Results 181 to 190 of about 6,098 (248)

Positive 14-3-3 protein in cerebrospinal fluid followed by poppy-induced delayed post-hypoxic leukoencephalopathy: A case report. [PDF]

Heliyon
Shen G, Dong H, Zhao J, Wu S, Lee KY, Chi L.   +5 more
europepmc   +1 more source

The Syndrome of Irreversible Lithium-Effectuated Neurotoxicity: A Scoping Review. [PDF]

Alpha Psychiatry
Konieczny K, Detraux J, Bouckaert F.
europepmc   +1 more source

The relationship of secondary dystonia and choreoathetosis with activity, participation and quality of life measures in children with dyskinetic cerebral palsy [PDF]

, 2014
Elegast Monbaliu, Paul De Cock, Lisa Mailleux, Els Ortibus, Katrijn Klingels, Hilde Feys   +5 more
openalex  

Mitochondrial Complex IV Deficiency Nuclear Type 11 Caused by a Novel Start-Lost Variant in the <i>COX20</i> Gene. [PDF]

Genes (Basel)
Kuchina A, Borovikov A, Sidorova O, Orlova M, Ryzhkova O, Zaigrin I, Murtazina A.   +6 more
europepmc   +1 more source

Presence and severity of dystonia and choreoathetosis overflow movements in participants with dyskinetic cerebral palsy and their relation with functional classification scales

, 2019
Inti Vanmechelen, Saranda Bekteshi, Kyra Bossier, Hilde Feys, Jan Deklerck, Elegast Monbaliu   +5 more
openalex   +2 more sources

Autosomal dominant Kufs disease in a Georgian adult woman: A case report. [PDF]

Epilepsy Behav Rep
Papiashvili N, Gagua S, Gonjilashvili N, Okujava N, Tsereteli A.   +4 more
europepmc   +1 more source

Complex movement disorders in early onset hypoparathyroidism. [PDF]

Arq Neuropsiquiatr
Sarmento F, Tamanini JVG, Gama SM, Freitas LF, Barsottini OGP, Pedroso JL.   +5 more
europepmc   +1 more source

Lesch-Nyhan syndrome a dental approach: case report. [PDF]

Afr Health Sci
Luz Campos PSS, da Silva LCP, Taitson PF, da Silva Oliveira LA, Bautista LC.   +4 more
europepmc   +1 more source

Beyond seizures: SCN8A heterozygous mutation presenting with epilepsy and paroxysmal dyskinesia. [PDF]

Ann Med Surg (Lond)
Zhang X, Yu T.
europepmc   +1 more source

Genetic Defects in Thyroid Hormone Supply. [PDF]

, 2014
FENZI, GIANFRANCO, MACCHIA, PAOLO EMIDIO, NETTORE, IMMACOLATA CRISTINA   +2 more
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