Filtros : "Medeiros Neto, Geraldo Antônio" "Journal of Endocrinological Investigation" Removido: "PEDIATRIA" Limpar

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  • Source: Journal of Endocrinological Investigation. Unidade: FM

    Assunto: ENDOCRINOLOGIA

    Acesso à fonteDOIHow to cite
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    • ABNT

      NOGUEIRA, C. R. et al. Autosomal recessive deficiency of combined pituitary hormones (except ACTH) in a consanguineous Brazilian kindred. Journal of Endocrinological Investigation, v. 21, p. 386-391, 1998Tradução . . Disponível em: https://doi.org/10.1007/bf03346922. Acesso em: 18 out. 2024.
    • APA

      Nogueira, C. R., Leite, C. C., Chedid, E. P. T., Liberman, B., Kopp, P., Pimentel Filho, F. R., & Medeiros Neto, G. A. (1998). Autosomal recessive deficiency of combined pituitary hormones (except ACTH) in a consanguineous Brazilian kindred. Journal of Endocrinological Investigation, 21, 386-391. doi:10.1007/bf03346922
    • NLM

      Nogueira CR, Leite CC, Chedid EPT, Liberman B, Kopp P, Pimentel Filho FR, Medeiros Neto GA. Autosomal recessive deficiency of combined pituitary hormones (except ACTH) in a consanguineous Brazilian kindred [Internet]. Journal of Endocrinological Investigation. 1998 ; 21 386-391.[citado 2024 out. 18 ] Available from: https://doi.org/10.1007/bf03346922
    • Vancouver

      Nogueira CR, Leite CC, Chedid EPT, Liberman B, Kopp P, Pimentel Filho FR, Medeiros Neto GA. Autosomal recessive deficiency of combined pituitary hormones (except ACTH) in a consanguineous Brazilian kindred [Internet]. Journal of Endocrinological Investigation. 1998 ; 21 386-391.[citado 2024 out. 18 ] Available from: https://doi.org/10.1007/bf03346922
  • Source: Journal of Endocrinological Investigation. Conference titles: Annual Meeting of the European Thyroid Association. Unidade: FM

    Assunto: ENDOCRINOLOGIA

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    • ABNT

      MEDEIROS NETO, Geraldo Antônio et al. Diagnosis of congenital hypothyriod goiter deficient tg as an endoplasmic reticulum storage disease (ersd) with induction of molecular chaperones. Journal of Endocrinological Investigation. Milano: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 18 out. 2024. , 1996
    • APA

      Medeiros Neto, G. A., Kim, P. S., Vono, J., Yoo, S. E., Targovnik, H. M., Hassam, A., & Arvam, P. (1996). Diagnosis of congenital hypothyriod goiter deficient tg as an endoplasmic reticulum storage disease (ersd) with induction of molecular chaperones. Journal of Endocrinological Investigation. Milano: Faculdade de Medicina, Universidade de São Paulo.
    • NLM

      Medeiros Neto GA, Kim PS, Vono J, Yoo SE, Targovnik HM, Hassam A, Arvam P. Diagnosis of congenital hypothyriod goiter deficient tg as an endoplasmic reticulum storage disease (ersd) with induction of molecular chaperones. Journal of Endocrinological Investigation. 1996 ;19( 6 suppl.): 25.[citado 2024 out. 18 ]
    • Vancouver

      Medeiros Neto GA, Kim PS, Vono J, Yoo SE, Targovnik HM, Hassam A, Arvam P. Diagnosis of congenital hypothyriod goiter deficient tg as an endoplasmic reticulum storage disease (ersd) with induction of molecular chaperones. Journal of Endocrinological Investigation. 1996 ;19( 6 suppl.): 25.[citado 2024 out. 18 ]
  • Source: Journal of Endocrinological Investigation. Conference titles: Annual Meeting of the European Thyroid Association. Unidade: FM

    Assunto: ENDOCRINOLOGIA

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    • ABNT

      REGO, K G M e SANTOS, C e MEDEIROS NETO, Geraldo Antônio. From genotype to phenotype: different mutations in the htpo gene induce heterogeneity in clinical presentation of total iodide organification defects. Journal of Endocrinological Investigation. Milano: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 18 out. 2024. , 1996
    • APA

