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Year Number of Results
2002 2
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2006 4
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2009 3
2010 10
2011 7
2012 2
2013 4
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2016 5
2017 4
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2019 10
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90 results

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Page 1
Broadening the PHIP-Associated Neurodevelopmental Phenotype.
Pascolini G, Scaglione GL, Chandramouli B, Castiglia D, Di Zenzo G, Didona B. Pascolini G, et al. Among authors: castiglia d. Children (Basel). 2024 Nov 17;11(11):1395. doi: 10.3390/children11111395. Children (Basel). 2024. PMID: 39594970 Free PMC article.
Mutation mechanisms.
Castiglia D, Zambruno G. Castiglia D, et al. Dermatol Clin. 2010 Jan;28(1):17-22. doi: 10.1016/j.det.2009.10.002. Dermatol Clin. 2010. PMID: 19945612 Review.
Histone deacetylase inhibition mitigates fibrosis-driven disease progression in recessive dystrophic epidermolysis bullosa.
Primerano A, De Domenico E, Cianfarani F, De Luca N, Floriddia G, Teson M, Cristofoletti C, Cardarelli S, Scaglione GL, Baldini E, Cangelosi D, Uva P, Reinoso Sánchez JF, Roubaty C, Dengjel J, Nyström A, Mastroeni S, Ulisse S, Castiglia D, Odorisio T. Primerano A, et al. Among authors: castiglia d. Br J Dermatol. 2024 Sep 18;191(4):568-579. doi: 10.1093/bjd/ljae225. Br J Dermatol. 2024. PMID: 38820176
Epidermolysis bullosa care in Italy.
Castiglia D, Zambruno G. Castiglia D, et al. Dermatol Clin. 2010 Apr;28(2):407-9, xiv-xv. doi: 10.1016/j.det.2010.02.016. Dermatol Clin. 2010. PMID: 20447515 Review.
Ichthyosis with confetti: clinics, molecular genetics and management.
Guerra L, Diociaiuti A, El Hachem M, Castiglia D, Zambruno G. Guerra L, et al. Among authors: castiglia d. Orphanet J Rare Dis. 2015 Sep 17;10:115. doi: 10.1186/s13023-015-0336-4. Orphanet J Rare Dis. 2015. PMID: 26381864 Free PMC article. Review.
Gamma-Secretase Inhibitors Downregulate the Profibrotic NOTCH Signaling Pathway in Recessive Dystrophic Epidermolysis Bullosa.
Condorelli AG, Nobili R, Muglia A, Scarpelli G, Marzuolo E, De Stefanis C, Rota R, Diociaiuti A, Alaggio R, Castiglia D, Odorisio T, El Hachem M, Zambruno G. Condorelli AG, et al. Among authors: castiglia d. J Invest Dermatol. 2024 Jul;144(7):1522-1533.e10. doi: 10.1016/j.jid.2023.10.045. Epub 2024 Jan 17. J Invest Dermatol. 2024. PMID: 38237731
Kindler syndrome: extension of FERMT1 mutational spectrum and natural history.
Has C, Castiglia D, del Rio M, Diez MG, Piccinni E, Kiritsi D, Kohlhase J, Itin P, Martin L, Fischer J, Zambruno G, Bruckner-Tuderman L. Has C, et al. Among authors: castiglia d. Hum Mutat. 2011 Nov;32(11):1204-12. doi: 10.1002/humu.21576. Epub 2011 Sep 20. Hum Mutat. 2011. PMID: 21936020 Review.
90 results