10 results match your criteria: "Marmara University School of Medicine Hospital[Affiliation]"

Article Synopsis
  • The study investigates the wall thickness of the inferior vena cava (IVC) in patients with Behçet's disease (BD) compared to healthy controls, revealing that BD patients have significantly thicker IVC walls.
  • Results showed that IVC wall thickness is associated with mucocutaneous and major organ involvement, indicating a correlation between vascular issues and BD symptoms.
  • The findings suggest that venous wall inflammation in BD affects not only lower extremity veins but also larger venous structures like the IVC, pointing to a widespread vascular inflammation in this disease.
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Article Synopsis
  • The study gathered data on 358 patients with polyarteritis nodosa (PAN) from nine countries, analyzing demographics, clinical features, and survival rates over 30 years.
  • Findings showed common symptoms such as constitutional issues, skin lesions, joint pain, and neurological problems, with a significant relapse rate of 48.5% during an average follow-up of nearly five years.
  • Survival rates for systemic PAN showed a decline over time, with important risk factors for mortality including older age, high serum creatinine levels, and involvement of the gastrointestinal system or central nervous system.
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Advances in the Treatment of Behcet's Disease.

Curr Rheumatol Rep

May 2021

Division of Rheumatology, Department of Internal Medicine, Marmara University School of Medicine Hospital, Fevzi Çakmak Mahallesi, Ust-Kaynarca, Pendik, Istanbul, Turkey.

Purpose Of Review: To assess current management of Behcet's disease (BD). Controversies on therapeutic approaches to different manifestations, whether conventional immunosuppressives (IS) or biologic agents, should be chosen, and options for refractory disease are discussed.

Recent Findings: Glucocorticoids are still the main agents for remission-induction and azathioprine the first-line conventional IS in maintenance phase to prevent relapses of major organ involvement.

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Objective: Kidney transplantation is the treatment of choice in end-stage renal disease. In Turkey, the inadequate cadaveric donor supply has resulted in transplantation from living kidney donors (LKD) in 80% of transplant operations. LKD candidates undergo a thorough general medical evaluation and are approved to donate their kidneys only if no contraindication is found.

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GNAS Spectrum of Disorders.

Curr Osteoporos Rep

June 2015

Pediatric Endocrinology, Marmara University School of Medicine Hospital, Istanbul, Turkey,

The GNAS complex locus encodes the alpha-subunit of the stimulatory G protein (Gsα), a ubiquitous signaling protein mediating the actions of many hormones, neurotransmitters, and paracrine/autocrine factors via generation of the second messenger cAMP. GNAS gives rise to other gene products, most of which exhibit exclusively monoallelic expression. In contrast, Gsα is expressed biallelically in most tissues; however, paternal Gsα expression is silenced in a small number of tissues through as-yet-poorly understood mechanisms that involve differential methylation within GNAS.

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GNAS is a complex imprinted locus leading to several different gene products that show exclusive monoallelic expression. GNAS also encodes the α-subunit of the stimulatory G protein (Gsα), a ubiquitously expressed signaling protein that is essential for the actions of many hormones and other endogenous molecules. Gsα is expressed biallelically in most tissues but its expression is silenced from the paternal allele in a small number of tissues.

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Postnatal establishment of allelic Gαs silencing as a plausible explanation for delayed onset of parathyroid hormone resistance owing to heterozygous Gαs disruption.

J Bone Miner Res

March 2014

Endocrine Unit, Department of Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA; Pediatric Endocrinology, Marmara University School of Medicine Hospital, Istanbul, Turkey.

Article Synopsis
  • Pseudohypoparathyroidism type-Ia (PHP-Ia) is caused by maternal mutations in the GNAS gene, resulting in a loss of function of Gαs, leading to resistance to parathyroid hormone (PTH) and hypocalcemia.
  • The PTH resistance in PHP-Ia manifests after early postnatal life, indicating that the silencing of the paternal Gαs allele in kidney cells occurs gradually rather than immediately after birth.
  • Studies show that while Gαs expression is mostly from the maternal allele in adulthood, both maternal and paternal alleles contribute equally at a postnatal age of 3 days, highlighting a delayed onset of PTH resistance in PHP-Ia patients.
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Cost-effectiveness of new pneumococcal conjugate vaccines in Turkey: a decision analytical model.

BMC Health Serv Res

November 2012

Department of Pediatrics and Pediatric Infectious Diseases, Marmara University School of Medicine Hospital, Altunizade, Pendik, Istanbul, 34662, Turkey.

Background: Streptococcus pneumoniae infections, which place a considerable burden on healthcare resources, can be reduced in a cost-effective manner using a 7-valent pneumococcal conjugate vaccine (PCV-7). We compare the cost effectiveness of a 13-valent PCV (PCV-13) and a 10-valent pneumococcal non-typeable Haemophilus influenzae protein D conjugate vaccine (PHiD-CV) with that of PCV-7 in Turkey.

Methods: A cost-utility analysis was conducted and a decision analytical model was used to estimate the proportion of the Turkish population <10 years old that would experience 10 mutually exclusive outcomes over the course of 1 year from a perspective of a healthcare system.

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Murine models indicate that Gαs and its extra-long variant XLαs, both of which are derived from GNAS, markedly differ regarding their cellular actions, but these differences are unknown. Here we investigated activation-induced trafficking of Gαs and XLαs, using immunofluorescence microscopy, cell fractionation, and total internal reflection fluorescence microscopy. In transfected cells, XLαs remained localized to the plasma membrane, whereas Gαs redistributed to the cytosol after activation by GTPase-inhibiting mutations, cholera toxin treatment, or G protein-coupled receptor agonists (isoproterenol or parathyroid hormone (PTH)(1-34)).

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It is now known that immunologic mechanisms have a role in the initiation of atherosclerotic processes. No antibodies against vascular endothelial cell (VEC) specific antigenic systems have been demonstrated in the pathogenesis of small vessel (lacunar) infarcts, though autoantibodies have been detected in 80% of patients with multi-infarct dementia. We studied VEC-specific antibodies in 17 patients with a diagnosis of vascular dementia; in 17 nondemented patients with small vessel infarcts and in 16 healthy, nondemented control group patients by using the Terasaki microtoxicity method.

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