Results 11 to 20 of about 13,156 (215)

Neuromyelitis optica spectrum disorder in a patient with ankylosing spondylitis: A case report

Clinical Case Reports, 2023
Key Clinical Message Neuromyelitis optica spectrum disorder is an autoimmune disease which tends to have other coexisting autoimmune or connective tissue diseases. However, coexisting with ankylosing spondylitis is rare. Here, we report a 57‐year‐old man
Mehri Salari, Bahareh Zaker Harofteh, Masoud Etemadifar   +2 more
doaj   +1 more source

Relapsing neuromyelitis optica spectrum disorder

Journal of Dr. NTR University of Health Sciences, 2021
Background: Neuromyelitis optica spectrum disorder (NMOSD) is a devastating inflammatory disorder of the central nervous system. Relapsing NMOSD (RNMOSD) is being reported frequently, leading to severe and permanent relapse related disability.
M Lakshmi Lavanya, G Butchi Raju, S Gopi, T Sateesh Kumar, U Aruna Kumari   +4 more
doaj   +1 more source

The efficacy of rituximab in the therapy of neuromyelitis optica in a patient with Sjogren's syndrome: case-report and literature review [PDF]

Терапевтический архив, 2018
This case is the first description of the successful anti-B-cell therapy with rituximab in a patient with Sjogrenʼs syndrome and neuromyelitis optica spectrum disorder in Russia.
A V Torgashina, V I Vasilyev
doaj   +1 more source

Fahr’s syndrome as a manifestation of autoimmune polyendocrine syndrome-1 and its unusual association with neuromyelitis optica spectrum disorder

Frontiers in Neuroscience, 2023
Fahr’s syndrome, also known as bilateral striopallidodendate calcinosis, is a rare inherited neurodegenerative illness characterized by abnormal calcium deposition in several areas of the brain, resulting in a wide range of neuropsychological symptoms ...
Ahmad Nawaz, Azba Ahmad, Ayesha Aslam, Safia Bano, Ahsan Numan, Eisham Sarmad   +5 more
doaj   +1 more source

Neuromyelitis Optica Spectrum Disorder

Cureus, 2023
Neuromyelitis optica spectrum disorder (NMOSD) is an autoimmune condition characterized by recurrent episodes of optic neuritis (ON) and transverse myelitis. This case report aims to highlight the importance of considering atypical presentations of NMOSD when confronted with MRI-detected Wernicke's encephalopathy.
Cazzaniga, Juliana, Jara Silva, Cesar E, Quinonez, Jonathan, Ruxmohan, Samir, Leyva, Melissa M, Fahs, Abrahim   +5 more
openaire   +2 more sources

Whole-Exome Sequencing Reveals a Missense Variant c.1612C>T (p.Arg538Cys) in the BTD Gene Leading to Neuromyelitis Optica Spectrum Disorder in Saudi Families

Frontiers in Pediatrics, 2022
Biotinidase deficiency is an autosomal recessive, multiple carboxylase deficiency usually associated with seizures, eczema, hypotonia, visual disturbances, hearing loss, and developmental delays. Only a handful of cases of biotinidase deficiency that had
Muhammad Imran Naseer, Muhammad Imran Naseer, Peter Natesan Pushparaj, Peter Natesan Pushparaj, Peter Natesan Pushparaj, Angham Abdulrahman Abdulkareem, Angham Abdulrahman Abdulkareem, Osama Y. Muthaffar   +7 more
doaj   +1 more source

Neuromyelitis optica spectrum disorder in three generations of a Chinese family [PDF]

, 2019
© 2019 Neuromyelitis optica spectrum disorder is an inflammatory demyelinating disease that is largely sporadic. Familial disease has been reported in one or two generations, although its basis remains unknown.
Dalton, Caroline, Fachim, H.A., Luo, Z., Reynolds, G.P., Sun, P., Wei, X., Yang, W., Zhang, S.   +7 more
core   +1 more source

Predictive Value of Serum Antibodies and Point Mutations of AQP4, AQP1 and MOG in A Cohort of Spanish Patients with Neuromyelitis Optica Spectrum Disorders [PDF]

, 2019
The detection of IgG aquaporin-4 antibodies in the serum of patients with Neuromyelitis optica (NMO) has dramatically improved the diagnosis of this disease and its distinction from multiple sclerosis.
Abril-Jaramillo, Javier, Casado Chocán, José Luis, Díaz Sánchez, María, Echevarría Irusta, Miriam, García Miranda, Pablo, García Sánchez, María Isabel, Lamas-Pérez, Lucía, Lebrato-Hernández, Lucía, Martínez Olivo, María del Mar, Morón Civanto, Francisco Jesús, Navarro, Gemma, Ramírez Lorca, Reposo, Romera, Mercedes, Suárez-Luna, Nela, Uclés Sánchez, Antonio José   +14 more
core   +1 more source

Clinical spectrum of myelin oligodendrocyte glycoprotein antibody-associated disease in Brazil: a single-center experience

Arquivos de Neuro-Psiquiatria, 2023
Background Anti-myelin oligodendrocyte glycoprotein (anti-MOG) antibody-associated disease (MOGAD) is an immune-mediated neurological disorder with a broad spectrum of clinical presentation that is often difficult to distinguish from other ...
Katharina Messias, Renata Moreto, Camila Aquino Cruz, Nathalia Rossoni Ronchi, Antonio Carlos dos Santos, André Messias, Vanessa Daccach Marques   +6 more
doaj   +1 more source

Pathophysiologisch-serologische, bildgebende und klinische Charakteristika der Neuromyelitis Optica [PDF]

, 2019
Hintergrund: Neuromyelitis optica-Spektrum-Erkrankungen (NMOSD) stellen eine Gruppe neuroinflammatorischer Erkrankungen dar, die mit dem klinischen Auftreten von Myelitiden und/oder Optikusneuritiden (ON) einhergeht.
Schumacher, Sophie
core   +1 more source