  • Ion Transport and Channel Regulation
  • Ion channel regulation and function
  • Cardiovascular Syncope and Autonomic Disorders
  • Cardiac Arrhythmias and Treatments
  • Pharmaceutical Practices and Patient Outcomes
  • Receptor Mechanisms and Signaling
  • Health and Wellbeing Research
  • Nuclear Receptors and Signaling
  • Genetic Syndromes and Imprinting
  • Circular RNAs in diseases
  • Biochemical Analysis and Sensing Techniques
  • Adrenal and Paraganglionic Tumors
  • Liver Disease Diagnosis and Treatment
  • Electrolyte and hormonal disorders
  • Human Health and Disease
  • Liver Disease and Transplantation
  • Growth Hormone and Insulin-like Growth Factors
  • Cytokine Signaling Pathways and Interactions
  • Apelin-related biomedical research
  • Nutrition and Health in Aging
  • Metabolism, Diabetes, and Cancer

Pamukkale University
2021-2024

Inonu University
2022

Gaziantep University
2015-2017

Gaziantep Children's Hospital
2017

Dokuz Eylül University
2014

Fine needle aspiration biopsy (FNAB) is a useful tool in the diagnosis of thyroid nodules. However, some limitations exist as approximately 25% cases cannot be distinguished with this method. Therefore, identification novel diagnostic markers very important improving papillary carcinoma (PTC) diagnosis. microRNAs (miRNAs) are small regulatory RNA molecules that have been involved variety biological processes, including tumorigenesis. Moreover, determination miRNAs prognostic, diagnostic, and...

10.1089/gtmb.2015.0062 article EN Genetic Testing and Molecular Biomarkers 2015-06-05

Chronic liver diseases have been shown to adversely affect the quality of life. Standardized tools for patient assessment are great importance treatment and follow-up these patients. In this study, we aimed determine validity reliability Liver Symptom Index 2.0 (LDSI 2.0) Turkish society, use in other studies daily clinical practice.A total 308 patients with chronic disease attending outpatient clinic Department Gastroenterology, Faculty Medicine, Dokuz Eylül University between September...

10.5152/tjg.2014.7509 article EN The Turkish Journal of Gastroenterology 2014-11-03

Graves' ophthalmopathy (GO) is the most common extrathyroidal manifestation of disease (GD). Severe identified in 3–5% patients with GD.1 GO usually present bilaterally, affecting their fifth and seventh decades. The highest risk severe eye involvement seen around age 60.2 Most GD who have do not require additional specific medical treatments. Conservative supportive procedures are satisfactory for patient comfort.3 Corticosteroids currently mainstay treatment moderate disease. However, side...

10.1136/postgradmedj-2016-134292 article EN Postgraduate Medical Journal 2016-08-26

Interferon-alpha (IFN-α) is an effective drug used for the treatment of chronic hepatitis C. So far its numerous side effects have been reported in literature. It may be difficult to always put IFN-induced thyroid diseases into a single classic disease table. There are atypical due IFN usage C virus. Herein, we present case with rare clinical table such as thyrotoxicosis observed following IFN-α therapy patient euthyroid nodular without autoimmune thyroiditis findings and use therapeutic...

10.1136/bcr-2017-221228 article EN BMJ Case Reports 2017-09-25

Objective: Diabetes mellitus (DM) is a complex syndrome caused by lack of insulin secretion and/or resistance and emerges with high blood glucose levels, along multiorgan involvement characterized micro/macro complications. Treatment process complications the disease are huge financial moral problems for society as well individuals. Material Methods: Mean platelet volume (MPV), red cell distribution width (RDW), glycosylated hemoglobin (HbA1c), neutrophil lymphocyte counts ratio (Neutrophil...

10.5336/intermed.2017-57111 article EN cc-by-nc-nd Turkiye Klinikleri Journal of Internal Medicine 2017-01-01

Searchable abstracts of presentations at key conferences in endocrinology ISSN 1470-3947 (print) | 1479-6848 (online)

10.1530/endoabs.37.ep609 article EN Endocrine Abstracts 2015-05-01

Abstract Objective Primary hypophysitis might be challenging to diagnose, and there is a lack of evidence regarding optimal treatment strategies due rarity the disease. We aim investigate clinical features compare outcomes different management primary in large group patients recruited on nationwide basis. Design A retrospective observational study. Methods The demographic, clinical, radiologic follow-up data were collected study protocol templates analyzed. Results One hundred thirteen...

10.1093/ejendo/lvae101 article EN European Journal of Endocrinology 2024-08-26

Thyrotoxic periodic paralysis (TPP) is the most common form of acquired hypokalaemic paralysis. The precipitating factors disease are a high-carbohydrate diet and exercise.1 2 Some TPP cases with normal potassium levels have also been reported, but diagnosis difficult rare.3 duration attacks typically few hours. Severity correlates serum level.4 It known that chronic use liquorice causes symptoms similar to mineralocorticoid secretion (apparent excess) syndrome, leading findings such as...

