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Acta Paediatrica (Oslo, Norway : 1992)
|
January 31, 2017
The clinical features of paediatric neural tube defects changed in a tertiary care centre between 1997 and 2015
Nina Haarup Gregersen, Kolja Kvist, Klaus Hindsø, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
December 4, 2014
A mitochondrial tRNA(Met) mutation causing developmental delay, exercise intolerance and limb girdle phenotype with onset in early childhood
Alfred Peter Born, Morten Duno, Jabin Rafiq, et al.
Ugeskrift for Laeger
|
April 19, 2017
[A Scandinavian guideline for initial management of minimal, mild and moderate head trauma in children]
Christina Rosenlund, Christina Engel Høi-Hansen, Kaare Engell Lundstrøm, et al.
Pharmacoeconomics
|
March 28, 2026
The Economic Burden of Duchenne Muscular Dystrophy: A Systematic Review
Erik Landfeldt, Maria Åberg, Luca Bello, et al.
European Journal of Pediatrics
|
January 21, 2022
Employment, health visits, mental health, and mortality in parents with a chronically ill child: a Danish nationwide population-based cohort study
Magnus Spangsberg Boesen, Lau Caspar Thygesen, Morten Blinkenberg, et al.
Danish Medical Journal
|
December 4, 2019
Everolimus as adjunctive treatment in tuberous sclerosis complex-associated epilepsy in children
Eva Martha Madsen Svarrer, Claudia Maria Fischer, Mikkel Grenaa Frederiksen, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
August 14, 2012
A novel RNASEH2B splice site mutation responsible for Aicardi-Goutieres syndrome in the Faroe Islands
Elsebet Ostergaard, Frodi Joensen, Karin Sundberg, et al.
Multiple Sclerosis and Related Disorders
|
December 10, 2020
Magnetic resonance imaging at baseline and follow-up to differentiate between pediatric monophasic acquired CNS demyelination and MS
Magnus Spangsberg Boesen, Morten Blinkenberg, Alfred Peter Born, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)
|
June 14, 2017
Pediatric-onset multiple sclerosis and other acquired demyelinating syndromes of the central nervous system in Denmark during 1977-2015: A nationwide population-based incidence study
Magnus Spangsberg Boesen, Melinda Magyari, Nils Koch-Henriksen, et al.
Multiple Sclerosis and Related Disorders
|
July 29, 2018
Increased cerebrospinal fluid chitinase 3-like 1 and neurofilament light chain in pediatric acquired demyelinating syndromes
Magnus Spangsberg Boesen, Poul Erik Hyldgaard Jensen, Melinda Magyari, et al.
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Search research articles
Search
Showing results (21-30 of 60) with videos related to
Sort By:
Page
of 6
Acta Paediatrica (Oslo, Norway : 1992)
|
January 31, 2017
The clinical features of paediatric neural tube defects changed in a tertiary care centre between 1997 and 2015
Nina Haarup Gregersen, Kolja Kvist, Klaus Hindsø, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
December 4, 2014
A mitochondrial tRNA(Met) mutation causing developmental delay, exercise intolerance and limb girdle phenotype with onset in early childhood
Alfred Peter Born, Morten Duno, Jabin Rafiq, et al.
Ugeskrift for Laeger
|
April 19, 2017
[A Scandinavian guideline for initial management of minimal, mild and moderate head trauma in children]
Christina Rosenlund, Christina Engel Høi-Hansen, Kaare Engell Lundstrøm, et al.
Pharmacoeconomics
|
March 28, 2026
The Economic Burden of Duchenne Muscular Dystrophy: A Systematic Review
Erik Landfeldt, Maria Åberg, Luca Bello, et al.
European Journal of Pediatrics
|
January 21, 2022
Employment, health visits, mental health, and mortality in parents with a chronically ill child: a Danish nationwide population-based cohort study
Magnus Spangsberg Boesen, Lau Caspar Thygesen, Morten Blinkenberg, et al.
Danish Medical Journal
|
December 4, 2019
Everolimus as adjunctive treatment in tuberous sclerosis complex-associated epilepsy in children
Eva Martha Madsen Svarrer, Claudia Maria Fischer, Mikkel Grenaa Frederiksen, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
August 14, 2012
A novel RNASEH2B splice site mutation responsible for Aicardi-Goutieres syndrome in the Faroe Islands
Elsebet Ostergaard, Frodi Joensen, Karin Sundberg, et al.
Multiple Sclerosis and Related Disorders
|
December 10, 2020
Magnetic resonance imaging at baseline and follow-up to differentiate between pediatric monophasic acquired CNS demyelination and MS
Magnus Spangsberg Boesen, Morten Blinkenberg, Alfred Peter Born, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)
|
June 14, 2017
Pediatric-onset multiple sclerosis and other acquired demyelinating syndromes of the central nervous system in Denmark during 1977-2015: A nationwide population-based incidence study
Magnus Spangsberg Boesen, Melinda Magyari, Nils Koch-Henriksen, et al.
Multiple Sclerosis and Related Disorders
|
July 29, 2018
Increased cerebrospinal fluid chitinase 3-like 1 and neurofilament light chain in pediatric acquired demyelinating syndromes
Magnus Spangsberg Boesen, Poul Erik Hyldgaard Jensen, Melinda Magyari, et al.
Page
of 6