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Topical steroid withdrawal: a survey of UK dermatologists' attitudes.
- Published in:
- Clinical & Experimental Dermatology, 2024, v. 49, n. 6, p. 607, doi. 10.1093/ced/llae045
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- Publication type:
- Article
Caring for babies born with epidermolysis bullosa.
- Published in:
- British Journal of Dermatology, 2024, v. 190, n. 5, p. 608, doi. 10.1093/bjd/ljae048
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- Publication type:
- Article
Do people with eczema and their carers understand topical steroid potency? Results of two surveys.
- Published in:
- Clinical & Experimental Dermatology, 2024, v. 49, n. 3, p. 267, doi. 10.1093/ced/llad372
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- Publication type:
- Article
O07 CHILD syndrome and ILVEN: disorders on the same spectrum?
- Published in:
- British Journal of Dermatology, 2024, v. 190, p. i3, doi. 10.1093/bjd/ljad483.007
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- Publication type:
- Article
P14 Midface Toddler Excoriation Syndrome (MiTES): a new mimic of non-accidental injury.
- Published in:
- British Journal of Dermatology, 2024, v. 190, p. i9, doi. 10.1093/bjd/ljad483.023
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- Publication type:
- Article
Topical steroid withdrawal is not a myth. Comment on '#corticophobia: a review on online misinformation related to topical steroids'.
- Published in:
- Clinical & Experimental Dermatology, 2023, v. 48, n. 6, p. 697, doi. 10.1093/ced/llad062
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- Publication type:
- Article
Potency of topical steroids should be clearly labelled on all packaging.
- Published in:
- British Journal of Dermatology, 2023, v. 188, n. 3, p. 427, doi. 10.1093/bjd/ljac104
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- Publication type:
- Article
Biallelic TUFT1 variants cause woolly hair, superficial skin fragility and desmosomal defects.
- Published in:
- British Journal of Dermatology, 2023, v. 188, n. 1, p. 75, doi. 10.1093/bjd/ljac026
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- Publication type:
- Article
Birth incidence and outcome of harlequin ichthyosis and collodion membrane in the UK and Ireland: a national 2-year prospective surveillance study.
- Published in:
- British Journal of Dermatology, 2023, v. 188, n. 1, p. 139, doi. 10.1093/bjd/ljac015
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- Publication type:
- Article
Topical steroid withdrawal syndrome: time to bridge the gap.
- Published in:
- British Journal of Dermatology, 2022, v. 187, n. 5, p. 780, doi. 10.1111/bjd.21770
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- Publication type:
- Article
Achenbach syndrome: no need for skin biopsy.
- Published in:
- Clinical & Experimental Dermatology, 2022, v. 47, n. 9, p. 1730, doi. 10.1111/ced.15269
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- Publication type:
- Article
Mutations in the ribosome biogenesis factor gene LTV1 are linked to LIPHAK syndrome, a novel poikiloderma-like disorder.
- Published in:
- Human Molecular Genetics, 2022, v. 31, n. 12, p. 1970, doi. 10.1093/hmg/ddab368
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- Publication type:
- Article
The epidemiology of epidermolysis bullosa in England and Wales: data from the national epidermolysis bullosa database*.
- Published in:
- British Journal of Dermatology, 2022, v. 186, n. 5, p. 843, doi. 10.1111/bjd.20958
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- Publication type:
- Article
Does SNAI2 mutation cause human piebaldism and Waardenburg syndrome?
- Published in:
- American Journal of Medical Genetics. Part A, 2020, v. 182, n. 12, p. 3074, doi. 10.1002/ajmg.a.61887
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- Publication type:
- Article
Skin lesions simulating child abuse.
- Published in:
- Indian Journal of Paediatric Dermatology, 2018, v. 19, n. 3, p. 187, doi. 10.4103/ijpd.IJPD_56_18
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- Publication type:
- Article
Congenital cutaneous lymphadenoma.
- Published in:
- Journal of Cutaneous Pathology, 2017, v. 44, n. 11, p. 954, doi. 10.1111/cup.13016
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- Publication type:
- Article
Topical Therapy in Atopic Dermatitis in Children.
- Published in:
- Indian Journal of Dermatology, 2016, v. 61, n. 6, p. 656, doi. 10.4103/0019-5154.193677
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- Publication type:
- Article
Steroid Sulfatase Deficiency and Androgen Activation Before and After Puberty.
- Published in:
- 2016
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- Publication type:
- journal article
Hereditary Vitamin D-Resistant Rickets Presenting as Alopecia.
- Published in:
- Pediatric Dermatology, 2014, v. 31, n. 4, p. 519, doi. 10.1111/pde.12327
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- Publication type:
- Article
Multiple cerebral abscesses in Papillon-Lefèvre syndrome.
- Published in:
- Child's Nervous System, 2013, v. 29, n. 8, p. 1227, doi. 10.1007/s00381-013-2152-2
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- Publication type:
- Article
Targeted Sequence Capture and High-Throughput Sequencing in the Molecular Diagnosis of Ichthyosis and Other Skin Diseases.
- Published in:
- Journal of Investigative Dermatology, 2013, v. 133, n. 2, p. 573, doi. 10.1038/jid.2012.332
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- Publication type:
- Article
RARE DERMATOLOGY SERVICES.
- Published in:
- Dermatological Nursing, 2012, v. 11, n. 2, p. 54
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- Publication type:
- Article
Revertant Mosaicism in Kindler Syndrome.
- Published in:
- 2012
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- Publication type:
- Letter
Identical Glycine Substitution Mutations in Type VII Collagen May Underlie Both Dominant and Recessive Forms of Dystrophic Epidermolysis Bullosa.
