BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

48 related articles for article (PubMed ID: 15283804)

  • 1. New clinical classification of stiff skin syndrome.
    Zhao Q; Chu Z; Li L; Feng C; Zhou H; Hu J; Zhao L; Che D; Zhang X; Peng B; Han Y; Geng S
    Arch Dermatol Res; 2024 Jun; 316(6):333. PubMed ID: 38844593
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Pro-Fibrotic Phenotype in a Patient with Segmental Stiff Skin Syndrome via TGF-β Signaling Overactivation.
    Fusco C; Nardella G; Augello B; Boccafoschi F; Palumbo O; Fusaro L; Notarangelo A; Barbano R; Parrella P; Annicchiarico G; De Meco C; Micale L; Graziano P; Castori M
    Int J Mol Sci; 2020 Jul; 21(14):. PubMed ID: 32698527
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Atypical presentation of scleroderma in infancy.
    Mishra N; Shrestha D; Poudyal RB; Shiva Raj KC
    Rheumatol Int; 2012 Apr; 32(4):1069-74. PubMed ID: 21327434
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mutations in fibrillin-1 cause congenital scleroderma: stiff skin syndrome.
    Loeys BL; Gerber EE; Riegert-Johnson D; Iqbal S; Whiteman P; McConnell V; Chillakuri CR; Macaya D; Coucke PJ; De Paepe A; Judge DP; Wigley F; Davis EC; Mardon HJ; Handford P; Keene DR; Sakai LY; Dietz HC
    Sci Transl Med; 2010 Mar; 2(23):23ra20. PubMed ID: 20375004
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Stiff skin syndrome versus scleroderma: a report of two cases.
    Azevedo VF; Serafini SZ; Werner B; Müller CS; Franchini CF; Morais RL
    Clin Rheumatol; 2009 Sep; 28(9):1107-11. PubMed ID: 19415378
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Familial inherited abnormalities: miscellaneous disorders.
    Candy DC; Howard FM; McNeish AS
    Clin Gastroenterol; 1982 Jan; 11(1):207-29. PubMed ID: 7037238
    [No Abstract]   [Full Text] [Related]  

  • 7. Familial epidermodysplasia verruciformis of Lewandowsky and Lutz.
    Rajagopalan K; Bahru J; Loo DS; Tay CH; Chin KN; Tan KK
    Arch Dermatol; 1972 Jan; 105(1):73-8. PubMed ID: 5009624
    [No Abstract]   [Full Text] [Related]  

  • 8. Systemic hyalinosis or fibromatosis hyalinica multiplex juvenilis as a congenital syndrome. A new entity based on the inborn error of the acid mucopolysaccharide metabolism in connective tissue cells?
    Ishikawa H; Mori S
    Acta Derm Venereol; 1973; 53(3):185-91. PubMed ID: 4124008
    [No Abstract]   [Full Text] [Related]  

  • 9. Congenital fascial dystrophy: the stiff skin syndrome.
    Helm TN; Wirth PB; Helm KF
    Cutis; 1997 Sep; 60(3):153-4. PubMed ID: 9314621
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Sebocystomatosis with congenital pachyonychia.
    Velasquez JP; Bustamante J
    Int J Dermatol; 1972; 11(2):77-81. PubMed ID: 5067395
    [No Abstract]   [Full Text] [Related]  

  • 11. Stiff skin syndrome is highly heterogeneous, and congenital fascial dystrophy is its distinct subset.
    Jablonska S; Blaszczyk M
    Pediatr Dermatol; 2004; 21(4):508-10. PubMed ID: 15283804
    [No Abstract]   [Full Text] [Related]  

  • 12. Congenital and genetic skin disorders with tumor formation.
    Reed WB; Boder E; Gardner M
    Birth Defects Orig Artic Ser; 1974; 10(4):265-84. PubMed ID: 4620305
    [TBL] [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.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 3.