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Journal Abstract Search

513 related items for PubMed ID: 25370770

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  • 3. [Cardiofaciocutaneous syndrome, a Noonan syndrome related disorder: clinical and molecular findings in 11 patients].
    Carcavilla A, García-Miñaúr S, Pérez-Aytés A, Vendrell T, Pinto I, Guillén-Navarro E, González-Meneses A, Aoki Y, Grinberg D, Ezquieta B.
    Med Clin (Barc); 2015 Jan 20; 144(2):67-72. PubMed ID: 25194980
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  • 4. Clinical and molecular analysis of RASopathies in a group of Turkish patients.
    Şimşek-Kiper PÖ, Alanay Y, Gülhan B, Lissewski C, Türkyilmaz D, Alehan D, Cetin M, Utine GE, Zenker M, Boduroğlu K.
    Clin Genet; 2013 Feb 20; 83(2):181-6. PubMed ID: 22420426
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  • 6. FOXI2: a possible gene contributing to ectodermal dysplasia.
    Kurban M, Zeineddine SB, Hamie L, Safi R, Abbas O, Kibbi AG, Bitar F, Nemer G.
    Eur J Dermatol; 2017 Dec 01; 27(6):641-645. PubMed ID: 29165300
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  • 8. Noonan syndrome and clinically related disorders.
    Tartaglia M, Gelb BD, Zenker M.
    Best Pract Res Clin Endocrinol Metab; 2011 Feb 01; 25(1):161-79. PubMed ID: 21396583
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  • 11. Genotype and phenotype spectrum of NRAS germline variants.
    Altmüller F, Lissewski C, Bertola D, Flex E, Stark Z, Spranger S, Baynam G, Buscarilli M, Dyack S, Gillis J, Yntema HG, Pantaleoni F, van Loon RL, MacKay S, Mina K, Schanze I, Tan TY, Walsh M, White SM, Niewisch MR, García-Miñaúr S, Plaza D, Ahmadian MR, Cavé H, Tartaglia M, Zenker M.
    Eur J Hum Genet; 2017 Jun 01; 25(7):823-831. PubMed ID: 28594414
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  • 13. Alterations in RAS-MAPK genes in 200 Spanish patients with Noonan and other neuro-cardio-facio-cutaneous syndromes. Genotype and cardiopathy.
    Ezquieta B, Santomé JL, Carcavilla A, Guillén-Navarro E, Pérez-Aytés A, Sánchez del Pozo J, García-Miñaur S, Castillo E, Alonso M, Vendrell T, Santana A, Maroto E, Galbis L.
    Rev Esp Cardiol (Engl Ed); 2012 May 01; 65(5):447-55. PubMed ID: 22465605
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  • 14. LYMPHODYSPLASIA AND KRAS MUTATION: A CASE REPORT AND LITERATURE REVIEW.
    Morcaldi G, Bellini T, Rossi C, Maghnie M, Boccardo F, Bonioli E, Bellini C.
    Lymphology; 2015 Sep 01; 48(3):121-7. PubMed ID: 26939159
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  • 17. Craniosynostosis in patients with RASopathies: Accumulating clinical evidence for expanding the phenotype.
    Ueda K, Yaoita M, Niihori T, Aoki Y, Okamoto N.
    Am J Med Genet A; 2017 Sep 01; 173(9):2346-2352. PubMed ID: 28650561
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  • 19. Non-hodgkin lymphoma in a patient with cardiofaciocutaneous syndrome.
    Ohtake A, Aoki Y, Saito Y, Niihori T, Shibuya A, Kure S, Matsubara Y.
    J Pediatr Hematol Oncol; 2011 Dec 01; 33(8):e342-6. PubMed ID: 20523244
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  • 20. A sibling pair with cardiofaciocutaneous syndrome (CFC) secondary to BRAF mutation with unaffected parents-the first cases of gonadal mosaicism in CFC?
    Geoghegan S, King G, Henchliffe J, Ramsden SC, Barry RJ, Green AJ, O'Connell SM.
    Am J Med Genet A; 2018 Jul 01; 176(7):1637-1640. PubMed ID: 29704308
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