Results 61 to 70 of about 1,990 (201)

Magnetic resonance imaging in five patients with a tumefactive demyelinating lesion in the central nervous system [PDF]

Arquivos de Neuro-Psiquiatria, 1999
Five patients with a tumefactive lesion were clinically followed from 1992 to 1993. Four patients were female; age ranged from 32 to 57 years, the duration of symptoms varied from 3 days to 3 years.
HELGA C. ALMEIDA SILVA, DAGOBERTO CALLEGARO, PAULO E. MARCHIORI, MILBERTO SCAFF, ANA MARIA C. TSANACLIS   +4 more
doaj   +1 more source

Encephalopathy with behavioral and psychiatric features–firstantibody proven case of Anti-NMDA receptor encephalitis from Pakistan [PDF]

, 2015
Background: Anti-N-methyl-D-aspartate (NMDA) receptor encephalitis is associated with psychiatric symptoms, memory disturbances, seizures, dyskinesia, and catatonia along with other constellation of symptoms.
Khan, Rizwanullah, Memon, Rabel Khalid, Siddiqui, Maimoona   +2 more
core   +1 more source

7 Tesla MRI of Balo's concentric sclerosis versus multiple sclerosis lesions [PDF]

, 2018
Background: Baló’s concentric sclerosis (BCS) is a rare condition characterized by concentrically layered white matter lesions. While its pathogenesis is unknown, hypoxia-induced tissue injury and chemotactic stimuli have been proposed as potential ...
Behrens, Janina R., Bellmann-Strobl, Judith, Giess, René M., Harms, Lutz, Jarius, Sven, Kuchling, Joseph, Niendorf, Thoralf, Ostendorf, Lennard, Paul, Friedemann, Ruprecht, Klemens, Scheel, Michael, Sinnecker, Tim, Wanner, Julia, Wildemann, Brigitte, Wuerfel, Jens   +14 more
core   +2 more sources

A rare case of simple hereditary recessive optic atrophy [PDF]

, 2015
Simple Autosomal Recessive Optic Atrophy (AROA) is a rare hereditary disorder that belongs to a group of disorders called Hereditary Optic Atrophy. Patients diagnosed with simple AROA have complete blindness since birth or from first few months of life ...
Arain, Fazal M., Chand, Prem, Choudary, Tanveer A.   +2 more
core   +1 more source

Defective sphingosine-1-phosphate receptor 1 (S1P1) phosphorylation exacerbates TH17-mediated autoimmune neuroinflammation [PDF]

, 2014
Sphingosine-1-phosphate (S1P) signaling regulates lymphocyte egress from lymphoid organs into systemic circulation. Sphingosine phosphate receptor 1 (S1P1) agonist, FTY-720 (Gilenya™) arrests immune trafficking and prevents multiple sclerosis (MS ...
Acharya, Swati, Arac, Ahmet, Axtell, Robert C., Blaho, Victoria A., Garris, Christopher S., Han, David K., Han, May H., Hla, Timothy, Ho, Peggy P., Huang, Yingxiang, Lewis, David B., Moon, Byoung San, Snyder, Michael P., Sobel, Raymond A., Steinberg, Gary K., Steinman, Lawrence, Wu, Linfeng   +16 more
core   +1 more source

Molecular imaging of multiple sclerosis: from the clinical demand to novel radiotracers

EJNMMI Radiopharmacy and Chemistry, 2019
Background Brain PET imaging with different tracers is mainly clinically used in the field of neurodegenerative diseases and brain tumors. In recent years, the potential usefulness of PET has also gained attention in the field of MS.
Matteo Bauckneht, Selene Capitanio, Stefano Raffa, Luca Roccatagliata, Matteo Pardini, Caterina Lapucci, Cecilia Marini, Gianmario Sambuceti, Matilde Inglese, Paolo Gallo, Diego Cecchin, Flavio Nobili, Silvia Morbelli   +12 more
doaj   +1 more source

