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 *

116 related articles for article (PubMed ID: 7574841)

  • 1. Congenital absence of skin and blistering in a neonate. Bart's syndrome and mandibulofacial dysostosis.
    Martin RW; Myers T; Shehata BM; Zemtsov A; Olson JL
    Arch Dermatol; 1995 Oct; 131(10):1197, 1200. PubMed ID: 7574841
    [No Abstract]   [Full Text] [Related]  

  • 2. [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; 16(2):149-54. PubMed ID: 3050332
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Do you know this syndrome? Bart's syndrome].
    Almeida NA; Serafini F; Marchiori J; Moro JG
    An Bras Dermatol; 2010; 85(1):119-21. PubMed ID: 20464103
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Congenital localized skin defect and epidermolysis bullosa hereditaria letalis.
    Skoven I; Drzewiecki KT
    Acta Derm Venereol; 1979; 59(6):533-7. PubMed ID: 94215
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Congenital localized absence of skin associated with blistering of the skin and mucous membranes: Bart's syndrome.
    Gharpuray MB; Tolat SN; Patki AH
    Cutis; 1989 Oct; 44(4):318-20. PubMed ID: 2805808
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Congenital transient mechanobullous dermatosis (Bart's syndrome). A clinical case and review of the literature].
    Patrizi A; Pauluzzi P; Dalla Casa P; Badiali De Giorgi L
    G Ital Dermatol Venereol; 1989 Oct; 124(10):447-50. PubMed ID: 2635690
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Dystrophic epidermolysis bullosa presenting with congenital localized absence of skin: report of four cases.
    Wojnarowska FT; Eady RA; Wells RS
    Br J Dermatol; 1983 Apr; 108(4):477-83. PubMed ID: 6838774
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Bart's syndrome associated with pyloric and choanal atresia.
    Narter F; Büyükbabani N; Yararlı H; Oztürk S; Ergüven M
    Turk J Pediatr; 2013; 55(2):214-7. PubMed ID: 24192685
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Congenital localized absence of the skin as a manifestation of epidermolysis bullosa.
    Kanzler MH; Smoller B; Woodley DT
    Arch Dermatol; 1992 Aug; 128(8):1087-90. PubMed ID: 1497364
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Bart's syndrome.
    Amichai B; Metzker A
    Int J Dermatol; 1994 Mar; 33(3):161-3. PubMed ID: 8169011
    [No Abstract]   [Full Text] [Related]  

  • 11. Bart's syndrome. Ultrastructure and genetic linkage.
    Zelickson B; Matsumura K; Kist D; Epstein EH; Bart BJ
    Arch Dermatol; 1995 Jun; 131(6):663-8. PubMed ID: 7778916
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Bart's Syndrome].
    Sich J; Hradecká V; Kokotková A; Danda J
    Cesk Dermatol; 1982 Jun; 57(3):170-4. PubMed ID: 7116474
    [No Abstract]   [Full Text] [Related]  

  • 13. Bart's syndrome: a mechanobullous disease of the newborn. Report of five cases and review.
    Sirota L; Dulitzky F; Metzker A
    Clin Pediatr (Phila); 1986 May; 25(5):252-4. PubMed ID: 3698444
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Bart's syndrome: report of a case.
    Carson KS
    Cutis; 1984 Oct; 34(4):410-2. PubMed ID: 6488896
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Epidermolysis bullosa dystrophica Bart (Bart syndrome)].
    Voss M
    Hautarzt; 1985 Jun; 36(6):351-3. PubMed ID: 4019188
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Bart's syndrome: microscopic, ultrastructural, and immunofluorescent mapping features.
    Butler DF; Berger TG; James WD; Smith TL; Stanely JR; Rodman OG
    Pediatr Dermatol; 1986 Feb; 3(2):113-8. PubMed ID: 3513144
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Dominant dystrophic epidermolysis bullosa with localized congenital absence of the skin. A case with an ultrastructure study].
    Nazzaro V; Blanchet-Bardon C; Deroubaix P; Mimoz C; Puissant A
    Ann Dermatol Venereol; 1986; 113(8):697-700. PubMed ID: 3800221
    [No Abstract]   [Full Text] [Related]  

  • 18. Bart syndrome with associated anomalies.
    Bart BJ; Lussky RC
    Am J Perinatol; 2005 Oct; 22(7):365-9. PubMed ID: 16215923
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A mechanobullous disease of the newborn. Bart's syndrome.
    Smith SZ; Cram DL
    Arch Dermatol; 1978 Jan; 114(1):81-4. PubMed ID: 339847
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Familial epidermolysis bullosa with aplasia cutis congenita: Bart's syndrome?
    Benvenuto C; Kraemer CK; Kruse RL; Cestari TF
    Skinmed; 2003; 2(5):319-21. PubMed ID: 14673268
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.