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Dermatology (Basel, Switzerland)|May 19, 2006
Sodium thiosulphate as a promising therapeutic option to treat calciphylaxisM Meissner, R Bauer, C Beier, et al.
Skinmed|March 29, 2023
Identification of a Novel <i>PLCD1</i> Variant in a Danish Family with Hereditary LeukonychiaSofie Lieberoth, Sheetal Kumar, Klaus Brusgaard, et al.
Journal of Photochemistry and Photobiology. B, Biology|June 2, 2001
Fluorescence staining of oral cancer using a topical application of 5-aminolevulinic acid: fluorescence microscopic studiesA Leunig, M Mehlmann, C Betz, et al.
Indian Journal of Dermatology|October 7, 2014
The First Report of KRT5 Mutation Underlying Acantholytic Dowling-Degos Disease with Mottled Hypopigmentation in an Indian FamilyShyam Verma, Sandra M Pasternack, Arno Rütten, et al.
Pediatric Dermatology|September 11, 2013
Alopecia and hypotrichosis as characteristic findings in Woodhouse-Sakati syndrome: report of a family with mutation in the C2orf37 geneArti Nanda, Sandra M Pasternack, Hassnaa Mahmoudi, et al.
Journal of Dermatological Science|August 19, 2019
UV-sensitive syndrome: Whole exome sequencing identified a nonsense mutation in the gene UVSSA in two consanguineous pedigrees from PakistanAmbreen Ijaz, Sabrina Wolf, Safur Rehman Mandukhail, et al.
Plos One|June 27, 2015
A Novel Locus for Ectodermal Dysplasia of Hair, Nail and Skin Pigmentation Anomalies Maps to Chromosome 18p11.32-p11.31Rabia Habib, Muhammad Ansar, Manuel Mattheisen, et al.
Archives of Dermatology|March 23, 2011
Efficacy of ablative laser treatment in Galli-Galli diseaseHarald Voth, Jennifer Landsberg, Guenter Reinhard, et al.
Nanoscale|March 16, 2016
Dimensionality effects on the luminescence properties of hBNLéonard Schué, Bruno Berini, Andreas C Betz, et al.
Archives of Dermatological Research|June 17, 2009
Novel mutations in the P2RY5 gene in one Turkish and two Indian patients presenting with hypotrichosis and woolly hairSandra M Pasternack, Sundaram Murugusundram, Sibylle Eigelshoven, et al.
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