69 results match your criteria: "Gulhane Military School of Medicine[Affiliation]"

Article Synopsis
  • The study looked at Familial Mediterranean fever (FMF), which is a disease where the body has improper inflammation, and focused on mutations in a specific part of the gene called exons.
  • Researchers checked data from over 2,200 FMF patients to see how different mutations affected their health.
  • They found that patients with mutations in exon 10 had worse symptoms than those with mutations in exon 2, meaning exon 10 mutations are associated with more severe cases of FMF.
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Comparison of early versus late onset familial Mediterranean fever.

Int J Rheum Dis

April 2018

Division of Rheumatology, Department of Internal Medicine, Eskisehir Osmangazi University, Eskisehir, Turkey.

Article Synopsis
  • The study investigates differences between early onset (≤20 years) and late onset (>20 years) Familial Mediterranean fever (FMF), focusing on patient demographics, clinical features, and genetic variations.
  • Out of 2,246 FMF patients in Turkey, 72.7% were in the early onset group, which experienced more severe symptoms and longer diagnosis delays, such as fever and arthritis.
  • Genetic analysis revealed that early onset patients had a higher prevalence of M694V mutations, suggesting this mutation may lead to more severe early disease manifestations.
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Background: Many factors contribute to the development of BPD basically by increasing inflammation in preterm lungs. However, premature neonates have insufficient anti-inflammatory capacity. We aimed to evaluate the effect of etanercept, an anti-TNF agent, on BPD development in newborn rat model with hyperoxia-induced lung injury.

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Risk factors for malignancy in systemic sclerosis patients.

Clin Rheumatol

June 2016

Department of Internal Medicine, Division of Rheumatology, Gaziantep University School of Medicine, Gaziantep, Turkey.

Systemic sclerosis (SSc) is an autoimmune connective tissue disease with multisystem involvement. An increased incidence of cancer in SSc patients compared with the general population has been reported in several reports. Our aims in this study were to determine the most common malignancies and to investigate the possible risk factors for the development of malignancy in patients with SSc.

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Characteristics Predicting Tuberculosis Risk under Tumor Necrosis Factor-α Inhibitors: Report from a Large Multicenter Cohort with High Background Prevalence.

J Rheumatol

March 2016

From the Division of Rheumatology, Department of Internal Medicine, Faculty of Medicine, Gaziantep University, Gaziantep; Division of Rheumatology, Department of Internal Medicine, Faculty of Medicine, Trakya University, Edirne; Division of Rheumatology, Department of Internal Medicine, Faculty of Medicine, Istanbul University; Division of Rheumatology, Department of Internal Medicine, Cerrahpasa Medical School, Istanbul University; Division of Rheumatology, Department of Internal Medicine, Fatih Sultan Mehmet Research and Training Hospital; Division of Rheumatology, Department of Internal Medicine, Faculty of Medicine, Marmara University, Istanbul; Division of Rheumatology, Department of Internal Medicine, Faculty of Medicine, Uludag University, Bursa; Division of Rheumatology, Department of Internal Medicine, Hacettepe University Hospital; Division of Rheumatology, Department of Internal Medicine, Gulhane Military School of Medicine; Division of Rheumatology, Department of Internal Medicine, Faculty of Medicine, Pamukkale University, Ankara; Division of Rheumatology, Department of Internal Medicine, Faculty of Medicine, Ege University; Division of Rheumatology, Department of Internal Medicine, Faculty of Medicine, Katip Celebi University, Izmir; Division of Rheumatology, Department of Internal Medicine, Faculty of Medicine, Sutcu Imam University, Kahramanmaras; Division of Rheumatology, Department of Internal Medicine, Faculty of Medicine, Mayis University, Samsun; Division of Rheumatology, Department of Internal Medicine, Faculty of Medicine, Kocaeli University, Izmit; Division of Rheumatology, Department of Internal Medicine, Faculty of Medicine, Akdeniz University, Antalya; Division of Rheumatology, Department of Internal Medicine, Faculty of Medicine, Cukurova University, Adana, Turkey.B. Kisacik, MD, Division of Rheumatology, Department of Internal Medicine, Faculty of Medicine, Gaziantep University; O.N. Pamuk, MD, Division of Rheumatology, Department of Int

Objective: Screening strategies for latent tuberculosis (TB) before starting tumor necrosis factor (TNF)-α inhibitors have decreased the prevalence of TB among patients who are treated with these agents. However, despite vigilant screening, TB continues to be an important problem, especially in parts of the world with a high background TB prevalence. The aim of this study was to determine the factors related to TB among a large multicenter cohort of patients who were treated with anti-TNF.

