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Journal Abstract Search

118 related items for PubMed ID: 4901597

  • 1. [Noonan's syndrome].
    Guibaud P.
    Pediatrie; 1969 Mar; 24(2):221-4. PubMed ID: 4901597
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  • 3. [Peripheral pulmonary stenosis, mental retardation and unusual facies. Apropos of a familial case].
    Rossignol AM, Rossignol B, Meaulle F, Plasse M, Denis B, Rambaud P, Bost M.
    Pediatrie; 1977 Mar; 32(7):643-50. PubMed ID: 928031
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  • 7. [Noonan syndrome in the differential diagnosis of Turner syndrome].
    Vergesslich KA, Schlemmer M, Wimmer M.
    Padiatr Padol; 1980 Mar; 15(3):195-203. PubMed ID: 7413223
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  • 8. [Role of cardiomyopathy in Noonan's syndrome. Apropos of a case].
    Rossignol AM, Rossignol B, Frappat P, Sandor C, Bost M.
    Pediatrie; 1976 Apr; 31(3):287-93. PubMed ID: 995583
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  • 13. [Combined aortic and pulmonary valve stenosis, changes in primary hemostasis and partial deficiency of factor XII in Noonan's syndrome].
    Mollica N, Antoncecchi S, Antoncecchi E, Bellantuono R, Castellaneta G, De Luca I.
    Minerva Cardioangiol; 1987 Jun; 35(6):311-5. PubMed ID: 3658194
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  • 14. Case records of the Massachusetts General Hospital. Weekly clinicopathological exercises. Case 28-1976.
    N Engl J Med; 1976 Jul 08; 295(2):92-9. PubMed ID: 944855
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  • 15. [Noonan's syndrome].
    Kazeĭ NS, Iskhakova FG, Chachiashvili MV.
    Med Sestra; 1983 Mar 08; 42(3):11-3. PubMed ID: 6551641
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  • 16. The Noonan syndrome.
    Fryns JP, Van der Hauwaert L, Van den Berghe H.
    Acta Paediatr Belg; 1977 Mar 08; 30(3):Suppl III:17-24. PubMed ID: 607763
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  • 18. [The Noonan syndrome (author's transl)].
    Neeb-Chrubasik S, Minne H, Kerner W.
    MMW Munch Med Wochenschr; 1980 Oct 24; 122(43):1508-10. PubMed ID: 6780845
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  • 19. Turner phenotype with normal sex chromosomal pattern and congenital heart disease (Noonan's syndrome).
    van der Horst RL.
    S Afr Med J; 1974 Feb 09; 48(6):219-22. PubMed ID: 4814498
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