Results 151 to 160 of about 3,018 (196)
Emerging Role of Biologic Drugs Targeting IL-17 and IL-23: Pityriasis Rubra Pilaris. [PDF]
Potestio L +8 more
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Severe atypical juvenile pityriasis rubra pilaris diagnosed in adulthood with a dramatic improvement with ustekinumab. [PDF]
McCarthy RL +5 more
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Loss-of-function mutations in Keratin 32 gene disrupt skin immune homeostasis in pityriasis rubra pilaris. [PDF]
Shi P +23 more
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Sezary syndrome initially presenting as pityriasis rubra pilaris: Clinicopathologic study of 3 cases. [PDF]
Alsawas M, Alzayadneh E, Mou E, Liu V.
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Pityriasis rubra pilaris secondary to viral infection
Kacper Pawlik +4 more
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Successful treatment of pityriasis rubra pilaris with brodalumab after nonresponse to IL-17A inhibition: A role for the innate cytokine IL-17C. [PDF]
Valido K +3 more
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Archives of Dermatology, 1971
To the Editor.— Regarding "Pityriasis Rubra Pilaris: Prolonged Treatment With Methotrexate" by Knowles and Chernosky in theArchives( 102 :603. 1970), and in view of some work I have done with vitamin A and reported cases of successful therapy with vitamin A, I would like to make these comments.
openaire +4 more sources
To the Editor.— Regarding "Pityriasis Rubra Pilaris: Prolonged Treatment With Methotrexate" by Knowles and Chernosky in theArchives( 102 :603. 1970), and in view of some work I have done with vitamin A and reported cases of successful therapy with vitamin A, I would like to make these comments.
openaire +4 more sources
Der Hautarzt, 2004
Pityriasis rubra pilaris (PRP) is a rare papulosquamous disease with typical onset during the first and fifth decades. The skin disorder normally starts on the scalp and spreads caudally within a few weeks. It often results in a generalized erythroderma with sharply demarcated islands of sparing ("nappes claires"). A 65-year-old patient with severe PRP
S, Artik +4 more
openaire +3 more sources
Pityriasis rubra pilaris (PRP) is a rare papulosquamous disease with typical onset during the first and fifth decades. The skin disorder normally starts on the scalp and spreads caudally within a few weeks. It often results in a generalized erythroderma with sharply demarcated islands of sparing ("nappes claires"). A 65-year-old patient with severe PRP
S, Artik +4 more
openaire +3 more sources

