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Pubmed for Handhelds

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Journal Abstract Search

155 related items for PubMed ID: 23095783

  • 21. Phylloid hypermelanosis: a cutaneous marker of several different disorders?
    Happle R, Franco-Guío MF, Santacoloma-Osorio G.
    Pediatr Dermatol; 2014; 31(4):504-6. PubMed ID: 23278628
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  • 22. Total Hemi-overgrowth in Pigmentary Mosaicism of the (Hypomelanosis of) Ito Type: Eight Case Reports.
    Pavone V, Signorelli SS, Praticò AD, Corsello G, Savasta S, Falsaperla R, Pavone P, Sessa G, Ruggieri M.
    Medicine (Baltimore); 2016 Mar; 95(10):e2705. PubMed ID: 26962770
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  • 25. Phylloid hypermelanosis: an unusual form of pigmentary mosaicism.
    Happle R.
    Dermatology; 2010 Mar; 220(2):183-5. PubMed ID: 20110629
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  • 30. Mosaic trisomy 7 in a patient with pigmentary abnormalities.
    Verghese S, Newlin A, Miller M, Burton BK.
    Am J Med Genet; 1999 Dec 22; 87(5):371-4. PubMed ID: 10594873
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  • 34. A patient with trisomy 13 mosaicism with an unusual skin pigmentary pattern and prolonged survival.
    González-del Angel A, Estandia-Ortega B, Gaviño-Vergara A, Sáez-de-Ocariz M, Velasco-Hernández Mde L, Salas-Labadía C.
    Pediatr Dermatol; 2014 Dec 22; 31(5):580-3. PubMed ID: 24846410
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  • 36. Hypomelanosis of Ito: pigmentary mosaicism with immature melanosome in keratinocytes.
    Devillers C, Quatresooz P, Hermanns-Lê T, Szepetiuk G, Lemaire R, Piérard-Franchimont C, Piérard GE.
    Int J Dermatol; 2011 Oct 22; 50(10):1234-9. PubMed ID: 21950289
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  • 40. High resolution microarray CGH and MLPA analysis for improved genotype/phenotype evaluation of two childhood genetic disorder cases: ring chromosome 19 and partial duplication 2q.
    Hermsen MA, Tijssen M, Acero IH, Meijer GA, Ylstra B, Toral JF.
    Eur J Med Genet; 2005 Oct 22; 48(3):310-8. PubMed ID: 16179226
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