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The Journal of Investigative Dermatology|January 1, 1994
Mutations in the rod 1A domain of keratins 1 and 10 in bullous congenital ichthyosiform erythroderma (BCIE)W H McLean, R A Eady, P J Dopping-Hepenstal, et al.Nature Genetics|September 7, 2001
Gene polymorphism in Netherton and common atopic diseaseA J Walley, S Chavanas, M F Moffatt, et al.European Journal of Pediatrics|May 30, 2015
Treatment of infantile haemangiomas: recommendations of a European expert groupPeter H Hoeger, John I Harper, Eulalia Baselga, et al.The British Journal of Dermatology|March 27, 2007
Keratitis-ichthyosis-deafness syndrome: disease expression and spectrum of connexin 26 (GJB2) mutations in 14 patientsJ Mazereeuw-Hautier, E Bitoun, J Chevrant-Breton, et al.Nature Genetics|June 3, 2000
Mutations in SPINK5, encoding a serine protease inhibitor, cause Netherton syndromeS Chavanas, C Bodemer, A Rochat, et al.The Journal of Investigative Dermatology|February 14, 2002
Netherton syndrome: disease expression and spectrum of SPINK5 mutations in 21 familiesEmmanuelle Bitoun, Stéphane Chavanas, Alan D Irvine, et al.European Journal of Medical Genetics|March 2, 2011
A proposal for classification of entities combining vascular malformations and deregulated growthCharlène E U Oduber, Chantal M A M van der Horst, J Henk Sillevis Smitt, et al.The British Journal of Dermatology|May 8, 1999
Skin fragility and hypohidrotic ectodermal dysplasia resulting from ablation of plakophilin 1J A McGrath, P H Hoeger, A M Christiano, et al.Aging and Cancer|October 3, 2022
Another Wrinkle with Age: Aged Collagen and Intra-peritoneal Metastasis of Ovarian CancerElizabeth I Harper, Tyvette S Hilliard, Emma F Sheedy, et al.Journal of Experimental & Clinical Cancer Research : CR|July 12, 2023
Host obesity alters the ovarian tumor immune microenvironment and impacts response to standard of care chemotherapyYueying Liu, Jing Yang, Tyvette S Hilliard, et al.Pageof 38