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Aim: To determine the incidence and outcomes of respiratory syncytial virus (RSV)-related acute lower respiratory tract infection (ALRI) including morbidity, nosocomial infection and mortality among newborn infants who were admitted to the neonatal intensive care units (NICUs).

Methods: A multicenter, prospective study was conducted in newborns who were hospitalized with community acquired or nosocomial RSV infection in 44 NICUs throughout Turkey. Newborns with ALRI were screened for RSV infection by Respi-Strip®-test.

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Background: Neonatal sepsis is an important cause of neonatal morbidity and mortality in the neonatal intensive care unit. Soluble triggering receptor expressed on myeloid cells-1 (sTREM-1) has been evaluated in sepsis and septic shock, and it was found to be valuable in distinguishing septic cases from nonseptic cases. Endocan is constitutively expressed by endothelial cells, and high levels of endocan may be of relevance for the promotion of systemic inflammation.

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The aim of this randomized controlled single-blind study is to explore whether addition of mud-pack and hot pool treatments to patient education make a significant difference in short and mild term outcomes of the patients with fibromyalgia. Seventy women with fibromyalgia syndrome were randomly assigned to either balneotherapy with mud-pack and hot pool treatments (35) or control (35) groups. After randomization, five patients from balneotherapy group and five patients from control group were dropped out from the study with different excuses.

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Behçet disease with vascular involvement: effects of different therapeutic regimens on the incidence of new relapses.

Medicine (Baltimore)

February 2015

From the Marmara University, School of Medicine, Department of Rheumatology Istanbul (FA-O, AK, HD); Selçuk University, School of Medicine, Department of Rheumatology Konya (SY); Pamukkale University, School of Medicine, Department of Rheumatology Denizli (AB, VÇ); Gaziantep University, School of Medicine, Department of Rheumatology Gaziantep (GK, BK, AMO); Kocaeli University, School of Medicine, Department of Rheumatology Kocaeli (AY, AÇ); Gulhane Military School of Medicine, Department of Rheumatology Ankara (MÇ, SY, SP); Çukurova University, School of Medicine, Department of Rheumatology Adana (FY, EE); Osmangazi University, School of Medicine, Department of Rheumatology Eskişehir (ŞYB, TK); Hacettepe University, School of Medicine, Department of Rheumatology Ankara (EB, UK, ÖK); Uludağ University, School of Medicine, Department of Rheumatology Bursa (BNC, YP); Ankara Numune Training and Research Hospital, Department of Rheumatology, Ankara (AO); Sütçü İmam University, School of Medicine, Department of Rheumatology, Kahramanmaraş (GYÇ); Bilim University, School of Medicine, Department of Rheumatology, Istanbul (YÇ); Hitit University Medical Faculty, Department of Rheumatology, Çorum (YK); and Ondokuz Mayıs University, School of Medicine, Department of Rheumatology, Samsun, Turkey (MS).

Vascular involvement is one of the major causes of mortality and morbidity in Behçet disease (BD). There are no controlled studies for the management of vascular BD (VBD), and according to the EULAR recommendations, only immunosuppressive (IS) agents are recommended. In this study, we aimed to investigate the therapeutic approaches chosen by Turkish physicians during the initial event and relapses of VBD and the association of different treatment options with the relapses retrospectively.

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Diagnostic value of elevated CXCR4 and CXCL12 in neonatal sepsis.

J Matern Fetal Neonatal Med

February 2015

Division of Neonatology, Department of Pediatrics, Gulhane Military School of Medicine, Ankara , Turkey .

Objective: Neonatal sepsis remains a major cause of morbidity and mortality in newborns. The chemokine CXCL12 and its receptor CXCR4 are now known to play an important role in inflammatory states. However, it is unclear how chemokines respond to late-onset neonatal sepsis.

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Background: Bronchopulmonary dysplasia (BPD) remains an important complication of preterm births. The soluble form of ST2 (sST2), interleukin-33 (IL-33), and soluble form of the urokinase plasminogen activator receptor (suPAR) have attracted increasing attention as biomarkers for different diseases. The aim of the current study was to assess the predictive value of plasma sST2, IL-33, and suPAR levels in patients with risk of BPD development.

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Crimean-Congo hemorrhagic fever virus (CCHFV), a member of the genus Nairovirus of the family Bunyaviridae, causes a severe disease in humans with high mortality rates. In Turkey, the number of patients with CCHF has increased since 2002. Here, we aimed to treat CCHF patients with CCHFV hyperimmunoglobulin.

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Reactive systemic (AA) amyloidosis leading to renal failure is the most severe complication of tumor necrosis factor receptor-associated periodic syndrome (TRAPS). There is now growing evidence to suggest that anti-tumor necrosis factor (anti-TNF) agents may be an attractive treatment option for amyloidosis not only in TRAPS but in several forms of secondary amyloidosis complicating inflammatory rheumatic diseases. In most of the reported cases, anti-TNF agents were deemed successful on the basis of regression of proteinuria and either improvement or stabilization of creatinine clearance, while objective proof of renal amyloid regression either by serum amyloid P scintigraphy or biopsy is limited.