      Rego, K. G. M., Santos, C., & Medeiros Neto, G. A. (1996). From genotype to phenotype: different mutations in the htpo gene induce heterogeneity in clinical presentation of total iodide organification defects. Journal of Endocrinological Investigation. Milano: Faculdade de Medicina, Universidade de São Paulo.
    • NLM

      Rego KGM, Santos C, Medeiros Neto GA. From genotype to phenotype: different mutations in the htpo gene induce heterogeneity in clinical presentation of total iodide organification defects. Journal of Endocrinological Investigation. 1996 ;19( 6 suppl.): 69.[citado 2024 out. 18 ]
    • Vancouver

      Rego KGM, Santos C, Medeiros Neto GA. From genotype to phenotype: different mutations in the htpo gene induce heterogeneity in clinical presentation of total iodide organification defects. Journal of Endocrinological Investigation. 1996 ;19( 6 suppl.): 69.[citado 2024 out. 18 ]
  • Source: Journal of Endocrinological Investigation. Unidade: FM

    Assunto: ENDOCRINOLOGIA

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    • ABNT

      KNOBEL, M et al. Prevalence of anti-thyroid peroxidade antibodies in autoimmune and nonautoimmune thyroid disorders in a relativity low iodine environment. Journal of Endocrinological Investigation, v. 17, p. 837-42, 1994Tradução . . Disponível em: https://doi.org/10.1007/bf03347788. Acesso em: 18 out. 2024.
    • APA

      Knobel, M., Barca, M. F., Pedrinola, F., & Medeiros Neto, G. A. (1994). Prevalence of anti-thyroid peroxidade antibodies in autoimmune and nonautoimmune thyroid disorders in a relativity low iodine environment. Journal of Endocrinological Investigation, 17, 837-42. doi:10.1007/bf03347788
    • NLM

      Knobel M, Barca MF, Pedrinola F, Medeiros Neto GA. Prevalence of anti-thyroid peroxidade antibodies in autoimmune and nonautoimmune thyroid disorders in a relativity low iodine environment [Internet]. Journal of Endocrinological Investigation. 1994 ;17 837-42.[citado 2024 out. 18 ] Available from: https://doi.org/10.1007/bf03347788
    • Vancouver

      Knobel M, Barca MF, Pedrinola F, Medeiros Neto GA. Prevalence of anti-thyroid peroxidade antibodies in autoimmune and nonautoimmune thyroid disorders in a relativity low iodine environment [Internet]. Journal of Endocrinological Investigation. 1994 ;17 837-42.[citado 2024 out. 18 ] Available from: https://doi.org/10.1007/bf03347788
  • Source: Journal of Endocrinological Investigation. Unidade: FM

    Assunto: ENDOCRINOLOGIA

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    • ABNT

      TARGOVNIK, H M et al. Human thyroid tissue do not express thyroalbumin. Journal of Endocrinological Investigation, v. 16, p. 415-9, 1993Tradução . . Disponível em: https://doi.org/10.1007/bf03348869. Acesso em: 18 out. 2024.
    • APA

      Targovnik, H. M., Frechtel, G. D., Varela, V., Wajchenberg, B. L., Vassart, G., Dumont, J., & Medeiros Neto, G. A. (1993). Human thyroid tissue do not express thyroalbumin. Journal of Endocrinological Investigation, 16, 415-9. doi:10.1007/bf03348869
    • NLM

      Targovnik HM, Frechtel GD, Varela V, Wajchenberg BL, Vassart G, Dumont J, Medeiros Neto GA. Human thyroid tissue do not express thyroalbumin [Internet]. Journal of Endocrinological Investigation. 1993 ;16 415-9.[citado 2024 out. 18 ] Available from: https://doi.org/10.1007/bf03348869
    • Vancouver

      Targovnik HM, Frechtel GD, Varela V, Wajchenberg BL, Vassart G, Dumont J, Medeiros Neto GA. Human thyroid tissue do not express thyroalbumin [Internet]. Journal of Endocrinological Investigation. 1993 ;16 415-9.[citado 2024 out. 18 ] Available from: https://doi.org/10.1007/bf03348869
  • Source: Journal of Endocrinological Investigation. Conference titles: Annual Meeting of the European Thyroid Association. Unidade: FM

