1,016 results match your criteria: "Inonu University School of Medicine & Liver Transplantation Institute[Affiliation]"

Study Design: Single-blinded, randomized controlled study.

Introduction: Carpal Tunnel Syndrome (CTS) causes pain and loss of function in the affected hand. The mobilization with movement (MWM) technique is a manual therapy method applied to correct joint movement limitation and to relieve pain and functional disorders.

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Background: The novel coronavirus disease 2019 (COVID-19) has a broad spectrum of clinical manifestations, the most common serious clinical manifestation of the coronavirus infection being pneumonia. Unfortunately, the optimal treatment approach is still uncertain. However, many studies have been conducted on the effectiveness of several medications in the treatment of COVID-19 infection.

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  • The study focuses on urinary tract infections (UTIs) in children and investigates the potential use of soluble Toll-like receptors (sTLR4, sTLR5) and interleukin 8 (IL-8) as biomarkers for diagnosing UTIs.
  • It involved 520 children, including those with UTIs, non-UTI infections, and healthy controls, measuring urine and serum levels of the biomarkers before and after treatment.
  • Results show that urine sTLR4 levels are higher in UTI patients, with a cut-off level identified to predict UTIs, especially higher in cases of pyelonephritis compared to cystitis, and decreasing post-treatment.
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Objective: This meta-analysis aims to review the effect of serial transabdominal amnioinfusion (TAI) on short-term and long-term perinatal outcomes in mid-trimester preterm premature rupture of membranes (PPROM).

Methods: Literature searches of PubMed, Web of Sciences, Scopus, and Cochrane Library were performed from their inception to April 2022. Studies comparing conventional treatment with serial TAI in women with proven PPROM at less than 26 + 0 weeks of gestation with oligohydramnios were included.

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Objective: The present study was aimed at investigating the effects of anti-seizure medications (ASMs), patient demographic characteristics, and the seizure type and frequency on the development of congenital malformations (CMs) in the infants of pregnant women with epilepsy (PWWE).

Methods: PWWE followed up at the neurology outpatient clinic of 21 centers between 2014 and 2019 were included in this prospective study. The follow-up of PWWE was conducted using structured, general pregnant follow-up forms prepared by the Pregnancy and Epilepsy Study Committee.

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Boron stress signal is transmitted through the TOR pathway.

J Trace Elem Med Biol

September 2023

Department of Genetics, Inonu University School of Medicine, Malatya 44280, Turkey; Department of Molecular Biology and Genetics, Izmir Institute of Technology, Izmir 35430, Turkey. Electronic address:

Although boron is an essential element for many organisms, an excess amount of it can cause toxicity, and the mechanism behind this toxicity is not yet fully understood. The Gcn4 transcription factor plays a crucial role in the boron stress response by directly activating the expression of the boron efflux pump Atr1. More than a dozen transcription factors and multiple cell signaling pathways have roles in regulating the Gcn4 transcription factor under various circumstances.

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Objective: The aim of this study is to clarify the role of different Doppler parameters such as umbilicocerebral ratio (UCR), cerebroplacentouterine ratio (CPUR), aortic isthmus, renal artery, and umbilical vein flow Doppler in predicting adverse neonatal outcomes in fetuses with late -onset fetal growth restriction.

Materials And Methods: The study included all patients diagnosed with fetal growth restriction at 32-39 weeks' gestation between 01/02/2020 and 01/02/2022 and treated at the Department of Obstetrics and Gynecology, Inonu University School of Medicine.

Results: Patients included in the study had a median gestational week at delivery of 37 (minimum 33+0-maximum 39+0), median CPR of 1.

