Gambaran klinis dan mutasi gen SCN1A yang berhubungan dengan spektrum generalized epilepsy with febrile seizure plus (GEFSplus)-severe myoclonic epilepsy in infancy (SMEI) pada anak
Saved in:
Main Authors: | , HERINI, E. Siti, , Promotor Prof. Dr. dr. Sutaryo, Sp.AK |
---|---|
Format: | Theses and Dissertations NonPeerReviewed |
Published: |
[Yogyakarta] : Universitas Gadjah Mada
2010
|
Subjects: | |
Online Access: | https://repository.ugm.ac.id/91515/ http://etd.ugm.ac.id/index.php?mod=penelitian_detail&sub=PenelitianDetail&act=view&typ=html&buku_id=49402 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | Universitas Gadjah Mada |
Similar Items
-
MUTASI GEN SCN1A (EKSON 11, 14, 23, DAN 25) YANG BERHUBUNGAN DENGAN SPEKTRUM GENERALIZED EPILEPSY WITH FEBRILE SEIZURE PLUS (GEFS+) PADA ANAK
by: , Elisabeth Siti Herini
Published: (2009) -
Juvenile myoclonic epilepsy.
by: Low, P.S.
Published: (2013) -
Juvenile myoclonic epilepsy.
by: Low, P.S.
Published: (2016) -
Seizures in myoclonic epilepsy with ragged-red fibers detected by DNA analysis : A case report
by: Oraporn Sitburana, et al.
Published: (2018) -
Spinocerebellar Ataxia type 17 presenting with progressive myoclonic epilepsy
by: Boongird A.
Published: (2023)