Detalhe da pesquisa
1.
Neurofilament light chain and total tau in the differential diagnosis and prognostic evaluation of acute and chronic inflammatory polyneuropathies.
Eur J Neurol
; 29(9): 2810-2822, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35638376
2.
Increasing involvement of CAPN1 variants in spastic ataxias and phenotype-genotype correlations.
Neurogenetics
; 22(1): 71-79, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33486633
3.
Chronic axonal idiopathic polyneuropathy: is it really benign.
Curr Opin Neurol
; 33(5): 562-567, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32773448
4.
Screening for Fabry disease and Hereditary ATTR amyloidosis in idiopathic small-fiber and mixed neuropathy.
Muscle Nerve
; 59(3): 354-357, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30246259
5.
Glycine receptor antibodies in PERM and related syndromes: characteristics, clinical features and outcomes.
Brain
; 137(Pt 8): 2178-92, 2014 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-24951641
6.
Low-dose rituximab treatment in a patient with anti-neurofascin-155 IgG4 autoimmune nodopathy.
J Neuroimmunol
; 389: 578326, 2024 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-38422690
7.
Neurodegenerative biomarkers outperform neuroinflammatory biomarkers in amyotrophic lateral sclerosis.
Amyotroph Lateral Scler Frontotemporal Degener
; 25(1-2): 150-161, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-37789557
8.
The path to diagnosis in ALS: delay, referrals, alternate diagnoses, and clinical progression.
Amyotroph Lateral Scler Frontotemporal Degener
; 24(1-2): 45-53, 2023 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-35343340
9.
Dying from ALS in Sweden: clinical status, setting, and symptoms.
Amyotroph Lateral Scler Frontotemporal Degener
; 24(3-4): 237-245, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35818691
10.
Validation of elevated levels of interleukin-8 in the cerebrospinal fluid, and discovery of new biomarkers in patients with GBS and CIDP using a proximity extension assay.
Front Immunol
; 14: 1241199, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-38077366
11.
Genome sequencing with comprehensive variant calling identifies structural variants and repeat expansions in a large fraction of individuals with ataxia and/or neuromuscular disorders.
Front Neurol
; 14: 1170005, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37273706
12.
Hereditary transthyretin amyloidosis in Sweden: Comparisons between a non-endemic and an endemic region.
Amyloid
; 29(4): 220-227, 2022 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-35438016
13.
ALS patients with concurrent neuroinflammatory disorders; a nationwide clinical records study.
Amyotroph Lateral Scler Frontotemporal Degener
; 23(3-4): 209-219, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-34852680
14.
Cardiac troponin T is elevated and increases longitudinally in ALS patients.
Amyotroph Lateral Scler Frontotemporal Degener
; 23(1-2): 58-65, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34151677
15.
T cell responses at diagnosis of amyotrophic lateral sclerosis predict disease progression.
Nat Commun
; 13(1): 6733, 2022 11 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-36347843
16.
Efficacy and Safety of Rituximab for New-Onset Generalized Myasthenia Gravis: The RINOMAX Randomized Clinical Trial.
JAMA Neurol
; 79(11): 1105-1112, 2022 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36121672
17.
Novel Mutation m.10372A>G in MT-ND3 Causing Sensorimotor Axonal Polyneuropathy.
Neurol Genet
; 7(2): e566, 2021 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-33732874
18.
Comparison Between Rituximab Treatment for New-Onset Generalized Myasthenia Gravis and Refractory Generalized Myasthenia Gravis.
JAMA Neurol
; 77(8): 974-981, 2020 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32364568
19.
Disability and health status in patients with chronic inflammatory demyelinating polyneuropathy.
Disabil Rehabil
; 31(9): 720-5, 2009.
Artigo
em Inglês
| MEDLINE | ID: mdl-19034780
20.
Measurement of sCD27 in the cerebrospinal fluid identifies patients with neuroinflammatory disease.
J Neuroimmunol
; 332: 31-36, 2019 07 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-30928869