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  • Fingolimod has been used for approximately ten years to treat multiple sclerosis but has been linked to elevated liver enzymes.
  • A case report details a 33-year-old woman who developed acute liver failure after taking Fingolimod and subsequently underwent liver transplantation.
  • There is currently no literature documenting instances of acute liver failure or the need for liver transplantation specifically related to Fingolimod treatment.
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  • The study focuses on the effectiveness and safety of TAF (tenofovir alafenamide) for chronic hepatitis B over 12 months in a real-life setting across 14 centers in Turkey, involving 480 patients.
  • It found that TAF treatment led to a notable increase in undetectable HBV DNA levels among patients, although the normalization of alanine transaminase (ALT) was not significantly different for those switching from another antiviral drug.
  • The results also indicated significant improvements in kidney and bone function shortly after switching to TAF, suggesting overall benefits for patients receiving this therapy.
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Background And Aim: Liver resection (LR) and liver transplantation (LT) are curative treatments for hepatocellular carcinoma (HCC). The main purpose of this study was to compare the survival of LR and LDLT in patients with HCC within the Milan criteria.

Materials And Methods: The results of the LR (n=67) and LDLT (n=391) groups were compared for overall survival (OS) and disease-free survival (DFS).

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Introduction: Cow's milk protein allergy (CMPA) is the most commonly encountered food allergy in the world, usually seen in infants under the age of 2 years. This study aims to determine the factors including COVID-19 affecting formula compliance of CMPA patients.

Methods: This study is a prospective, observational study based on 10 different Paediatric Allergy-Immunology clinics in Turkey.

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Context: The aims of the study are to compare characteristics of subacute thyroiditis (SAT) related to different etiologies, and to identify predictors of recurrence of SAT and incident hypothyroidism.

Methods: This nationwide, multicenter, retrospective cohort study included 53 endocrinology centers in Turkey. The study participants were divided into either COVID-19-related SAT (Cov-SAT), SARS-CoV-2 vaccine-related SAT (Vac-SAT), or control SAT (Cont-SAT) groups.

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Background: The study's objective is to evaluate if Molsidomine (MOL), an anti-oxidant, anti-inflammatory, and anti-apoptotic drug, is effective in treating hyperoxic lung injury (HLI).

Methods: The study consisted of four groups of neonatal rats characterized as the Control, Control+MOL, HLI, HLI + MOL groups. Near the end of the study, the lung tissue of the rats were evaluated with respect to apoptosis, histopathological damage, anti-oxidant and oxidant capacity as well as degree of inflammation.

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Thromboembolism in Children.

Indian J Pediatr

July 2024

Department of Pediatric Hematology and Oncology, Inonu University School of Medicine, Malatya, Turkey.

Objective: To study pediatric patients who were diagnosed with thrombosis between January 2009 and March 2020.

Methods: Patients were evaluated with respect to thrombophilic risk factors, localization of the thrombus, response to treatment, and recurrence rates during the last 11 y.

Results: Among 84 patients, 59 (70%) had venous thrombosis and 20 (24%) had arterial thrombosis.

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Article Synopsis
  • - The study aimed to analyze the effectiveness of adding pertuzumab (P) to trastuzumab (H) and neoadjuvant chemotherapy (NCT) in achieving pathological complete response (pCR) in HER2+ breast cancer patients.
  • - Involving 1,528 female patients, the results showed that those receiving NCT-HP had a significantly higher pCR rate (66.4%) compared to those on NCT-H (56.8%) and fewer relapses (4.5% vs. 12.2%).
  • - Key factors predicting pCR included invasive ductal carcinoma type, lower tumor grades, and the use of paclitaxel, reinforcing the benefits of adding pertuzumab in
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  • The blood-brain barrier (BBB) regulates the central nervous system and is linked to neurodevelopmental disorders (NDDs), especially in infants with intracerebral hemorrhage (ICH).
  • Researchers identified a rare disease trait in 13 individuals from 8 families due to a genetic variant in the ESAM gene, affecting endothelial cell function and leading to developmental issues.
  • The study highlights the connection between endothelial dysfunction and NDDs, suggesting the emergence of a new category of diseases called "tightjunctionopathies."
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  • Autosomal recessive congenital ichthyosis (ARCI) is a skin disorder characterized by abnormal scaling and has three main forms: lamellar ichthyosis, congenital ichthyosiform erythroderma, and harlequin ichthyosis.
  • The condition is caused by mutations in several genes, with the most severe form (harlequin ichthyosis) primarily linked to specific mutations in one gene, which can also lead to the other two forms.
  • A study involving 64 patients identified 34 novel mutations, expanding the known mutations associated with this condition and showing a connection between the type of mutation and the severity of the skin condition.
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Objective: Bernard-Soulier syndrome (BSS) is one of the rare inherited platelet disorders that is characterized by macrothrombocytopenia and adhesion abnormality due to the absence or malfunctioning of the membrane GPIb-IX-V complex. There is no high-quality evidence on obstetric management of BSS owing to its rarity. Here we report an uncomplicated delivery of an adolescent with BSS and review the literature on the topic of BSS and pregnancy.

