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Journal Abstract Search

242 related items for PubMed ID: 16860226

  • 1. Noonan-like/multiple giant cell lesion syndrome: report of a case and review of the literature.
    Wolvius EB, de Lange J, Smeets EE, van der Wal KG, van den Akker HP.
    J Oral Maxillofac Surg; 2006 Aug; 64(8):1289-92. PubMed ID: 16860226
    [No Abstract] [Full Text] [Related]

  • 2. Noonan-like syndrome mutations in PTPN11 in patients diagnosed with cherubism.
    Jafarov T, Ferimazova N, Reichenberger E.
    Clin Genet; 2005 Aug; 68(2):190-1. PubMed ID: 15996221
    [No Abstract] [Full Text] [Related]

  • 3. Acute myeloid leukemia in an adult Noonan syndrome patient with PTPN11 mutation.
    Matsubara K, Yabe H, Ogata T, Yoshida R, Fukaya T.
    Am J Hematol; 2005 Jun; 79(2):171-2. PubMed ID: 15929108
    [No Abstract] [Full Text] [Related]

  • 4. Case report: Noonan-like multiple central giant cell granuloma syndrome.
    Bitton N, Alexander S, Ruggiero S, Parameswaran A, Russo A, Ferguson F.
    Pediatr Dent; 2012 Jun; 34(5):144-7. PubMed ID: 23211900
    [Abstract] [Full Text] [Related]

  • 5. SOS1: a new player in the Noonan-like/multiple giant cell lesion syndrome.
    Hanna N, Parfait B, Talaat IM, Vidaud M, Elsedfy HH.
    Clin Genet; 2009 Jun; 75(6):568-71. PubMed ID: 19438935
    [Abstract] [Full Text] [Related]

  • 6. Double-chambered right ventricle in an adult with Noonan syndrome.
    Patel AM, Kim JB, Roberts AE, Aragam J.
    Cardiol Rev; 2006 Jun; 14(5):e16-20. PubMed ID: 16924159
    [Abstract] [Full Text] [Related]

  • 7. Phenotypic and genotypic characterisation of Noonan-like/multiple giant cell lesion syndrome.
    Lee JS, Tartaglia M, Gelb BD, Fridrich K, Sachs S, Stratakis CA, Muenke M, Robey PG, Collins MT, Slavotinek A.
    J Med Genet; 2005 Feb; 42(2):e11. PubMed ID: 15689434
    [No Abstract] [Full Text] [Related]

  • 8. Acute lymphoblastic leukaemia in Noonan syndrome.
    Roti G, La Starza R, Ballanti S, Crescenzi B, Romoli S, Foá R, Tartaglia M, Aversa F, Fabrizio Martelli M, Mecucci C.
    Br J Haematol; 2006 May; 133(4):448-50. PubMed ID: 16643459
    [No Abstract] [Full Text] [Related]

  • 9. Severe aortic valvar stenosis in familial Noonan syndrome with mutation of the PTPN11 gene.
    Abadir S, Edouard T, Julia S.
    Cardiol Young; 2007 Feb; 17(1):95-7. PubMed ID: 17184563
    [Abstract] [Full Text] [Related]

  • 10. Bilateral central giant cell granulomas of the mandible in an 8-year-old girl with Noonan syndrome (Noonan-like/multiple giant cell lesion syndrome).
    Edwards PC, Fox J, Fantasia JE, Goldberg J, Kelsch RD.
    Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2005 Mar; 99(3):334-40. PubMed ID: 15716842
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  • 14. The spectrum of cardiac anomalies in Noonan syndrome as a result of mutations in the PTPN11 gene.
    Sznajer Y, Keren B, Baumann C, Pereira S, Alberti C, Elion J, Cavé H, Verloes A.
    Pediatrics; 2007 Jun; 119(6):e1325-31. PubMed ID: 17515436
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  • 15. [Noonan syndrome].
    Ogata T.
    Nihon Rinsho; 2006 Jun 28; Suppl 2():505-10. PubMed ID: 16817452
    [No Abstract] [Full Text] [Related]

  • 16. Germline KRAS mutations cause Noonan syndrome.
    Schubbert S, Zenker M, Rowe SL, Böll S, Klein C, Bollag G, van der Burgt I, Musante L, Kalscheuer V, Wehner LE, Nguyen H, West B, Zhang KY, Sistermans E, Rauch A, Niemeyer CM, Shannon K, Kratz CP.
    Nat Genet; 2006 Mar 28; 38(3):331-6. PubMed ID: 16474405
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  • 20. A case of neurofibromatosis-Noonan syndrome with a central giant cell granuloma.
    Yazdizadeh M, Tapia JL, Baharvand M, Radfar L.
    Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2004 Sep 28; 98(3):316-20. PubMed ID: 15356469
    [Abstract] [Full Text] [Related]

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