J
John A. McGrath
Researcher at King's College London
Publications - 674
Citations - 26684
John A. McGrath is an academic researcher from King's College London. The author has contributed to research in topics: Epidermolysis bullosa & Mutation. The author has an hindex of 75, co-authored 631 publications receiving 24078 citations. Previous affiliations of John A. McGrath include Ninewells Hospital & Southampton General Hospital.
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Treatment of excessive granulation tissue with EMLA cream and 95% silver-nitrate pencils.
John A. McGrath,O. Schofield +1 more
TL;DR: Simple, pain-free treatment in patients using EMLA® cream for excessive granulation tissue occurring in dystropbic epidermolysis bullosa, junctional epiderMolysis Bullosa (non-Herlitz form) and pyoderma gangrenosum was used and clinical results were clearly superior to similar areas treated with a topical-steroid-antibiotic combination commonly used as a standard treatment.
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New insights into hereditary angio-oedema: Molecular diagnosis and therapy.
TL;DR: Understanding the pathogenesis of HAE is leading to the introduction of new therapies that target the bradykinin receptor or inhibit kallikrein activity, innovations that will hopefully reduce morbidity and mortality in this group of severe genetic disease.
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Ichthyosis Prematurity Syndrome: From Fetus to Adulthood
TL;DR: Citing this paper Please note that where the full-text provided on King's Research Portal is the Author Accepted Manuscript or Post-Print version this may differ from the final Published version.
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Induced Pluripotent Stem Cell Differentiation and Three-Dimensional Tissue Formation Attenuate Clonal Epigenetic Differences in Trichohyalin
Anastasia Petrova,Antonio Capalbo,Laureen Jacquet,Simon Hazelwood-Smith,Dimitra Dafou,Carl Hobbs,Matthew Arno,Alessio Farcomeni,Liani Devito,Heba Badraiq,Michael A. Simpson,John A. McGrath,Wei Li Di,Jeffrey B. Cheng,Theodora M. Mauro,Dusko Ilic +15 more
TL;DR: Analysis of two induced pluripotent stem cell lines used in engineering of 3D human epidermal equivalent (HEE), which more closely approximates epidermis, found that differentiation and tissue formation may mitigate variations in the iPSC methylome.
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Strategies to identify disease genes.
TL;DR: This review aims to summarize both traditional and current strategies for identifying susceptibility and monogenetic disease genes and describes how these strategies have evolved in tune with the ever-expanding wealth of information now available at the authors' fingertips.