Below are the most recent publications written about "Pigmentation Disorders" by people in Profiles.
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De Antonis C, Hyde JT, Lee JB, Hsu S. An unusual presentation of pigmented purpuric lichenoid dermatitis. Dermatol Online J. 2023 Oct 15; 29(5).
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Colucciello M. ACUTE RETINAL PIGMENT EPITHELIITIS: ASSOCIATION WITH ACUTE COXSACKIE A VIRUS INFECTION. Retin Cases Brief Rep. 2023 Sep 01; 17(5):504-506.
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Vempuluru VS, Laiton A, Milman T, Lee JB, Eagle RC, Shields CL. Exogenous Ochronosis With Ocular Involvement From Chronic Use of Teavigo. Ophthalmic Plast Reconstr Surg. 2023 Sep-Oct 01; 39(5):e139-e142.
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Saffarian Z, Samii R, Hadizadeh A, Ghanadan A, Vahidnezhad H. Purpuric dermatosis and lymphocytic vasculopathy following SARS-CoV-2 vaccination: Report of two patients. Dermatol Ther. 2022 11; 35(11):e15898.
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Dagnewu KY, Ayele A, Liu L, Pramanik R, Onoufriadis A, Abebe E, McGrath JA. Griscelli syndrome type 3 in Ethiopian sisters resulting from a homozygous missense mutation in MLPH. Int J Dermatol. 2020 Mar; 59(3):e55-e57.
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Camp DA, Lally SE, Shields CL. Heterochromia following intravitreal chemotherapy in two cases. J AAPOS. 2019 08; 23(4):241-243.
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Saleem MD, Oussedik E, Schoch JJ, Berger AC, Picardo M. Acquired disorders with depigmentation: A systematic approach to vitiliginoid conditions. J Am Acad Dermatol. 2019 May; 80(5):1215-1231.e6.
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Sahu S, Gochoco A, Santa E, Sahu J. An Unusual Presentation of Subungual Pigmentation: Cotton Sock Debris Mimicking Subungual Hemorrhage With Concern for Subungual Melanoma. Dermatol Surg. 2017 05; 43(5):753-755.
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Lee JYW, Eldeeb MS, Hsu CK, Saito R, Abouzeid SA, McGrath JA. Further evidence for genotype-phenotype disparity in Griscelli syndrome. Br J Dermatol. 2017 04; 176(4):1086-1089.
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Lee JYW, Hsu CK, Michael M, Nanda A, Liu L, McMillan JR, Pourreyron C, Takeichi T, Tolar J, Reid E, Hayday T, Blumen SC, Abu-Mouch S, Straussberg R, Basel-Vanagaite L, Barhum Y, Zouabi Y, Al-Ajmi H, Huang HY, Lin TC, Akiyama M, Lee JYY, McLean WHI, Simpson MA, Parsons M, McGrath JA. Large Intragenic Deletion in DSTYK Underlies Autosomal-Recessive Complicated Spastic Paraparesis, SPG23. Am J Hum Genet. 2017 Feb 02; 100(2):364-370.