27 results match your criteria: "Goztepe Medicalpark Hospital[Affiliation]"

Objectives: To determine the effects of hyperandrogenemia and other phenotypic parameters on endometrial vitamin D receptor (VDR-X2 and VDR-X4) expression in women with polycystic ovary syndrome (PCOS) undergoing ovarian stimulation and total embryo freezing.

Methods: Forty-four PCOS patients were divided into four phenotypes according to the criteria for hyperandrogenemia (HA), ovulatory dysfunction (OD), and polycystic ovary morphology (PCOM): phenotype A (HA+OD+PCOM), phenotype B (HA+OD), phenotype C (HA+PCOM), and phenotype D (OD+PCOM). Endometrial VDR expression was determined by real-time PCR and immunohistochemistry.

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Objective: The aim of the study was to determine the expression pattern of long pentraxin 3 (PTX3) mRNA in cumulus cells (CCs) isolated from metaphase II oocytes of women with unilateral endometrioma undergoing controlled ovarian stimulation using a gonadotropin-releasing hormone antagonist (GnRHa) protocol.

Patients And Methods: A total of 60 CC samples, 30 from the affected ovary and 30 from the contralateral ovary, were collected from 12 patients with unilateral endometrioma who underwent flexible GnRHa protocol with recombinant human chorionic gonadotropin (rhCG) trigger. Thirty CC samples collected from the left ovary of 12 women with male factor infertility were used as external controls.

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Cardiovascular disease (CVD) is a major cause of death in the female population. The current study aimed to examine the relationship between CVD risk and novel endothelial dysfunction biomarkers [i.e.

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Polycystic Ovary Syndrome Accompanied by Hyperandrogenemia or Metabolic Syndrome Triggers Glomerular Podocyte Injury.

Diagnostics (Basel)

October 2024

Department of Anatomy, Histology, Pathology, and Forensic Medicine, Faculty of Medicine, University of Sofia "St. Kliment Ohridski", 1407 Sofia, Bulgaria.

To determine whether the urinary excretion of podocyte degradation products varies according to PCOS phenotype and metabolic syndrome (MetS). The concentrations of podocalyxin (PDX) and nephrin, chronic markers of podocyte damage, and neutrophil gelatinase-associated lipocalin (NGAL), a marker of acute glomerular damage, were analyzed in the morning urine samples of 50 PCOS patients and 50 healthy controls matched by age and BMI. Albuminuria was assessed by calculating the urine albumin-creatinine ratio (uACR).

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Background And Objective: Artificial intelligence (AI) advancements continue to have a profound impact on modern society, driving significant innovation and development across various fields. We sought to appraise the reliability of the information offered by Chat Generative Pre-Trained Transformer (ChatGPT) regarding diseases commonly associated with sports surgery. We hypothesized that ChatGPT could offer high-quality information on sports-related diseases and be used in patient education.

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Brugada syndrome (BS) is characterized by ST segment elevation in right precordial leads (V1-V3), ventricular tachycardia (VT), ventricular fibrillation (VF), and sudden cardiac death (SCD) in individuals without structural heart disease. The aim of this study is to contribute to the controversial issue of finding the most valuable marker that can predict poor prognosis during follow-up in patients with a diagnosis of BS. A total of 68 patients diagnosed with BS or had Brugada-type ECG change between January 1997 and July 2012 at the Department of Cardiology of Başkent University Faculty of Medicine, Ankara, Turkey, were included in this cohort study.

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Objective: Differences in individual muscle/fat volumes may change the effectiveness of chemotherapy. In this study, the relationship between trunkal muscle and fat volume and body mass index (BMI) obtained before receiving neoadjuvant chemotherapy (NCT) in patients with breast cancer and complete pathological response (pCR) was investigated.

Materials And Methods: The volumes of psoas, abdominal and paraspinal muscles, and trunkal subcutaneous and visceral fat were calculated using CoreSlicer AI 2.

