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 *

265 related articles for article (PubMed ID: 23461053)

  • 1. Cutis tricolor.
    Torchia D; Schachner LA; Izakovic J
    Cutis; 2013 Jan; 91(1):11-6. PubMed ID: 23461053
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Cutis tricolor parvimaculata: a distinct neurocutaneous syndrome?
    Larralde M; Happle R
    Dermatology; 2005; 211(2):149-51. PubMed ID: 16088163
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A novel association of an uncommon pigmentation pattern: coexistence of cutis tricolor with intracranial teratoma and holoprosencephaly.
    Tekin B; Yucelten AD; Bayri Y
    Dermatol Online J; 2014 Oct; 20(10):. PubMed ID: 25525998
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Complex malformation (Ruggieri-Happle) phenotype with "cutis tricolor" in a 10-year-old girl.
    Nicita F; Spalice A; Roggini M; Papetti L; Ursitti F; Tarani L; Ruggieri M
    Brain Dev; 2012 Nov; 34(10):869-72. PubMed ID: 22370055
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Familial cutis tricolor: a possible example of paradominant inheritance.
    Baba M; Seçkin D; Akçali C; Happle R
    Eur J Dermatol; 2003; 13(4):343-5. PubMed ID: 12948912
    [TBL] [Abstract][Full Text] [Related]  

  • 6. "Cutis tricolor": congenital hyper- and hypopigmented macules associated with a sporadic multisystem birth defect: an unusual example of twin spotting?
    Happle R; Barbi G; Eckert D; Kennerknecht I
    J Med Genet; 1997 Aug; 34(8):676-8. PubMed ID: 9279762
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Cutis tricolor: congenital hyper- and hypopigmented lesions in a background of normal skin with and without associated systemic features: further expansion of the phenotype.
    Ruggieri M
    Eur J Pediatr; 2000 Oct; 159(10):745-9. PubMed ID: 11039129
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Hypomelanosis of ito-whorled hyperpigmentation combination: a mirror image presentation.
    Thapa R; Dhar S; Malakar R; Chakrabartty S
    Pediatr Dermatol; 2007; 24(5):572-3. PubMed ID: 17958820
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Late-onset amyloidosis cutis dyschromica: an unusual case.
    Kutlu Ö; Çetinkaya PÖ; Ünverdi H; Vahapoğlu G; Ekşioğlu M
    Dermatol Online J; 2019 Apr; 25(4):. PubMed ID: 31046910
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Cutis tricolor parvimaculata in ring chromosome 15 syndrome: A case report.
    Ribeiro Dias Barroso C; Silveira Gomes L; Abrantes Silvestre V; Yamada Utagawa C
    Pediatr Dermatol; 2018 May; 35(3):e204-e205. PubMed ID: 29658137
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Visual Dermatology: An 8-Year-Old Girl With Symmetric Pigmented and Hypopigmented Patches.
    Ortega-Quijano D
    J Cutan Med Surg; 2019; 23(6):644. PubMed ID: 31729909
    [No Abstract]   [Full Text] [Related]  

  • 13. Neurological manifestations in individuals with pure cutaneous or syndromic (Ruggieri-Happle syndrome) phenotypes with "cutis tricolor": a study of 14 cases.
    Lionetti E; Pavone P; Kennerknecht I; Failla G; Schepis C; De Pasquale R; Pavone L; Ruggieri M
    Neuropediatrics; 2010 Aug; 41(2):60-5. PubMed ID: 20799151
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Spectrum of skeletal abnormalities in a complex malformation syndrome with "cutis tricolor" (Ruggieri-Happle syndrome).
    Ruggieri M; Roggini M; Kennerknecht I; Polizzi A; Distefano A; Pavone V
    Acta Paediatr; 2011 Jan; 100(1):121-7. PubMed ID: 21143296
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Amyloidosis cutis dyschromia: a rare form of primary cutaneous amyloidosis.
    Al-Dawsari NA; Shahab RK
    Dermatol Online J; 2014 Apr; 20(4):22328. PubMed ID: 24746296
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Cutis tricolor coexistent with cutis marmorata telangiectatica congenita: "phacomatosis achromico-melano-marmorata".
    Boente Mdel C; Obeid R; Asial RA; Bibas-Bonet H; Coronel AM; Happle R
    Eur J Dermatol; 2008; 18(4):394-6. PubMed ID: 18573710
    [TBL] [Abstract][Full Text] [Related]  

  • 17.
    Ruggieri M; Polizzi A; Schepis C; Morano M; Strano S; Belfiore G; Palmucci S; Foti PV; Pirrone C; Roggini M; David E; Salpietro V; Milone P
    Quant Imaging Med Surg; 2016 Oct; 6(5):525-534. PubMed ID: 27942472
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Dyschromatosis universalis hereditaria: a case report.
    Kumar S; Rajendra O; Prasad H
    Int J Dermatol; 2014 Mar; 53(3):342-5. PubMed ID: 24320734
    [No Abstract]   [Full Text] [Related]  

  • 19. An unusual presentation of primary cutaneous amyloidosis.
    Garg T; Marak A; Ahmed R; Chander R; Jain M
    Dermatol Online J; 2017 Aug; 23(8):. PubMed ID: 29469741
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Analysis of 36 cases of Blaschkoid dyspigmentation: reading between the lines of Blaschko.
    Cohen J; Shahrokh K; Cohen B
    Pediatr Dermatol; 2014; 31(4):471-6. PubMed ID: 25039703
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.