Detalhe da pesquisa
1.
Redefining migraine prevention: early treatment with anti-CGRP monoclonal antibodies enhances response in the real world.
J Neurol Neurosurg Psychiatry
; 2024 May 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-38777579
2.
Current clinical practice in disabling and chronic migraine in the primary care setting: results from the European My-LIFE anamnesis survey.
BMC Neurol
; 21(1): 1, 2021 Jan 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33390161
3.
Need of guidance in disabling and chronic migraine identification in the primary care setting, results from the european MyLife anamnesis survey.
BMC Fam Pract
; 22(1): 54, 2021 03 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-33743604
4.
Prophylactic Allogeneic Hematopoietic Stem Cell Therapy for CSF1R-Related Leukoencephalopathy.
Mov Disord
; 37(5): 1108-1109, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35587623
5.
Hereditary diffuse leukoencephalopathy with spheroids with phenotype of primary progressive multiple sclerosis.
Eur J Neurol
; 22(2): 328-333, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25311247
6.
Sequence variants in eukaryotic translation initiation factor 4-gamma (eIF4G1) are associated with Lewy body dementia.
Acta Neuropathol
; 125(3): 425-38, 2013 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-23124435
7.
A woman in her 70s with chronic walking difficulties.
Tidsskr Nor Laegeforen
; 135(19): 1753-5, 2015 Oct 20.
Artigo
em Inglês, Norueguês
| MEDLINE | ID: mdl-26486671
8.
A SCA7 premutation may be a novel Mendelian modifier of MS course: A case report.
Mult Scler Relat Disord
; 31: 148-150, 2019 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-30999137
9.
An AARS variant as the likely cause of Swedish type hereditary diffuse leukoencephalopathy with spheroids.
Acta Neuropathol Commun
; 7(1): 188, 2019 11 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-31775912
10.
A novel de novo pathogenic mutation in the CACNA1A gene.
Mov Disord
; 27(12): 1578-9, 2012 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-23038654
11.
Different stages of white matter changes in the original HDLS family revealed by advanced MRI techniques.
J Neuroimaging
; 24(5): 444-52, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-23751174
12.
Stora regionala orättvisor gällande behandling av huvudvärk.
Lakartidningen
; 1152018 05 09.
Artigo
em Sueco
| MEDLINE | ID: mdl-29762814
13.
Autosomal dominant cerebellar ataxia type III: a review of the phenotypic and genotypic characteristics.
Orphanet J Rare Dis
; 8: 14, 2013 Jan 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-23331413
14.
Parkinsonian features in hereditary diffuse leukoencephalopathy with spheroids (HDLS) and CSF1R mutations.
Parkinsonism Relat Disord
; 19(10): 869-77, 2013 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-23787135
15.
Autosomal dominant Parkinson's disease.
Parkinsonism Relat Disord
; 18 Suppl 1: S7-10, 2012 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-22166459
16.
Hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS): a misdiagnosed disease entity.
J Neurol Sci
; 314(1-2): 130-7, 2012 Mar 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-22050953
17.
MRI characteristics and scoring in HDLS due to CSF1R gene mutations.
Neurology
; 79(6): 566-74, 2012 Aug 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-22843259
18.
Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids.
Nat Genet
; 44(2): 200-5, 2011 Dec 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-22197934
19.
Microglia: multiple roles in surveillance, circuit shaping, and response to injury.
Neurology
; 82(20): 1846, 2014 May 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-24843036
20.
An adult-onset leukoencephalopathy with axonal spheroids and pigmented glia accompanied by brain calcifications: a case report and a literature review of brain calcifications disorders.
J Neurol
; 260(10): 2665-8, 2013 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-24036850