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 *

162 related articles for article (PubMed ID: 6374321)

  • 21. Three homozygous PTC mutations in the collagen type VII gene of patients affected by recessive dystrophic epidermolysis bullosa: analysis of transcript levels in dermal fibroblasts.
    Gardella R; Zoppi N; Ferraboli S; Marini D; Tadini G; Barlati S; Colombi M
    Hum Mutat; 1999; 13(6):439-52. PubMed ID: 10408773
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Therapeutic considerations in recessive dystrophic epidermolysis bullosa.
    Bauer EA; Cooper TW
    Arch Dermatol; 1981 Sep; 117(9):529-30. PubMed ID: 6271076
    [No Abstract]   [Full Text] [Related]  

  • 23. [Course observations in 3 siblings with epidermolysis bullosa hereditaria dystrophica (Hallopeau-Siemens)].
    Schirren C; Grässner H; Grässner K
    Z Hautkr; 1975 Mar; 50(5):183-92. PubMed ID: 1229228
    [No Abstract]   [Full Text] [Related]  

  • 24. Lethal epidermolytic epidermolysis bullosa: a new autosomal recessive type of epidermolysis bullosa.
    Salih MA; Lake BD; el Hag MA; Atherton DJ
    Br J Dermatol; 1985 Aug; 113(2):135-43. PubMed ID: 4027181
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Efficacy of systemic phenytoin in the treatment of junctional epidermolysis bullosa.
    Fine JD; Johnson L
    Arch Dermatol; 1988 Sep; 124(9):1402-6. PubMed ID: 3415285
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Compound heterozygosity for a nonsense mutation and a splice site mutation in the type VII collagen gene (COL7A1) in recessive dystrophic epidermolysis bullosa.
    Tamai K; Ishida-Yamamoto A; Matsuo S; Iizuka H; Hashimoto I; Christiano AM; Uitto J; McGrath JA
    Lab Invest; 1997 Feb; 76(2):209-17. PubMed ID: 9042157
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Acantholytic epidermolysis bullosa.
    Hoffman MD; Fleming MG; Pearson RW
    Arch Dermatol; 1995 May; 131(5):586-9. PubMed ID: 7741547
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Epidermolysis bullosa simplex localisata associated with anodontia, hair and nail disorders: a new syndrome.
    Gamborg Nielsen P; Sjölund E
    Acta Derm Venereol; 1985; 65(6):526-30. PubMed ID: 2420118
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Epidermolysis bullosa of the newborn].
    Quiroga Cantú M; Ortíz Jalomo R; Hinojosa Garza S
    Bol Med Hosp Infant Mex; 1979; 36(5):863-70. PubMed ID: 465188
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [A case of recessive dystrophic epidermolysis bullosa with a vegetative variant].
    Pincelli C; Zucchi M; Girolomoni G; Bertazzoni MG
    G Ital Dermatol Venereol; 1985; 120(2):125-9. PubMed ID: 4007953
    [No Abstract]   [Full Text] [Related]  

  • 31. Epidermolysis bullosa pruriginosa: a rare presentation with asymptomatic lesions.
    Ghosh S; Chaudhuri S; Jain VK
    Indian J Dermatol Venereol Leprol; 2013; 79(2):235-7. PubMed ID: 23442465
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Pseudosyndactyly and musculoskeletal contractures in inherited epidermolysis bullosa: experience of the National Epidermolysis Bullosa Registry, 1986-2002.
    Fine JD; Johnson LB; Weiner M; Stein A; Cash S; Deleoz J; Devries DT; Suchindran C
    J Hand Surg Br; 2005 Feb; 30(1):14-22. PubMed ID: 15620486
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Bullous scabies in hereditary dystrophic epidermolysis bullosa].
    Ponce-Navárez E; Przybilla B
    Hautarzt; 1981 Feb; 32(2):96-7. PubMed ID: 7228670
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Studies on two siblings with recessive dystrophic epidermolysis bullosa (Hallopeau-Siemens) and the plasminogen activator and its inhibitor in the lesion.
    Kaneko F; Tsukinaga I; Ando M; Ohkawara A; Oguchi H; Oikawa K; Nagai M
    Dermatologica; 1989; 178(3):156-63. PubMed ID: 2498140
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Epidermolysis bullosa letalis in two brothers.
    Esterly NB; Hruby MA
    Birth Defects Orig Artic Ser; 1974; 10(10):154-7. PubMed ID: 4462628
    [No Abstract]   [Full Text] [Related]  

  • 36. Cause-specific risks of childhood death in inherited epidermolysis bullosa.
    Fine JD; Johnson LB; Weiner M; Suchindran C
    J Pediatr; 2008 Feb; 152(2):276-80. PubMed ID: 18206702
    [TBL] [Abstract][Full Text] [Related]  

  • 37. "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]  

  • 38. Epidermolysis bullosa: treatment with vitamin E, preliminary results.
    Degreef H; Flour M
    Arch Belg Dermatol; 1974; 30(2):83-7. PubMed ID: 4470373
    [No Abstract]   [Full Text] [Related]  

  • 39. 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]  

  • 40. [Study on COL7A1 gene mutation in a epidermolysis bullosa pruriginosa family].
    Chen X; Li G; Zhu X
    Zhonghua Yi Xue Za Zhi; 2000 Nov; 80(11):869-71. PubMed ID: 11218887
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.