142 related articles for article (PubMed ID: 24117545)
1. Bullous dermolysis of the newborn: four new cases and clinical review.
Radkevich-Brown O; Shwayder T
Pediatr Dermatol; 2013; 30(6):736-40. PubMed ID: 24117545
[TBL] [Abstract][Full Text] [Related]
2. Autosomal dominant bullous dermolysis of the newborn associated with a heterozygous missense mutation p.G1673R in type VII collagen.
Frew J; Lim SW; Klausseger A; Chow CW; Tran K; Su J; Orchard D; Varigos G; Sawamura D; Nishie W; Shimizu H; Murrell DF
Australas J Dermatol; 2011 Nov; 52(4):e1-4. PubMed ID: 22070715
[TBL] [Abstract][Full Text] [Related]
3. Transient bullous dermolysis of the newborn in three generations.
Fassihi H; Diba VC; Wessagowit V; Dopping-Hepenstal PJ; Jones CA; Burrows NP; McGrath JA
Br J Dermatol; 2005 Nov; 153(5):1058-63. PubMed ID: 16225626
[TBL] [Abstract][Full Text] [Related]
4. Bullous dermolysis of the newborn and dystrophic epidermolysis bullosa pruriginosa within the same family: two phenotypes associated with a COL7A1 mutation.
Murase K; Kanoh H; Ishii N; Hashimoto T; Nakano H; Sawamura D; Seishima M
Acta Derm Venereol; 2011 Oct; 91(6):730-1. PubMed ID: 21629976
[No Abstract] [Full Text] [Related]
5. Intraepidermal Type VII Collagen by Immunofluorescence Mapping: A Specific Finding for Bullous Dermolysis of the Newborn.
Heinecke G; Marinkovich MP; Rieger KE
Pediatr Dermatol; 2017 May; 34(3):308-314. PubMed ID: 28523885
[TBL] [Abstract][Full Text] [Related]
6. Recessive bullous dermolysis of the newborn in preterm siblings with a missense mutation in type VII collagen.
Boccaletti V; Zambruno G; Castiglia D; Magnani C; Tognetti E; Fabrizi G; Cortelazzi C; Pagliarello C; Di Nuzzo S
Pediatr Dermatol; 2015; 32(2):e42-7. PubMed ID: 25639640
[TBL] [Abstract][Full Text] [Related]
7. Three new cases of transient bullous dermolysis of the newborn.
Hanson SG; Fine JD; Levy ML
J Am Acad Dermatol; 1999 Mar; 40(3):471-6. PubMed ID: 10071321
[TBL] [Abstract][Full Text] [Related]
8. A novel glycine mutation in the COL7A1 gene leading to dominant dystrophic epidermolysis bullosa with intra-familial phenotypical heterogeneity.
Riedl E; Klausegger A; Bauer JW; Foedinger D; Kittler H
Pediatr Dermatol; 2009; 26(1):115-7. PubMed ID: 19250433
[TBL] [Abstract][Full Text] [Related]
9. Transient bullous dermolysis of the newborn: a novel de novo mutation in the COL7A1 gene.
Shi BJ; Zhu XJ; Liu Y; Hao J; Yan GF; Wang SP; Wang XY; Diao QC
Int J Dermatol; 2015 Apr; 54(4):438-42. PubMed ID: 25800346
[TBL] [Abstract][Full Text] [Related]
10. A novel pathogenic mutation in the COL7A1 gene resulting in mild autosomal dominant bullous dermolysis of the newborn.
Lor M; Liu M; Kuklinski LF; Hogeling M
Pediatr Dermatol; 2020 Sep; 37(5):955-957. PubMed ID: 32542816
[TBL] [Abstract][Full Text] [Related]
11. A Japanese family with dominant pretibial dystrophic epidermolysis bullosa: Identification of a new glycine substitution in the triple-helical collagenous domain of type VII collagen.
