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Observations on Keratosis Follicularis
Archives of Dermatology, 1960Keratosis follicularis, commonly referred to as Darier's disease, is a rare, persistent, cutaneous disorder characterized by malodorous, greasy, crusted, sometimes pustular, hyperkeratotic brownish-red papules located primarily on the scalp, face, retroauricular areas and the trunk.
J N, PENROD +2 more
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Archives of Dermatology and Syphilology, 1943
In 1938 Peck 1 studied a case of Darier's disease in a man aged 25. It occurred to him that since the chief pathologic change is a follicular dyskeratosis, the disease might possibly be due to vitamin A deficiency. He therefore tried the effect of large doses of this vitamin and obtained considerable clinical improvement.
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In 1938 Peck 1 studied a case of Darier's disease in a man aged 25. It occurred to him that since the chief pathologic change is a follicular dyskeratosis, the disease might possibly be due to vitamin A deficiency. He therefore tried the effect of large doses of this vitamin and obtained considerable clinical improvement.
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Unilateral Keratosis Follicularis
Archives of Dermatology, 1977To the Editor.— Keratosis follicularis (Darier's disease) usually presents as a symmetrical eruption of keratotic, often greasy, follicular and perifollicular papules. Sites of predilection are the chest, upper back, extremities, scalp, and inguinal area. It is thought to be transmitted as an autosomal dominant with incomplete penetrance.
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Unilateral keratosis follicularis.
Cutis, 1985Unilateral keratosis follicularis is considered a localized variant of Darier's disease and should be included in the differential diagnosis of zosteriform keratotic eruptions. The authors present a case report and review the treatment; topical retinoic acid appears to be the treatment of choice.
J A, Moore, R H, Schosser
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KERATOSIS FOLLICULARIS SINE DYSKERATOSIS
Archives of Dermatology and Syphilology, 1932Recently a patient was seen in consultation in the clinic with an eruption that appeared to fulfil clinically all the diagnostic criteria of keratosis follicularis (Darier). However, further study of the case, including microscopic examination of a biopsy specimen, proved my tentative diagnosis to be incorrect.
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Phase 3 Trials of Tirbanibulin Ointment for Actinic Keratosis
New England Journal of Medicine, 2021Andrew Blauvelt
exaly
Keratosis follicularis spinulosa decalvans.
European Journal of Pediatric Dermatology, 2018Keratosis follicularis spinulosa decalvans is a dominant X-linked hereditary disorder thus affecting less severely females, but it can be autosomal dominant or more often sporadic. Its boundaries with other forms of keratosis follicularis atrophicans are not clear and there is overlapping with other diseases included in the group of lichen planopilaris,
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