Infantile spasmer

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Standard

Infantile spasmer. / Préel, Marie; Møller, Rikke S; Miranda, Maria J; Hoei-Hansen, Christina Engel.

I: Ugeskrift for Laeger, Bind 182, Nr. 15, V10190597, 2020.

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt

Harvard

Préel, M, Møller, RS, Miranda, MJ & Hoei-Hansen, CE 2020, 'Infantile spasmer', Ugeskrift for Laeger, bind 182, nr. 15, V10190597. <https://ugeskriftet.dk/files/scientific_article_files/2020-03/ufl-10-19-0597-file005-digital_tv_.pdf>

APA

Préel, M., Møller, R. S., Miranda, M. J., & Hoei-Hansen, C. E. (2020). Infantile spasmer. Ugeskrift for Laeger, 182(15), [V10190597]. https://ugeskriftet.dk/files/scientific_article_files/2020-03/ufl-10-19-0597-file005-digital_tv_.pdf

Vancouver

Préel M, Møller RS, Miranda MJ, Hoei-Hansen CE. Infantile spasmer. Ugeskrift for Laeger. 2020;182(15). V10190597.

Author

Préel, Marie ; Møller, Rikke S ; Miranda, Maria J ; Hoei-Hansen, Christina Engel. / Infantile spasmer. I: Ugeskrift for Laeger. 2020 ; Bind 182, Nr. 15.

Bibtex

@article{4c456b4b7b2b4c4fb19a26347eca4250,
title = "Infantile spasmer",
abstract = "Infantile spasms (IS) is a severe developmental and epileptic encephalopathy, occurring mainly in children aged 3-18 months. IS have multiple aetiologies, and the treatment differs accordingly. Early diagnosis and treatment may improve the outcome, but many patients are initially misdiagnosed. Evaluation includes seizure semiology, electroencephalography, cerebral magnetic resonance imaging and genetic and metabolic testing. Treatment varies among centres, and initial treatment may include vigabatrin and/or corticosteroids. In recent years, as summarised in this review, knowledge has substantially increased regarding genetic aetiologies and treatment regimens.",
author = "Marie Pr{\'e}el and M{\o}ller, {Rikke S} and Miranda, {Maria J} and Hoei-Hansen, {Christina Engel}",
year = "2020",
language = "Dansk",
volume = "182",
journal = "Ugeskrift for Laeger",
issn = "0041-5782",
publisher = "Almindelige Danske Laegeforening",
number = "15",

}

RIS

TY - JOUR

T1 - Infantile spasmer

AU - Préel, Marie

AU - Møller, Rikke S

AU - Miranda, Maria J

AU - Hoei-Hansen, Christina Engel

PY - 2020

Y1 - 2020

N2 - Infantile spasms (IS) is a severe developmental and epileptic encephalopathy, occurring mainly in children aged 3-18 months. IS have multiple aetiologies, and the treatment differs accordingly. Early diagnosis and treatment may improve the outcome, but many patients are initially misdiagnosed. Evaluation includes seizure semiology, electroencephalography, cerebral magnetic resonance imaging and genetic and metabolic testing. Treatment varies among centres, and initial treatment may include vigabatrin and/or corticosteroids. In recent years, as summarised in this review, knowledge has substantially increased regarding genetic aetiologies and treatment regimens.

AB - Infantile spasms (IS) is a severe developmental and epileptic encephalopathy, occurring mainly in children aged 3-18 months. IS have multiple aetiologies, and the treatment differs accordingly. Early diagnosis and treatment may improve the outcome, but many patients are initially misdiagnosed. Evaluation includes seizure semiology, electroencephalography, cerebral magnetic resonance imaging and genetic and metabolic testing. Treatment varies among centres, and initial treatment may include vigabatrin and/or corticosteroids. In recent years, as summarised in this review, knowledge has substantially increased regarding genetic aetiologies and treatment regimens.

M3 - Tidsskriftartikel

C2 - 32286217

VL - 182

JO - Ugeskrift for Laeger

JF - Ugeskrift for Laeger

SN - 0041-5782

IS - 15

M1 - V10190597

ER -

ID: 269794603