Epilepsy: Transition from pediatric to adult care. Recommendations of the Ontario epilepsy implementation task force.

about

Epilepsy: Transition from pediatric to adult care. Recommendations of the Ontario epilepsy implementation task force.

Item

http://www.wikidata.org/entity/Q39417475

description

2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年論文

@yue

2017年論文

@zh-hant

2017年論文

@zh-hk

2017年論文

@zh-mo

2017年論文

@zh-tw

2017年论文

@wuu

2017年论文

@zh

2017年论文

@zh-cn

name

Epilepsy: Transition from pedi ...... psy implementation task force.

@en

Epilepsy: Transition from pedi ...... psy implementation task force.

@nl

type

Item

label

Epilepsy: Transition from pedi ...... psy implementation task force.

@en

Epilepsy: Transition from pedi ...... psy implementation task force.

@nl

prefLabel

Epilepsy: Transition from pedi ...... psy implementation task force.

@en

Epilepsy: Transition from pedi ...... psy implementation task force.

@nl

P1476

Epilepsy: Transition from pedi ...... psy implementation task force.

@en

P2093

Anastasia Vogt

http://www.w3.org/2001/XMLSchema#string

Anne S Bassett

http://www.w3.org/2001/XMLSchema#string

Ayman Hassan

http://www.w3.org/2001/XMLSchema#string

Berge A Minassian

http://www.w3.org/2001/XMLSchema#string

Bernard Lawless

http://www.w3.org/2001/XMLSchema#string

Beverly Guttman

http://www.w3.org/2001/XMLSchema#string

Danielle M Andrade

http://www.w3.org/2001/XMLSchema#string

Dolly Menna-Dack

http://www.w3.org/2001/XMLSchema#string

Eduard Bercovici

http://www.w3.org/2001/XMLSchema#string

Esther Bui

http://www.w3.org/2001/XMLSchema#string

P2860

De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy

De novo loss-of-function mutations in CHD2 cause a fever-sensitive myoclonic epileptic encephalopathy sharing features with Dravet syndrome

Transition: driving and exercise

Models for transition clinics

Psychogenic nonepileptic seizures in children: a review

De novo pathogenic SCN8A mutation identified by whole-genome sequencing of a family quartet affected by infantile epileptic encephalopathy and SUDEP

In silico prioritization based on coexpression can aid epileptic encephalopathy gene discovery

Arrhythmia in heart and brain: KCNQ1 mutations link epilepsy and sudden unexplained death.

Differences between mistimed and unwanted pregnancies among women who have live births

Burden analysis of rare microdeletions suggests a strong impact of neurodevelopmental genes in genetic generalised epilepsies

P304

1502-1517

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1111/EPI.13832

http://www.w3.org/2001/XMLSchema#string

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

Peter Szatmari

P577

2017-07-06T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

28681381

http://www.w3.org/2001/XMLSchema#string