These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

136 related articles for article (PubMed ID: 22481662)

  • 21. Light and transmission electron microscopy of generalized dystrophic epidermolysis bullosa (Pasini's albopapuloid subtype).
    Almeida HL; Nudelmann L; Rocha NM; Castro LA
    An Bras Dermatol; 2012; 87(2):285-7. PubMed ID: 22570034
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. A case of epidermolysis bullosa hereditaria--dominant dystrophic type of Cockayne and Touraine.
    Yotsumoto S; Setoyama M; Hisadome H; Tashiro M; Murata F
    Dermatology; 1993; 186(3):201-4. PubMed ID: 8453148
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Esophageal stenosis in childhood: dystrophic epidermolysis bullosa without skin blistering due to collagen VII mutations.
    Zimmer KP; Schumann H; Mecklenbeck S; Bruckner-Tuderman L
    Gastroenterology; 2002 Jan; 122(1):220-5. PubMed ID: 11781296
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Splice site mutation in COL7A1 resulting in aberrant in-frame transcripts identified in a case of recessive dystrophic epidermolysis bullosa, pretibial.
    Masunaga T; Kubo A; Ishiko A
    J Dermatol; 2018 Jun; 45(6):742-745. PubMed ID: 29500833
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. The G2028R glycine substitution mutation in COL7A1 leads to marked inter-familiar clinical heterogeneity in dominant dystrophic epidermolysis bullosa.
    Nakamura H; Sawamura D; Goto M; Sato-Matsumura KC; LaDuca J; Lee JY; Masunaga T; Shimizu H
    J Dermatol Sci; 2004 May; 34(3):195-200. PubMed ID: 15113589
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Moderation of phenotypic severity in dystrophic and junctional forms of epidermolysis bullosa through in-frame skipping of exons containing non-sense or frameshift mutations.
    McGrath JA; Ashton GH; Mellerio JE; Salas-Alanis JC; Swensson O; McMillan JR; Eady RA
    J Invest Dermatol; 1999 Sep; 113(3):314-21. PubMed ID: 10469327
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Exon 87 skipping of the COL7A1 gene in dominant dystrophic epidermolysis bullosa.
    Koga H; Hamada T; Ishii N; Fukuda S; Sakaguchi S; Nakano H; Tamai K; Sawamura D; Hashimoto T
    J Dermatol; 2011 May; 38(5):489-92. PubMed ID: 21352278
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Multiple Milia as an Isolated Skin Manifestation of Dominant Dystrophic Epidermolysis Bullosa: Evidence of Phenotypic Variability.
    Akasaka E; Nakano H; Takagi Y; Toyomaki Y; Sawamura D
    Pediatr Dermatol; 2017 Mar; 34(2):e106-e108. PubMed ID: 28008652
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Premature termination codons on both alleles of the type VII collagen gene (COL7A1) in three brothers with recessive dystrophic epidermolysis bullosa.
    Christiano AM; Suga Y; Greenspan DS; Ogawa H; Uitto J
    J Clin Invest; 1995 Mar; 95(3):1328-34. PubMed ID: 7883979
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. A recurrent frameshift mutation in exon 19 of the type VII collagen gene (COL7A1) in Mexican patients with recessive dystrophic epidermolysis bullosa.
    Mellerio JE; Salas-Alanis JC; Amaya-Guerra M; Tamez E; Ashton GH; Mohammedi R; Eady RA; McGrath JA
    Exp Dermatol; 1999 Feb; 8(1):22-9. PubMed ID: 10206718
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Modulation of disease severity of dystrophic epidermolysis bullosa by a splice site mutation in combination with a missense mutation in the COL7A1 gene.
    Winberg JO; Hammami-Hauasli N; Nilssen O; Anton-Lamprecht I; Naylor SL; Kerbacher K; Zimmermann M; Krajci P; Gedde-Dahl T; Bruckner-Tuderman L
    Hum Mol Genet; 1997 Jul; 6(7):1125-35. PubMed ID: 9215684
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Pretibial dystrophic epidermolysis bullosa: a recessively inherited COL7A1 splice site mutation affecting procollagen VII processing.
    Betts CM; Posteraro P; Costa AM; Varotti C; Schubert M; Bruckner-Tuderman L; Castiglia D
    Br J Dermatol; 1999 Nov; 141(5):833-9. PubMed ID: 10583163
    [TBL] [Abstract][Full Text] [Related]  

  • 36. A scleroderma-like variant of recessive dystrophic epidermolysis bullosa?
    Ishikawa O; Warita S; Ohnishi K; Miyachi Y
    Br J Dermatol; 1993 Nov; 129(5):602-5. PubMed ID: 8251361
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Dystrophic epidermolysis bullosa inversa: a case report.
    Altomare GF; Polenghi M; Pigatto PD; Nazzaro V; Piattoni F
    Dermatologica; 1990; 181(2):145-8. PubMed ID: 2173667
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Late-onset pretibial recessive dystrophic epidermolysis bullosa.
    Mahto A; McGrath JA; Deroide F; Rustin MH
    Clin Exp Dermatol; 2013 Aug; 38(6):630-2. PubMed ID: 23786535
    [TBL] [Abstract][Full Text] [Related]  

  • 39. "Sporadic" dystrophic epidermolysis bullosa: a new dominant or mitis recessive mutation?
    Vaccaro M; Moretti G; Guarneri F; Cannavò S; Magaudda L
    Eur J Dermatol; 2000 Aug; 10(6):436-8. PubMed ID: 10980463
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Dystrophic epidermolysis bullosa phenotypes in a large consanguineous Tunisian family.
    Ouragini H; Cherif F; Kassar S; Floriddia G; Pascucci M; Daoud W; Osman-Dhahri AB; Boubaker S; Castiglia D; Abdelhak S
    J Dermatol Sci; 2009 May; 54(2):114-20. PubMed ID: 19261445
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.