Results 171 to 180 of about 12,825 (214)

Multiple cerebral cavernomas in linear scleroderma: an unusual association

Arquivos de Neuro-Psiquiatria
Gabriela Rodrigues Tomaz, Maria Eduarda Slhessarenko Fraife Barreto, Rafael Tuzino Leite Neves Maffei, Renato Barradas Rodrigues, Sebastião Boanerges de Araujo Neto, Marianna Pinheiro Moraes de Moraes, José Luiz Pedroso, Orlando Graziani Povoas Barsottini   +7 more
doaj   +1 more source

Serum Neurofilament Light Levels in Patients with Cerebrotendinous Xanthomatosis: a Pilot Study. [PDF]

Cerebellum
Camelo-Filho AE, Sá Barreto Lima PLG, da Rosa RF, Miyajima OR, Marcucci MHB, de Oliveira Scott SS, de Arruda Furtado LET, Frota AF, Soares MVR, Macedo DS, Pessoa A, Nóbrega PR, Braga-Neto P.   +12 more
europepmc   +1 more source

Treatment of primary adult-onset neurodegenerative cerebellar ataxias. [PDF]

Neurotherapeutics
Ariello LE, Rastall DPW, Rosenthal LS.
europepmc   +1 more source

Protein-First, but Not Protein-Only: Rethinking Neurodegenerative Diseases Through Transgenic Mouse Models. [PDF]

Neurol Int
Zeng CW.
europepmc   +1 more source

Exome Sequencing uncovers Homozygous Stop-Gained variant in the <i>SYNE1</i> Gene Leading to Spinocerebellar Ataxia. [PDF]

Pak J Med Sci
Haque A, Alam MZ, Bibi F, Muthaffar OY, Rasool M, Imran Naseer M.   +5 more
europepmc   +1 more source

Cerebellar ataxias and functional movement disorders: navigating clinical overlap. [PDF]

BMJ Neurol Open
Erdlenbruch F, Thieme A, Depienne C, Timmann D, Popkirov S.   +4 more
europepmc   +1 more source

Hereditary neurodegenerative disorders with spastic-ataxic manifestations: genetic and clinical insights into previously reported variants. [PDF]

Neurogenetics
Ahmad R, Ayaz K, Khan MN, Naeem M, Houlden H.   +4 more
europepmc   +1 more source

ON/OFF Phenomenon in 4-Aminopyridine Therapy in Spinocerebellar Ataxia 27B: Therapeutic and Diagnostic Insights. [PDF]

Mov Disord Clin Pract
Caneda C, Bertoncello E, Peghin A, Satolli S, Santorelli FM, Tinazzi M, Di Vico IA.   +6 more
europepmc   +1 more source

Novel homozygous <i>SYNE1</i> missense variant in late onset autosomal recessive cerebellar ataxia 1: a case report. [PDF]

Ther Adv Neurol Disord
Selmaj I, Himmelreich N, Selmaj K.
europepmc   +1 more source

Peripheral Neuropathy-Predominant Adult-Onset Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay: Novel Variant in the SACS gene. [PDF]

Ann Indian Acad Neurol
Dash A, Mustafa F, Agarwal A, Garg D, Pandit AK, Srivastava AK, Radhakrishnan DM.   +6 more
europepmc   +1 more source