Results 191 to 200 of about 13,652 (256)

Case report of paroxysmal dystonia in a child with KBG syndrome: Expansion of the phenotype and utility of whole exome sequencing. [PDF]

Medicine (Baltimore)
Dantam CR, Wilkes E, Summers HN, Morris CA, Ahad RF.   +4 more
europepmc   +1 more source

Efficacy of Deep Brain Stimulation for the Treatment of Monogenic Dystonia Symptoms: A Systematic Review. [PDF]

Eur J Neurol
Indelicato E, Carmona-Hidalgo B, Quintero J, Escobar JDO, Koy A, Salamon A, Tacik P, Muñoz-Delgado L, Giannini G, Reich M, Albanese A, Bäumer T, Grandas F, Jech R, Leonardos A, Mir P, Pérez-Dueñas B, Perez-Sanchez JR, Valldeoriola F, Zanni G, Vidailhet M, Rodríguez-López R, Blasco-Amaro JA, Reinhard C, Boesch S, European Reference Network for Rare Neurological Diseases (ERN‐RND).   +25 more
europepmc   +1 more source

Botulinum toxin paralysis of the orbicularis muscle [PDF]

, 1993
Evinger, C., Horn, Anja K. E., Porter, J. D.   +2 more
core  

Targeted intervention by using neuromodulation in the management of oro-mandibular dystonia with co-morbid bipolar disorder: A case study. [PDF]

Indian J Psychiatry
Joshi M, Chaudhary P, Kar SK, Pandey S.
europepmc   +1 more source

Neurogenetic Disorders with Hearing Loss: Mechanisms, Classifications, and Emerging Insights. [PDF]

Curr Neurol Neurosci Rep
Owrang D, Vona B.
europepmc   +1 more source

The Associations Between Depression, Subjective Sleep Quality, and Health-Related Quality of Life in Patients with Meige Syndrome: A Cross-Sectional Study. [PDF]

Nat Sci Sleep
Li M, Li J, Li M, Li J, Yu Y, Yang K, Zhou L, Li S, Li Y, Li Q, Wei J, Li H.   +11 more
europepmc   +1 more source

Neurorehabilitation in Dystonia Care: Key Questions of Who Benefits, What Modalities, and When to Intervene. [PDF]

Dystonia
Kamo H, Nagaki K, Kraus AR, Warren L, Wagle Shukla A.   +4 more
europepmc   +1 more source

Hemifacial Spasm and Blepharospasm: Divergent Social Cognition Performance Despite Similar Neurocognitive Profiles. [PDF]

Brain Behav
Çelik S.
europepmc   +1 more source

A novel NKX2-1 frameshift variant expanding the genetic landscape of benign hereditary chorea. [PDF]

Neurol Sci
Aloisio S, De Riggi M, Martini A, Grandolfo S, Birreci D, Angelini L, Cinicola BL, Spalice A, Bologna M.   +8 more
europepmc   +1 more source