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Vestibular cortex lesions affect the perception of verticality
Seventy‐one patients with unilateral supratentorial infarctions were evaluated with respect to static vestibular function in the roll plane, including determinations of the subjective visualExpand
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[Frontotemporal lobar degeneration].
Case 1: 77 year-old, right-handed woman complaining a three year history of behavioral disinhibition, hyperorality, repetitive movements, stereotypic speech and delusional misidentification.Expand
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Isolation of the gene for McLeod syndrome that encodes a novel membrane transport protein
McLeod syndrome is an X-linked multisystem disorder characterized by abnormalities in the neuromuscular and hematopoietic systems. We have assembled a cosmid contig of 360 kb that encompasses theExpand
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Motor recovery following capsular stroke. Role of descending pathways from multiple motor areas.
The functional anatomy of motor recovery was studied by assessing motor function quantitatively in 23 patients following capsular or striatocapsular stroke. While selective basal ganglia lesionsExpand
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A Pan-European Study of the C9orf72 Repeat Associated with FTLD: Geographic Prevalence, Genomic Instability, and Intermediate Repeats
We assessed the geographical distribution of C9orf72 G4C2 expansions in a pan‐European frontotemporal lobar degeneration (FTLD) cohort (n = 1,205), ascertained by the European Early‐Onset DementiaExpand
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Clinical features and molecular bases of neuroacanthocytosis
The term acanthocytosis is derived from the Greek for "thorn" and is used to describe a peculiar spiky appearance of erythrocytes. Acanthocytosis is found to be associated with at least threeExpand
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Imaging cortical anatomy by high-resolution MR at 3.0T: detection of the stripe of Gennari in visual area 17.
The brain can be parcellated into numerous anatomical and functional subunits. The classic work by Brodmann (Vergleichende Lokalisationslehre der Grosshirnrinde in ihren Prinzipien dargestellt aufExpand
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McLeod neuroacanthocytosis: Genotype and phenotype
McLeod syndrome is caused by mutations of XK, an X‐chromosomal gene of unknown function. Originally defined as a peculiar Kell blood group variant, the disease affects multiple organs, including theExpand
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Neuroacanthocytosis Syndromes
Neuroacanthocytosis (NA) syndromes are a group of genetically defined diseases characterized by the association of red blood cell acanthocytosis and progressive degeneration of the basal ganglia. NAExpand
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The pattern of cognitive performance in CADASIL: a monogenic condition leading to subcortical ischemic vascular dementia.
OBJECTIVE Subcortical ischemic vascular lesions, which are closely related to small vessel disease, are a common substrate of cognitive impairment and dementia. Cerebral autosomal dominantExpand
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