Migraine prophylactic management in neurology and primary care (2006-2015).

Abstract:

:

journal_name

J Neurol

journal_title

Journal of neurology

authors

Jackson JL,Kay C,Scholcoff C,Nickoloff S,Fletcher K

doi

10.1007/s00415-018-9066-6

subject

pub_date

2018-12-01 00:00:00

pages

3019-3021

issue

12

eissn

0340-5354

issn

1432-1459

pii

10.1007/s00415-018-9066-6

journal_volume

265

pub_type

信件
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    abstract::Stroke in young adults is not a rare entity, and often provides difficult management decisions for neurologists. The knowledge gained from stroke in older adults does not transfer easily to this younger group given the different causes of stroke observed. Cardiac causes of stroke are common in this group, but often co...

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  • Correction to: The immediate impact of the COVID‑19 pandemic on motor neuron disease services and mortality in Scotland.

    abstract::The article The immediate impact of the COVID‑19 pandemic on motor neuron disease services and mortality in Scotland, written by Stella A. Glasmacher, Juan Larraz, Arpan R. Mehta, Patrick K. A. Kearns, Michael Wong, Judith Newton, Richard Davenport, George Gorrie, Ian Morrison, Javier Carod Artal, Siddharthan Chandran...

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    authors: Glasmacher SA,Larraz J,Mehta AR,Kearns PKA,Wong M,Newton J,Davenport R,Gorrie G,Morrison I,Carod Artal J,Chandran S,Pal S,CARE-MND Consortium.

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  • Juvenile-onset bulbospinal muscular atrophy with deafness: Vialetta-van Laere syndrome or Madras-type motor neuron disease?

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  • Treatment of chronic relapsing inflammatory demyelinating polyneuropathy by cyclosporin A and plasma exchange. A case report.

    abstract::A patient with chronic relapsing inflammatory demyelinating polyneuropathy was successfully treated with plasma exchanges and cyclosporin A (CsA). Dynamometric measurements of hand force during the time of CsA treatment showed a highly significant correlation between hand force and CsA blood levels. The largest influe...

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    authors: Hefter H,Sprenger KB,Arendt G,Hafner D

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  • Antibodies and neuronal autoimmune disorders of the CNS.

    abstract::We review the neuronal antibodies described in CNS disorders in order to clarify their diagnostic value, emphasize potentials pitfalls and limitations in the diagnosis of paraneoplastic neurological syndromes (PNS), and examine the current evidence for a possible pathogenic role. We propose to classify the neuronal an...

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    authors: Graus F,Saiz A,Dalmau J

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  • How predictors and patterns of stroke recurrence after a TIA differ during the first year of follow-up.

    abstract::The highest risk of subsequent stroke after a TIA occurs within the first week after the index event. However, the risk of stroke recurrence (SR) remains high during the first year of follow-up. We studied the temporal pattern and predictors of SR (at 7 days and from 7 days to 1-year follow-up). Between April 2008 and...

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    authors: Purroy F,Jiménez Caballero PE,Gorospe A,Torres MJ,Alvarez-Sabin J,Martínez-Sánchez P,Cánovas D,Freijo M,Egido JA,Ramírez-Moreno JM,Alonso-Arias A,Rodríguez-Campello A,Casado-Naranjo I,Martí-Fàbregas J,Silva Y,Cardona P,Mo

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  • Diagnosis, investigation and management of hereditary spastic paraplegias in the era of next-generation sequencing.

    abstract::The hereditary spastic paraplegias (HSPs) are a group of genetic conditions in which spastic paralysis of the legs is the principal clinical feature. This is caused by a relatively selective distal axonal degeneration involving the longest axons of the corticospinal tracts. Consequently, these conditions provide an op...

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    authors: Hensiek A,Kirker S,Reid E

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  • Selection of thrombogenetic antiphospholipid antibodies in cerebrovascular disease patients.

    abstract:BACKGROUND AND PURPOSE:The association between anticardiolipin antibodies (aCL) and thrombosis is well recognized, but its role as an independent risk factor for stroke is not. The study's aim was to investigate the presence of antiphospholipid antibodies (aPL) and ischemic vascular events by using both traditional mea...

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    doi:10.1007/s00415-003-1045-9

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  • Mastication-induced vertigo and nystagmus.

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  • Coenzyme Q in serum and muscle of 5 patients with Kearns-Sayre syndrome and 12 patients with ophthalmoplegia plus.

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  • Clinical experience with high-dose idebenone in Friedreich ataxia.

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    pub_type: 杂志文章,评审

    doi:10.1007/s00415-015-7825-1

    authors: Gold DR,Zee DS

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    abstract::Neuroinflammation (microglial activation) and subclinical nigrostriatal dysfunction have been reported in subjects at risk of Parkinsonism. Eight non-manifesting carriers (NMCs) of LRRK2 G2019S mutation had 11C-PK11195 and 18F-DOPA PET to assess microglial activation and striatal dopamine system integrity, respectivel...

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    doi:10.1007/s00415-020-09830-3

    authors: Gersel Stokholm M,Garrido A,Tolosa E,Serradell M,Iranzo A,Østergaard K,Borghammer P,Møller A,Parbo P,Stær K,Brooks DJ,Martí MJ,Pavese N

    更新日期:2020-08-01 00:00:00

  • Effects of a short outpatient rehabilitation treatment on disability of multiple sclerosis patients--a randomised controlled trial.

    abstract::It is well known that neurorehabilitation can reduce disability or improve handicap of people with multiple sclerosis (MS). The aim of this study was to evaluate the effectiveness of a short period (6 weeks) of a tailored, individualised outpatient rehabilitation program in people with progressive MS. A randomised-con...

    journal_title:Journal of neurology

    pub_type: 临床试验,杂志文章,随机对照试验

    doi:10.1007/s00415-003-1097-x

    authors: Patti F,Ciancio MR,Cacopardo M,Reggio E,Fiorilla T,Palermo F,Reggio A,Thompson AJ

    更新日期:2003-07-01 00:00:00

  • PEN-2 gene mutation in a familial Alzheimer's disease case.

    abstract::Genetic evidence indicates a central role of cerebral accumulation of beta-amyloid (Abeta) in the pathogenesis of Alzheimer's disease (AD). Beside presenilin 1 and 2, three other recently discovered proteins (Aph 1, PEN 2 and nicastrin) are associated with gamma-secretase activity, the enzymatic complex generating Abe...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-005-0799-7

    authors: Sala Frigerio C,Piscopo P,Calabrese E,Crestini A,Malvezzi Campeggi L,Civita di Fava R,Fogliarino S,Albani D,Marcon G,Cherchi R,Piras R,Forloni G,Confaloni A

    更新日期:2005-09-01 00:00:00

  • A new mutation in GJC2 associated with subclinical leukodystrophy.

    abstract::Recessive mutations in GJC2, the gene-encoding connexin 47 (Cx47), cause Pelizaeus-Merzbacher-like disease type 1, a severe dysmyelinating disorder. One recessive mutation (p.Ile33Met) has been associated with a much milder phenotype--hereditary spastic paraplegia type 44. Here, we present evidence that a novel Arg98L...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-014-7429-1

    authors: Abrams CK,Scherer SS,Flores-Obando R,Freidin MM,Wong S,Lamantea E,Farina L,Scaioli V,Pareyson D,Salsano E

    更新日期:2014-10-01 00:00:00