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Year Number of Results
1988 1
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2006 2
2008 1
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2013 1
2014 2
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2017 4
2018 6
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2020 2
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2023 5
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39 results

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Page 1
Clopidogrel and Aspirin in Acute Ischemic Stroke and High-Risk TIA.
Johnston SC, Easton JD, Farrant M, Barsan W, Conwit RA, Elm JJ, Kim AS, Lindblad AS, Palesch YY; Clinical Research Collaboration, Neurological Emergencies Treatment Trials Network, and the POINT Investigators. Johnston SC, et al. N Engl J Med. 2018 Jul 19;379(3):215-225. doi: 10.1056/NEJMoa1800410. Epub 2018 May 16. N Engl J Med. 2018. PMID: 29766750 Free PMC article. Clinical Trial.
Refractory Hailey-Hailey disease cleared with upadacitinib.
Murphy L, Ch'en P, Song EJ. Murphy L, et al. JAAD Case Rep. 2023 Sep 27;41:64-67. doi: 10.1016/j.jdcr.2023.09.011. eCollection 2023 Nov. JAAD Case Rep. 2023. PMID: 37869368 Free PMC article. No abstract available.
Human embryonic stem cell-derived cardiomyocytes restore function in infarcted hearts of non-human primates.
Liu YW, Chen B, Yang X, Fugate JA, Kalucki FA, Futakuchi-Tsuchida A, Couture L, Vogel KW, Astley CA, Baldessari A, Ogle J, Don CW, Steinberg ZL, Seslar SP, Tuck SA, Tsuchida H, Naumova AV, Dupras SK, Lyu MS, Lee J, Hailey DW, Reinecke H, Pabon L, Fryer BH, MacLellan WR, Thies RS, Murry CE. Liu YW, et al. Nat Biotechnol. 2018 Aug;36(7):597-605. doi: 10.1038/nbt.4162. Epub 2018 Jul 2. Nat Biotechnol. 2018. PMID: 29969440 Free PMC article.
Dupilumab in the treatment of genodermatosis: A systematic review.
Wu PC, Dai YX, Li CL, Chen CC, Chang YT, Ma SH. Wu PC, et al. J Dtsch Dermatol Ges. 2023 Jan;21(1):7-17. doi: 10.1111/ddg.14924. Epub 2023 Jan 19. J Dtsch Dermatol Ges. 2023. PMID: 36657040 Review.
The assessed genodermatoses included Netherton syndrome, epidermolysis bullosa pruriginosa, hyper-IgE syndrome, Hailey-Hailey disease, and severe eczema associated with genetic disorders. ...In conclusion, Dupilumab may have a potential therapeutic role in certain g …
The assessed genodermatoses included Netherton syndrome, epidermolysis bullosa pruriginosa, hyper-IgE syndrome, Hailey-Hailey …
A novel splice-site mutation in the ATP2C1 gene of a Chinese family with Hailey-Hailey disease.
Xiao H, Huang X, Xu H, Chen X, Xiong W, Yang Z, Deng X, He Z, Deng H. Xiao H, et al. J Cell Biochem. 2019 Mar;120(3):3630-3636. doi: 10.1002/jcb.27640. Epub 2018 Sep 11. J Cell Biochem. 2019. PMID: 30654607
Hailey-Hailey disease (HHD), also known as familial benign chronic pemphigus, is an autosomal dominant genodermatosis. ...
Hailey-Hailey disease (HHD), also known as familial benign chronic pemphigus, is an autosomal dominant genodermatosis. ...
Variable Response to Naltrexone in Patients With Hailey-Hailey Disease.
Cao S, Lilly E, Chen ST. Cao S, et al. JAMA Dermatol. 2018 Mar 1;154(3):362-363. doi: 10.1001/jamadermatol.2017.5463. JAMA Dermatol. 2018. PMID: 29344611 Free PMC article.
This case series presents 3 cases of patients with Hailey-Hailey disease demonstrating varying responses to naltrexone....
This case series presents 3 cases of patients with Hailey-Hailey disease demonstrating varying responses to naltrexone....
INFLUENCE OF HEALTH TECHNOLOGY ASSESSMENT AND ITS MEASUREMENT.
Hailey D, Werkö S, Rosén M, Macpherson K, Myles S, Gallegos Rivero V, Hipólito-Olivares C, Sihvo S, Pwu J, Yang WW, Chen YC, Perez Galán A, Aleman A, Villamil E. Hailey D, et al. Int J Technol Assess Health Care. 2016 Jan;32(6):376-384. doi: 10.1017/S0266462316000611. Int J Technol Assess Health Care. 2016. PMID: 28124969 Review.
Cryo-EM structures of human SPCA1a reveal the mechanism of Ca2+/Mn2+ transport into the Golgi apparatus.
Chen Z, Watanabe S, Hashida H, Inoue M, Daigaku Y, Kikkawa M, Inaba K. Chen Z, et al. Sci Adv. 2023 Mar 3;9(9):eadd9742. doi: 10.1126/sciadv.add9742. Epub 2023 Mar 3. Sci Adv. 2023. PMID: 36867705 Free PMC article.
Detrimental mutations of the ATP2C1 gene encoding SPCA1 cause Hailey-Hailey disease. Here, using nanobody/megabody technologies, we determined cryo-electron microscopy structures of human SPCA1a in the ATP and Ca(2+)/Mn(2+)-bound (E1-ATP) state and the metal-free ph …
Detrimental mutations of the ATP2C1 gene encoding SPCA1 cause Hailey-Hailey disease. Here, using nanobody/megabody technologie …
39 results