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 *

115 related articles for article (PubMed ID: 2498140)

  • 41. HLA antigens and dominant dystrophic epidermolysis bullosa in a family study.
    Ozawa A; Matsuo I; Niizuma K; Ohkido M; Nose Y; Tsuji K
    Tissue Antigens; 1978 Sep; 12(3):233-5. PubMed ID: 83022
    [No Abstract]   [Full Text] [Related]  

  • 42. Squamous cell carcinoma complicating recessive dystrophic epidermolysis bullosa-Hallopeau-Siemens: a report of four cases.
    Dammak A; Zribi J; Boudaya S; Mseddi M; Meziou TJ; Masmoudi A; Ellouze Z; Keskes H; Turki H
    Int J Dermatol; 2009 Jun; 48(6):588-91. PubMed ID: 19538366
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Gastrointestinal manifestations in the Hallopeau-Siemens variant of recessive dystrophic epidermolysis bullosa.
    Wong WL; Entwisle K; Pemberton J
    Br J Radiol; 1993 Sep; 66(789):788-93. PubMed ID: 8220949
    [TBL] [Abstract][Full Text] [Related]  

  • 44. [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]  

  • 45. Verruciform xanthoma. Occurrence in eroded skin in a patient with recessive dystrophic epidermolysis bullosa.
    Cooper TW; Santa Cruz DJ; Bauer EA
    J Am Acad Dermatol; 1983 Apr; 8(4):463-7. PubMed ID: 6853779
    [TBL] [Abstract][Full Text] [Related]  

  • 46. [Syndromes 13. Epidermolysis bullosa].
    Meijndert L; Jonkman MF
    Ned Tijdschr Tandheelkd; 1999 Aug; 106(8):302-5. PubMed ID: 11930425
    [TBL] [Abstract][Full Text] [Related]  

  • 47. The largest family of the Americas with dominant dystrophic epidermolysis bullosa pruriginosa: a 18-year longitudinal genotype-phenotype study.
    Fortuna G; Di Lorenzo M; Cepeda-Valdes R; Garcia-Garcia C; Salas-Alanis JC
    J Dermatol Sci; 2013 Sep; 71(3):217-21. PubMed ID: 23688405
    [No Abstract]   [Full Text] [Related]  

  • 48. Occurrence of hereditary nephritis, pretibial epidermolysis bullosa and beta-thalassemia minor in two siblings with end-stage renal disease.
    Kagan A; Feld S; Chemke J; Bar-Khayim Y
    Nephron; 1988; 49(4):331-2. PubMed ID: 3412548
    [No Abstract]   [Full Text] [Related]  

  • 49. Therapeutic efficacy of phenytoin in recessive dystrophic epidermolysis. A comparison of short- and long-term treatment.
    Cooper TW; Bauer EA
    Arch Dermatol; 1984 Apr; 120(4):490-5. PubMed ID: 6703753
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Premature termination codons in the type VII collagen gene (COL7A1) underlie severe, mutilating recessive dystrophic epidermolysis bullosa.
    Christiano AM; Anhalt G; Gibbons S; Bauer EA; Uitto J
    Genomics; 1994 May; 21(1):160-8. PubMed ID: 8088783
    [TBL] [Abstract][Full Text] [Related]  

  • 51. 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]  

  • 52. Phenytoin therapy of recessive dystrophic epidermolysis bullosa. Clinical trial and proposed mechanism of action on collagenase.
    Bauer EA; Cooper TW; Tucker DR; Esterly NB
    N Engl J Med; 1980 Oct; 303(14):776-81. PubMed ID: 6251365
    [TBL] [Abstract][Full Text] [Related]  

  • 53. [A case of dystrophic hereditary bullous epidermolysis].
    Ciesielska M
    Czas Stomatol; 1984 Apr; 37(4):297-305. PubMed ID: 6597080
    [No Abstract]   [Full Text] [Related]  

  • 54. Evidence for a functional defect of the lamina lucida in recessive dystrophic epidermolysis bullosa demonstrated by suction blisters.
    Tidman MJ; Eady RA
    Br J Dermatol; 1984 Oct; 111(4):379-87. PubMed ID: 6487542
    [TBL] [Abstract][Full Text] [Related]  

  • 55. The clinical spectrum of dystrophic epidermolysis bullosa.
    Horn HM; Tidman MJ
    Br J Dermatol; 2002 Feb; 146(2):267-74. PubMed ID: 11903238
    [TBL] [Abstract][Full Text] [Related]  

  • 56. [Gastrointestinal manifestations of recessive dystrophic epidermolysis bullosa].
    Michel-Aceves R; Ramírez-Mayans JA; Casaubón-Garcín P; Rivera-Echegoyen M; Antonieta Mora M
    Bol Med Hosp Infant Mex; 1990 Jan; 47(1):20-5. PubMed ID: 2186753
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Anchoring fibrils and type VII collagen are absent from skin in severe recessive dystrophic epidermolysis bullosa.
    Bruckner-Tuderman L; Mitsuhashi Y; Schnyder UW; Bruckner P
    J Invest Dermatol; 1989 Jul; 93(1):3-9. PubMed ID: 2746005
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Interfering factors in the assay of plasminogen activators by the fibrin plate method. Occurrence of different inhibitors against tissue plasminogen activator and urokinase.
    Wijngaards G
    Thromb Haemost; 1979 May; 41(3):590-600. PubMed ID: 111368
    [TBL] [Abstract][Full Text] [Related]  

  • 59. 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]  

  • 60. Recessive dystrophic epidermolysis bullosa. Evidence for increased collagenase as a genetic characteristic in cell culture.
    Bauer EA; Eisen AZ
    J Exp Med; 1978 Nov; 148(5):1378-87. PubMed ID: 214508
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.