[HTML][HTML] Epilepsy genetics and precision medicine in adults: a new landscape for developmental and epileptic encephalopathies

� Beltr�n-Corbellini, � Aledo-Serrano…�- Frontiers in�…, 2022 - frontiersin.org
This review aims to provide an updated perspective of epilepsy genetics and precision
medicine in adult patients, with special focus on developmental and epileptic�…

Transition to adult medical care for adolescents with epilepsy

RPJ Geerlings, AP Aldenkamp, PHN De With…�- Epilepsy & Behavior, 2015 - Elsevier
Introduction During transition to adult medical care, the adolescent with epilepsy is
especially prone to emotional, mental, physical, and social developmental difficulties�…

Whole‐exome sequencing in adult patients with developmental and epileptic encephalopathy: it is never too late

R Minardi, L Licchetta, MC Baroni, T Pippucci…�- Clinical�…, 2020 - Wiley Online Library
Developmental and epileptic encephalopathies (DEE) encompass rare, sporadic
neurodevelopmental disorders and usually with pediatric onset. As these conditions are�…

Dravet syndrome: early electroclinical findings and long‐term outcome in adolescents and adults

F Darra, D Battaglia, C Dravet, M Patrini, F Offredi…�- …, 2019 - Wiley Online Library
To describe the outcome of Dravet syndrome (DS) in adolescents and adults we conducted
a longitudinal retrospective study of two independent cohorts of 34 adolescents (group 1)�…

Epilepsy: addressing the transition from pediatric to adult care

S Rajendran, A Iyer�- Adolescent health, medicine and therapeutics, 2016 - Taylor & Francis
Adolescence is a period of rapid change, both physical and psychosocial for any young
person. It can be challenging when they have ongoing health problems and when their care�…

Helping families cope with the severe stress of Dravet syndrome

P Camfield, C Camfield, K Nolan�- Canadian Journal of Neurological�…, 2016 - cambridge.org
A child with Dravet syndrome shakes family life to the core. Dravet syndrome usually has
three phases:(1) up to 1-1� years: with episodes of febrile status epilepticus but normal�…

Dravet Syndrome: An Electroclinical, Genetic, Treatment, and Outcome Study of 35 Patients in Argentina

RH Caraballo, G Veneruzzo, M Loos…�- Journal of Pediatric�…, 2024 - thieme-connect.com
We analyzed the electroclinical features, molecular findings, treatment, disease course, and
outcomes of patients with Dravet syndrome (DS) with positive genetic markers seen at a�…

[BOOK][B] Transitionsmedizin: Multiprofessionelle Begleitung junger Erwachsener mit chronischer Krankheit

M Oldhafer - 2015 - books.google.com
Endlich erwachsen, aber immer noch chronisch krank! Der Wechsel von der Jugend-in die
Erwachsenenmedizin–Transition–ist f�r chronisch kranke Jugendliche schwierig: Sie f�hlen�…

[HTML][HTML] Evidence review: Transition from paediatric to adult epilepsy services

NGC UK - 2022 - ncbi.nlm.nih.gov
The NICE guideline “Transition from children's to adults' services for young people using
health or social care services” sets out generic guidance covering the period before, during�…

[HTML][HTML] Evidence review: Information and support

NGC UK - 2022 - ncbi.nlm.nih.gov
The need for up-to-date and accurate information and support when needed for anyone
living with epilepsy is well recognised. People with epilepsy and their family and/or carers�…