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Background: A fine-tuned pro-inflammatory and anti-inflammatory balance in the follicular unit is essential for cumulus expansion and successful ovulation. While the long pentraxin 3 (PTX3) gene is required for the expansion of cumulus cells (CCs), ovulation, resumption of meiosis and fertilization, the vitamin D receptor gene (VDR-X2) is required for intra-follicle redox balance. This study was planned to determine the expression pattern of VDR-X2 and PTX3 mRNA in CCs isolated from germinal vesicle (GV), metaphase I (MI), and metaphase II (MII) oocytes of PCOS patients with ovulatory dysfunction.

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Endometrial Injury Upregulates Expression of Receptivity Genes in Women with Implantation Failure.

Int J Environ Res Public Health

February 2023

Department of Obstetrics and Gynecology, CERICSAL (Centro di RIcerca Clinica SALentino), "Veris Delli Ponti Hospital", 73020 Lecce, Italy.

Background: Homeobox genes A10 (HOXA10) and A11 (HOXA11), members of the abdominal B gene family, are responsible for embryonic survival and implantation. This study was planned to investigate whether endometrial injury alters the expression of both transcripts in women with implantation failure.

Methods: A total of 54 women with implantation failure were divided into two equal groups as experimental (scratching) and sham (no scratching).

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Background: This study aimed to compare the kidney paired donation (KPD) program recipients with the traditional living donor kidney transplantation (LDKT) recipients regarding patient and graft survival.

Methods: We retrospectively analyzed 141 recipients of the KPD program and 141 classic LDKT recipients that we matched for age and sex as controls between July 2005 and June 2019. We compared the 2 transplant groups for patient and kidney survival using the Kaplan-Maier test.

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Objective: To reveal whether hysteroscopic removal of the International Federation of Gynecology and Obstetrics (FIGO) types 0 and 1 fibroids makes any changes in the expression of homeobox genes (HOXA10, HOXA11), leukemia inhibitory factor, and nuclear factor-kappa B (NF-kB).

Design: A case-control study.

Setting: University-based in vitro fertilisation center.

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Objectives: Despite the development of diagnosis and treatment methods, the psychological effects of infertility on women were not adequately addressed. This study investigated the effect of male and female factor infertility on women's anxiety, depression, self-esteem, quality of life, and sexual function parameters.

Methods: In this prospective, cross-sectional study, 480 women [n = 234, with male factor infertility (MFI) (MFI group) and n = 246, with female factor infertility (FFI) (FFI group)], who could not conceive despite unprotected intercourse for 1 year, and 242 fertile healthy women (control group) who had children within the last 1 year were included.

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Best Practice Recommendations for Geriatric Dysphagia Management with 5 Ws and 1H.

Ann Geriatr Med Res

June 2022

Department of Physical Medicine and Rehabilitation, Ankara Diskapi Yildirim Beyazit Training and Research Hospital, University of Health Sciences Turkey, Ankara, Turkey.

Background: Dysphagia is a geriatric syndrome. Changes in the whole body that occur with aging also affect swallowing functions and cause presbyphagia. This condition may progress to oropharyngeal and/or esophageal dysphagia in the presence of secondary causes that increase in incidence with aging.

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Article Synopsis
  • - NEMO deficiency, caused by mutations in the IKBKG gene, leads to serious immunodeficiency, making patients susceptible to recurrent infections, but also presents with severe inflammatory issues, the reasons for which are not well understood.
  • - A study on a 12-year-old male with NEMO deficiency analyzed his immune profile before and after undergoing hematopoietic stem cell transplantation (HSCT), measuring responses to NF-kB activators and examining specific immune cell populations.
  • - Findings showed that even with immune deficiency, there were high levels of certain inflammatory markers and a significant presence of low-density granulocytes, indicating an abnormal immune response that normalized post-transplant, suggesting these factors may contribute to tissue damage associated with
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Article Synopsis
  • This study investigates the outcomes of fragmented electrogram (FE)-guided ganglionated plexus (GP) ablation for treating vagally mediated bradyarrhythmia (VMB) performed by both experienced and inexperienced operators.
  • Data from 47 patients across 16 cardiac hospitals showed that while the number of ablation points was similar, experienced operators had significantly better acute responses compared to novices.
  • The study concludes that FE-guided GP ablation can be successfully performed by inexperienced operators, but procedural time and acute responses differ significantly between them and more experienced practitioners.
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Article Synopsis
  • Biallelic mutations in the IL21R gene lead to combined immunodeficiency, often resulting in severe infections including cryptosporidiosis, with a study analyzing 13 patients revealing eight unique mutations.
  • Common symptoms included recurrent bacterial, fungal, and viral infections, with additional issues like asthma and skin diseases, while many patients showed low antibody levels and immune cell deficiencies.
  • Hematopoietic stem cell transplantation (HSCT) had a poor success rate, with only 33.3% survival among transplanted patients and 57.1% mortality in non-transplanted cases, highlighting the impact of organ damage from chronic infections on outcomes.
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Introduction: Childhood obesity can cause hyperlipidemia and hepatic steatosis at early age and chronic disease complications in adult life. We aimed to evaluate the relationship between abdominal subcutaneous fat thickness (ASFT) and hepatic steatosis, serum lipid and transaminase levels in obese children.

