Artículos de revistas
Noonan's Syndrome [síndrome De Noonan]
Registro en:
Revista Brasileira De Medicina. , v. 53, n. 1-2, p. 31 - 34, 1996.
347264
2-s2.0-5244297013
Autor
Disarz A.E.
Andrade R.G.
Disarz E.M.C.L.
Institución
Resumen
[No abstract available] 53 1-2 31 34 Noonan, J.A., Ehmke, D.A., Associated noncardiac malformations in children with congenital heart disease (1963) J. Pediatr, 63, pp. 468-470 Bernier-Buzzanga, J., Su, W.P.D., Noonan's syndrome with Extensive Verrucae (1990) Cutis, 46 (3), pp. 171-270 Portmann, D., Herman, D., Rodrigues, E., Portmann, M., Sindrome de Noonan e manifestações otorrinolaringológicas. Apresentação de um caso (1993) Rev. Bras. de Otorrinolaringologia, 59 (4), pp. 281-283 Grob, J.J., Laure, M., Berge, G., Taramasco, M., Bore, P., Benderitter, T., Andrac, L., Bonerandi, J.J., Les signes cutanés du Syndrome de Noonan (1988) Ann. Dermatol. 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Child., 133, pp. 846-850 Noonan, J.A., Hypertelorism with Turner phenotype: A new syndrome with associated congenital heart disease (1968) Am. J. Dis. Child., 116, pp. 373-380 Miller, M., Motulsky, A.C., Noonan syndrome in an adult family presenting with chronic lymphedema (1978) Am. J. Med., 65, pp. 379-383 White, S.E., Lymphedema in Noonan's syndrome (1984) Int. J. Dermatol., 23, pp. 656-657 Nielsen, D.B., Sex chromosome abnormalities and Noonan syndrome (1980) Arizona Med., 37, pp. 486-490 Rigs Jr., W., Roentgen findings in Noonan's syndrome (1970) Radiology, 96, pp. 393-395 Celermajer, J.M., Blowder, J.D., Cohen, D.H., Pulmonans stenosis in patients with the Turner phenotype in the male (1968) Am. J. Dis. Child., 116, pp. 351-358 Hirsch, H.D., Gelband, H., Garcia, O., Rapidly progressive obstructive cardiomyopathy in infants with Noonan's syndrome: Report of two cases (1975) Circulation, 52, pp. 1161-1165 Jackson, G., Anand, I.S., Oram, S., Asymetric septal hypertrophy and propanolol treatment in a case of Ulrich - Noonan syndrome (1979) Br. Heart J., 42, pp. 611-614 Wright, N.L., Summitt, R.L., Ainger, L.E., Noonan's syndrome and Ebstein's malformation of the tricuspid valve (1968) Am. J Dis. Child., 116, pp. 367-372 Towne, W.D., Fabian, J.S., Rosen, K.M., Systolic prolapse of the mitral valve in Noonan's syndrome (1975) Am. Heart J., 90, pp. 499-502 Witt, D.R., Hoyme, H.E., Zonana, J., Lymphedema in Noonan syndrome: Clues to pathogenesis and prenatal diagnosis and review of the literature (1987) A. J. Ned. Genet, 27, pp. 841-856 Hernandez, R.J., Stern, A.M., Rosenthal, A., Pulmonary lymphangiectasis in Noonan syndrome (1980) A. J. 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J., 171, pp. 294-296 Vesterhus, P., Aarskog, D., Noonan's syndrome and autoimmune thyreoiditis (1973) J. Pedriatr., 83, pp. 237-240 Nora, J.J., Nora, A.H., Sinha, A.K., The Ulrich-Noonan syndrome (Turner phenotype) (1974) Am. J. Dis. Child., 127, pp. 48-55 Cunning, W.A., Simpson, J.S., Intestinal diverticulosis in Noonan's syndrome (1977) Br. J. Radiol., 50, pp. 64-65 Lanning, P., Simila, S., Suramo, I., Lymphatic abnormalities in Noonan's syndrome (1978) Pediatr. Radiol, 7, pp. 106-109 Smith, S., Schulman, A., Weir, E.K., Lymphatic abnormalities in Noonan syndrome: A case report (1979) S. Afr. Med. J., 56, pp. 271-274 Johansson, B.W., Mandahl, N., Ulrich-Noonan syndrome (1980) Acta Med. Scand., 207, pp. 505-510 King, J.O., Denborough, M.A., Anesthetic-induced malignant hyperpyrexia in children (1973) J. Pediatr., 83, pp. 37-40 Pinsky, L., Levy, E., Malignant hyperpyrexia or the XX-XY Turner phenotype? (1973) J. Pediatr., 83, pp. 896-897. , Letter to the editor Kobayashi, I., Aikawa, T., Takemiya, T., Noonan's syndrome with syringomyelia (1986) JPN J. Psychiatry Neurol., 40, pp. 101-104 Mendez, H.M.M., Opitz, J.M., Noonan syndrome: A review (1985) Am. J. Med. Genet., 21, pp. 493-506 Kobylinski, O., Ueber eine flughautahnliche Ausbreitung am Haise (1883) Arch. Anthropol., 14, pp. 342-348 Nora, J.J., Fraser, F.C., (1981) Medical Genetics: Principles and Practice. 2nd. Ed., , Philadelphia: Lea and Febiger Cortada, X., Tayse, K., Hartmann, A.F., Familial Williams syndrome (1980) Clin. Genet., 18, pp. 173-176 Escobar, V., Weaver, D.D., Aarskog syndrome. New findings and genetic analysis (1978) Jama, 240, pp. 2638-2641 Spiegel, P.G., Pekman, W.M., Rich, B.H., Versteeg, C.N., Nelson, V., Dudikov, M., The orthopedic aspects of the fetal alcohol syndrome (1973) Clin. Orthop., 139, pp. 58-63 Myhre, S.A., Williams, R., Teratogenic effects associated with maternal primidone therapy (1981) J. 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