Detalhe da pesquisa
1.
Low skeletal muscle mass and liver fibrosis in children with cerebral palsy.
Eur J Pediatr
; 182(11): 5047-5055, 2023 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-37656239
2.
Metabolic assessment in children with neuromuscular disorders shows risk of liver enlargement, steatosis and fibrosis.
Acta Paediatr
; 112(4): 846-853, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36579362
3.
Employment, health visits, mental health, and mortality in parents with a chronically ill child: a Danish nationwide population-based cohort study.
Eur J Pediatr
; 181(4): 1547-1555, 2022 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-35059826
4.
Infections seem to be more frequent before onset of pediatric multiple sclerosis: A Danish nationwide nested case-control study.
Mult Scler
; 25(6): 783-791, 2019 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29770725
5.
Children with dyskinetic cerebral palsy are severely affected as compared to bilateral spastic cerebral palsy.
Acta Paediatr
; 108(10): 1850-1856, 2019 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-30933377
6.
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.
Mult Scler
; 24(8): 1077-1086, 2018 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-28608742
7.
Succinate-CoA ligase deficiency due to mutations in SUCLA2 and SUCLG1: phenotype and genotype correlations in 71 patients.
J Inherit Metab Dis
; 39(2): 243-52, 2016 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-26475597
8.
Mutations in COA3 cause isolated complex IV deficiency associated with neuropathy, exercise intolerance, obesity, and short stature.
J Med Genet
; 52(3): 203-7, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25604084
9.
LAMA2-related myopathy: Frequency among congenital and limb-girdle muscular dystrophies.
Muscle Nerve
; 52(4): 547-53, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-25663498
10.
Children and adolescents previously treated with glucocorticoids display lower verbal intellectual abilities.
Acta Paediatr
; 104(8): 784-91, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-25801849
11.
Infrastructuring precision medicine: Making gene therapies for rare diseases workable in practice.
Soc Sci Med
; 351: 116966, 2024 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-38759386
12.
Burden of Disease of Duchenne Muscular Dystrophy in Denmark - A National Register-Based Study of Individuals with Duchenne Muscular Dystrophy and their Closest Relatives.
J Neuromuscul Dis
; 11(2): 443-457, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38217608
13.
Acetaminophen treatment in children and adults with spinal muscular atrophy: a lower tolerance and higher risk of hepatotoxicity.
Neuromuscul Disord
; 34: 9-18, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-38052667
14.
Homozygous splice variant (c.1741-6G>A) of the COL6A1 gene in three patients with Ullrich congenital muscular dystrophy.
Neuromuscul Disord
; 33(7): 539-545, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37315421
15.
Nonpharmacological Interventions to Reduce Sedation and General Anesthesia in Pediatric MRI: A Meta-analysis.
Hosp Pediatr
; 13(10): e301-e313, 2023 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37727937
16.
School performance and psychiatric comorbidity in childhood absence epilepsy: A Danish cohort study.
Eur J Paediatr Neurol
; 42: 75-81, 2023 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-36584475
17.
The clinical features of paediatric neural tube defects changed in a tertiary care centre between 1997 and 2015.
Acta Paediatr
; 106(5): 837-840, 2017 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-28135771
18.
A novel RNASEH2B splice site mutation responsible for Aicardi-Goutieres syndrome in the Faroe Islands.
Acta Paediatr
; 101(11): e509-13, 2012 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-22882256
19.
Validation of Pediatric Idiopathic Generalized Epilepsy Diagnoses from the Danish National Patient Register During 1994â2019.
Clin Epidemiol
; 14: 501-509, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35469145
20.
School performance and psychiatric comorbidity in juvenile absence epilepsy and juvenile myoclonic epilepsy: a Danish population-based cohort study.
J Neurol
; 269(9): 4997-5007, 2022 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-35595971