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Year Number of Results
2000 1
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2013 2
2015 1
2019 1
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2023 1
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11 results

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Inherited skin disorders presenting with poikiloderma.
Rayinda T, van Steensel M, Danarti R. Rayinda T, et al. Int J Dermatol. 2021 Nov;60(11):1343-1353. doi: 10.1111/ijd.15498. Epub 2021 Mar 19. Int J Dermatol. 2021. PMID: 33739439 Review.
Prompt diagnosis at the time of presentation could help to prevent complications and mitigate the course of the disease. This review discusses these to help the practicing clinician manage patients presenting with the symptom. ...
Prompt diagnosis at the time of presentation could help to prevent complications and mitigate the course of the disease. This review …
The roles of cytokines in photoaging.
Kondo S. Kondo S. J Dermatol Sci. 2000 Mar;23 Suppl 1:S30-6. doi: 10.1016/s0923-1811(99)00076-6. J Dermatol Sci. 2000. PMID: 10764989 Review.
However, cytokines are the major orchestrators of the host defense processes and are involved in response to exogenous and endogenous insults, and repair and restore homeostasis. Therefore, cytokines may be beneficial in the course of photoaging. Considering the complex cy …
However, cytokines are the major orchestrators of the host defense processes and are involved in response to exogenous and endogenous insult …
Mandibuloacral dysplasia type A in childhood.
Garavelli L, D'Apice MR, Rivieri F, Bertoli M, Wischmeijer A, Gelmini C, De Nigris V, Albertini E, Rosato S, Virdis R, Bacchini E, Dal Zotto R, Banchini G, Iughetti L, Bernasconi S, Superti-Furga A, Novelli G. Garavelli L, et al. Am J Med Genet A. 2009 Oct;149A(10):2258-64. doi: 10.1002/ajmg.a.33005. Am J Med Genet A. 2009. PMID: 19764019
Mandibuloacral dysplasia type A (MADA) is characterized by growth retardation, postnatal onset of craniofacial anomalies with mandibular hypoplasia, progressive acral osteolysis, and skin changes including mottled pigmentation, skin atrophy, and lipodystrophy. Owing to its slowly …
Mandibuloacral dysplasia type A (MADA) is characterized by growth retardation, postnatal onset of craniofacial anomalies with mandibular hyp …
Safety and efficacy of a novel multimodality hydroquinone-free skin brightener over six months.
Bruce S. Bruce S. J Drugs Dermatol. 2013 Mar;12(3):S27-31. J Drugs Dermatol. 2013. PMID: 23545930 Clinical Trial.
METHODS: Subjects were instructed to apply skin brightening complex to the entire face twice daily and to follow a standard skin care regimen (facial cleanser, moisturizer, and sunscreen) during the course of the study. The study was conducted over a 12-week period and con …
METHODS: Subjects were instructed to apply skin brightening complex to the entire face twice daily and to follow a standard skin care regime …
A novel mutation and large size polymorphism affecting the V2 domain of keratin 1 in an African-American family with severe, diffuse palmoplantar keratoderma of the ichthyosis hystrix Curth-Macklin type.
Richardson ES, Lee JB, Hyde PH, Richard G. Richardson ES, et al. J Invest Dermatol. 2006 Jan;126(1):79-84. doi: 10.1038/sj.jid.5700025. J Invest Dermatol. 2006. PMID: 16417221 Free article.
We have studied a family with severe, diffuse, nonepidermolytic PPK and verrucous hyperkeratotic plaques over the joints and in flexures and identified a new KRT1 gene mutation that is predicted to completely alter the K1 tail domain. In addition, a new K1 size polymorphis …
We have studied a family with severe, diffuse, nonepidermolytic PPK and verrucous hyperkeratotic plaques over the joints and in flexures and …
11 results