BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

316 related articles for article (PubMed ID: 2662909)

  • 1. Autosomal recessive epidermolysis bullosa simplex. Generalized phenotypic features suggestive of junctional or dystrophic epidermolysis bullosa, and association with neuromuscular diseases.
    Fine JD; Stenn J; Johnson L; Wright T; Bock HG; Horiguchi Y
    Arch Dermatol; 1989 Jul; 125(7):931-8. PubMed ID: 2662909
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Generalized atrophic benign epidermolysis bullosa.
    Hintner H; Wolff K
    Arch Dermatol; 1982 Jun; 118(6):375-84. PubMed ID: 7092249
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Epidermolysis bullosa simplex: identification of a kindred with autosomal recessive transmission of the Weber-Cockayne variety.
    Fine JD; Johnson L; Wright T; Horiguchi Y
    Pediatr Dermatol; 1989 Mar; 6(1):1-5. PubMed ID: 2539587
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Epidermolysis bullosa simplex associated with muscular dystrophy with recessive inheritance.
    Niemi KM; Sommer H; Kero M; Kanerva L; Haltia M
    Arch Dermatol; 1988 Apr; 124(4):551-4. PubMed ID: 3355199
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Epidermolysis bullosa with late-onset muscular dystrophy and plectin deficiency.
    Yiu EM; Klausegger A; Waddell LB; Grasern N; Lloyd L; Tran K; North KN; Bauer JW; McKelvie P; Chow CW; Ryan MM; Murrell DF
    Muscle Nerve; 2011 Jul; 44(1):135-41. PubMed ID: 21674528
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 19-DEJ-1, a hemidesmosome-anchoring filament complex-associated monoclonal antibody. Definition of a new skin basement membrane antigenic defect in junctional and dystrophic epidermolysis bullosa.
    Fine JD; Horiguchi Y; Couchman JR
    Arch Dermatol; 1989 Apr; 125(4):520-3. PubMed ID: 2649012
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Epidermolysis bullosa simplex associated with muscular dystrophy: a new case.
    Patrizi A; Di Lernia V; Neri I; Badiali De Giorgi L; Masi M
    Pediatr Dermatol; 1994 Dec; 11(4):342-5. PubMed ID: 7899187
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [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]  

  • 9. Ophthalmologic Approach in Epidermolysis Bullosa: A Cross-Sectional Study With Phenotype-Genotype Correlations.
    Mellado F; Fuentes I; Palisson F; I Vergara J; Kantor A
    Cornea; 2018 Apr; 37(4):442-447. PubMed ID: 29384803
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Evaluation and treatment of the newborn with epidermolysis bullosa.
    Gonzalez ME
    Semin Perinatol; 2013 Feb; 37(1):32-9. PubMed ID: 23419761
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The eye in epidermolysis bullosa.
    Tong L; Hodgkins PR; Denyer J; Brosnahan D; Harper J; Russell-Eggitt I; Taylor DS; Atherton D
    Br J Ophthalmol; 1999 Mar; 83(3):323-6. PubMed ID: 10365041
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Oral soft tissues in hereditary epidermolysis bullosa.
    Wright JT; Fine JD; Johnson LB
    Oral Surg Oral Med Oral Pathol; 1991 Apr; 71(4):440-6. PubMed ID: 2052329
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Inherited epidermolysis bullosa: new diagnostic criteria and classification.
    Intong LR; Murrell DF
    Clin Dermatol; 2012; 30(1):70-7. PubMed ID: 22137229
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Congenital muscular dystrophy and epidermolysis bullosa simplex.
    Kletter G; Evans OB; Lee JA; Melvin B; Yates AB; Bock HG
    J Pediatr; 1989 Jan; 114(1):104-7. PubMed ID: 2909695
    [No Abstract]   [Full Text] [Related]  

  • 15. Genetic abnormalities and clinical classification of epidermolysis bullosa.
    Mitsuhashi Y; Hashimoto I
    Arch Dermatol Res; 2003 Apr; 295 Suppl 1():S29-33. PubMed ID: 12677430
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Dystrophic epidermolysis bullosa.
    Burkhart CG; Ruppert ES
    Clin Pediatr (Phila); 1981 Aug; 20(8):493-6. PubMed ID: 7249491
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Using immunofluorescence (antigen) mapping in the diagnosis and classification of epidermolysis bullosa: a first report from Iran.
    Barzegar M; Asadi-Kani Z; Mozafari N; Vahidnezhad H; Kariminejad A; Toossi P
    Int J Dermatol; 2015 Oct; 54(10):e416-23. PubMed ID: 26220012
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Oral health status in patients with inherited epidermolysis bullosa: a comparative multicenter study.
    Joseph C; Marty M; Dridi SM; Verhaeghe V; Bailleul-Forestier I; Chiaverini C; Hubiche T; Mazereeuw-Hautier J; Deny O; Declerck D; Kémoun P
    Quintessence Int; 2023 Jan; 54(1):34-43. PubMed ID: 36268944
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The generalized atrophic benign form of junctional epidermolysis bullosa. Experience with four patients in the United States.
    Paller AS; Fine JD; Kaplan S; Pearson RW
    Arch Dermatol; 1986 Jun; 122(6):704-10. PubMed ID: 3521495
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Epidermolysis bullosa simplex generalisata: importance of immunofluorescence studies in early diagnosis.
    Baker H
    Arch Dermatol Res; 1982; 272(3-4):393-9. PubMed ID: 6762155
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.