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dominant dystrophic epidennoly-sis 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
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
Epidermolysis bullosa. II. Type VII collagen mutations and phenotype-genotype correlations in the dystrophic subtypes.
Varki R, Sadowski S, Uitto J, Pfendner E.
J Med Genet. 2007 Mar;44(3):181-92. doi: 10.1136/jmg.2006.045302. Epub 2006 Sep 13.
PMID:16971478
Epidermolysis Bullosa.
Khanna D, Bardhan A.
2024 Jan 11. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan–.
PMID:38261681
Beremagene Geperpavec: First Approval.
Dhillon S.
Drugs. 2023 Aug;83(12):1131-1135. doi: 10.1007/s40265-023-01921-5.
PMID:37432558
Genotype and phenotype correlations in 441 patients with epidermolysis bullosa from China.
Chen F, Wei R, Deng D, Zhang X, Cao Y, Pan C, Wang Y, Cao Q, Wang J, Zeng M, Huang L, Gu Y, Yao Z, Li M.
J Eur Acad Dermatol Venereol. 2023 Feb;37(2):411-419. doi: 10.1111/jdv.18692. Epub 2022 Nov 5.
PMID:36287101
Dominant dystrophic epidermolysis bullosa is associated with glycolytically active GATA3+ T helper 2 cells which may contribute to pruritus in lesional skin.
Aala WJF, Hou PC, Hong YK, Lin YC, Lee YR, Tu WT, Papanikolaou M, Benzian-Olsson N, Onoufriadis A, I Chen Harn H, Hwang DY, Cheng SM, Lu K, Chen PC, McGrath JA, Hsu CK.
Br J Dermatol. 2024 Jul 16;191(2):252-260. doi: 10.1093/bjd/ljae110.
PMID:38477474
Dystrophic Epidermolysis Bullosa.
Lucky AW, Pope E, Crawford S.
2006 Aug 21 [updated 2025 May 8]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025.
PMID:20301481
Dominant Dystrophic Epidermolysis Bullosa with a Mutation in COL7A1 Confirmed by Diagnostic Exome Sequencing.
Won SH, Bae KN, Son JH, Shin K, Kim HS, Ko HC, Kim BS, Kim MB.
Chonnam Med J. 2022 Jan;58(1):66-67. doi: 10.4068/cmj.2022.58.1.66. Epub 2022 Jan 25.
PMID:35169569
Epidermolysis Bullosa Acquisita Develops in Dominant Dystrophic Epidermolysis Bullosa.
Hayashi R, Natsuga K, Watanabe M, Iwata H, Shinkuma S, Ito A, Masui Y, Ito M, Shimomura Y.
J Invest Dermatol. 2016 Jan;136(1):320-3. doi: 10.1038/JID.2015.370.
PMID:26763454
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