10.1136/postgradmedj-2016-134716 article EN Postgraduate Medical Journal 2017-03-03

Searchable abstracts of presentations at key conferences in endocrinology ISSN 1470-3947 (print) | 1479-6848 (online)

10.1530/endoabs.37.ep231 article EN Endocrine Abstracts 2015-05-01

Aim: Type 2 diabetes mellitus (T2DM) is one of the most common chronic diseases in older adults.With advancing age, polypharmacy and proteinenergy malnutrition associated with can be seen frequently T2DM patients due to metabolic causes may adversely affect prognosis.In this study, it was aimed evaluate relationship between patients.Materials Methods: Three hundred twenty-one aged 65 years over, diagnosed receiving oral anti-diabetic drug therapy, who applied Internal Medicine Geriatrics...

10.4274/nkmj.galenos.2022.19483 article EN cc-by-nc-nd Namık Kemal Tıp Dergisi 2022-06-22

Searchable abstracts of presentations at key conferences in endocrinology ISSN 1470-3947 (print) | 1479-6848 (online)

10.1530/endoabs.37.ep1190 article EN Endocrine Abstracts 2015-05-01

Searchable abstracts of presentations at key conferences in endocrinology ISSN 1470-3947 (print) | 1479-6848 (online)

10.1530/endoabs.37.ep901 article EN Endocrine Abstracts 2015-05-01

Tiroid hastalıkları, özellikle hipotiroidi, üreme çağındaki kadınlarda ve gebelerde sık görülen endokrin bozukluklardan biridir. Gebe kadınların %3-5?inde subklinik %0,3-0,5?inde aşikar hipotiroidi görülmektedir. Gebelerde tanısında TSH, sT4 veya TT4 kullanılmaktadır. Hipotiroidi, erken geç obstetrik komplikasyonlara neden olabilmektedir. Annede anemi, spontan abortus, konjestif kalp yetmezliği, preeklampsi, postpartum hemoraji, plasental anomali gestasyonel hipertansiyon olabilirken;...

10.5336/endocrin.2015-47689 article TR cc-by-nc-nd Turkiye Klinikleri Journal of Endocrinology 2016-01-01

Searchable abstracts of presentations at key conferences in endocrinology ISSN 1470-3947 (print) | 1479-6848 (online)

10.1530/endoabs.37.ep952 article EN Endocrine Abstracts 2015-05-01

Abstract Purpose To investigate the effects of combination thyroid replacement treatment on left atrial volume (LAV), diastolic functions, and electromechanical delays in women with low triiodothyronine (T3) levels. Methods The study consisted forty-seven female patients primer hypothyroidism. who had T3 levels, despite using tetraiodothyronine (T4) for a while normal thyrotropin (TSH) T4 levels levothyroxine (LT4) started therapy were included study. Biochemical samples (TSH, free T4, T3)...

10.21203/rs.3.rs-2456721/v1 preprint EN cc-by Research Square (Research Square) 2023-01-11

Bartter syndrome  and Gitelman syndrome  are rare autosomal recessive syndromes. In extremely cases, GS may diagnosed with growth retardation and diabetes mellitus. this 3-case series, was identified at 17-year follow-up of our dizygotic twin patients BS and glucose metabolism disorder was developed.  Whereas, 3RD. patient in adulthood period developed mellitus after 8 years follow up. Chronic hypopotassemia has been shown to cause ın several articles....

10.17546/msd.292428 article EN Medical Science and Discovery 2017-02-28

Searchable abstracts of presentations at key conferences in endocrinology ISSN 1470-3947 (print) | 1479-6848 (online)

10.1530/endoabs.49.ep1003 article EN Endocrine Abstracts 2017-05-03

Bartter syndrome and Gitelman are rare autosomal recessive syndromes. In extremely cases, GS may diagnosed with growth retardation diabetes mellitus. this 3-case series, was identified at 17-year follow-up of our dizygotic twin patients BS glucose metabolism disorder developed. Whereas, 3RD. patient in adulthood period developed mellitus after 8 years follow up. Chronic hypopotassemia has been shown to cause ın several articles. Potassium plays an important role insulin, IGF-1 hormone cycle....

10.36472/msd.v4i2.182 article EN Medical Science and Discovery 2017-02-28

Abstract Purpose: The aim of this study is; To examine the destruction insulin receptor substrate-1 (IRS-1) molecule, which is one mechanisms that cause resistance in diabetes and obesity, its effect to reduce destruction. For purpose, effects exercise, metformin, exenatide pioglitazone treatments on IRS-1 ubiquitination pancreas, muscle adipose tissue were investigated an obese diabetic animal model. Method: Obese rat model was used study. This characterised by resistance. molecular...

10.1210/jendso/bvab048.893 article EN cc-by-nc-nd Journal of the Endocrine Society 2021-05-01
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