The UK Working Party's Diagnostic Criteria for Atopic Dermatitis. I. Derivation of a minimum set of discriminators for atopic dermatitis
…, EA Bingham, AY Finlay, AC Pembroke… - British journal of …, 1994 - academic.oup.com
A working party of 13 dermatologists, two family practitioners and a paediatrician was assembled,
with the aim of developing a minimum list of reliable discriminators for atopic dermatitis…
with the aim of developing a minimum list of reliable discriminators for atopic dermatitis…
The UK Working Party's diagnostic criteria for atopic dermatitis. III. Independent hospital validation
HC Williams, PG Jburney, AC Pembroke… - British journal of …, 1994 - academic.oup.com
In order to qualify as a case of atopic dermatitis, we propose that an individual must have an
itchy skin condition plus three or more of the following: history of flexural involvement, a …
itchy skin condition plus three or more of the following: history of flexural involvement, a …
Validation of the UK diagnostic criteria for atopic dermatitis in a population setting
HC Williams, PGJ Burney, AC Pembroke… - British Journal of …, 1996 - academic.oup.com
One reason why so little is known about the epidemiology of atopic dermatitis (AD) is lack of
suitable diagnostic criteria. A simple list of diagnostic criteria for AD for use in …
suitable diagnostic criteria. A simple list of diagnostic criteria for AD for use in …
London-born black Caribbean children are at increased risk of atopic dermatitis
HC Williams, AC Pembroke, H Forsdyke… - Journal of the American …, 1995 - Elsevier
Background: Previous reports suggest that atopic dermatitis is more common in black Caribbean
children born in the United Kingdom than in white children. It is unclear whether these …
children born in the United Kingdom than in white children. It is unclear whether these …
[HTML][HTML] Localization of a gene (MCUL1) for multiple cutaneous leiomyomata and uterine fibroids to chromosome 1q42. 3-q43
…, HM Nelson, E Healy, AC Pembroke… - The American Journal of …, 2001 - cell.com
Dominant transmission of multiple uterine and cutaneous smooth-muscle tumors is seen in
the disorder multiple leiomyomatosis (ML). We undertook a genomewide screen of 11 …
the disorder multiple leiomyomatosis (ML). We undertook a genomewide screen of 11 …
FACE—facial Afro‐Caribbean childhood eruption
HC Williams, J Ashworth, AC Pembroke… - Clinical and …, 1990 - Wiley Online Library
Five cases of a distinctive facial eruption in Afro‐Caribbean children are described. Distinctive
features include monomorphic papules that are confined to the face, especially around …
features include monomorphic papules that are confined to the face, especially around …
The successful use of minocycline in pyoderma gangrenosum—a report of seven cases and review of the literature
…, RAC Graham-Brown, AC Pembroke - Journal of …, 1989 - Taylor & Francis
We report seven cases in which minocycline was successfully used to treat pyoderma
gangrenosum. This more than doubles the six previously reported cases. Minocycline is …
gangrenosum. This more than doubles the six previously reported cases. Minocycline is …
[PDF][PDF] Phrynoderma and perforating folliculitis due to vitamin A deficiency in a diabetic
SM Neill, AC Pembroke… - Journal of the Royal …, 1988 - journals.sagepub.com
Discussion The 5 cases previously reported were all males aged 57-77 years. Four out of
the 5 had eosinophilia and 4 lymphopenia (2 marked and 2 borderline). The patient without …
the 5 had eosinophilia and 4 lymphopenia (2 marked and 2 borderline). The patient without …
Eruptive angiomata in malignant disease
AC Pembroke, K Grice, AV Levantine… - Clinical and …, 1978 - academic.oup.com
We report the eruption of multiple angiomata in four patients with the following malignant
diseases: Hodgkin's disease, chronic lymphatic leukaemia, probable disseminated melanoma, …
diseases: Hodgkin's disease, chronic lymphatic leukaemia, probable disseminated melanoma, …
Heterozygous germline missense mutation in the p63 gene underlying EEC syndrome
…, JE Mellerio, AC Pembroke… - Clinical and …, 2000 - academic.oup.com
Mutations in the p63 gene have recently been delineated as the molecular basis for some
cases of the ectrodactyly, ectodermal dysplasia and cleft lip/palate (EEC) syndrome, an …
cases of the ectrodactyly, ectodermal dysplasia and cleft lip/palate (EEC) syndrome, an …