- Published in:
- Acta Dermato-Venereologica, 2011, v. 91, n. 3, p. 262, doi. 10.2340/00015555-1053
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- Publication type:
- Article
Dilated Cardiomyopathy In Epidermolysis Bullosa: A Retrospective, Multicenter Study-Response.
- Published in:
- Pediatric Dermatology, 2010, v. 27, n. 6, p. 679, doi. 10.1111/j.1525-1470.2010.01339.x
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- Publication type:
- Article
Diarrhea Associated with Propranolol Treatment for Hemangioma of Infancy (HOI).
- Published in:
- Pediatric Dermatology, 2010, v. 27, n. 5, p. 558, doi. 10.1111/j.1525-1470.2010.01221.x
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- Publication type:
- Article
Links Between Granuloma Annulare, Necrobiosis Lipoidica Diabeticorum and Childhood Diabetes: A Matter of Time?
- Published in:
- Pediatric Dermatology, 2010, v. 27, n. 2, p. 178, doi. 10.1111/j.1525-1470.2010.01099.x
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- Publication type:
- Article
A New Way to Classify Genetic Skin Disease.
- Published in:
- Journal of Investigative Dermatology, 2009, v. 129, n. 11, p. 2543, doi. 10.1038/jid.2009.292
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- Publication type:
- Article
Degos disease: a new simulator of non-accidental injury.
- Published in:
- Developmental Medicine & Child Neurology, 2009, v. 51, n. 8, p. 647, doi. 10.1111/j.1469-8749.2009.03349.x
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- Publication type:
- Article
End-stage renal failure in adolescence with Sjögren’s syndrome autoantibodies SSA and SSB.
- Published in:
- 2007
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- Publication type:
- Report
The gene encoding R-spondin 4 (RSPO4), a secreted protein implicated in Wnt signaling, is mutated in inherited anonychia.
- Published in:
- Nature Genetics, 2006, v. 38, n. 11, p. 1245, doi. 10.1038/ng1883
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- Publication type:
- Article
Atlas of Genodermatoses.
- Published in:
- 2006
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- Publication type:
- Book Review
Germline LEMD3 mutations are rare in sporadic patients with isolated melorheostosis.
- Published in:
- Human Mutation, 2006, v. 27, n. 3, p. 290, doi. 10.1002/humu.9403
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- Publication type:
- Article
Gonosomal Mosaicism for a Nonsense Mutation (R1947X) in the NF1 Gene in Segmental Neurofibromatosis Type 1.
- Published in:
- Journal of Investigative Dermatology, 2005, v. 125, n. 3, p. 463, doi. 10.1111/j.0022-202X.2005.23834.x
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- Publication type:
- Article
Two New XPD Patients Compound Heterozygous for the Same Mutation Demonstrate Diverse Clinical Features.
- Published in:
- Journal of Investigative Dermatology, 2005, v. 125, n. 1, p. 86, doi. 10.1111/j.0022-202X.2005.23745.x
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- Publication type:
- Article
Pyogenic Skin Infections as a Presentation of Papillon-Lefèvre Syndrome: Phenotypic Variability or Under-Reporting?
- Published in:
- Periodontal Practice Today, 2005, v. 2, n. 3, p. 191
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- Publication type:
- Article
Skin and kin.
- Published in:
- 2005
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- Publication type:
- journal article
Skin and kin.
- Published in:
- Journal of the Royal Society of Medicine, 2005, v. 98, n. 5, p. 200, doi. 10.1177/014107680509800507
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- Publication type:
- Article
A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis.
- Published in:
- 2004
- By:
- Publication type:
- Letter
An Atlas of Diseases of the Nail.
- Published in:
- 2004
- By:
- Publication type:
- Book Review
Recurrent Mutations in Kindlin-1, a Novel Keratinocyte Focal Contact Protein, in the Autosomal Recessive Skin Fragility and Photosensitivity Disorder, Kindler Syndrome.
- Published in:
- Journal of Investigative Dermatology, 2004, v. 122, n. 1, p. 78, doi. 10.1046/j.0022-202X.2003.22136.x
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- Publication type:
- Article
The Desktop Guide to Complementary and Alternative Medicine: an Evidence-based Approach.
- Published in:
- 2001
- By:
- Publication type:
- Book Review
Book review and Erratum.
- Published in:
- 2001
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- Publication type:
- Book Review
Sturge-Weber syndrome.
- Published in:
- 2000
- By:
- Publication type:
- Book Review
Missense Mutations in Keratin 17 Cause Either Pachyonychia Congenita Type 2 or a Phenotype Resembling Steatocystoma Multiplex.
- Published in:
- 1997
- By:
- Publication type:
- Report
A Recurrent Homozygous Nonsense Mutation within the LAMA3 Gene as a Cause of Herlitz Junctional Epidermolysis Bullosa in Patients of Pakistani Ancestry: Evidence for a Founder Effect.
- Published in:
- Journal of Investigative Dermatology, 1996, v. 106, n. 4, p. 781, doi. 10.1111/1523-1747.ep12346349
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- Publication type:
- Article
Genetic Disorders of the Skin (Book).
- Published in:
- 1992
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- Publication type:
- Book Review
Precocious puberty in a boy with a widespread linear epidermal naevus.
- Published in:
- British Journal of Dermatology, 1991, v. 125, n. 2, p. 178, doi. 10.1111/j.1365-2133.1991.tb06068.x
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- Publication type:
- Article
Dermatology and the human gene map.
- Published in:
- British Journal of Dermatology, 1991, v. 124, n. 1, p. 3, doi. 10.1111/j.1365-2133.1991.tb03274.x
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- Publication type:
- Article
Letter to the Editors.
- Published in:
- Clinical Genetics, 1990, v. 38, n. 4, p. 318, doi. 10.1111/j.1399-0004.1990.tb03587.x
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- Publication type:
- Article