Results 221 to 230 of about 39,513 (283)

A novel de Novo KCNC1 mutation (c.1147 C > T) presenting with epilepsy and ADHD: a case report and literature review. [PDF]

BMC Neurol
Huang C, Kang Y, Peng R, Zhong H, Zeng N, Zhang L, Chen X, Du S.   +7 more
europepmc   +1 more source

Effects of bolus injection rate on the pharmacodynamics and pharmacokinetics of propofol, etomidate and sufentanil in rats. [PDF]

Front Vet Sci
Liu S, Gong D, Li X, Qiu F, Zhang W.
europepmc   +1 more source

Navigating the diagnostic challenges of myoclonus in neurodegenerative disorders: video-EEG/polygraphy, clinical vignettes, and narrative analysis. [PDF]

Front Neurol
d'Orsi G, Di Claudio MT, Soccio AA, Palumbo V, Ferro CP, Costantino U, Latino R, Fogli D.   +7 more
europepmc   +1 more source

Survival Following a Tricyclic Antidepressant Overdose Presenting With Serotonin Syndrome-Like Symptoms and Critical Illness Polyneuropathy: A Case Report. [PDF]

Cureus
Nakamura S, Okuda R, Takama T, Kakihana Y, Niiyama S.   +4 more
europepmc   +1 more source

Prion Diseases-When Proteins Turn Lethal: Creutzfeldt-Jakob Disease (CJD) and the Quest for Classification, Diagnosis, Therapeutic Approaches, and Emerging Research. [PDF]

Molecules
Ramesh TS, Bartusik-Aebisher D, Dynarowicz K, Aebisher D.   +3 more
europepmc   +1 more source

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Myoclonus

Continuum, 2013
Myoclonus remains a challenging movement phenotype to characterize, evaluate, and treat. A systematic assessment of the temporal sequence, phenomenology, and distribution of movements can assist in the rational approach to diagnosis and management.Cortical forms of myoclonus are increasingly recognized as primarily cerebellar disorders.
Alberto J, Espay, Robert, Chen
openaire   +2 more sources