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dystrophic epidermolysis bullosa相关文献:
Epidermolysis Bullosa: Pediatric Perspectives.
Hon KL, Chu S, Leung AKC.
Curr Pediatr Rev. 2022;18(3):182-190. doi: 10.2174/1573396317666210525161252.
PMID:34036913
In vivo topical gene therapy for recessive dystrophic epidermolysis bullosa: a phase 1 and 2 trial.
Gurevich I, Agarwal P, Zhang P, Dolorito JA, Oliver S, Liu H, Reitze N, Sarma N, Bagci IS, Sridhar K, Kakarla V, Yenamandra VK, O'Malley M, Prisco M, Tufa SF, Keene DR, South AP, Krishnan SM, Marinkovich MP.
Nat Med. 2022 Apr;28(4):780-788. doi: 10.1038/s41591-022-01737-y. Epub 2022 Mar 28.
PMID:35347281
Herpes simplex virus gene therapy for dystrophic epidermolysis bullosa (DEB).
Epstein AL, Haag-Molkenteller C.
Cell. 2023 Aug 17;186(17):3523-3523.e1. doi: 10.1016/j.cell.2023.07.031.
PMID:37595560
Practical considerations relevant to treatment with the gene therapy beremagene geperpavec-svdt for dystrophic epidermolysis bullosa.
Paller AS, Guide SV, Ayala D, Gonzalez ME, Lucky AW, Bagci IS, Marinkovich MP.
J Dermatolog Treat. 2024 Dec;35(1):2350232. doi: 10.1080/09546634.2024.2350232. Epub 2024 May 9.
PMID:38724041
Dystrophic Epidermolysis Bullosa Inversa - Case Report and Review of the Literature.
Merzel Šabović EK, Luzar B, Wechtersbach K, Dolenc-Voljč M.
Acta Dermatovenerol Croat. 2022 Nov;30(3):151-156.
PMID:36812272
Dystrophic epidermolysis bullosa: from disease biology to biologic therapy.
Samuelov L.
Br J Dermatol. 2024 Jul 16;191(2):159-160. doi: 10.1093/bjd/ljae182.
PMID:38680069
Dystrophic Epidermolysis Bullosa.
Yadav RS, Jayswal A, Shrestha S, Gupta SK, Paudel U.
JNMA J Nepal Med Assoc. 2018 Sep-Oct;56(213):879-882. doi: 10.31729/jnma.3791.
PMID:31065125
Dystrophic epidermolysis bullosa - From biochemistry to interventions.
Nyström A.
Matrix Biol. 2025 Apr;136:111-126. doi: 10.1016/j.matbio.2025.02.001. Epub 2025 Feb 6.
PMID:39922469
Recessive Dystrophic Epidermolysis Bullosa: Advances in the Laboratory Leading to New Therapies.
Woodley DT, Chen M.
J Invest Dermatol. 2015 Jul;135(7):1705-1707. doi: 10.1038/jid.2015.149.
PMID:26066885
Identical glycine substitution mutations in type VII collagen may underlie both dominant and recessive forms of dystrophic epidermolysis bullosa.
Almaani N, Liu L, Dopping-Hepenstal PJ, Lai-Cheong JE, Wong A, Nanda A, Moss C, Martinéz AE, Mellerio JE, McGrath JA.
Acta Derm Venereol. 2011 May;91(3):262-6. doi: 10.2340/00015555-1053.
PMID:21448560
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