Kategori "Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı" İçin Listeleme
Toplam kayıt 1696, listelenen: 1041-1060
-
Monitoring and prognostic evaluation of patients with congenital hypothyroidism treated in a pediatric endocrinology unit
(TURKISH J PEDIATRICS, 2013)In this study, the etiological factors, diagnostic approaches, dose, and duration of treatment were compared between cases with transient and permanent congenital hypothyroidism (CH) with respect to prognosis. One hundred ... -
Morphometric and ultrastructural analysis of the effect of bromocriptine and cyclosporine on the vasospastic femoral artery of rats
(E-CENTURY PUBLISHING CORP, 2015)Vasospasm is the main causes of mortality and morbidity in patiens with subarachnoid hemorrhage (SAH). The arterial narrowing mechanism that develops after SAH is not yet fully understood but many studies showed that ... -
Motor skills, language development, and visual processing in preterm and full-term infants
(Springer, 2021)Language development is intertwined with motor development. This study examined how visual processing might mediate the relation between language development and motor skills in preterm (PT, n = 34, Mean gestational age = ... -
Motor skills, language development, and visual processing in preterm and full-term infants
(Springer, 2023)Language development is intertwined with motor development. This study examined how visual processing might mediate the relation between language development and motor skills in preterm (PT, n = 34, Mean gestational age = ... -
MR imaging pattern of tibial subchondral bone structure: considerations of meniscal coverage and integrity
(Springer, 2020)Objectives To compare regional differences in subchondral trabecular structure using high-resolution MRI in meniscus-covered/meniscus-uncovered tibia in cadaveric knees with intact/torn menisci. Materials and methods 3D ... -
MR spectroscopy findings in lafora disease: Short communication
(2009)Our aim was to investigate the [1H] MR spectroscopy (MRS) findings of Lafora Disease (LD), which is a disabling form of progressive myoclonic epilepsy. METHODS Twelve patients diagnosed with LD and 12 control subjects ... -
MRI of Pancreas in Patients with Chronic Pancreatitis and Healthy Volunteers: Can Pancreatic Signal Intensity and Contrast Enhancement Patterns be Valuable Predictors of Early Chronic Pancreatitis?
(BENTHAM SCIENCE PUBL LTD, 2017)Background: Chronic pancreatitis is a progressive inflammatory disease of the pancreatic parenchyma and ductal structures. Typical MR imaging features of chronic pancreatitis include dilatation of the main pancreatic duct ... -
Multi-parametric evaluation of autologous cultivated Limbal epithelial cell transplantation outcomes of Limbal stem cell deficiency due to chemical burn
(Bmc, 2020)Background the sparsity of established tools for the grading of limbal stem cell deficiency hinder objective assessments of the clinical outcome of cultivated limbal epithelial cell transplantation. To advance towards the ... -
A multicenter retrospective analysis of patients with nasopharyngeal carcinoma treated in IMRT era from a nonendemic population: Turkish Society for Radiation Oncology Head and Neck Cancer Group Study (TROD 01-001)
(Wiley, 2023)BackgroundWe aimed to evaluate patients with nasopharyngeal carcinoma (NPC) in a nonendemic population. MethodsIn a national, retrospective, multicenteric study, 563 patients treated with intensity modulated radiotherapy ... -
Multiple muscle hypoplasia in Poland's syndrome
(2008)Poland's syndrome is a nonhereditary congenital disorder with unknown etiology, characterized by unilateral absence of pectoralis major muscle and various deformities of the ipsilateral upper extremity. The most common ... -
Multiple muscle hypoplasia in Poland's syndrome [Multipl kas hipoplazili Poland sendromu]
(2008)Poland's syndrome is a nonhereditary congenital disorder with unknown etiology, characterized by unilateral absence of pectoralis major muscle and various deformities of the ipsilateral upper extremity. The most common ... -
Multiple-level cement vertebroplasty in patients with vertebral commpression fractures from osteodystrophy in chronic liver disease
(ACTA MEDICA BELGICA, 2008)Multiple compression fractures of osteoporotic vertebrae are common in patients with a liver transplant or with chronic liver disease. The authors describe two such patients, treated with percutaneous cement vertebroplasty ... -
Multisystem inflammatory syndrome in children associated with Bacille Calmette-Guérin scar: a case presentation
(BioMed Central Ltd, 2023)Background: During Coronavirus disease of 2019 (COVID-19) pandemic, the WHO reported a noticeable increase in Kawasaki disease prevalence in countries where Kawasaki disease is rare. This newly seen disease, unlike typical ... -
Muscle Transposition and Circumferential Vacuum-Assisted Closure to Salvage the Knee Joint in Transtibial Amputation of the Leg: Case Report
(SAGE PUBLICATIONS INC, 2011)Degloving injury is the avulsion of the skin off the underlying muscle and bone, which may also involve the latter structures in high-energy trauma. This study reports the case of a 33-year-old male patient who sustained ... -
Mutation of SGK3, a Novel Regulator of Renal Phosphate Transport, Causes Autosomal Dominant Hypophosphatemic Rickets
(Endocrine Soc, 2020)Context. Hypophosphatemic rickets (HR) is a group of rare hereditary renal phosphate wasting disorders caused by mutations in PHEX, FGF23, DMP1, ENPP1, CLCN5, SLC9A3R1, SLC34A1, or SLC34A3. Objective. A large kindred with ... -
Mutation spectrum of congenital heart disease in a consanguineous Turkish population
(Wiley, 2022)Backgrounds: While many studies agree that consanguinity increases the rate of congenital heart disease (CHD), few genome analyses have been conducted with consanguineous CHD cohorts. Methods: We recruited 73 CHD probands ... -
Mutations in MBOAT7, Encoding Lysophosphatidylinositol Acyltransferase I, Lead to Intellectual Disability Accompanied by Epilepsy and Autistic Features
(CELL PRESS, 2016)The risk of epilepsy among individuals with intellectual disability (ID) is approximately ten times that of the general population. From a cohort of >5,000 families affected by neurodevelopmental disorders, we identified ... -
Mycophenolate mofetil as a novel immunosuppressant in the treatment of neuro-Behcet's disease with parenchymal involvement: presentation of four cases
(CLINICAL & EXPER RHEUMATOLOGY, 2011)Background. Behcet's disease is a inultisystemic, relapsing, inflammatory disorder of unknown origin. Among Turkish cohorts, 5-15% of patients show involvement of the central nervous system (CNS) at some time during their ... -
Mycophenolate mofetil as a novel immunosuppressant in the treatment of neuro-Behçet's disease with parenchymal involvement: Presentation of four cases
(2011)Background. Behçet's disease is a multisystemic, relapsing, inflammatory disorder of unknown origin. Among Turkish cohorts, 5-15% of patients show involvement of the central nervous system (CNS) at some time during their ... -
Mycotic Ascending Aortic Pseudoaneurysm Causing a Large Mediastinal Abscess
(WILEY, 2009)(ECHOCARDIOGRAPHY, Volume 26, July 2009).