Browsing Dahili Tıp Bilimleri Bölümü Bildiri Koleksiyonu by Issue Date
Now showing items 1-20 of 30
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Concomitant autoimmune diseases in patients with sarcoidosis
(Bmj Publishing Group, 2017)Sarcoidosis is a chronic granulomatous disease characterized by non-caseating granuloma formation. It can mimic many rheumatic diseases and/or may be coexist with them. There are limited data in the literature about the ... -
Demographic, clinical, and laboratory characteristics of elderly onset psoriatic arthritis
(Bmj Publishing Group, 2017)Background: Psoriatic arthritis (PsA) is a chronic inflamatory disease characterized with axial and peripheral joints involvement. It is rarely affects patients older than 65 years old. Objectives: The purpose of this study ... -
Development of independent mu/treatment time verification algorithm for non-imrt treatment planning: a clinical experience
(Amer Inst Physics, 2018)The aim of this study is to develop an algorithm for independent MU/treatment time (TT) verification for non-IMRT treatment plans, as a part of QA program to ensure treatment delivery accuracy. Two radiotherapy delivery ... -
Assessment of serum vitamin D in pediatric hematopoietic stem cell transplantation patients and its relation with complications
(Nature Publishing Group, 2018)Recently, evaluation of serum vitamin D level in pediatric hematopoietic stem cell transplantation (HSCT) patients gained popularity, as there is close relation with development of GVHD and complications. Our aim was ... -
Malignancy in patients with sarcoidosis: a retrospective cohort study from Turkey
(Bmj Publishing Group, 2018)The relationship between sarcoidosis and malignancy is not clear yet. There is debate with different speculations in the literature in this regard, that this association may be just a coincidence and/or common pathogenetic ... -
The results of rituximab therapy in the patients with steroid dependent nephrotic syndrome
(Springer, 2018): The patients with steroid dependent nephritic syndrome (SDNS) require prolonged steroid therapy. To reduce the side effects of prolonged steroid therapy, alternative treatments which have steroidsparing effect are ... -
The evaluation of left ventricular functions in children with steroid-sensitive nephrotic syndrome
(Springer, 2018): Nephrotic syndrome has been associated with increased risk of cardiovascular diseases (CVD), which may be attributable to the hypoalbuminemia, dyslipidemia, hypercoagulopathy or inflammatory activation. In childhood ... -
A single center study of the patients with cystinuria
(Springer, 2018)be partially treated with bicarbonate, bone marrow transplantation or possibly gene therapy. -
The clinical significance of jak2v617f mutation for philadelphia-negative chronic myeloproliferative neoplasms in patients with splanchic vein thrombosis
(Cig Media Group, Lp, 2019)Context: High prevalence of JAK2V617F mutation in splanchic vein thrombosis (SVT), including Budd-Chiari syndrome (BCS) and portal vein thrombosis (PVT) raised suspicion of an underlying Philadelphiaenegative chronic ... -
Catheter-directed gastric artery embolization with octreotide acetate loaded PLA/PLGA (poly[lactide-co-glycolide] acid) microspheres with slow sustained-release properties suppresses the plasma concentration of ghrelin, which results in weight loss
(Science Direct, 2019)Purpose: The objective of the present work was to formulate slow- and sustained-release octreotide acetate-loaded PLA/PLGA (polylactide)(poly (Lactic-co- Glycolic) acid) microspheres and prospectively test the effects ... -
Multifunctional iron oxide nanoparticle-embedded PVP-HEC microparticles as a drug-eluting embolic material
(Science Direct, 2019)To develop MRI imageable novel HEC-PVP-magnetic embolic particles intended for transcatheter arterial chemoembolization and magnetic ablation -
Donor lymphocyte infusion administrations after allogeneic stem cell transplantations in pediatrics: a single center experience
(Nature Publishing Group, 2019)Loss of chimerism is one of the major problems after allogeneic stem cell transplantation(SCT). Donor- lymphocyte infusions(DLI) are used as a treatment after taper or stopping immunosuppression. In this study, DLI ... -
Comparison of allogeneic stem cell transplantation results from related or unrelated donors in beta-thalassemia major
(Nature Publishing Group, 2019)Although there have been significant improvements with conventional therapies in beta thalassemia major, hematopoietic stem cell transplantation is only curative therapy. Related donors are preferred to diminish ... -
Comparison of turkish stem cell coordination center (TURKOK) with Istanbul university bone marrow bank (TRIS); A single center experience in match unrelated donors
(Nature Publishing Group, 2019)Match family donors are the preferable options in allogenic stem cell transplant. However, in the absence of donor relatives match unrelated donors have been an option. In this study, the donor screening, transplant ... -
Extracorporeal photopheresis treatment for steroid resistant graft versus host disease in pediatrics: single center experience
(Nature Publishing Group, 2019)Background: Steroid resistant graft vs host disease (GVHD) is defined as unresolved or worsened symptomatology of GVHD at day 14 despite effective immunosuppression with steroid therapy. Second line immunosuppressive agents, ... -
Hit three birds with one stone: successful stem cell transplantation from one family donor to three siblings
(Nature Publishing Group, 2019)Background: Thalassemia major is a single gene related hereditary hemoglobinopaty required life long regular transfusions with chelation therapies. Stem cell transplantation is the only curative treatment of the disease. ... -
A Case of Gonadotropin-independent precocious puberty due to germ cell tumor in the frontal lobe
(Karger, 2019)It is known that gonadotropin-independent or peripheral precocious puberty (PPP) may develop due to tumors that secrete beta human chorionic gonadotropin (Beta-HCG) -
Perinatal form hypophosphatasia caused by a novel large duplication of ALPL gene and two year follow-up under enzyme replacement therapy; a case report
(Karger, 2019)Hypophosphatasia is a rare disease caused by mutations in the gene encoding tissuenonspecific isoenzyme of alkaline phosphatase. Duplications of the ALPL gene account for fewer than 1% of the mutations causing HPP. It has ... -
Effectiveness and safety transarterial embolization with bleomycin-loaded PLA/PLGA (polylactic acid)(poly[lactic-co-glycolic acid]) microspheres for treatment of vascular malformation using a porcine spleen model
(Science Direct, 2019)To prospectively study the effectiveness and safety of Bleomycin-loaded PLA/PLGA microparticles in the porcine spleen model
