Results 131 to 140 of about 101,774 (257)

<i>HSD17B4</i>-Related Disorder: Defining the Phenotype in Adult-Onset Patients. [PDF]

Neurol Genet
Falcone GMI, Tessa A, Rizzo C, Semeraro M, Barghigiani M, Santorelli FM, Musumeci O.   +6 more
europepmc   +1 more source

Establishing Sensory Neurons as Therapeutic Targets in Peripheral Neuropathy Driven by Polyglutamine Expanded Murine ATXN3

Annals of Neurology, EarlyView.
Repeat expansion disorders frequently involve peripheral neuropathy, yet mechanisms remain unclear. Using a spinocerebellar ataxia type 3 (SCA3) Knock‐In Atxn3Q300/Q6, we identify progressive sensorimotor deficits, peripheral nerve pathology, and dorsal root ganglia RNA splicing dysregulation.
Juan P. Mato, John M. Hayes, Jacen Emerson, Maeha Sridharan, Toluwani Adelaja, Arsal Naeem, Alexandra F. Putka, Hayley S. McLoughlin   +7 more
wiley   +1 more source

A Case of Persistent Ataxia and Atypical Brain Lesions: From the National Multiple Sclerosis Society Case Conference Proceedings. [PDF]

Neurol Neuroimmunol Neuroinflamm
Rodin RE, Manzano GS, Klawiter EC, Chwalisz BK, Zamvil SS, Goldman MD, Riley C, Chitnis T.   +7 more
europepmc   +1 more source

Synaptophysin autoantibodies mediate synaptic dysfunction in cerebellar ataxia. [PDF]

Cell Rep Med
Ho S, Wong HK, Shqau D, Winklmeier S, Grobe-Einsler M, Rostasy K, Kümpfel T, Thaler FS, Brimberg L, Schneider MA, Muley T, Vural A, Seifert-Held T, Endmayr V, Höftberger R, Faber J, Klopstock T, Frahm S, Gerdes LA, Meinl E, Mader S.   +20 more
europepmc   +1 more source

Early Neuroimmune Modulation in Hereditary Cerebellar Ataxias: Experimental Opportunities in Zebrafish Models. [PDF]

Cells
Naef V, Giacich M, Damiani D, Santorelli FM.   +3 more
europepmc   +1 more source

Tissue Damage in Rheumatoid Arthritis Is Genetically Linked to Low Peptidylglycine Alpha‐Amidating Monooxygenase Activity in Synovial Fibroblasts

Arthritis &Rheumatology, EarlyView.
Objective Both susceptibility to, and severity of, rheumatoid arthritis (RA) is associated with the rs26232 C allele. Our primary aim was to identify the biologic mechanism underlying this association. Methods Expression of surrounding genes was compared among rs26232 genotypes.
Kevin J. Sheridan, Emma R. Dorris, Maria Inês Pimenta, Jemma Falkov, Matthew Fisher, Sam Pledger, Hector Devey, Munitta Muthana, Denis C. Shields, Richard E. Mains, Betty A. Eipper, Christopher D. Buckley, Anthony G. Wilson   +12 more
wiley   +1 more source

Quantitative susceptibility mapping reveals widespread brain iron abnormalities in sporadic patients with early-stage amyotrophic lateral sclerosis. [PDF]

Brain Commun
Ma M, Zhao B, Gao N, Sun X, Shao K, Lin P, Li W, Zhao Y, Yu D, Yan C, Liu S, Yun Y.   +11 more
europepmc   +1 more source

Development of interactive MRI‐based 3D visualization tools for neuroanatomy education in Latin America

Anatomical Sciences Education, EarlyView.
Abstract The study of neuroanatomy is fundamental in many scientific fields. Despite this, it is a challenging subject for students. As technology evolves, it is being increasingly incorporated into educational methods, including the teaching of neuroanatomy. Three‐dimensional (3D) visualizations are well suited for displaying neuroanatomy.
Merlin J. Fair, Diego Cureño, Alejandro De León Cuevas, Paola Ocampo Luna, Marta Bianciardi, María G. García‐Gomar   +5 more
wiley   +1 more source

Suspicion of cerebellar diseases

Practica Oto-Rhino-Laryngologica, 1978
Sakata, Kazuki, Nakajo, Takeshi
openaire   +3 more sources

Congenital central nervous system malformations in piedmontese calves-part 1. structural brain disorders. [PDF]

Front Vet Sci
Ferrini S, Scaglione F, Cagnotti G, Borriello G, Cantile C, Castelli M, Catania AM, Di Muro G, Grego E, Manassero L, Quaglino A, Tessarolo C, Tomassone L, Valazza A, Bellino C, D'Angelo A.   +15 more
europepmc   +1 more source