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期刊名:British journal of dermatology

缩写:BRIT J DERMATOL

ISSN:0007-0963

e-ISSN:1365-2133

IF/分区:9.6/Q1

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共收录本刊相关文章索引11177
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Jawad Khan,Dorottya Godor,Arjun Ramaiya et al. Jawad Khan et al.
An 18-year-old girl with extreme anorexia nervosa (BMI 13 kg/m2, 37.9 kilograms) was admitted for nutritional stabilisation. She reported a two-week history of abdominal pain, reduced urine output and a widespread rash on her abdomen, arms ...
Razan Dodein,Alya Abdul-Wahab Razan Dodein
Congenital milium of the nipple is a rare condition, with limited cases reported. We present two cases highlighting an uncommon presentation of an otherwise common neonatal condition. Case 1: A 10-month-old female had a few-millimeter pearl...
Pooja Jassal-Prior,Luke Carson,Suzy Leech et al. Pooja Jassal-Prior et al.
Acrodermatitis enteropathica (AE) is a rare disorder of zinc deficiency which may be hereditary or acquired. Hereditary AE is an autosomal recessive disorder caused by defects in the zinc transporter gene SLC39A4, resulting in impaired inte...
Melissa Freneat,Tess McPherson,James Davison et al. Melissa Freneat et al.
An infant of 19 months presented to dermatology with a widespread psoriasiform rash favouring inguinal and neck flexures. There was a known family history of psoriasis but no other concerns reported. This progressed to become erythrodermic ...
Pratima Poudel,Celia Moss,Malobi Ogboli Pratima Poudel
Restrictive dermopathy (RD) is a rare, lethal, congenital autosomal recessive laminopathy syndrome characterized by generalised tight translucent skin, dysmorphic facies, arthrogryposis multiplex congenita, and pulmonary hypoplasia. It is c...
Laura Howells,Jane Ravenscroft,Amanda Roberts et al. Laura Howells et al.
Background: Eczema patients and their carers often have questions where there is no good evidence base to advise them. Aim: Rapid Eczem...
Lorna Holcroft,Anne Doolan,Ann O&#x;Sullivan Lorna Holcroft
Introduction: The underdeveloped structural connections between the epidermis and the dermis in preterm babies, means that they are more vulnerable to skin injury than term infants and adults.1 The reported prevalence of ...
Anamika Kunnumpurath,Vani Agarwal,Maria Zahoor et al. Anamika Kunnumpurath et al.
Incontinentia Pigmenti (IP) is a rare X-linked genetic disorder characterised by four stages of cutaneous involvement: vesicular, verrucous, hyperpigmented and hypopigmented (Scheuerle AE, Ursini MV. Incontinentia Pigmenti. In: GeneReviews ...
Natalie King Stokes,Claire O&#x;Neill,Mary Glover et al. Natalie King Stokes et al.
Incontinentia pigmenti (IP) is a rare X-linked dominant genetic condition affecting the skin, teeth, eyes and central nervous system. It is most frequently caused by a common deletion of exons 4-10 in the IKBKG gene. Skin manifestations cla...
Jasmine Sofela,Hannah Cookson Jasmine Sofela
7-year old female develops inflamed well demarcated annular patches with golden crust on the plantar surface of both feet. Treated initially for infected discoid eczema in the community. Unresponsive to topical corticosteroids and oral anti...