Marburg variant of multiple sclerosis; a diagnostic and therapeutic challenge [PDF]

, 2015
Marburg variant of multiple sclerosis (MS) is a highly aggressive, fulminant demyelinating disease with very high morbidity and mortality. Early diagnosis and aggressive management is vital to limit severe disability and improve the outcome. We present a
Imtiaz, Sadia, MD, Arsalan Ahmad, Siddiqui, Maimoona   +2 more
core   +1 more source

Errors in neuroradiology [PDF]

, 2015
Approximately 4 % of radiologic interpretation in daily practice contains errors and discrepancies that should occur in 2-20 % of reports. Fortunately, most of them are minor degree errors, or if serious, are found and corrected with sufficient ...
Briganti, F, Brunese, L, Caranci, F, Gatta, G, Leone, G, Pinto, A, Reginelli, A, Squillaci, E, Tedeschi, E   +8 more
core   +2 more sources

Pediatric multiple sclerosis: update on diagnostic criteria, imaging, histopathology and treatment choices [PDF]

, 2016
Pediatric multiple sclerosis (MS) represents less than 5% of the MS population, but patients with pediatric-onset disease reach permanent disability at a younger age than adult onset patients.
A Ghezzi, A Ghezzi, A Ghezzi, A Ghezzi, A Langer-Gould, A Langer-Gould, A Rovira, A Scalfari, A Scalfari, A Waldman, AH Beecham, AJ Thompson, AK Probstel, B Banwell, B Banwell, B Banwell, B Huppke, B Kornek, BF Popescu, BT Gudbjornsson, C Lechner, C Lucchinetti, C Renoux, C Tornatore, CF Lucchinetti, CF Lucchinetti, CG Lee, CH Polman, CH Polman, CM Dalton, CM Lill, Cris S. Constantinescu, D Chabas, D Miller, DA Hafler, DH Miller, DH Miller, DM Wingerchuk, E Piscolla, EA Yeh, EA Yeh, EM Hennes, F Yang, FD Lublin, G Alper, G Bloomgren, G Filippini, H Butzkueven, Huei-Shyong Wang, I Kister, I Metz, I-Jun Chou, IA Ketelslegers, IA Ketelslegers, J Kira, J Kitley, J Kitley, J O’Mahony, J Palace, J Shimizu, JA Cohen, JK Swanton, JP Fryer, JW Peterson, K Chalmoukou, K Rostasy, KE Harding, L Belbasis, L Bo, L Kappos, L Mantia La, LB Krupp, LH Verhey, M Absinta, M Absoud, M Absoud, M Jurynczyk, M Reindl, MA Friese, MC Mayer, MF Liao, MH Barnett, MH Sun, MW Koch, N Collongues, N Heussinger, O Aktas, O Stuve, P Duquette, P Huppke, P Waters, PJ Waters, PW Schaefer, R Ali, RC Dale, RF Neuteboom, RM Ransohoff, S Bigi, S Jarius, S Lulu, S Pfeifenbring, S Ramanathan, SV Ramagopalan, T Chitnis, T Kanda, T Olsson, T Plavina, TE Lotze, William P. Whitehouse, Y Mikaeloff, Y Mikaeloff, Y Sadaka, YD Fragoso   +112 more
core   +2 more sources

Neuromyelitis Optica Mimicking Multiple Sclerosis: A Case Report and a Comprehensive Review of the Literature

Clinical Case Reports, Volume 13, Issue 10, October 2025.
Post‐gadolinium enhancement of the spinal cord seen in NMO. ABSTRACT Neuromyelitis optica spectrum disorder (NMOSD) may mimic other neurological conditions, including multiple sclerosis (MS). We report a 25‐year‐old woman with hypothyroidism and depression who presented with progressive quadriparesis.
Sunil Thatal, Susmin Karki, Asmita Parajuli, Sweta Bhandari, Bibek K. C., Dibasha Adhikari, Navin Kumar Sah   +6 more
wiley   +1 more source