Scorza FA

References (3)

Title : MEGDEL Syndrome - Finsterer_2020_Pediatr.Neurol_110_25
Author(s) : Finsterer J , Scorza FA , Fiorini AC , Scorza CA
Ref : Pediatr Neurol , 110 :25 , 2020
Abstract :
PubMedSearch : Finsterer_2020_Pediatr.Neurol_110_25
PubMedID: 32684373
Gene_locus related to this paper: human-SERAC1

Title : Dystonia is a Common Phenotypic Feature of MEGDEL Syndrome - Finsterer_2018_Tremor.Other.Hyperkinet.Mov.(N.Y)_8_568
Author(s) : Finsterer J , Scorza FA , Fiorini AC , Scorza CA , Almeida AC
Ref : Tremor Other Hyperkinet Mov (N Y) , 8 :568 , 2018
Abstract :
PubMedSearch : Finsterer_2018_Tremor.Other.Hyperkinet.Mov.(N.Y)_8_568
PubMedID: 29971201
Gene_locus related to this paper: human-SERAC1

Title : Long-term cosequences of intrahippocampal kainate injection in the Proechimys guyannensis rodent - Arida_2005_Epilepsy.Res_65_201
Author(s) : Arida RM , Scorza FA , Carvalho Rde A , Cavalheiro EA
Ref : Epilepsy Research , 65 :201 , 2005
Abstract :
PubMedSearch : Arida_2005_Epilepsy.Res_65_201
PubMedID: 16084693