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Journal Abstract Search

398 related items for PubMed ID: 20447504

  • 1. Gene therapy for recessive dystrophic epidermolysis bullosa.
    Titeux M, Pendaries V, Hovnanian A.
    Dermatol Clin; 2010 Apr; 28(2):361-6, xii. PubMed ID: 20447504
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  • 2. Mild recessive dystrophic epidermolysis bullosa associated with two compound heterozygous COL7A1 mutations.
    von Bartenwerffer W, Has C, Arin MJ, Tantcheva-Poór I, Kreuter A, Kremer K, Arshah T, Hoffmann M, Eming SA, Kohlhase J, Krieg T, Bruckner-Tuderman L, Hartmann K.
    Eur J Dermatol; 2011 Apr; 21(2):170-2. PubMed ID: 21382783
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  • 3. Mutation analysis and characterization of COL7A1 mutations in dystrophic epidermolysis bullosa.
    Dang N, Murrell DF.
    Exp Dermatol; 2008 Jul; 17(7):553-68. PubMed ID: 18558993
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  • 4. Dystrophic epidermolysis bullosa with one dominant and one recessive mutation of the COL7A1 gene in a child with deafness.
    Weinel S, Lucky AW, Uitto J, Pfendner EG, Choo D.
    Pediatr Dermatol; 2008 Jul; 25(2):210-4. PubMed ID: 18429782
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  • 5. Restoration of type VII collagen expression and function in dystrophic epidermolysis bullosa.
    Chen M, Kasahara N, Keene DR, Chan L, Hoeffler WK, Finlay D, Barcova M, Cannon PM, Mazurek C, Woodley DT.
    Nat Genet; 2002 Dec; 32(4):670-5. PubMed ID: 12426566
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  • 8. Gene therapy: pursuing restoration of dermal adhesion in recessive dystrophic epidermolysis bullosa.
    Cutlar L, Greiser U, Wang W.
    Exp Dermatol; 2014 Jan; 23(1):1-6. PubMed ID: 24107073
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  • 14. Stable nonviral genetic correction of inherited human skin disease.
    Ortiz-Urda S, Thyagarajan B, Keene DR, Lin Q, Fang M, Calos MP, Khavari PA.
    Nat Med; 2002 Oct; 8(10):1166-70. PubMed ID: 12244305
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  • 15. Long-term follow-up of patients with recessive dystrophic epidermolysis bullosa in the Netherlands: expansion of the mutation database and unusual phenotype-genotype correlations.
    van den Akker PC, van Essen AJ, Kraak MM, Meijer R, Nijenhuis M, Meijer G, Hofstra RM, Pas HH, Scheffer H, Jonkman MF.
    J Dermatol Sci; 2009 Oct; 56(1):9-18. PubMed ID: 19665875
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  • 16. X-linked ichthyosis along with recessive dystrophic epidermolysis bullosa in the same patient.
    Hernández-Martín A, Cuadrado-Corrales N, Ciria-Abad S, Arias-Palomo D, Mascaró-Galy JM, Escámez MJ, García M, Del Río M, Torrelo A, González-Sarmiento R.
    Dermatology; 2010 Oct; 221(2):113-6. PubMed ID: 20523032
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  • 18. Denuded congenital lesions: recessive dystrophic epidermolysis bullosa.
    Fleming KF, Wu JJ, Dyson SW, Dadras SS, Metz BJ.
    Dermatol Online J; 2009 Apr 15; 15(4):4. PubMed ID: 19450397
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  • 20. Compound heterozygosity in sibling patients with recessive dystrophic epidermolysis bullosa associated with a mild phenotype.
    Shibusawa Y, Negishi I, Ishikawa O.
    Int J Dermatol; 2006 Mar 15; 45(3):302-5. PubMed ID: 16533235
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