Report of the 13th Annual International Pachyonychia Congenita Consortium Symposium
dc.contributor.author | Rittié, L. | |
dc.contributor.author | Kaspar, R.L. | |
dc.contributor.author | Sprecher, E. | |
dc.contributor.author | Smith, F.J.D. | |
dc.date.accessioned | 2017-06-16T20:16:50Z | |
dc.date.available | 2018-07-09T17:42:25Z | en |
dc.date.issued | 2017-05 | |
dc.identifier.citation | Rittié, L. ; Kaspar, R.L.; Sprecher, E.; Smith, F.J.D. (2017). "Report of the 13th Annual International Pachyonychia Congenita Consortium Symposium." British Journal of Dermatology 176(5): 1144-1147. | |
dc.identifier.issn | 0007-0963 | |
dc.identifier.issn | 1365-2133 | |
dc.identifier.uri | https://hdl.handle.net/2027.42/137611 | |
dc.publisher | Wiley Periodicals, Inc. | |
dc.title | Report of the 13th Annual International Pachyonychia Congenita Consortium Symposium | |
dc.type | Article | en_US |
dc.rights.robots | IndexNoFollow | |
dc.subject.hlbsecondlevel | Dermatology | |
dc.subject.hlbtoplevel | Health Sciences | |
dc.description.peerreviewed | Peer Reviewed | |
dc.description.bitstreamurl | https://deepblue.lib.umich.edu/bitstream/2027.42/137611/1/bjd15417.pdf | |
dc.description.bitstreamurl | https://deepblue.lib.umich.edu/bitstream/2027.42/137611/2/bjd15417_am.pdf | |
dc.identifier.doi | 10.1111/bjd.15417 | |
dc.identifier.source | British Journal of Dermatology | |
dc.identifier.citedreference | Eliason MJ, Leachman SA, Feng BJ et al. A review of the clinical phenotype of 254 patients with genetically confirmed pachyonychia congenita. J Am Acad Dermatol 2012; 67: 680 – 6. | |
dc.identifier.citedreference | McLean WH, Hansen CD, Eliason MJ et al. The phenotypic and molecular genetic features of pachyonychia congenita. J Invest Dermatol 2011; 131: 1015 – 17. | |
dc.identifier.citedreference | Wilson NJ, O’Toole EA, Milstone LM et al. The molecular genetic analysis of the expanding pachyonychia congenita case collection. Br J Dermatol 2014; 171: 343 – 55. | |
dc.identifier.citedreference | Kerns ML, Hakim JM, Lu RG et al. Oxidative stress and dysfunctional NRF2 underlie pachyonychia congenita phenotypes. J Clin Invest 2016; 126: 2356 – 66. | |
dc.identifier.citedreference | Lu CP, Polak L, Rocha AS et al. Identification of stem cell populations in sweat glands and ducts reveals roles in homeostasis and wound repair. Cell 2012; 150: 136 – 50. | |
dc.identifier.citedreference | Wallis T, Poole CD, Hoggart B. Can skin disease cause neuropathic pain? A study in pachyonychia congenita. Clin Exp Dermatol 2016; 41: 26 – 33. | |
dc.identifier.citedreference | Shinkuma S, Guo Z, Christiano AM. Site‐specific genome editing for correction of induced pluripotent stem cells derived from dominant dystrophic epidermolysis bullosa. Proc Natl Acad Sci USA 2016; 113: 5676 – 81. | |
dc.identifier.citedreference | Guedes AG, Morisseau C, Sole A et al. Use of a soluble epoxide hydrolase inhibitor as an adjunctive analgesic in a horse with laminitis. Vet Anaesth Analg 2013; 40: 440 – 8. | |
dc.identifier.citedreference | Duverger O, Ohara T, Shaffer JR et al. Hair keratin mutations in tooth enamel increase dental decay risk. J Clin Invest 2014; 124: 5219 – 24. | |
dc.identifier.citedreference | Gonzalez‐Ramos J, Sendagorta‐Cudos E, Gonzalez‐Lopez G et al. Efficacy of botulinum toxin in pachyonychia congenita type 1: report of two new cases. Dermatol Ther 2016; 29: 32 – 6. | |
dc.identifier.citedreference | Swartling C, Vahlquist A. Treatment of pachyonychia congenita with plantar injections of botulinum toxin. Br J Dermatol 2006; 154: 763 – 5. | |
dc.identifier.citedreference | Swartling C, Karlqvist M, Hymnelius K et al. Botulinum toxin in the treatment of sweat‐worsened foot problems in patients with epidermolysis bullosa simplex and pachyonychia congenita. Br J Dermatol 2010; 163: 1072 – 6. | |
dc.identifier.citedreference | Tariq S, Schmitz ML, Kanjia MK. Chronic foot pain due to pachyonychia congenita in a pediatric patient: a successful management strategy. A A Case Rep 2016; 6: 305 – 7. | |
dc.identifier.citedreference | Bunick CG, Milstone LM. The x‐ray crystal structure of the keratin 1–keratin 10 helix 2B heterodimer reveals molecular surface properties and biochemical insights into human skin disease. J Invest Dermatol 2017; 137: 142 – 50. | |
dc.identifier.citedreference | Pan B, Byrnes K, Schwartz M et al. Peripheral neuropathic changes in pachyonychia congenita. Pain 2016; 157: 2843 – 53. | |
dc.owningcollname | Interdisciplinary and Peer-Reviewed |
Files in this item
Remediation of Harmful Language
The University of Michigan Library aims to describe library materials in a way that respects the people and communities who create, use, and are represented in our collections. Report harmful or offensive language in catalog records, finding aids, or elsewhere in our collections anonymously through our metadata feedback form. More information at Remediation of Harmful Language.
Accessibility
If you are unable to use this file in its current format, please select the Contact Us link and we can modify it to make it more accessible to you.