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Molecular and functional aspects of the hairless (hr) gene in laboratory rodents and humans.
Panteleyev AA, Paus R, Ahmad W, Sundberg JP, Christiano AM. Panteleyev AA, et al. Exp Dermatol. 1998 Oct;7(5):249-67. doi: 10.1111/j.1600-0625.1998.tb00295.x-i1. Exp Dermatol. 1998. PMID: 9832313 Review.
Multiple familial cutaneous glomangioma: a pedigree of 4 generations and critical analysis of histologic and genetic differences of glomus tumors.
Blume-Peytavi U, Adler YD, Geilen CC, Ahmad W, Christiano A, Goerdt S, Orfanos CE. Blume-Peytavi U, et al. J Am Acad Dermatol. 2000 Apr;42(4):633-9. J Am Acad Dermatol. 2000. PMID: 10727310
Progressive symmetrical erythrokeratoderma: report of a Turkish family and evaluation for loricrin and connexin gene mutations.
Akman A, Masse M, Mihci E, Richard G, Christiano AM, Balle BJ, Ciftcioglu MA, Alpsoy E. Akman A, et al. Clin Exp Dermatol. 2008 Aug;33(5):582-4. doi: 10.1111/j.1365-2230.2008.02728.x. Epub 2008 May 7. Clin Exp Dermatol. 2008. PMID: 18462442
Novel compound heterozygous mutations in the desmoplakin gene cause hair shaft abnormalities and culminate in lethal cardiomyopathy.
Yesudian PD, Cabral RM, Ladusans E, Spinty S, Gibbs J, Fryer A, Christiano AM, Mendelsohn SS. Yesudian PD, et al. Clin Exp Dermatol. 2014 Jun;39(4):506-8. doi: 10.1111/ced.12329. Clin Exp Dermatol. 2014. PMID: 24825141
A novel mutation in the 12(R)-lipoxygenase (ALOX12B) gene underlies nonbullous congenital ichthyosiform erythroderma.
Ashoor G, Massé M, García Luciano LM, Sheffer R, Martinez-Mir A, Christiano AM, Zlotogorski A. Ashoor G, et al. Br J Dermatol. 2006 Jul;155(1):198-200. doi: 10.1111/j.1365-2133.2006.07188.x. Br J Dermatol. 2006. PMID: 16792775 No abstract available.
Identification of mutations in the COL7A1 gene in a proband with mild recessive dystrophic epidermolysis bullosa and aortic insufficiency.
Horev L, Waran Lalin T, Martinez-Mir A, Bagheri BA, Tadin-Strapps M, Schneiderman PI, Grossman ME, Bickers DR, Christiano AM. Horev L, et al. Clin Exp Dermatol. 2003 Jan;28(1):80-4. doi: 10.1046/j.1365-2230.2003.01190.x. Clin Exp Dermatol. 2003. PMID: 12558638
Novel mutation in the human hairless gene once more erroneously diagnosed and treated as 'alopecia areata'.
Roelandt T, Kraemer L, Van Neste D, Lissens W, Roseeuw D, Christiano AM, Hachem JP. Roelandt T, et al. Br J Dermatol. 2008 Apr;158(4):834-5. doi: 10.1111/j.1365-2133.2007.08413.x. Epub 2008 Jan 30. Br J Dermatol. 2008. PMID: 18241276 No abstract available.
A recurrent splice-site mutation in the human hairless gene underlies congenital atrichia in Irish families.
O'Regan GM, Zurada J, Martinez-Mir A, Christiano AM, Irvine AD. O'Regan GM, et al. Br J Dermatol. 2007 Apr;156(4):744-7. doi: 10.1111/j.1365-2133.2006.07742.x. Epub 2007 Jan 30. Br J Dermatol. 2007. PMID: 17263802 No abstract available.
Clinical and molecular diagnostic criteria of congenital atrichia with papular lesions.
Zlotogorski A, Panteleyev AA, Aita VM, Christiano AM. Zlotogorski A, et al. J Invest Dermatol. 2001 Dec;117(6):1662-5. doi: 10.1046/j.0022-202x.2001.01618.x. J Invest Dermatol. 2001. PMID: 11886538
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