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Andrew G. Roberts

University Hospital of Wales
University of Wales

34

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Characterization of a large genomic deletion in four Irish families with C7 deficiency.

2012 Molecular Immunology
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Seasonal Palmar Keratoderma in Erythropoietic Protoporphyria Indicates Autosomal Recessive Inheritance

2009 Journal of Investigative Dermatology
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Seasonal Palmar Keratoderma in Erythropoietic Protoporphyria Indicates Autosomal Recessive

2009 Journal of Investigative Dermatology
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Complement component C7 deficiency in four Irish families: The characterisation of a large genomic deletion within the C7 gene

2009 Molecular Immunology
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Prevalence of mutations leading to complete C6 deficiency (C6Q0) in the Western Cape, South Africa and detection of novel mutations leading to C6Q0 in an Irish family

2007 Molecular Immunology
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Depletion of iNOS-derived nitric oxide by prostaglandin H synthase-2 in inflammation-activated J774.2 macrophages through lipohydroperoxidase turnover

2005 Biochemical Journal
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Hepatoerythropoietic porphyria: a missense mutation in the UROD gene is associated with mild disease and an unusual porphyrin excretion pattern

2004 British Journal of Dermatology
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The 16189 variant of mitochondrial DNA occurs more frequently in C282Y homozygotes with haemochromatosis than those without iron loading.

2004 Journal of Medical Genetics
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Alternative splicing and tissue-specific transcription of human and rodent ubiquitous 5-aminolevulinate synthase (ALAS1) genes.

2001 Biochimica et Biophysica Acta
- Andrew G. Roberts
- George H. Elder
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Advanced cardiac life support

2000 Journal of Clinical Nursing
- Andrew G. Roberts
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