Familial and sporadic fatal insomnia (Q28185765)

Fatal familial insomnia and dysautonomia with selective degeneration of thalamic nuclei

Europe PubMed Central

title

Familial and sporadic fatal insomnia (English)

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1

Pasquale Montagna

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Pietro Cortelli

object named as

Pietro Cortelli

series ordinal

3

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Elio Lugaresi

series ordinal

4

object named as

Elio Lugaresi

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Pierluigi Gambetti

series ordinal

2

object named as

Pierluigi Gambetti

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language of work or name

English

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publication date

March 2003

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published in

Lancet Neurology

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volume

2

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issue

3

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page(s)

167-76

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cites work

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"Fatal familial insomnia": neuropsychological study of a disease with thalamic degeneration

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Fatal familial insomnia: a second kindred with mutation of prion protein gene at codon 178

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Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphism

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Allelic origin of the abnormal prion protein isoform in familial prion diseases

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Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphism

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Clinical features of fatal familial insomnia: phenotypic variability in relation to a polymorphism at codon 129 of the prion protein gene.

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A subtype of sporadic prion disease mimicking fatal familial insomnia.

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Prion protein conformation in a patient with sporadic fatal insomnia

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First experimental transmission of fatal familial insomnia

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Transmission of fatal familial insomnia to laboratory animals.

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Evidence for the conformation of the pathologic isoform of the prion protein enciphering and propagating prion diversity

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Fatal familial insomnia: clinical, neuropathological, and genetic description of a Spanish family.

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New mutation in scrapie amyloid precursor gene (at codon 178) in Finnish Creutzfeldt-Jakob kindred

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Fatal familial insomnia: a new Austrian family

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Novel twelve-generation kindred of fatal familial insomnia from germany representing the entire spectrum of disease expression.

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Fatal familial insomnia: a seventh family.

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Fatal familial insomnia with a mutation at codon 178 of the prion protein gene: first report from Japan

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Analysis of the prion protein gene in thalamic dementia

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Thalamic form of Creutzfeldt-Jakob disease or fatal insomnia? Report of a sporadic case with normal prion protein genotype.

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The thalamus participates in the regulation of the sleep-waking cycle. A clinico-pathological study in fatal familial thalamic degeneration.

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Motor overactivity and loss of motor circadian rhythm in fatal familial insomnia: an actigraphic study.

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Diurnal blood pressure variation and hormonal correlates in fatal familial insomnia.

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Fatal familial insomnia: sleep, neuroendocrine and vegetative alterations

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Dissociated 24-hour patterns of somatotropin and prolactin in fatal familial insomnia.

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Diffuse thalamic degeneration in fatal familial insomnia. A morphometric study

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Selective neuronal vulnerability in human prion diseases. Fatal familial insomnia differs from other types of prion diseases

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Clinical findings in sporadic Creutzfeldt-Jakob disease correlate with thalamic pathology

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A PrP gene codon 178 base substitution and a 24-bp interstitial deletion in familial Creutzfeldt-Jakob disease

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Afferent projections to the mediodorsal and anterior thalamic nuclei in the cat. Anatomical-clinical correlations.

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Distribution of cardiovascular related cells within the human thalamus

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Fatal familial insomnia: genetic, neuropathologic, and biochemical study of a patient from a new Italian kindred

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Fatal familial insomnia: clinical and pathologic heterogeneity in genetic half brothers

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