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Objective: Several lines of evidence point to a polarized T-helper-1 (Th1) immune response in Behçet's disease (BD). Interferon (IFN)-alpha which has an ability to promote strong Th1 type immune response has been shown to increase in patients with BD. In order to clarify if plasmacytoid dendritic cells (pDCs) abnormally respond to a stimulus in patients with BD, we investigated the levels of intracellular IFN-alpha and beta in pDCs with or without CpG D ODN stimulation.

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The Fukuyama type congenital muscular dystrophy (FCMD) is a rare autosomal recessive disorder characterized by cranial, cerebellar and ocular malformations and congenital muscular dystrophy. Hyperekplexia is characterized by transient, generalized rigidity in response to unexpected loud noises or sudden tactile stimulation. Herein, we report an infant who had typical clinical features of FCMD with hyperekplexia.

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Ankle fractures and fracture dislocations are common injuries in orthopaedic practice however pure ankle dislocation without an associated fracture is extremely rare. There are a few cases reporting such a lesion in the literature. Also this injuries are generally open high energy trauma injuries.

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Introduction: In this study, we investigated D-dimer serum level as a diagnostic parameter for acute appendicitis.

Materials And Methods: Forty-nine patients were enrolled in the study. Patients were classified according to age; sex; duration between the beginning of pain and referral to a hospital or clinic; Alvarado scores; and in physical examination, presence of muscular defense, the number of leukocytes, preoperative ultrasonography, and D-dimer levels of histopathologic study groups were analyzed.

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Purpose: Acute appendicitis is one of the most common surgical emergencies. Diagnosis is usually made depending on the presenting history, clinical evaluation, and laboratory tests. The aim of this study was to investigate the role of urinary 5-hydroxyindoleacetic acid (U-5-HIAA) in the early diagnosis of acute appendicitis.

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The objective of the study was to investigate the response rate to non-steroidal anti-inflammatory drugs (NSAIDs) and the clinical parameters that might predict this response in patients with active ankylosing spondylitis. This is a prospective, observational, 3-month study that was conducted in a single center. Ninety-five consecutive patients with active ankylosing spondylitis were included in the study.

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Ulnar artery aneurysm in a patient with Behçet's disease.

Rheumatol Int

January 2010

Division of Rheumatology, Department of Internal Medicine, Gulhane Military School of Medicine, Etlik, 06100 Ankara, Turkey.

Behçet's disease is a systemic disease characterized by oral aphthosis, genital ulcers, ocular lesions, gastrointestinal, musculoskeletal, neurological and major vessel involvement. Arterial involvement, aneurysms and arterial thrombosis have been reported in 1.5-3% of patients.

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Osteopoikilosis (OPK) is a rare benign sclerosing disease of the skeleton and inherited as an autosomal dominant trait. OPK is associated with inflammatory rheumatic disorders, such as rheumatoid arthritis, scleroderma, reactive arthritis and familial Mediterranean fever (FMF). We report a rare case of OPK coexistent with ankylosing spondylitis and FMF.

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The assessment of disease activity in Behçet's disease (BD), either by BD Current Activity Form (BDCAF) or Iranian BD Dynamic Measure (IBDDAM), depends largely on the history of the clinical features. Accuracy of recall of a retrospective questionnaire might influence its reliability to some extent. The aim of this study was to investigate whether patients with BD can recall the items included in both of the disease activity forms accurately.

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Congenital afibrinogenemia is a rare disorder characterized by the absence in circulating fibrinogen, a hexamer composed of two sets of three polypeptides (Aalpha, Bbeta and gamma). Although predisposition to thrombosis is a well known feature of dysfibrinogenemia, the relatively frequent thrombotic manifestations seen in congenital afibrinogenemia are puzzling. We herein report a mutational analysis of a young afibrinogenemic man from Turkey with multiple thrombo-embolic events involving both arteries and veins.

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[Evaluation of patient quality of life after total hip arthroplasty].

Acta Orthop Traumatol Turc

August 2008

Department of Orthopedics and Traumatology (Ortopedi ve Travmatoloji Anabilim Dali), Gülhane Military School of Medicine, Ankara, Turkey.

Objectives: We evaluated the effect of total hip arthroplasty on patient quality of life.

Methods: The study included 30 patients (6 men, 24 women; mean age 62 years; range 36 to 82 years) undergoing total hip arthroplasty. The Medical Outcomes Study Short-Form 36-Item Health Survey (SF-36) was administered to the patients before and after 1.

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