Absence Epilepsy and Paroxysmal Dyskinesia

Pediatric Neurology Briefs ◽

10.15844/pedneurbriefs-16-12-6 ◽

2002 ◽

Vol 16 (12) ◽

pp. 92

Author(s):

J Gordon Millichap

Keyword(s):

Absence Epilepsy ◽

Paroxysmal Dyskinesia

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Early-onset Absence Epilepsy and Paroxysmal Dyskinesia

Epilepsia ◽

10.1046/j.1528-1157.2002.13802.x ◽

2002 ◽

Vol 43 (10) ◽

pp. 1224-1229 ◽

Author(s):

Renzo Guerrini ◽

Rocio Sanchez-Carpintero ◽

Thierry Deonna ◽

Margherita Santucci ◽

Kailash P. Bhatia ◽

...

Keyword(s):

Early Onset ◽

Absence Epilepsy ◽

Paroxysmal Dyskinesia

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Ethosuximide, Valproic Acid, and Lamotrigine in Childhood Absence Epilepsy

Yearbook of Neurology and Neurosurgery ◽

10.1016/j.yneu.2010.12.021 ◽

2011 ◽

Vol 2011 ◽

pp. 35-36

Author(s):

M.J. Brodie

Keyword(s):

Valproic Acid ◽

Absence Epilepsy ◽

Childhood Absence Epilepsy

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Two epileptic syndromes, one brain: Childhood absence epilepsy and benign childhood epilepsy with centrotemporal spikes

Yearbook of Neurology and Neurosurgery ◽

10.1016/j.yneu.2012.05.084 ◽

2012 ◽

Vol 2012 ◽

pp. 11-12

Author(s):

J. Kevill

Keyword(s):

Absence Epilepsy ◽

Childhood Epilepsy ◽

Childhood Absence Epilepsy ◽

Epileptic Syndromes

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Narrowing down the candidate region for childhod absence epilepsy in 8q24 and characterization of a candidate gene, T-STAR

Neuroscience Research ◽

10.1016/s0168-0102(00)81566-7 ◽

2000 ◽

Vol 38 ◽

pp. S120

Author(s):

Y Sugimoto

Keyword(s):

Candidate Gene ◽

Absence Epilepsy ◽

Candidate Region

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Early-Onset Absence Epilepsy Caused by Mutations in the Glucose Transporter GLUT1

Yearbook of Neurology and Neurosurgery ◽

10.1016/s0513-5117(09)79174-4 ◽

2010 ◽

Vol 2010 ◽

pp. 42-43

Author(s):

M.J. Brodie

Keyword(s):

Early Onset ◽

Glucose Transporter ◽

Absence Epilepsy ◽

Glucose Transporter Glut1 ◽

Transporter Glut1

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Paroxysmal dyskinesia due to PRRT2 mutation in 15-year-old female patient with benign familial infantile convulsions

Neuropediatrics ◽

10.1055/s-0033-1337706 ◽

2013 ◽

Vol 44 (02) ◽

Author(s):

F Brueckner ◽

B Kohl ◽

B Püst ◽

S Gassner ◽

S Biskup ◽

...

Keyword(s):

Female Patient ◽

Paroxysmal Dyskinesia

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Biallelic PDE2A Mutations: A New Cause of Intellectual Disability with Paroxysmal Dyskinesia and/or Epilepsy

10.1055/s-0039-1685434 ◽

2019 ◽

Author(s):

D. Doummar ◽

C. Dentel ◽

V. Bouilleret ◽

B. Dozieres-Puyravel ◽

H. Nasser ◽

...

Keyword(s):

Intellectual Disability ◽

Paroxysmal Dyskinesia

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TYPICAL IDIOPATHIC ABSENCE EPILEPSY: A NOT SO BENIGN CONDITION

Neuropediatrics ◽

10.1055/s-2006-945561 ◽

2006 ◽

Vol 37 (S 1) ◽

Author(s):

B Echenne ◽

A Roubertie ◽

C Cieuta-Walti ◽

R Cheminal-Lancelot ◽

G Sébire

Keyword(s):

Absence Epilepsy ◽

Benign Condition

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Is a cortical focus driving a cortico-thalamic circuit in human absence epilepsy?

Frontiers in Neuroscience ◽

10.3389/conf.fnins.2010.05.00010 ◽

1900 ◽

Vol 4 ◽

Author(s):

Van Luijtelaar Gilles

Keyword(s):

Absence Epilepsy ◽

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Faculty Opinions recommendation of A multicenter, randomized, placebo-controlled trial of levetiracetam in children and adolescents with newly diagnosed absence epilepsy.

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature ◽

10.3410/f.10255956.11049054 ◽

2011 ◽

Author(s):

Selim Benbadis

Keyword(s):

Children And Adolescents ◽

Controlled Trial ◽

Absence Epilepsy ◽

Newly Diagnosed

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