Results 61 to 70 of about 530 (127)
peer-reviewedNetherton syndrome is an autosomal recessive multisystemic disorder characterized by congenital ichthyosiform erythroderma, hair shaft defects and atopy, caused by mutations within the human SPINK5 gene.
FALLON, PADRAIC
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Clinico Epidemiological Profile of Dermatological Manifestations in Preschool going Children in a Tertiary Health Care Centre [PDF]
BACKGROUND: Dermatological manifestations during the childhood period include a variety of infectious and non infectious diseases. There is variation in the pattern of dermatoses, with eczemas being the most common skin disorder in developed countries ...
Siddhant Sunil Mahajan,
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Measuring the impact of pruritus in patients with epidermolysis bullosa: evaluation with an itch-specific instrument. [PDF]
Alheggi A +6 more
europepmc +1 more source
Recent genetic findings demonstrate an important role for the epidermal protein filaggrin in the aetiology of atopic diseases, including asthma as well as eczema.
Weller, R., McLean, W.H.I.
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La risposta cutanea dermografica nei pazienti con orticaria o psoriasi
Background: physical urticarias (Us) represent about 20% of all cases of acute or chronic Us. Among these patients, the most common are those affected by immediate dermographism.
AYALA, FABIO, DI MASO, ANNA MARIA
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Systemic Salicylate Toxicity From Topical Emollient Use in an Infant With Suspected Ichthyosis. [PDF]
Pullukat K, Husien T.
europepmc +1 more source
Cochlear implantation in syndromic patients: difficulties and lessons learnt. [PDF]
Saleeb MF +4 more
europepmc +1 more source
POF1B protein distribution in normal and pathological skin
In this study a rabbit polyclonal antibody anti human POF1B, raised against the corresponding fusion protein, was used to characterize on frozen sections the tissue distribution of the protein in normal and pathological skin conditions in which there are
P. della Mina +5 more
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