Zobrazeno 1 - 10
of 199
pro vyhledávání: '"Kilidireas C"'
Tumefactive demyelinating lesions (TDL) represent a diagnostic dilemma for clinicians, and in rare atypical cases a collaboration of a neuroradiologist, a neurologist, and a neuropathologist is warranted for accurate diagnosis. Recent advances in neu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::1e4465277b5da3014090028c532a0d68
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3219794
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3219794
Aims: Our goal was to expand the spectrum of clinico-radiologic characteristics and the possible therapeutic choices in patients with tumefactive demyelinating lesions (TDLs). Methods: A retrospective analysis of 50 patients with at least one TDL was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::83ff2bd0ea00b1710e215eeee79e35f4
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3020502
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3020502
We aimed to determine whether Alemtuzumab-induced immune reconstitution affects immunoglobulin and complement levels in the serum of Relapsing-Remitting Multiple Sclerosis (RRMS) patients. IgG4-levels were increased 24-months after treatment initiati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::acec632867896b09b41ecdad85f32546
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:2996959
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:2996959
Background: Cortical demyelination and meningeal inflammation have been detected neuropathologically in multiple sclerosis (MS) and recently in myelin oligodendrocyte glycoprotein antibody disease (MOGAD). Objectives: To assess in vivo cortical and l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::1c4fed75a688e39dcc3958c63d628523
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:2997299
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:2997299
Atypical forms of demyelinating diseases with tumor-like lesions and aggressive course represent a diagnostic and therapeutic challenge for neurologists. Herein, we describe a 50-year-old woman presenting with subacute onset of left hemiparesis, memo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::59bc750134b0e4dc98231f06a08956a0
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:2997512
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:2997512
Background: Baló’s Concentric Sclerosis (BCS) is a rare heterogeneous demyelinating disease with a variety of phenotypes on Magnetic Resonance Imaging (MRI). Existing literature lacks data especially on the therapeutic approach of the disease whic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::b22541591cafa8741e834591e4c8ac88
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3103490
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3103490
IgG4-related disease (IgG4-RD) is a disorder with various clinical manifestations. Central nervous system (CNS) involvement is well recognized, with hypertrophic pachymeningitis and hypophysitis being the most common manifestations. Spinal cord invol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::c5f1e651b61499f594c83cf71aa897c9
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3003369
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3003369
Autor:
Anagnostouli, M. Vakrakou, A.G. Zambelis, T. Boufidou, F. Nikolaou, C. Karandreas, N. Kilidireas, C.
Purpose: The comorbidity of myasthenia gravis (MG), with other autoimmune disorders like systemic lupus erythematosus (SLE), is relatively frequent but the co-occurrence with chronic inflammatory demyelinating polyneuropathy (CIDP) along with various
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::6a2c99f5971d66326dc69424a932bf1a
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:2997649
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:2997649
Background and purpose: Glial fibrillary acidic protein (GFAP) is an intracellular protein of the astrocytic cytoskeleton. Recently, autoantibodies to GFAP detected by cell-based assay in cerebrospinal fluid (CSF) or serum have been implicated in cer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::13f988e022ca3775424d1ea9e8f149b0
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:2997418
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:2997418