(Q48113682)

8 February 2018

title

Narcolepsy is a common phenotype in HSAN IE and ADCA-DN. (English)

1 reference

8 February 2018

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6

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8 February 2018

Rocco Liguori

10

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8 February 2018

Vincenzo Donadio

11

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8 February 2018

Piero Parchi

12

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8 February 2018

Juliane Winkelmann

18

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8 February 2018

Giuseppe Plazzi

22

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8 February 2018

Chiara La Morgia

Chiara La Morgia

3

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Caterina Tonon

Caterina Tonon

5

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Fabio Pizza

Fabio Pizza

2

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Valerio Carelli

Valerio Carelli

21

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Marco Seri

Marco Seri

8

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Emmanuel Mignot

20

Emmanuel Mignot

1 reference

8 February 2018

Christian Franceschini

4

Christian Franceschini

1 reference

8 February 2018

Keivan Kaveh Moghadam

1

Keivan Kaveh Moghadam

1 reference

8 February 2018

Ferdinando Cornelio

13

Ferdinando Cornelio

1 reference

8 February 2018

Piero Barboni

7

Piero Barboni

1 reference

8 February 2018

Simona Ferrari

9

Simona Ferrari

1 reference

8 February 2018

author name string

Domenico Inzitari

14

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8 February 2018

Andrea Mignarri

15

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8 February 2018

Giuseppe Capocchi

16

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8 February 2018

Maria Teresa Dotti

17

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8 February 2018

Ling Lin

19

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8 February 2018

language of work or name

English

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publication date

10 April 2014

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8 February 2018

published in

Brain

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8 February 2018

volume

137

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8 February 2018

issue

Pt 6

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8 February 2018

page(s)

1643-1655

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8 February 2018

The control region of mitochondrial DNA shows an unusual CpG and non-CpG methylation pattern

cites work

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWU069

Cerebrospinal fluid and plasma biomarkers in Alzheimer disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWU069

The Mitochondrial Proteome and Human Disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWU069

Mitochondrial dysfunction as a cause of optic neuropathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWU069

A narcolepsy susceptibility locus maps to a 5 Mb region of chromosome 21q.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWU069

Modulation of lymphatic muscle contractility by the neuropeptide substance P

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWU069

Tauopathy in human and experimental variant Creutzfeldt-Jakob disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWU069

Raised CSF phospho-tau concentrations in variant Creutzfeldt-Jakob disease: diagnostic and pathological implications

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWU069

Epigenetic switching by the metabolism-sensing factors in the generation of orexin neurons from mouse embryonic stem cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWU069

Hereditary sensory neuropathy with deafness and dementia: a clinical and neuroimaging study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWU069

A missense mutation in myelin oligodendrocyte glycoprotein as a cause of familial narcolepsy with cataplexy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWU069

Autonomic regulation of lymphatic flow in the lower extremity demonstrated on lymphoscintigraphy in patients with reflex sympathetic dystrophy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWU069

Cutting edge: TCR stimulation is sufficient for induction of Foxp3 expression in the absence of DNA methyltransferase 1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWU069

Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing loss

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWU069

DNMT1 mutation hot spot causes varied phenotypes of HSAN1 with dementia and hearing loss.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWU069

Common variants in P2RY11 are associated with narcolepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWU069

The autoimmune basis of narcolepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWU069

Distinctive patterns of DNA methylation associated with Parkinson disease: identification of concordant epigenetic changes in brain and peripheral blood leukocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWU069

Autosomal dominant cerebellar ataxia deafness and narcolepsy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWU069

Genetic and familial aspects of narcolepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWU069

The role of cerebrospinal fluid hypocretin measurement in the diagnosis of narcolepsy and other hypersomnias

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWU069

Polysomnographic and neurometabolic features may mark preclinical autosomal dominant cerebellar ataxia, deafness, and narcolepsy due to a mutation in the DNA (cytosine-5-)-methyltransferase gene, DNMT1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWU069

Symptomatic narcolepsy, cataplexy and hypersomnia, and their implications in the hypothalamic hypocretin/orexin system

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWU069

A novel de novo exon 21 DNMT1 mutation causes cerebellar ataxia, deafness, and narcolepsy in a Brazilian patient

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWU069

A mutation in a case of early onset narcolepsy and a generalized absence of hypocretin peptides in human narcoleptic brains

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWU069

Narcolepsy as an adverse event following immunization: case definition and guidelines for data collection, analysis and presentation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWU069

DNA methyltransferase 1, cytosine methylation, and cytosine hydroxymethylation in mammalian mitochondria

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWU069

DNA methylation status of nuclear-encoded mitochondrial genes underlies the tissue-dependent mitochondrial functions

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWU069

Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWU069

Hereditary sensory neuropathy with sensorineural deafness and early-onset dementia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWU069

Novel mutation in the replication focus targeting sequence domain of DNMT1 causes hereditary sensory and autonomic neuropathy IE.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWU069

21 January 2018

Identifiers

DOI

10.1093/BRAIN/AWU069

1 reference

8 February 2018

1 reference

8 February 2018