Hamada T; Fukuda S; Ishii N; Abe T; Nagata K; Koro O; Hatano Y; Nakano H; Sawamura D; Hashimoto T
J Dermatol Sci; 2009 Jun; 54(3):212-4. PubMed ID: 19269793
[No Abstract] [Full Text] [Related]
12. Novel COL7A1 mutation in a family with bullous dermolysis of the newborn: Phenotypic variability associated with a COL7A1 mutation within the same family.
Takashima S; Shinkuma S; Fujita Y; Natsuga K; Nomura T; Hida T; Ishikawa S; Nakamura H; Abe R; Shimizu H
J Dermatol; 2018 Sep; 45(9):e260-e261. PubMed ID: 29574987
[No Abstract] [Full Text] [Related]
13. Review of collagen VII sequence variants found in Australasian patients with dystrophic epidermolysis bullosa reveals nine novel COL7A1 variants.
Dang N; Klingberg S; Marr P; Murrell DF
J Dermatol Sci; 2007 Jun; 46(3):169-78. PubMed ID: 17425959
[TBL] [Abstract][Full Text] [Related]
14. Two cases of recessive dystrophic epidermolysis bullosa diagnosed as severe generalized.
Ohashi M; Shu E; Nagai M; Murase K; Nakano H; Tamai K; Sawamura D; Hiroka T; Seishima M; Kitajima Y; Aoyama Y
J Dermatol; 2011 Sep; 38(9):893-9. PubMed ID: 21658117
[TBL] [Abstract][Full Text] [Related]
15. A case of recessive dystrophic epidermolysis bullosa caused by compound heterozygous mutations in the COL7A1 gene.
Suzuki S; Shimomura Y; Yamamoto Y; Kariya N; Shibuya M; Ito M; Fujiwara H
Br J Dermatol; 2006 Oct; 155(4):838-40. PubMed ID: 16965439
[No Abstract] [Full Text] [Related]
16. First report of COL7A1 mutations in two patients with recessive dystrophic epidermolysis bullosa from Peru.
Saeidian AH; Youssefian L; Rosales-Solis GM; Vahidnezhad H; Atanasova VS; Uitto J; South AP; Salas-Alanis JC
Clin Exp Dermatol; 2018 Aug; 43(6):719-722. PubMed ID: 29427316
[No Abstract] [Full Text] [Related]
17. Mild dystrophic epidermolysis bullosa associated with homozygous gene mutation c.6216+5G>T in type VII collagen ultrastructurally suggestive of the decreased number of anchoring fibrils.
Komori T; Dainichi T; Otsuka A; Nakano H; Sawamura D; Ishida-Yamamoto A; Kabashima K
J Dermatol; 2018 Nov; 45(11):e305-e306. PubMed ID: 29696689
[No Abstract] [Full Text] [Related]
18. Revertant mosaicism in recessive dystrophic epidermolysis bullosa.
Almaani N; Nagy N; Liu L; Dopping-Hepenstal PJ; Lai-Cheong JE; Clements SE; Techanukul T; Tanaka A; Mellerio JE; McGrath JA
J Invest Dermatol; 2010 Jul; 130(7):1937-40. PubMed ID: 20357813
[No Abstract] [Full Text] [Related]
19. Immunohistochemical, ultrastructural, and molecular features of Kindler syndrome distinguish it from dystrophic epidermolysis bullosa.
Shimizu H; Sato M; Ban M; Kitajima Y; Ishizaki S; Harada T; Bruckner-Tuderman L; Fine JD; Burgeson R; Kon A; McGrath JA; Christiano AM; Uitto J; Nishikawa T
Arch Dermatol; 1997 Sep; 133(9):1111-7. PubMed ID: 9301588
[TBL] [Abstract][Full Text] [Related]
20. Scanning electron microscopy of a blister roof in dystrophic epidermolysis bullosa.
Almeida HL; Monteiro L; Marques e Silva R; Rocha NM; Scheffer H
An Bras Dermatol; 2013; 88(6):966-8. PubMed ID: 24474107
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
