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Inflammatory myopathies: Clinical, diagnostic and therapeutic aspects

Muscle & nerve, 2003-04, Vol.27 (4), p.407-425

2003

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Sporadic inclusion body myositis: HLA-DRB1 allele interactions influence disease risk and clinical phenotype

Neuromuscular disorders : NMD, 2009-11, Vol.19 (11), p.763-765

2009

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Patterns of muscle involvement in inclusion body myositis: Clinical and magnetic resonance imaging study

Muscle & nerve, 2001-11, Vol.24 (11), p.1526-1534

2001

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Progressive myopathy with up-regulation of MHC-I associated with statin therapy

Neuromuscular disorders : NMD, 2007-02, Vol.17 (2), p.194-200

2007

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Paraspinal and scapular myopathy associated with scleroderma

Journal of clinical neuromuscular disease, 2010-06, Vol.11 (4), p.213-222

2010

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Seasonal occurrence of relapses in inflammatory myopathies: a preliminary study

Journal of neurology, 2002-04, Vol.249 (4), p.441-444

2002

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Prevalence of sporadic inclusion body myositis in Western Australia

Muscle & nerve, 2000-06, Vol.23 (6), p.970-972

2000

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Familial inclusion body myositis in a mother and son with different ancestral MHC haplotypes

Neuromuscular disorders : NMD, 2006-11, Vol.16 (11), p.754-758

2006

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Treatment of inflammatory myopathies

Muscle & nerve, 1997-06, Vol.20 (6), p.651-664

1997

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632: Statins may initiate a persisting immune-mediated myopathy and myositis: a study of 10 cases

Journal of clinical neuroscience, 2007, Vol.14 (10), p.1029-1029

2007

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3. Polymyalgia rheumatics and giant cell arteritis

Medical journal of Australia, 1996-10, Vol.165 (8), p.438-442

Zilko, Paul J

1996

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3. Polymyalgia rheumatics and giant cell arteritis: Old age, myalgia, headache — variations on a theme?

Medical journal of Australia, 1996-10, Vol.165 (8), p.438-442

Zilko, Paul J

1996

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Polymyalgia rheumatica and giant cell arteritis

Medical journal of Australia, 1996-10, Vol.165 (8), p.438-442

Zilko, P J

1996

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Frequency of relapses in patients with polymyositis and dermatomyositis

Muscle & nerve, 1998-12, Vol.21 (12), p.1668-1672

1998

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Apolipoprotein E ϵ4 in inclusion body myositis

Annals of neurology, 1995-12, Vol.38 (6), p.957-959

1995

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Idiopathic inflammatory myopathies: optimum immunosuppressive treatment

BioDrugs : clinical immunotherapeutics, biopharmaceuticals, and gene therapy, 1997-04, Vol.7 (4), p.262-272

1997

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Inflammatory Myopathy

Current treatment options in neurology, 1999-07, Vol.1 (3), p.263-272

1999

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Penicillamine-associated myasthenia gravis, antiacetylcholine receptor and antistriational antibodies

The American journal of medicine, 1977-11, Vol.63 (5), p.689-694

1977

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Amyloidosis associated with dermatomyositis and features of multiple myeloma

The American journal of medicine, 1975-09, Vol.59 (3), p.448-452

1975

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Amyloidosis associated with dermatomyositis and features of multiple myeloma: The progression of amyloidosis associated with corticosteroid and cytotoxic drug therapy

The American journal of medicine, 1975-01, Vol.59 (3), p.448-452

1975

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Accounting for cryptic population substructure enhances detection of inbreeding depression with genomic inbreeding coefficients: an example from a critically endangered marsupial

Molecular ecology, 2020-08, Vol.29 (16), p.2978-2993

2020

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Genetic control of suppressor lymphocyte function in myasthenia gravis: relationship of impaired suppressor function to HLA-B8/DRW3 and cold reactive lymphocytotoxic antibodies

Clinical immunology and immunopathology, 1979-10, Vol.14 (2), p.222-230

1979

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Ankylosing spondylitis in HLA-B27-positive individuals: use in diagnosis

BMJ, 1979-01, Vol.1 (6156), p.125-125

1979

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Genetic control of suppressor lymphocyte function in myasthenia gravis: Relationship of impaired suppressor function to [formula omitted] and cold reactive lymphocytotoxic antibodies

Clinical immunology and immunopathology, 1979-10, Vol.14 (2), p.222-230

1979

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Applying Population Viability Analysis to Inform Genetic Rescue That Preserves Locally Unique Genetic Variation in a Critically Endangered Mammal

Diversity (Basel), 2021-08, Vol.13 (8), p.382

2021

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Neurosciences & Neurology
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Biological And Medical Sciences
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Medical Sciences
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Neurosciences
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Aged
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Diseases Of Striated Muscles. Neuromuscular Diseases
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Adult
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Dermatomyositis
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Muscle, Skeletal - Pathology
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Polymyositis
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Aged, 80 And Over
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Anti-Inflammatory Agents - Therapeutic Use
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Inflammatory myopathies: Clinical, diagnostic and therapeutic aspects

Sporadic inclusion body myositis: HLA-DRB1 allele interactions influence disease risk and clinical phenotype

Patterns of muscle involvement in inclusion body myositis: Clinical and magnetic resonance imaging study

Progressive myopathy with up-regulation of MHC-I associated with statin therapy

Paraspinal and scapular myopathy associated with scleroderma

Seasonal occurrence of relapses in inflammatory myopathies: a preliminary study

Prevalence of sporadic inclusion body myositis in Western Australia

Familial inclusion body myositis in a mother and son with different ancestral MHC haplotypes

Treatment of inflammatory myopathies

632: Statins may initiate a persisting immune-mediated myopathy and myositis: a study of 10 cases

3. Polymyalgia rheumatics and giant cell arteritis

3. Polymyalgia rheumatics and giant cell arteritis: Old age, myalgia, headache — variations on a theme?

Polymyalgia rheumatica and giant cell arteritis

Frequency of relapses in patients with polymyositis and dermatomyositis

Apolipoprotein E ϵ4 in inclusion body myositis

Idiopathic inflammatory myopathies: optimum immunosuppressive treatment

Inflammatory Myopathy

Penicillamine-associated myasthenia gravis, antiacetylcholine receptor and antistriational antibodies

Amyloidosis associated with dermatomyositis and features of multiple myeloma

Amyloidosis associated with dermatomyositis and features of multiple myeloma: The progression of amyloidosis associated with corticosteroid and cytotoxic drug therapy

Accounting for cryptic population substructure enhances detection of inbreeding depression with genomic inbreeding coefficients: an example from a critically endangered marsupial

Genetic control of suppressor lymphocyte function in myasthenia gravis: relationship of impaired suppressor function to HLA-B8/DRW3 and cold reactive lymphocytotoxic antibodies

Ankylosing spondylitis in HLA-B27-positive individuals: use in diagnosis

Genetic control of suppressor lymphocyte function in myasthenia gravis: Relationship of impaired suppressor function to [formula omitted] and cold reactive lymphocytotoxic antibodies

Applying Population Viability Analysis to Inform Genetic Rescue That Preserves Locally Unique Genetic Variation in a Critically Endangered Mammal

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