HLA associations with inclusion body myositis (Q24681826)

2

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P J Zilko

3

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W Ollier

4

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F L Mastaglia

Clinical and Experimental Immunology

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language of work or name

English

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publication date

October 1994

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published in

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volume

98

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issue

1

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page(s)

40-5

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cites work

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Inclusion body myositis: an underdiagnosed condition?

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HLA-linked congenital adrenal hyperplasia results from a defective gene encoding a cytochrome P-450 specific for steroid 21-hydroxylation

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Inflammatory and non-inflammatory inclusion body myositis. Characterization of the mononuclear cells and expression of the immunoreactive class I major histocompatibility complex product

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Haplospecific polymorphism between HLA B and tumor necrosis factor

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Association of tumor necrosis factor (TNF) and class II major histocompatibility complex alleles with the secretion of TNF-a and TNF-0 by human mononuclear cells: a possible link to insulin-dependent diabetes mellitus

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HLA antigens and Bf allotypes in SLE: evidence for the association being with specific haplotypes

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Disease associations with complotypes, supratypes and haplotypes

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

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Rearrangement of 21-hydroxylase genes in disease-associated MHC supratypes

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Immunogenetic associations of scleroderma-related antinuclear antibodies

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C4 DNA RFLP reference typing report

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Inclusion body myositis

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12 December 2020