Detalhe da pesquisa
1.
Do Early Relapses Predict the Risk of Long-Term Relapsing Disease in an Adult and Paediatric Cohort with MOGAD?
Ann Neurol
; 94(3): 508-517, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37394961
2.
Evolution of brain MRI lesions in paediatric myelin-oligodendrocyte glycoprotein antibody-associated disease (MOGAD) and its relevance to disease course.
J Neurol Neurosurg Psychiatry
; 95(5): 426-433, 2024 Apr 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-37979966
3.
The emerging spectrum of fetal acetylcholine receptor antibody-related disorders (FARAD).
Brain
; 146(10): 4233-4246, 2023 10 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-37186601
4.
Antineurofascin IgG2-associated paediatric autoimmune nodopathy.
Dev Med Child Neurol
; 65(8): 1118-1122, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-36631915
5.
Muscle cramps and contractures: causes and treatment.
Pract Neurol
; 23(1): 23-34, 2023 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-36522175
6.
Early predictors of disability of paediatric-onset AQP4-IgG-seropositive neuromyelitis optica spectrum disorders.
J Neurol Neurosurg Psychiatry
; 93(1): 101-111, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34583946
7.
Isolated central nervous system familial hemophagocytic lymphohistiocytosis (fHLH) presenting as a mimic of demyelination in children.
Mult Scler
; 28(4): 669-675, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-34704499
8.
Pregnancy outcomes in patients with congenital myasthenic syndromes.
Muscle Nerve
; 66(3): 345-348, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35661384
9.
The clinical spectrum of the congenital myasthenic syndrome resulting from COL13A1 mutations.
Brain
; 142(6): 1547-1560, 2019 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31081514
10.
Prevalence and incidence of neuromyelitis optica spectrum disorder, aquaporin-4 antibody-positive NMOSD and MOG antibody-positive disease in Oxfordshire, UK.
J Neurol Neurosurg Psychiatry
; 91(10): 1126-1128, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32576617
11.
A study of referral bias in NMOSD and MOGAD cohorts.
Mult Scler Relat Disord
; 85: 105553, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38552551
12.
Expanding the phenotype of DYNC1H1-associated diseases with a rare variant resulting in spinal muscular atrophy with lower extremity predominance (SMA-LED) and upper motor neuron signs.
Turk J Pediatr
; 65(3): 531-535, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37395972
13.
Congenital myasthenic syndromes: a retrospective natural history study of respiratory outcomes in a single centre.
Brain Commun
; 5(6): fcad299, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-38035366
14.
Care Recommendations for the Investigation and Management of Children With Skeletal Muscle Channelopathies.
Pediatr Neurol
; 145: 102-111, 2023 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-37315339
15.
Expanding the phenotype of children presenting with hypoventilation with biallelic TBCK pathogenic variants and literature review.
Neuromuscul Disord
; 33(1): 50-57, 2023 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36522252
16.
Risdiplam: an investigational survival motor neuron 2 (SMN2) splicing modifier for spinal muscular atrophy (SMA).
Expert Opin Investig Drugs
; 31(5): 451-461, 2022 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-35316106
17.
Early clinical and pre-clinical therapy development in Nemaline myopathy.
Expert Opin Ther Targets
; 26(10): 853-867, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-36524401
18.
SARS-CoV-2 vaccination and new-onset myasthenia gravis: A report of 7 cases and review of the literature.
Neuromuscul Disord
; 32(10): 785-789, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-36130855
19.
Rituximab in juvenile myasthenia gravis-an international cohort study and literature review.
Eur J Paediatr Neurol
; 40: 5-10, 2022 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-35835035
20.
Factors Associated With Relapse and Treatment of Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease in the United Kingdom.
JAMA Netw Open
; 5(1): e2142780, 2022 01 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35006246