Ara
Toplam kayıt 204, listelenen: 61-70
Cerebral Venous Sinus Thrombosis With Internal Jugular Venous Thrombosis In A Male Patient With Nephrotic Syndrome
(Turkish Neurosurgical Soc, 2015)
Cerebral venous sinus thrombosis with internal jugular vein thrombosis is not reported as a complication in nephrotic syndrome. We report a 40-year-old male with nephrotic syndrome, who had headache during his hospitalization. ...
Early Onset Collagen Vi Myopathies: Genetic and Clinical Correlations
(Wiley, 2010)
Objective: Mutations in the genes encoding the extracellular matrix protein collagen VI (ColVI) cause a spectrum of disorders with variable inheritance including Ullrich congenital muscular dystrophy, Bethlem myopathy, and ...
Cranial Metastatic Alveolar Rhabdomyosarcoma Mimicking Hematological Malignancy In An Adolescent Boy
(Springer, 2014)
Widespread alveolar rhabdomyosarcoma (ARMS) with bone marrow involvement and with an unknown primary tumor, especially presenting with acute tumor lysis syndrome can be easily misdiagnosed as a hematological malignancy. ...
Fukuyama Type Congenital Muscular-Dystrophy In A Turkish Child
(Canadian J Neurol Sci Inc, 1990)
Atypical Choroid Plexus Papilloma: Clinical Experience in the Cpt-Siop-2000 Study
(Springer, 2009)
Atypical choroid plexus papilloma (APP) represents a novel intermediate-grade subtype of choroid plexus tumor (CPT), the clinical outcome of which has not been described yet. We present the first analysis of a group of APP ...
Cardiac and Pulmonary Investigations in Bethlem Myopathy
(Amer Medical Assoc, 2006)
Background: Bethlem myopathy is considered a relatively mild neuromuscular disorder without significant cardiac and respiratory involvement. Objective: To investigate cardiac and respiratory involvement in Bethlem myopathy. ...
Assessment of Whole-Brain White Matter By DTI in Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay
(Amer Soc Neuroradiology, 2013)
BACKGROUND AND PURPOSE: Extension and characteristics of WM involvement other than the brain stem remain inadequately investigated in ARSACS. The aim of this study was to investigate whole-brain WM alterations in patients ...
Disease Course And Treatment Responses In Children With Relapsingmyelin Oligodendrocyte Glycoprotein Antibody-Associated Disease
(Amer Medical Assoc, 2018)
IMPORTANCE Myelin oligodendrocyte glycoprotein antibodies (MOG-Abs) are consistently identified in a range of demyelinating disorders in adults and children. Current therapeutic strategies are largely center specific, and ...
Electrophysiological Subtypes And Prognostic Factors Of Childhood Guillain-Barre Syndrome
(Aves, 2018)
Introduction: We assessed the clinical, epidemiologic, electrophysiological and prognostic characteristics of childhood Guillain-Barre Syndrome admitted to 13 pediatric neurology centers in Turkey. Method: Using a standard ...
Genotype-Phenotype Analysis Of Human Frontoparietal Polymicrogyria Syndromes
(Wiley, 2005)
Human cerebral cortical polymicrogyria is a heterogeneous disorder, with only one known gene (GPR56) associated with an apparently distinctive phenotype, termed bilateral frontoparietal polymicrogyria (BFPP). To define the ...