Search Results - "Almaani, N."

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  1. 1

    A systematic review of the literature on the treatment of pityriasis rubra pilaris type 1 with TNF-antagonists by Petrof, G., Almaani, N., Archer, C.B., Griffiths, W.A.D., Smith, C.H.

    “…Background  Adult pityriasis rubra pilaris (PRP) type 1 is a rare chronic papulosquamous disorder with clinical and histological parallels with psoriasis…”
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    Journal Article
  2. 2

    Prurigo Pigmentosa: A Clinicopathological Report of Three Middle Eastern Patients by Almaani, N., Msallam, H., Al-Tarawneh, A. H.

    “…Prurigo pigmentosa is a unique cutaneous inflammatory disorder characterized by a sudden onset of pruritic and erythematous macules, urticarial papules, and…”
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  3. 3

    The relevance of patch testing in peristomal dermatitis by Al-Niaimi, F., Beck, M., Almaani, N., Samarasinghe, V., Williams, J., Lyon, C.

    Published in British journal of dermatology (1951) (01-07-2012)
    “…Summary Background  Skin disorders are a common problem for ostomates, resulting in more than a third of visits to a stoma nurse. Irritant reactions,…”
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    Journal Article
  4. 4

    Identical Glycine Substitution Mutations in Type VII Collagen May Underlie Both Dominant and Recessive Forms of Dystrophic Epidermolysis Bullosa by ALMAANI, Noor, LIU, Lu, DOPPING-HEPENSTAL, Patricia J. C, LAI-CHEONG, Joey E, WONG, Alvin, NANDA, Arti, MOSS, Celia, MARTINEZ, Anna E, MELLERIO, Jemima E, MCGRATH, John A

    Published in Acta dermato-venereologica (01-05-2011)
    “…Autosomal dominant and recessive forms of dystrophic epidermolysis bullosa (DEB) result from mutations in the type VII collagen gene (COL7A1). Although…”
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  5. 5

    Erythema gyratum repens associated with pityriasis rubra pilaris by Almaani, N., Robson, A., Sarkany, R., Griffiths, W. A. D.

    Published in Clinical and experimental dermatology (01-03-2011)
    “…Summary Erythema gyratum repens (EGR) is a rare cutaneous eruption characterized by serpiginous morphology and a migrating scaly border. It is one of the most…”
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    Autosomal dominant junctional epidermolysis bullosa by Almaani, N., Liu, L., Dopping-Hepenstal, P.J.C., Lovell, P.A., Lai-Cheong, J.E., Graham, R.M., Mellerio, J.E., McGrath, J.A.

    Published in British journal of dermatology (1951) (01-05-2009)
    “…Summary Background  Epidermolysis bullosa (EB) encompasses a heterogeneous group of inherited skin disorders associated with trauma‐induced blistering. The…”
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  9. 9

    Epidermolysis bullosa pruriginosa in association with lichen planopilaris by Almaani, N., Liu, L., Perez, A., Robson, A., Mellerio, J. E., McGrath, J. A.

    Published in Clinical and experimental dermatology (01-12-2009)
    “…Summary Epidermolysis bullosa pruriginosa (EBP) is a clinical variant of dominant or occasionally recessive, dystrophic epidermolysis bullosa (EB). Clinically,…”
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    Journal Article
  10. 10

    Bullous pemphigoid in a patient with suspected non-Herlitz junctional epidermolysis bullosa by Pérez, A., Almaani, N., Stefanato, C. M., Bhogal, B., Groves, R. W., Mellerio, J. E., McGrath, J. A.

    Published in Clinical and experimental dermatology (01-12-2010)
    “…Summary A 56‐year‐old man with lifelong trauma‐induced blisters, nail dystrophy and dental enamel hypoplasia presented with a new spontaneous blistering…”
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