Results 191 to 200 of about 6,098 (248)

Mutations Identified by Whole-Exome Sequencing in a Norwegian Patient with Sporadic Ataxia and Edema [PDF]

core   +1 more source

Ciprofloxacin-associated choreoathetosis in a haemodialysis patient

, 2013
Ahad Abdalla, Shazrul Ramly, Peter Boers, Liam Casserly   +3 more
openalex   +1 more source

A Novel Variant in SQSTM1 Gene Causing Neurodegeneration with Ataxia, Dystonia, and Gaze Palsy in a Peruvian Family. [PDF]

Mov Disord Clin Pract
Chacaltana-Vinas C, Ramirez-Pajares P, Manrique-Palomino A, Clause AR, Chawla A, Thorpe E, Taft R, Rivera-Valdivia A, Sarapura-Castro E, Bazalar-Montoya J, Cornejo-Olivas M.   +10 more
europepmc   +1 more source

Rare GNAO1 Variant Presenting with Deep Brain Stimulation-Responsive Jaw-Opening Dystonia. [PDF]

Mov Disord Clin Pract
Maass F, Biskup S, Malinova V, Weinrich C, van Riesen C.   +4 more
europepmc   +1 more source

Exploring the Genetic Landscape of Chorea in Infancy and Early Childhood: Implications for Diagnosis and Treatment. [PDF]

Curr Issues Mol Biol
Spoto G, Ceraolo G, Butera A, Di Rosa G, Nicotera AG.   +4 more
europepmc   +1 more source

Ceftriaxone-induced encephalopathy in a patient with a normal renal function. [PDF]

BMJ Case Rep
Zarauskas A, Rodrigues B, Alvarez V.
europepmc   +1 more source

Protocol for combined N-of-1 trials to assess cerebellar neurostimulation for movement disorders in children and young adults with dyskinetic cerebral palsy. [PDF]

BMC Neurol
San Luciano M, Oehrn CR, Wang SS, Tolmie JS, Wiltshire A, Graff RE, Zhu J, Starr PA.   +7 more
europepmc   +1 more source