Works matching DE "FACIAL manifestations of general diseases"


Results: 93
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    Pigmented facial plaques.

    Published in:
    Clinical & Experimental Dermatology, 2010, v. 35, n. 7, p. 805, doi. 10.1111/j.1365-2230.2010.03821.x
    By:
    • Simpson, R. C.;
    • Crichlow, S.;
    • Harman, K. E.
    Publication type:
    Article
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    Germline KRAS and BRAF mutations in cardio-facio-cutaneous syndrome.

    Published in:
    Nature Genetics, 2006, v. 38, n. 3, p. 294, doi. 10.1038/ng1749
    By:
    • Niihori, Tetsuya;
    • Aoki, Yoko;
    • Narumi, Yoko;
    • Neri, Giovanni;
    • Cavé, Hélène;
    • Verloes, Alain;
    • Okamoto, Nobuhiko;
    • Hennekam, Raoul C. M.;
    • Gillessen-Kaesbach, Gabriele;
    • Wieczorek, Dagmar;
    • Kavamura, Maria Ines;
    • Kurosawa, Kenji;
    • Ohashi, Hirofumi;
    • Wilson, Louise;
    • Heron, Delphine;
    • Bonneau, Dominique;
    • Corona, Giuseppina;
    • Kaname, Tadashi;
    • Naritomi, Kenji;
    • Baumann, Clarisse
    Publication type:
    Article
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    Leonine facies.

    Published in:
    2021
    By:
    • Qin Jian Low;
    • Seng Wee Cheo;
    • Wen Yee Evelyn Yap;
    • Low, Qin Jian;
    • Cheo, Seng Wee;
    • Yap, Wen Yee Evelyn
    Publication type:
    journal article
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    Clinical features.

    Published in:
    Indian Journal of Dermatology, Venereology & Leprology, 2009, v. 75, p. S13
    Publication type:
    Article
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    Superficial Peeling.

    Published in:
    Journal of Dermatologic Surgery & Oncology, 1989, v. 15, n. 9, p. 924, doi. 10.1111/j.1524-4725.1989.tb03179.x
    By:
    • Stagnone, James J.
    Publication type:
    Article
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    (28) Facial leiomyomas.

    Published in:
    British Journal of Dermatology, 1991, v. 125, p. 60, doi. 10.1111/j.1365-2133.1991.tb05498.x
    By:
    • Tatnall, F. M.;
    • Leigh, I. M.
    Publication type:
    Article
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    Marcus Gunn syndrome.

    Published in:
    Eye (0950-222X), 2004, v. 18, n. 1, p. 88, doi. 10.1038/sj.eye.6700509
    By:
    • Davis, G.;
    • Chen, C.;
    • Selva, D.
    Publication type:
    Article
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    Facial Asymmetry in a Newly Born Baby: Diagnostic Challenge!

    Published in:
    Clinical Medicine Insights: Case Reports, 2022, v. 15, p. 1, doi. 10.1177/11795476221088487
    By:
    • Kamal, Naglaa M;
    • Omair, Maher MR;
    • Attar, Ruwayd;
    • Abosabie, Salma AS;
    • Asiri, Nawras M;
    • Sherief, Laila M;
    • El-Shabrawi, Mortada
    Publication type:
    Article
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    Rare GABRA3 variants are associated with epileptic seizures, encephalopathy and dysmorphic features.

    Published in:
    2017
    By:
    • Niturad, Cristina Elena;
    • Lev, Dorit;
    • Kalscheuer, Vera M.;
    • Charzewska, Agnieszka;
    • Schubert, Julian;
    • Lerman-Sagie, Tally;
    • Kroes, Hester Y.;
    • Oegema, Renske;
    • Traverso, Monica;
    • Specchio, Nicola;
    • Lassota, Maria;
    • Chelly, Jamel;
    • Bennett-Back, Odeya;
    • Carmi, Nirit;
    • Koffler-Brill, Tal;
    • Iacomino, Michele;
    • Trivisano, Marina;
    • Capovilla, Giuseppe;
    • Striano, Pasquale;
    • Nawara, Magdalena
    Publication type:
    journal article
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    Complex translocation disrupting TCF4 and altering TCF4 isoform expression segregates as mild autosomal dominant intellectual disability.

    Published in:
    2016
    By:
    • Maduro, Valerie;
    • Pusey, Barbara N.;
    • Cherukuri, Praveen F.;
    • Atkins, Paul;
    • du Souich, Christèle;
    • Rupps, Rosemarie;
    • Limbos, Marjolaine;
    • Adams, David R.;
    • Bhatt, Samarth S.;
    • Eydoux, Patrice;
    • Links, Amanda E.;
    • Lehman, Anna;
    • Malicdan, May C.;
    • Mason, Christopher E.;
    • Morimoto, Marie;
    • Mullikin, James C.;
    • Sear, Andrew;
    • Van Karnebeek, Clara;
    • Stankiewicz, Pawel;
    • Gahl, William A.
    Publication type:
    journal article
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