(Q47969615)

7 February 2018

title

HLA allele distribution distinguishes sporadic inclusion body myositis from hereditary inclusion body myopathies (English)

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7 February 2018

main subject

inclusion body myositis

1 reference

Koffman BM

1

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7 February 2018

Sivakumar K

2

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7 February 2018

Simonis T

3

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7 February 2018

Stroncek D

4

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7 February 2018

Dalakas MC

5

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7 February 2018

publication date

1 April 1998

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7 February 2018

Journal of Neuroimmunology

published in

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7 February 2018

volume

84

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7 February 2018

issue

2

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7 February 2018

page(s)

139-142

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7 February 2018

Monoclonal antibody analysis of mononuclear cells in myopathies. V: Identification and quantitation of T8+ cytotoxic and T8+ suppressor cells

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0165-5728%2897%2900245-2

7 January 2021

"Rimmed vacuole myopathy" sparing the quadriceps. A unique disorder in Iranian Jews

1 reference

https://api.crossref.org/works/10.1016%2FS0165-5728%2897%2900245-2

7 January 2021

Major histocompatibility complex genes in systemic lupus erythematosus, Sjögren's syndrome, and polymyositis

1 reference

https://api.crossref.org/works/10.1016%2FS0165-5728%2897%2900245-2

7 January 2021

Nomenclature for factors of the HLA system, 1995

1 reference

https://api.crossref.org/works/10.1016%2FS0165-5728%2897%2900245-2

7 January 2021

Polymyositis, dermatomyositis and inclusion-body myositis

1 reference

https://api.crossref.org/works/10.1016%2FS0165-5728%2897%2900245-2

7 January 2021

Disease associations with complotypes, supratypes and haplotypes

1 reference

https://api.crossref.org/works/10.1016%2FS0165-5728%2897%2900245-2

7 January 2021

HLA associations with inclusion body myositis

1 reference

https://api.crossref.org/works/10.1016%2FS0165-5728%2897%2900245-2

7 January 2021

The immunobiology of muscle

1 reference

https://api.crossref.org/works/10.1016%2FS0165-5728%2897%2900245-2

7 January 2021

Susceptibility to IDDM is marked by MHC supratypes rather than individual alleles

1 reference

https://api.crossref.org/works/10.1016%2FS0165-5728%2897%2900245-2

7 January 2021

Immune-mediated conditions and antibodies associated with sporadic inclusion body myositis

1 reference

https://api.crossref.org/works/10.1016%2FS0165-5728%2897%2900245-2

7 January 2021

Restricted use of T cell receptor V genes in endomysial infiltrates of patients with inflammatory myopathies

1 reference

https://api.crossref.org/works/10.1016%2FS0165-5728%2897%2900245-2

7 January 2021

Inclusion body myositis. Observations in 40 patients

1 reference

https://api.crossref.org/works/10.1016%2FS0165-5728%2897%2900245-2

7 January 2021

Hereditary inclusion body myopathy maps to chromosome 9p1-q1

1 reference

https://api.crossref.org/works/10.1016%2FS0165-5728%2897%2900245-2

7 January 2021

Familial inclusion body myositis: Evidence for autosomal dominant inheritance

1 reference

https://api.crossref.org/works/10.1016%2FS0165-5728%2897%2900245-2

7 January 2021

The αβ T-Cell Receptor Repertoire in Inclusion Body Myositis: Diverse Patterns of Gene Expression by Muscle-infiltrating Lymphocytes

1 reference

https://api.crossref.org/works/10.1016%2FS0165-5728%2897%2900245-2

7 January 2021

B-Lymphocyte Alloantigens Associated with Systemic Lupus Erythematosus

1 reference

https://api.crossref.org/works/10.1016%2FS0165-5728%2897%2900245-2

7 January 2021

Vacuolar myopathy sparing the quadriceps.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-5728%2897%2900245-2

7 January 2021

Contribution of genes of the major histocompatibility complex to susceptibility and disease phenotype in inflammatory bowel disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-5728%2897%2900245-2

7 January 2021

Inclusion body myositis: new concepts

1 reference

https://api.crossref.org/works/10.1016%2FS0165-5728%2897%2900245-2

7 January 2021

The spectrum of familial inclusion body myopathies in 13 families and a description of a quadriceps-sparing phenotype in non-Iranian Jews

1 reference

https://api.crossref.org/works/10.1016%2FS0165-5728%2897%2900245-2

7 January 2021

An inflammatory, familial, inclusion body myositis with autoimmune features and a phenotype identical to sporadic inclusion body myositis. Studies in three families

1 reference

https://api.crossref.org/works/10.1016%2FS0165-5728%2897%2900245-2

7 January 2021

10.1016/S0165-5728(97)00245-2

Identifiers

DOI

1 reference

7 February 2018

1 reference

7 February 2018