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.


PUBMED FOR HANDHELDS

Journal Abstract Search


312 related items for PubMed ID: 3355199

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4. [Incidence of hereditary dystrophic bullous epidermolysis and progressive muscular dystrophy in one family].
    de Weerdt CJ, Castelein S.
    Ned Tijdschr Geneeskd; 1972 Jul 22; 116(30):1264-8. PubMed ID: 5041295
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. [Epidermolysis bullosa dystrophica inversa: report on 2 sisters].
    Hashimoto I, Anton-Lamprecht I, Hofbauer M.
    Hautarzt; 1976 Nov 22; 27(11):532-7. PubMed ID: 1002472
    [Abstract] [Full Text] [Related]

  • 8. Epidermolysis bullosa in Finland. Clinical features, morphology and relation to collagen metabolism.
    Kero M.
    Acta Derm Venereol Suppl (Stockh); 1984 Nov 22; 110():1-51. PubMed ID: 6331034
    [Abstract] [Full Text] [Related]

  • 9. [Epidermolysis bullosa and congenital skin aplasia (Bart's syndrome). Report of 3 cases].
    Tincopa-Wong OW, Peláez-Gutiérrez R, Esparza-Urtecho W, Meléndez-Guevara G, Paoli-Razuri C, Sánchez-Aznarán N.
    Med Cutan Ibero Lat Am; 1988 Nov 22; 16(2):149-54. PubMed ID: 3050332
    [Abstract] [Full Text] [Related]

  • 10. 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 22; 125(7):931-8. PubMed ID: 2662909
    [Abstract] [Full Text] [Related]

  • 11. Novel compound heterozygous mutations in the plectin gene in epidermolysis bullosa with muscular dystrophy and the use of protein truncation test for detection of premature termination codon mutations.
    Dang M, Pulkkinen L, Smith FJ, McLean WH, Uitto J.
    Lab Invest; 1998 Feb 22; 78(2):195-204. PubMed ID: 9484717
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. [Dowling-Meara dominant epidermolysis bullosa. An intraepidermal epidermolysis bullosa which hides its prognosis well].
    Blanchet-Bardon C, Nazzaro V, Raynaud F, Hubert S, Mimoz C.
    Ann Dermatol Venereol; 1987 Feb 22; 114(3):341-8. PubMed ID: 3605965
    [Abstract] [Full Text] [Related]

  • 20. Epidermolysis bullosa hereditaria et albopapuloides (Pasini).
    Acta Derm Venereol; 1968 Feb 22; 48(4):373. PubMed ID: 4179051
    [No Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 16.