(Q21261507)

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Custom CGH array profiling of copy number variations (CNVs) on chromosome 6p21.32 (HLA locus) in patients with venous malformations associated with multiple sclerosis

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scholarly article

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Custom CGH array profiling of copy number variations (CNVs) on chromosome 6p21.32 (HLA locus) in patients with venous malformations associated with multiple sclerosis (English)

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multiple sclerosis

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10

object named as

Paolo Zamboni

author given names

Paolo

author last names

Zamboni

1 reference

Dimensions Publication ID

17 August 2022

Matteo Bovolenta

object named as

Matteo Bovolenta

2

author given names

Matteo

author last names

Bovolenta

1 reference

Dimensions Publication ID

17 August 2022

object named as

Donato Gemmati

8

author given names

Donato

author last names

Gemmati

1 reference

Dimensions Publication ID

17 August 2022

author name string

Alessandra Ferlini

1

author given names

Alessandra

author last names

Ferlini

1 reference

Dimensions Publication ID

17 August 2022

Marcella Neri

3

author given names

Marcella

author last names

Neri

1 reference

Dimensions Publication ID

17 August 2022

Francesca Gualandi

4

author given names

Francesca

author last names

Gualandi

1 reference

Dimensions Publication ID

17 August 2022

Alessandra Balboni

5

author given names

Alessandra

author last names

Balboni

1 reference

Dimensions Publication ID

17 August 2022

Anton Yuryev

6

author given names

Anton

author last names

Yuryev

1 reference

Dimensions Publication ID

17 August 2022

Fabrizio Salvi

7

author given names

Fabrizio

author last names

Salvi

1 reference

Dimensions Publication ID

17 August 2022

Alberto Liboni

9

author given names

Alberto

author last names

Liboni

1 reference

Dimensions Publication ID

17 August 2022

language of work or name

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publication date

2010

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BMC Medical Genetics

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11

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1

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64

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Chronic cerebrospinal venous insufficiency in patients with multiple sclerosis

1 reference

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Variation analysis and gene annotation of eight MHC haplotypes: the MHC Haplotype Project

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19 March 2017

Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants

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19 March 2017

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

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19 March 2017

The big idea: iron-dependent inflammation in venous disease and proposed parallels in multiple sclerosis

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19 March 2017

SP100 inhibits ETS1 activity in primary endothelial cells

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19 March 2017

Diagnostic criteria for multiple sclerosis: 2005 revisions to the “McDonald Criteria”

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19 March 2017

Detection of large-scale variation in the human genome

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19 March 2017

Intracranial venous haemodynamics in multiple sclerosis

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19 March 2017

Multiple sclerosis

1 reference

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19 March 2017

Rating neurologic impairment in multiple sclerosis: An expanded disability status scale (EDSS)

1 reference

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19 March 2017

Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2880319

19 March 2017

Risk alleles for multiple sclerosis identified by a genomewide study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2880319

7 April 2017

Anomalous venous blood flow and iron deposition in multiple sclerosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2880319

12 September 2017

Venous collateral circulation of the extracranial cerebrospinal outflow routes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2880319

12 September 2017

Molecular mechanisms of T-cell receptor and costimulatory molecule ligation/blockade in autoimmune disease therapy

1 reference

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12 September 2017

Epistasis among HLA-DRB1, HLA-DQA1, and HLA-DQB1 loci determines multiple sclerosis susceptibility

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2880319

12 September 2017

Targeting the immune system in cancer

1 reference

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12 September 2017

An extension to a statistical approach for family based association studies provides insights into genetic risk factors for multiple sclerosis in the HLA-DRB1 gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2880319

12 September 2017

The value of cerebral Doppler venous haemodynamics in the assessment of multiple sclerosis.

1 reference

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12 September 2017

A novel custom high density-comparative genomic hybridization array detects common rearrangements as well as deep intronic mutations in dystrophinopathies

1 reference

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12 September 2017

Doppler haemodynamics of cerebral venous return

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2880319

12 September 2017

Identification of a novel risk locus for multiple sclerosis at 13q31.3 by a pooled genome-wide scan of 500,000 single nucleotide polymorphisms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2880319

12 September 2017

T cell-mediated help against tumors

1 reference

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12 September 2017

HLA class I alleles tag HLA-DRB1*1501 haplotypes for differential risk in multiple sclerosis susceptibility

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2880319

12 September 2017

The genetics of multiple sclerosis: SNPs to pathways to pathogenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2880319

12 September 2017

Copy-number variation in sporadic amyotrophic lateral sclerosis: a genome-wide screen

1 reference

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12 September 2017

Human disease classification in the postgenomic era: a complex systems approach to human pathobiology

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12 September 2017

Multiple sclerosis--the plaque and its pathogenesis

1 reference

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12 September 2017

The role of iron in the pathogenesis of experimental allergic encephalomyelitis and multiple sclerosis

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12 September 2017

Role of MRI in multiple sclerosis II: brain and spinal cord atrophy

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12 September 2017

Analysis of genome-wide copy number variation in Irish and Dutch ALS populations

1 reference

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27 September 2017

Multiple Sclerosis Severity Score: using disability and disease duration to rate disease severity.

1 reference

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27 September 2017

Refining genetic associations in multiple sclerosis

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-11-64

21 January 2018

Identification of candidate genes for sporadic amyotrophic lateral sclerosis by array comparative genomic hybridization.

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-11-64

21 January 2018

The unsolved puzzle of multiple sclerosis and venous function.

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-11-64

21 January 2018

Quantitative in vivo magnetic resonance imaging of multiple sclerosis at 7 Tesla with sensitivity to iron

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-11-64

21 January 2018

Iron deposits surrounding multiple sclerosis plaques.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2880319

29 November 2018

The multiple sclerosis severity score (MSSS) predicts disease severity over time

1 reference

https://pubmed.ncbi.nlm.nih.gov/20426824

12 December 2020

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Heat shock protein inhibitors and vaccines as new agents in cancer treatment

1 reference

https://pubmed.ncbi.nlm.nih.gov/20426824

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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10.1186/1471-2350-11-64

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release_2ei64u3qcrcvzgv5gvhrntnicq

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