Results 171 to 180 of about 15,320 (235)

Genetic and clinical insights into <i>MAST4</i>-related neurodevelopmental disorders. [PDF]

Front Pediatr
Zheng X, Fan F, Lei B, Xu Y, Peng M, Zhou Y.   +5 more
europepmc   +1 more source

Familial West syndrome and dystonia caused by an Aristaless related homeobox gene mutation [PDF]

, 2018
Boltshauser, Eugen, Gross, Claudia, Hehr, Ute, Schmitt, Bernhard, Uyanik, Goekhan, Winkler, Jürgen, Wohlrab, Gabriele   +6 more
core  

Imaging Findings of Vigabatrin-Associated Neurotoxicity in a 12-Month-Old With Infantile Epileptic Spasm Syndrome. [PDF]

Cureus
Nedimyer Horner J, Asfour MA, Silva G, Chandra T.   +3 more
europepmc   +1 more source

Genetic etiologies with a large NGS panel in a monocentric cohort of 1000 patients with pediatric onset epilepsies. [PDF]

Epilepsia Open
Barcia G, Chemaly N, Gobin-Limballe S, Losito E, Aubart M, Sarda E, Assouline Z, Plante-Bordeneuve P, Hully M, Barrois R, Barnerias C, Sareidaki D, Zeitoun DC, Eisermann M, Fourrage C, Hanein S, Rio M, Boddaert N, Desguerre I, Kaminska A, Steffann J, Nabbout R.   +21 more
europepmc   +1 more source

Interdependence of clinical factors predicting cognition in children with tuberous sclerosis complex [PDF]

core   +1 more source

Predictive model for initial response to first-line treatment in children with infantile epileptic spasms syndrome. [PDF]

Ital J Pediatr
Ge W, Wan L, Wang Z, Fu L, Yang G.
europepmc   +1 more source

Developmental Outcome at 36 Months in Tuberous Sclerosis: Are There any Modifiable Predictors? [PDF]

Epilepsy Curr
Joshi C.
europepmc   +1 more source

Burden of illness in tuberous sclerosis complex-associated epilepsy: a systematic literature review of epidemiology, health-related quality of life, costs and resource use. [PDF]

Orphanet J Rare Dis
Furber A, Martin A, Bertuzzi A, Wesson F, Harrison M, Bowditch S, Siddiqui J.   +6 more
europepmc   +1 more source