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zadetkov: 152
1.
  • Microvascular Pathology and... Microvascular Pathology and Morphometrics of Sporadic and Hereditary Small Vessel Diseases of the Brain
    Craggs, Lucinda J.L.; Yamamoto, Yumi; Deramecourt, Vincent ... Brain pathology, September 2014, Letnik: 24, Številka: 5
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    Small vessel diseases (SVDs) of the brain are likely to become increasingly common in tandem with the rise in the aging population. In recent years, neuroimaging and pathological studies have ...
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2.
  • Hippocampal Neuronal Atroph... Hippocampal Neuronal Atrophy and Cognitive Function in Delayed Poststroke and Aging-Related Dementias
    GEMMELL, Elizabeth; BOSOMWORTH, Helen; ALLAN, Louise ... Stroke, 03/2012, Letnik: 43, Številka: 3
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    We have previously shown delayed poststroke dementia in elderly (≥75 years old) stroke survivors is associated with medial temporal lobe atrophy; however, the basis of the structural and functional ...
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3.
  • On the identification of lo... On the identification of low allele frequency mosaic mutations in the brains of Alzheimer's disease patients
    Sala Frigerio, Carlo; Lau, Pierre; Troakes, Claire ... Alzheimer's & dementia, November 2015, Letnik: 11, Številka: 11
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    Abstract Introduction The cause of sporadic Alzheimer's disease (AD) remains unclear. Given the growing evidence that protein aggregates can spread in a “prion-like” fashion, we reasoned that a small ...
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4.
  • Phenotype variability in pr... Phenotype variability in progranulin mutation carriers: a clinical, neuropsychological, imaging and genetic study
    Le Ber, Isabelle; Camuzat, Agnès; Hannequin, Didier ... Brain (London, England : 1878), 03/2008, Letnik: 131, Številka: 3
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    Frontotemporal dementia (FTD), characterized by behavioural and language disorders, is a clinically, genetically and pathologically heterogeneous group of diseases. The most recently identified of ...
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5.
  • Adult Niemann-Pick disease ... Adult Niemann-Pick disease type C in France: clinical phenotypes and long-term miglustat treatment effect
    Nadjar, Yann; Hütter-Moncada, Ana Lucia; Latour, Philippe ... Orphanet journal of rare diseases, 10/2018, Letnik: 13, Številka: 1
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    Niemann-Pick disease type C (NP-C) is a neurodegenerative lysosomal lipid storage disease caused by autosomal recessive mutations in the NPC1 or NPC2 genes. The clinical presentation and evolution of ...
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6.
  • Different tau species lead ... Different tau species lead to heterogeneous tau pathology propagation and misfolding
    Dujardin, Simon; Bégard, Séverine; Caillierez, Raphaëlle ... Acta neuropathologica communications, 11/2018, Letnik: 6, Številka: 1
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    Tauopathies are a heterogeneous group of pathologies characterized by tau aggregation inside neurons. Most of them are sporadic but certain tauopathies rely on tau gene (MAPT) mutations. They ...
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7.
  • Intraventricular dopamine i... Intraventricular dopamine infusion alleviates motor symptoms in a primate model of Parkinson's disease
    Moreau, Caroline; Rolland, Anne Sophie; Pioli, Elsa ... Neurobiology of disease, 06/2020, Letnik: 139
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    Continuous compensation of dopamine represents an ideal symptomatic treatment for Parkinson's disease (PD). The feasibility in intracerebroventricular administration (i.c.v.) of dopamine previously ...
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8.
  • Magnetic resonance imaging ... Magnetic resonance imaging changes following natalizumab discontinuation in multiple sclerosis patients with progressive multifocal leukoencephalopathy
    Hodel, Jérôme; Bapst, Blanche; Outteryck, Olivier ... Multiple sclerosis, 12/2018, Letnik: 24, Številka: 14
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    Background: Detecting early progressive multifocal leukoencephalopathy-immune reconstitution inflammatory syndrome (PML-IRIS) is clinically relevant. Objective: Evaluating magnetic resonance imaging ...
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9.
  • Human subiculo-fornico-mami... Human subiculo-fornico-mamillary system in Alzheimer’s disease: Tau seeding by the pillar of the fornix
    Thierry, Manon; Boluda, Susana; Delatour, Benoît ... Acta neuropathologica, 03/2020, Letnik: 139, Številka: 3
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    In Alzheimer’s disease (AD), Tau and Aβ aggregates involve sequentially connected regions, sometimes distantly separated. These alterations were studied in the pillar of the fornix (PoF), an axonal ...
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10.
  • The TMEM240 Protein, Mutate... The TMEM240 Protein, Mutated in SCA21, Is Expressed in Purkinje Cells and Synaptic Terminals
    Homa, Mégane; Loyens, Anne; Eddarkaoui, Sabiha ... Cerebellum (London, England), 06/2020, Letnik: 19, Številka: 3
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    A variety of missense mutations and a stop mutation in the gene coding for transmembrane protein 240 ( TMEM240 ) have been reported to be the causative mutations of spinocerebellar ataxia 21 (SCA21). ...
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zadetkov: 152

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