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2001 1
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2010 1
2016 1
2019 1
2024 0

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Topical Retinoids: Therapeutic Mechanisms in the Treatment of Photodamaged Skin.
Riahi RR, Bush AE, Cohen PR. Riahi RR, et al. Am J Clin Dermatol. 2016 Jun;17(3):265-76. doi: 10.1007/s40257-016-0185-5. Am J Clin Dermatol. 2016. PMID: 26969582 Review.
Photodamage of the skin occurs as a consequence of cumulative exposure to solar ultraviolet radiation (UVR) and is characterized by deep wrinkles, easy bruising, inelasticity, mottled pigmentation, roughness, and telangiectasias. The mechanism of UVR-induced photoda …
Photodamage of the skin occurs as a consequence of cumulative exposure to solar ultraviolet radiation (UVR) and is characterized by deep wri …
Photoaging: pathogenesis, prevention, and treatment.
Kang S, Fisher GJ, Voorhees JJ. Kang S, et al. Clin Geriatr Med. 2001 Nov;17(4):643-59, v-vi. doi: 10.1016/s0749-0690(05)70091-4. Clin Geriatr Med. 2001. PMID: 11535421 Review.
Premature skin aging, or photoaging, results largely from repeated exposure to ultraviolet (UV) radiation from the sun. Photoaging is characterized clinically by wrinkles, mottled pigmentation, rough skin, and loss of skin tone; the major histologic alterations lie …
Premature skin aging, or photoaging, results largely from repeated exposure to ultraviolet (UV) radiation from the sun. Photoaging is charac …
Mandibuloacral dysplasia type B (MADB): a cohort of eight patients from Suriname with a homozygous founder mutation in ZMPSTE24 (FACE1), clinical diagnostic criteria and management guidelines.
Hitzert MM, van der Crabben SN, Baldewsingh G, van Amstel HKP, van den Wijngaard A, van Ravenswaaij-Arts CMA, Zijlmans CWR. Hitzert MM, et al. Orphanet J Rare Dis. 2019 Dec 19;14(1):294. doi: 10.1186/s13023-019-1269-0. Orphanet J Rare Dis. 2019. PMID: 31856865 Free PMC article.
BACKGROUND: Mandibuloacral Dysplasia with type B lipodystrophy (MADB) is a rare premature aging disorder with an autosomal recessive inheritance pattern. MADB is characterized by brittle hair, mottled, atrophic skin, generalized lipodystrophy, insulin resistance, metabolic …
BACKGROUND: Mandibuloacral Dysplasia with type B lipodystrophy (MADB) is a rare premature aging disorder with an autosomal recessive inherit …
Identification of novel and known KRT5 and KRT14 mutations in 53 patients with epidermolysis bullosa simplex: correlation between genotype and phenotype.
Arin MJ, Grimberg G, Schumann H, De Almeida H Jr, Chang YR, Tadini G, Kohlhase J, Krieg T, Bruckner-Tuderman L, Has C. Arin MJ, et al. Br J Dermatol. 2010 Jun;162(6):1365-9. doi: 10.1111/j.1365-2133.2010.09657.x. Epub 2010 Feb 25. Br J Dermatol. 2010. PMID: 20199538
Three novel deletion/insertion mutations, among them one in-frame duplication, were associated with the rare phenotype of EBS with mottled pigmentation. We identified for the first time a patient with compound heterozygosity for KRT5 mutations causing Dowling-Degos …
Three novel deletion/insertion mutations, among them one in-frame duplication, were associated with the rare phenotype of EBS with mottle …
Our approach to non-ablative treatment of photoaging.
Weiss RA, Weiss MA, Beasley KL, Munavalli G. Weiss RA, et al. Lasers Surg Med. 2005 Jul;37(1):2-8. doi: 10.1002/lsm.20199. Lasers Surg Med. 2005. PMID: 16035079
CONCLUSIONS: Significant improvement in the appearance of signs and symptoms of photoaging, including telangiectasias, mottled pigmentation, irregular surface texture, wrinkling and skin sagging can achieved by relatively non-invasive means....
CONCLUSIONS: Significant improvement in the appearance of signs and symptoms of photoaging, including telangiectasias, mottled pig …