Population And Methods: A retrospective study was conducted with children (aged 4-18 years) who presented to outpatient clinic due to obesity.

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Aims: Mahaim-type accessory pathways (MAPs) are generally right-sided due to the embryological differentiation, but left-sided localization is also possible. This study aims to compare the clinical and electrophysiological characteristics of right- and left-sided MAPs.

Methods: Of 251 patients diagnosed with AP by electrophysiological study between November 2015 and February 2020, 12 patients with MAP were included (right sided n = 8, left sided n = 4).

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In tension gastrothorax, the abdominal contents are displaced into the thorax, leading to a mediastinal shift that arises from the pressure placed on the intrathoracic region. This condition is often due to a congenital or acquired (secondary to surgery) diaphragmatic defect and is rarely seen secondary to trauma. A 40-year-old man presented to the emergency department after an in-vehicle traffic accident.

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Objective: The main objective of this study is to evaluate the availability of lateral antebrachial cutaneous nerve (LACN) autograft for acute or delayed repair of segmented digital nerve injuries.

Patients And Methods: 13 digital nerve defects of 11 patients; treated with interposition of LACN graft that harvested from ipsilateral extremity were included in the study. Mean follow up period was 35, 7 months.

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Epithelioid hemangioendotheliomas are uncommon vascular neoplasms and their spinal location is even rarer. We report clinical course of a 31-year-old man with an epithelioid hemangioendothelioma at the cranio-cervical junction. A cervical magnetic resonance imaging revealed tumor that caused posterior cervical cord compression.

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Outcome of hematopoietic cell transplantation for DNA double-strand break repair disorders.

J Allergy Clin Immunol

January 2018

Institute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, United Kingdom; Primary Immunodeficiency Group, Institute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, United Kingdom. Electronic address:

Background: Rare DNA breakage repair disorders predispose to infection and lymphoreticular malignancies. Hematopoietic cell transplantation (HCT) is curative, but coadministered chemotherapy or radiotherapy is damaging because of systemic radiosensitivity. We collected HCT outcome data for Nijmegen breakage syndrome, DNA ligase IV deficiency, Cernunnos-XRCC4-like factor (Cernunnos-XLF) deficiency, and ataxia-telangiectasia (AT).

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Neonatal meningoencephalitis is a severe condition for the developing brain of a newborn. Radiologic findings of necrosis and liquefaction due to hemorrhagic meningoencephalitis may be confused with brain abcess. In this article, we report a neonate having liquefaction necrosis due to hemorrhagic meningoencephalitis mimicing intracranial abscess due to Proteus mirabilis.

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Objectives: The aim of this study was to determine long term follow up of the patients who had femoral head osteonecrosis and had been treated with free vascularized fibular grafting.

Patients And Methods: We retrospectively reviewed 28 hips of 21 patients who had undergone free vascularized fibular grafting for the treatment of osteonecrosis of femoral head. There were 16 male and 5 female patients.

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Objective: The aim of this study was to determine long-term follow-up results of patients with femoral head osteonecrosis who were treated with free vascularized fibular grafting (FVFG).

Methods: The results of 28 hips of 21 patients (16 male, 5 female) who underwent FVFG for treatment of osteonecrosis of the femoral head were retrospectively reviewed. Mean age of patients at time of surgery was 30.

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