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 *

161 related articles for article (PubMed ID: 12220272)

  • 1. Cole disease: hypopigmentation with punctate keratosis of the palms and soles.
    Vignale R; Yusín A; Panuncio A; Abulafia J; Reyno Z; Vaglio A
    Pediatr Dermatol; 2002; 19(4):302-6. PubMed ID: 12220272
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Hypopigmentation with punctate keratosis of the palms and soles.
    Cole LA
    Arch Dermatol; 1976 Jul; 112(7):998-100. PubMed ID: 132904
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Cole disease: guttate hypopigmentation and punctate palmoplantar keratoderma.
    Moore MM; Orlow SJ; Kamino H; Wang N; Schaffer JV
    Arch Dermatol; 2009 Apr; 145(4):495-7. PubMed ID: 19380683
    [No Abstract]   [Full Text] [Related]  

  • 4. ENPP1 Mutation Causes Recessive Cole Disease by Altering Melanogenesis.
    Chourabi M; Liew MS; Lim S; H'mida-Ben Brahim D; Boussofara L; Dai L; Wong PM; Foo JN; Sriha B; Robinson KS; Denil S; Common JE; Mamaï O; Ben Khalifa Y; Bollen M; Liu J; Denguezli M; Bonnard C; Saad A; Reversade B
    J Invest Dermatol; 2018 Feb; 138(2):291-300. PubMed ID: 28964717
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Hyper- and hypopigmented macules over palms and soles since birth--a case of dyschromatosis symmetrica hereditaria.
    Hemmati I; Lam J
    Dermatol Online J; 2009 Nov; 15(11):5. PubMed ID: 19951641
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Palmoplantar hyperkeratoses and hypopigmentation. Cole disease.
    Schmieder A; Hausser I; Schneider SW; Goerdt S; Peitsch WK
    Acta Derm Venereol; 2011 Oct; 91(6):737-8. PubMed ID: 21597676
    [No Abstract]   [Full Text] [Related]  

  • 7. A new variant of punctate acrokeratoderma associated with a pigmentary disorder.
    Satoh T; Yokozeki H; Katayama I; Nishioka K
    Br J Dermatol; 1993 Jun; 128(6):693-5. PubMed ID: 8338755
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Cole disease: a case report and literature review.
    Kim JM; Cho HH; Ko HC
    J Eur Acad Dermatol Venereol; 2015 Dec; 29(12):2492-3. PubMed ID: 25065726
    [No Abstract]   [Full Text] [Related]  

  • 9. Punctate hyperkeratosis of the palms and soles. An ultrastructural study.
    Rubenstein DJ; Schwartz RA; Hansen RC; Payne CM
    J Am Acad Dermatol; 1980 Jul; 3(1):43-9. PubMed ID: 6156960
    [TBL] [Abstract][Full Text] [Related]  

  • 10. X-linked dominant inheritance in palmoplantar keratoderma with leukokeratosis: a study of the pedigree of two cases.
    Sharma PK; Rath N; Chauhan R; Sharma SK; Kar HK
    J Dermatol; 2003 Nov; 30(11):816-21. PubMed ID: 14684940
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Comprehensive understanding of idiopathic guttate hypomelanosis: clinical and histopathological correlation.
    Kim SK; Kim EH; Kang HY; Lee ES; Sohn S; Kim YC
    Int J Dermatol; 2010 Feb; 49(2):162-6. PubMed ID: 20465639
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Hyperpigmentation in a Chinese family with autosomal dominant Cole disease.
    Li Z; Wang L; Wang S
    Exp Dermatol; 2022 Feb; 31(2):248-254. PubMed ID: 34297442
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Hereditary palmoplantar (epidermolytic) keratoderma: illustration through a familial report.
    Sehgal VN; Sardana K; Sharma S; Raut D
    Skinmed; 2004; 3(6):323-30; quiz 331-2. PubMed ID: 15538081
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Congenital hypopigmentation, hyperpigmentation, and punctate palmoplantar keratoderma.
    Nair N; Chang J; Evans MS
    Pediatr Dermatol; 2022 May; 39(3):476-477. PubMed ID: 36156296
    [No Abstract]   [Full Text] [Related]  

  • 15. Keratosis punctata palmoplantaris controlled with topical retinoids: a case report and review of the literature.
    Kong MS; Harford R; O'Neill JT
    Cutis; 2004 Sep; 74(3):173-9. PubMed ID: 15499759
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A novel ENPP1 mutation identified in a multigenerational family affected by Cole disease.
    Gabaton N; Kannu P; Pope E; Shugar A; Lara-Corrales I
    Pediatr Dermatol; 2020 Sep; 37(5):868-871. PubMed ID: 32598042
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Expanding the phenotype associated with a desmoplakin dominant mutation: Carvajal/Naxos syndrome associated with leukonychia and oligodontia.
    Boulé S; Fressart V; Laux D; Mallet A; Simon F; de Groote P; Bonnet D; Klug D; Charron P
    Int J Cardiol; 2012 Nov; 161(1):50-2. PubMed ID: 22795705
    [No Abstract]   [Full Text] [Related]  

  • 18. Abnormal keratinization and cutaneous inflammation in Mal de Meleda.
    Kudo M; Ishiura N; Tamura-Nakano M; Shimizu T; Kamata M; Akasaka E; Nakano H; Okuma Y; Tada Y; Okochi H; Tamaki T
    J Dermatol; 2020 May; 47(5):554-558. PubMed ID: 32157724
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Epidermolysis bullosa herpetiformis with mottled pigmentation and an unusual punctate keratoderma.
    Medenica-Mojsilović L; Fenske NA; Espinoza CG
    Arch Dermatol; 1986 Aug; 122(8):900-8. PubMed ID: 2943231
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Reticulate acropigmentation of Dohi: a case report of autosomal recessive inheritance.
    Alfadley A; Al Ajlan A; Hainau B; Pedersen KT; Al Hoqail I
    J Am Acad Dermatol; 2000 Jul; 43(1 Pt 1):113-7. PubMed ID: 10863235
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.