Movement Disorders
|
0.410 |
Biomarker
|
group |
HPO |
|
|
|
Movement Disorders
|
0.410 |
CausalMutation
|
group |
CLINVAR |
Cognitive development in Dravet syndrome: a retrospective, multicenter study of 26 patients.
|
21269283 |
2011 |
Movement Disorders
|
0.410 |
GeneticVariation
|
group |
CLINVAR |
Cognitive development in Dravet syndrome: a retrospective, multicenter study of 26 patients.
|
21269283 |
2011 |
Movement Disorders
|
0.410 |
CausalMutation
|
group |
CLINVAR |
Cryptogenic epileptic syndromes related to SCN1A: twelve novel mutations identified.
|
18413471 |
2008 |
Movement Disorders
|
0.410 |
GeneticVariation
|
group |
CLINVAR |
Cryptogenic epileptic syndromes related to SCN1A: twelve novel mutations identified.
|
18413471 |
2008 |
Movement Disorders
|
0.410 |
GeneticVariation
|
group |
CLINVAR |
De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy.
|
11359211 |
2001 |
Movement Disorders
|
0.410 |
CausalMutation
|
group |
CLINVAR |
De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy.
|
11359211 |
2001 |
Movement Disorders
|
0.410 |
GeneticVariation
|
group |
CLINVAR |
Dravet syndrome and parent associations: the IDEA League experience with comorbid conditions, mortality, management, adaptation, and grief.
|
21463290 |
2011 |
Movement Disorders
|
0.410 |
CausalMutation
|
group |
CLINVAR |
Dravet syndrome and parent associations: the IDEA League experience with comorbid conditions, mortality, management, adaptation, and grief.
|
21463290 |
2011 |
Movement Disorders
|
0.410 |
CausalMutation
|
group |
CLINVAR |
Dravet syndrome--from epileptic encephalopathy to channelopathy.
|
24836964 |
2014 |
Movement Disorders
|
0.410 |
GeneticVariation
|
group |
CLINVAR |
Dravet syndrome--from epileptic encephalopathy to channelopathy.
|
24836964 |
2014 |
Movement Disorders
|
0.410 |
GeneticVariation
|
group |
CLINVAR |
Generalized epilepsy with febrile seizures plus. A genetic disorder with heterogeneous clinical phenotypes.
|
9126059 |
1997 |
Movement Disorders
|
0.410 |
CausalMutation
|
group |
CLINVAR |
Generalized epilepsy with febrile seizures plus. A genetic disorder with heterogeneous clinical phenotypes.
|
9126059 |
1997 |
Movement Disorders
|
0.410 |
CausalMutation
|
group |
CLINVAR |
Genotype-phenotype associations in SCN1A-related epilepsies.
|
21248271 |
2011 |
Movement Disorders
|
0.410 |
GeneticVariation
|
group |
CLINVAR |
Genotype-phenotype associations in SCN1A-related epilepsies.
|
21248271 |
2011 |
Movement Disorders
|
0.410 |
GeneticVariation
|
group |
CLINVAR |
Idiopathic epilepsies with seizures precipitated by fever and SCN1A abnormalities.
|
17561957 |
2007 |
Movement Disorders
|
0.410 |
CausalMutation
|
group |
CLINVAR |
Idiopathic epilepsies with seizures precipitated by fever and SCN1A abnormalities.
|
17561957 |
2007 |
Movement Disorders
|
0.410 |
CausalMutation
|
group |
CLINVAR |
Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2.
|
10742094 |
2000 |
Movement Disorders
|
0.410 |
GeneticVariation
|
group |
CLINVAR |
Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2.
|
10742094 |
2000 |
Movement Disorders
|
0.410 |
Biomarker
|
group |
CTD_human |
Paroxysmal movement disorders in severe myoclonic epilepsy in infancy.
|
12907273 |
2003 |
Movement Disorders
|
0.410 |
CausalMutation
|
group |
CLINVAR |
Prognostic, clinical and demographic features in SCN1A mutation-positive Dravet syndrome.
|
22719002 |
2012 |
Movement Disorders
|
0.410 |
GeneticVariation
|
group |
CLINVAR |
Prognostic, clinical and demographic features in SCN1A mutation-positive Dravet syndrome.
|
22719002 |
2012 |
Movement Disorders
|
0.410 |
CausalMutation
|
group |
CLINVAR |
Progressive gait deterioration in adolescents with Dravet syndrome.
|
22409937 |
2012 |
Movement Disorders
|
0.410 |
GeneticVariation
|
group |
CLINVAR |
Progressive gait deterioration in adolescents with Dravet syndrome.
|
22409937 |
2012 |
Movement Disorders
|
0.410 |
GeneticVariation
|
group |
CLINVAR |
SCN1A duplications and deletions detected in Dravet syndrome: implications for molecular diagnosis.
|
19400878 |
2009 |