Results 71 to 80 of about 5,913 (240)

CARD14 gain-of-function mutation alone is sufficient to drive IL-23/IL-17-mediated psoriasiform skin inflammation in vivo [PDF]

, 2018
Rare autosomal dominant mutations in the gene encoding the keratinocyte signaling molecule, Caspase Recruitment Domain-Containing Protein 14 (CARD14), have been associated with an increased susceptibility to psoriasis but the physiological impact of ...
Cheng, Phil, Contassot, Emmanuel, French, Lars E, Kiefer, Betina, Meier, Barbara, Mellett, Mark, Mohanan, Deepa, Nobbe, Stephan, Ospelt, Caroline, Satoh, Takashi K, Schairer, Rebekka, Thome, Margot   +11 more
core   +1 more source

Systemic sclerosis in a patient with pityriasis rubra pilaris [PDF]

The Pan African Medical Journal, 2010
Pityriasis rubra pilaris (PRP) is a rare, chronic erythematous squamous disorder of unknown etiology. It has been found in association with several autoimmune diseases, including thyroiditis, myositis, myasthenia gravis and vitiligo.
Hamida Turki, Zouhir Bahloul, Makram Frigui, Hatem Masmoudi, Faten Frikha   +4 more
doaj  

Papulosquamous: clinicopathological [PDF]

, 2017
Background: Papulosquamous disorders comprise a group of dermatoses that have distinct morphologic features. The characteristic primary lesion of these disorders is a papule, usually erythematous, that has a variable amount of scaling on the surface ...
Narayankar, Shilpa Laxmikant, Pandit, Gopal Ambadasrao   +1 more
core   +2 more sources

An expert system for the differential diagnosis of erythemato-squamous diseases [PDF]

, 2000
Cataloged from PDF version of article.This paper presents an expert system for differential diagnosis of erythemato-squamous diseases incorporating decisions made by three classification algorithms: nearest neighbor classifier, naive Bayesian classifier ...
Emeksiz, N., Guvenir, H. A.
core   +1 more source

Pityriasis Rubra Pilaris

, 2015
Pityriasis rubra pilaris (PRP) is a chronic, inflammatory, papulosquamous disorder of keratinization of unknown etiology. It appears both in hereditary and in acquired form. According to the classification by Griffiths, there are six types of PRP: classical adult (type I), atypical adult (type II), classical juvenile (type III), circumscribed juvenile (
Petrov, Andrej, Pljakoska, Vesna
openaire   +3 more sources

A Perspective on the Use of NB-UVB Phototherapy vs. PUVA Photochemotherapy [PDF]

, 2018
Narrowband UVB (NB-UVB) phototherapy and psoralen-UVA (PUVA) photochemotherapy are widely used phototherapeutic modalities for a range of skin diseases.
Ahmad, Archier, Archier, Aslam, Atzmony, Aydogan, Behrens-Williams, Berroeta, Bhatnagar, Bhatnagar, Bilsland, Bilsland, Bishnoi, Boswell, Brazzelli, Bruynzeel, Calzavara-Pinton, Calzavara-Pinton, Cameron, Cameron, Carter, Chalmers, Chauhan, Chen, Clayton, Collins, Cunningham, Dawe, Dawe, Dawe, Dawe, De, Decock, Der-Petrossian, Diederen, El-Mofty, Engin, Farnaghi, Fernandez-Guarino, Foerster, Garritsen, George, Godt, Gordon, Grandi, Green, Grundmann-Kollmann, Halpern, Harrop, Healy, Hearn, Hindson, Hindson, Hofer, Holme, Hoot, Hudson-Peacock, Ibbotson, Ibbotson, Iraji, Karvonen, Kerscher, Khafagy, Knobler, Kolde, Larko, Lever, Lindelof, Ling, Man, Man, Man, Man, Markham, Mastalier, Mckenna, Menage, Messenger, Millington, Mobacken, Mohamed, Morgado-Carrasco, Murray, Norris, Olsen, Parrish, Pavlovsky, Radakovic, Robinson, Roelandts, Roelandts, Ros, Rosen, Rosen, Rosen, Salem, Sapam, Sevrain, Sezer, Sivaramakrishnan, Snellman, Solak, Stern, Stern, Stern, Stern, Stern, Stern, Tanew, Tanew, Taylor, Tegner, Tzaneva, Van, Van, Wackernagel, Warren, Westerhof, Yones, Yones   +119 more
core   +3 more sources

Secukinumab for the treatment of adult‐onset pityriasis rubra pilaris: a single‐arm clinical trial with transcriptomic analysis *

British Journal of Dermatology, 2022
The pathogenesis of pityriasis rubra pilaris (PRP) is not completely understood, but interleukin (IL)‐17 has been shown to play a critical role. There are no reliable immunomodulatory agents to treat PRP.
Blake W. Boudreaux, T. Pincelli, Puneet K Bhullar, Meera H. Patel, C. Brumfiel, Xing Li, M. Heckman, M. Pittelkow, A. Mangold, J. Sluzevich   +9 more
semanticscholar   +1 more source

Classical Juvenile Pityriasis Rubra Pilaris Treated With Secukinumab: Case Report and a Review of Biological Treatments in the Pediatric Population

Pediatric Dermatology, EarlyView.
ABSTRACT Pityriasis rubra pilaris (PRP) is a rare, chronic papulosquamous disorder with limited treatment options in pediatric patients. We report the case of a 9‐year‐old boy with juvenile PRP (type III), who achieved complete disease remission after treatment with secukinumab, an IL‐17A inhibitor, following initial therapeutic resistance to topical ...
Zeno Fratton, Giuseppe Stinco, Enzo Errichetti   +2 more
wiley   +1 more source

Gluten‐related skin disorders: clinical presentation, diagnostic and treatments

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 23, Issue 7, Page 857-867, July 2025.
Summary Gluten‐related disorders (GRDs) encompass a spectrum of clinical manifestations triggered by gluten ingestion in genetically susceptible individuals. These disorders include celiac disease (CD) and non‐celiac gluten sensitivity (NCGS) and present with both intestinal and extraintestinal symptoms, including skin manifestations.
Dario Didona, Roberto Maglie, Farzan Solimani   +2 more
wiley   +1 more source

Pityriasis rubra pilaris (Devergie's disease): clinical case [PDF]

Саратовский научно-медицинский журнал, 2016
Pityriasis rubra pilaris (Devergie's disease) is a rare chronic papulosquamous skin disease, it is of unknown etiology, leading to palmoplantar keratoderma, erythroderma and ectropion. Due to its rarity and difficulty in differentiating it with psoriasis,
Galkina ЕМ, Utz SR, BakulevAL, Minyonok ТА.   +3 more
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