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Unlabelled: This study aimed to investigate the coexistence of pilonidal sinus disease (PSD) and hirsutism in female patients.

Materials And Methods: The demographic and clinical data of 164 female patients who underwent surgery for PSD between January 2007 and May 2014 were evaluated for this retrospective cross-sectional study. Data collected for this study were age, BMI, the modified Ferriman and Gallwey scale (mFGS) for hirsutism, main symptoms, type of surgery, early postoperative complications (wound infection, wound dehiscence), recurrence, and follow-up.

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International Forum: The Turkish perspective on apheresis activity: The Turkish apheresis registry report.

Transfus Apher Sci

April 2023

University of Health Sciences, Ankara Oncology Training and Research Hospital, Department of Hematology & Apheresis & Bone Marrow Transplantation Unit, Ankara, Turkey; Ankara Yildirim Beyazit University, School of Medicine, Department of Internal Medicine, Division of Hematology, Ankara, Turkey.

Therapeutic apheresis is an extracorporeal treatment that selectively removes abnormal cells or harmful substances in the blood that are associated with or cause certain diseases. During the last decades the application of therapeutic apheresis has expanded to a broad spectrum of hematological and non-hematological diseases due to various studies on the clinical efficacy of this procedure. In this context there are more than 30 centers performing therapeutic apheresis and registered in the apheresis database in Turkey.

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Objective: To evaluate autopsy reports of the deaths due to electrocution in terms of body mass index, body surface area, and organ weights with a biophysical perspective.

Methods: The retrospective study was conducted in Malatya, Turkiye, and comprised autopsy reports of electrocution cases that were obtained from the local branch of the Council of Forensic Medicine related to the period from 2012 to 2019. Organ weights and ventricular thicknesses were compared in terms of body mass index and body surface area.

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This multicenter, cross-sectional study aimed to determine and examine the privacy awareness and patient rights education of healthcare professionals working in intensive care units (ICUs). The primary purpose of this study was to determine the privacy awareness of healthcare professionals working in the ICU. In addition, the secondary aim was to examine the relationship between patient rights education and awareness scores, as well as to question the need for privacy awareness education.

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Background: In this retrospective study, we evaluated the effect of ferritin levels on the outcomes of autologous stem cell transplantation in patients with MM or lymphoma.

Methods: In this study, 170 patients with measured ferritin levels within one month before transplantation who underwent ASCT with the diagnosis of MM or lymphoma were evaluated. The cut-off value of ferritin was determined as 500 ng/mL to evaluate the transplant outcomes in both groups.

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Background: Although the underlying genetic causes of intellectual disability (ID) continue to be rapidly identified, the biological pathways and processes that could be targets for a potential molecular therapy are not yet known. This study aimed to identify ID-related shared pathways and processes utilizing enrichment analyses.

Methods: In this multicenter study, causative genes of patients with ID were used as input for Disease Ontology (DO), Gene Ontology (GO), and Kyoto Encyclopedia of Genes and Genomes enrichment analysis.

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Thymic Seminoma with Regressive Changes Obscured by Granulomatous Reaction.

J Coll Physicians Surg Pak

December 2022

Department of Pathology, School of Medicine, Inonu University, Malatya, Turkey.

Primary thymic seminoma is an exceedingly rare tumour. There are few case reports about mediastinal thymic seminoma accompanied by secondary changes. We report a case of a 29-year male admitted to our hospital because of chest pain and dyspnea for 8 months.

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