Emma K. Wedgeworth
St John's Institute Of Dermatology, Guy's And St Thomas' NHS Foundation Trust
London, ENG, United Kingdom
London, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 9 publications
Does the gene matter? Genotype-phenotype and genotype-outcome associations in congenital melanocytic naevi.
Journal: The British journal of dermatology
Published: May 02, 2019
A case of toxic epidermal necrolysis and vanishing bile duct syndrome, requiring liver transplantation.
Journal: Journal of the European Academy of Dermatology and Venereology : JEADV
Published: April 21, 2017
The Role of Topical Timolol in the Treatment of Infantile Hemangiomas: A Systematic Review and Meta-analysis.
Journal: Acta dermato-venereologica
Published: April 20, 2017
Predictive phenotyping of inherited ichthyosis by next-generation DNA sequencing.
Journal: The British journal of dermatology
Published: June 14, 2016
Propranolol in the treatment of infantile haemangiomas: lessons from the European Propranolol In the Treatment of Complicated Haemangiomas (PITCH) Taskforce survey.
Journal: The British journal of dermatology
Published: October 05, 2015
Clinical features and WNT10A mutations in seven unrelated cases of Schöpf-Schulz-Passarge syndrome.
Journal: The British journal of dermatology
Published: May 25, 2014
The missense mutation p.R1303Q in type XVII collagen underlies junctional epidermolysis bullosa resembling Kindler syndrome.
Journal: The Journal of investigative dermatology
Published: September 06, 2013
A cutaneous lymphoma international prognostic index (CLIPi) for mycosis fungoides and Sezary syndrome.
Journal: European journal of cancer (Oxford, England : 1990)
Published: April 05, 2013
MBTPS2 mutation in a British pedigree with keratosis follicularis spinulosa decalvans.
Journal: Clinical and experimental dermatology
Published: July 24, 2012
Showing 1-9 of 9
Last Updated: 09/26/2026