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searching for Rolandic epilepsy 6 found (23 total)

C16orf78 (1,197 words) [view diff] case mismatch in snippet view article find links to article

duplication of the C16orf78 gene was associated with at least one case of Rolandic Epilepsy. C16orf78 has no known paralogs in humans. C16orf78 has over 80 orthologs

Nuclear receptor 4A2 (2,159 words) [view diff] exact match in snippet view article find links to article

of function of NR4A2 is associated with intellectual deficiency, rolandic epilepsy, and language impairment". Clinical Case Reports. 7 (8): 1582–1584

James Rutka (1,582 words) [view diff] exact match in snippet view article find links to article

S.; Rutka, J.T. (2009). "Neurosurgical management of intractable Rolandic epilepsy in children; role of resection in eloquen cortex". J Neurosurg Pediatr

Paroxysmal exercise-induced dystonia (2,211 words) [view diff] exact match in snippet view article find links to article

Bonanni P, Nardocci N, et al. (March 1999). "Autosomal recessive rolandic epilepsy with paroxysmal exercise-induced dystonia and writer's cramp: delineation

Georg Winterer (1,815 words) [view diff] exact match in snippet view article find links to article

16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy. Hum Mol Genet 23:6069-80 with Quednow, BB, Brinkmeyer J, Mobascher

List of OMIM disorder codes (18,877 words) [view diff] exact match in snippet view article find links to article

268300; ESCO2 Robinow syndrome, autosomal recessive; 268310; ROR2 Rolandic epilepsy, mental retardation, and speech dyspraxia; 300643; SRPX2 Rothmund–Thomson