    Assunto: ENDOCRINOLOGIA

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    • ABNT

      TARGOVNIK, H M et al. Nonsense mutation with preferential production of a 171 nt deleted tg 'ANTIND.M RNA' as cause of human congenital goiter. Journal of Endocrinological Investigation. Milano: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 18 out. 2024. , 1992
    • APA

      Targovnik, H. M., Varela, V., Cochaux, P., & Medeiros Neto, G. A. (1992). Nonsense mutation with preferential production of a 171 nt deleted tg 'ANTIND.M RNA' as cause of human congenital goiter. Journal of Endocrinological Investigation. Milano: Faculdade de Medicina, Universidade de São Paulo.
    • NLM

      Targovnik HM, Varela V, Cochaux P, Medeiros Neto GA. Nonsense mutation with preferential production of a 171 nt deleted tg 'ANTIND.M RNA' as cause of human congenital goiter. Journal of Endocrinological Investigation. 1992 ;15( 5 suppl.2): 39.[citado 2024 out. 18 ]
    • Vancouver

      Targovnik HM, Varela V, Cochaux P, Medeiros Neto GA. Nonsense mutation with preferential production of a 171 nt deleted tg 'ANTIND.M RNA' as cause of human congenital goiter. Journal of Endocrinological Investigation. 1992 ;15( 5 suppl.2): 39.[citado 2024 out. 18 ]
  • Source: Journal of Endocrinological Investigation. Conference titles: International Symposium Molecular and Celllar Biology of Thyroid Disease. Unidade: FM

    Assunto: ENDOCRINOLOGIA

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    • ABNT

      HAKOYAMA, M M et al. Altered thyroid autoimmunity in the presence of active and inactive pituitary grawth hormone producing tumours. Journal of Endocrinological Investigation. Pisa: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 18 out. 2024. , 1992
    • APA

      Hakoyama, M. M., Schenberg, M., Knobel, M., & Medeiros Neto, G. A. (1992). Altered thyroid autoimmunity in the presence of active and inactive pituitary grawth hormone producing tumours. Journal of Endocrinological Investigation. Pisa: Faculdade de Medicina, Universidade de São Paulo.
    • NLM

      Hakoyama MM, Schenberg M, Knobel M, Medeiros Neto GA. Altered thyroid autoimmunity in the presence of active and inactive pituitary grawth hormone producing tumours. Journal of Endocrinological Investigation. 1992 ;15( 6 suppl.3): se 1992.[citado 2024 out. 18 ]
    • Vancouver

      Hakoyama MM, Schenberg M, Knobel M, Medeiros Neto GA. Altered thyroid autoimmunity in the presence of active and inactive pituitary grawth hormone producing tumours. Journal of Endocrinological Investigation. 1992 ;15( 6 suppl.3): se 1992.[citado 2024 out. 18 ]
  • Source: Journal of Endocrinological Investigation. Unidade: FM

    Assunto: ENDOCRINOLOGIA

    Acesso à fonteDOIHow to cite
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    • ABNT

      SUGAWARA, M et al. Thyroid peroxidase in endemic goiter tissue. Journal of Endocrinological Investigation, v. 13, p. 893-9, 1990Tradução . . Disponível em: https://doi.org/10.1007/bf03349648. Acesso em: 18 out. 2024.
    • APA

      Sugawara, M., Summer, C. N., Kobayashi, A., Murakami, S., Kuma, K., & Medeiros Neto, G. A. (1990). Thyroid peroxidase in endemic goiter tissue. Journal of Endocrinological Investigation, 13, 893-9. doi:10.1007/bf03349648
    • NLM

      Sugawara M, Summer CN, Kobayashi A, Murakami S, Kuma K, Medeiros Neto GA. Thyroid peroxidase in endemic goiter tissue [Internet]. Journal of Endocrinological Investigation. 1990 ;13 893-9.[citado 2024 out. 18 ] Available from: https://doi.org/10.1007/bf03349648
    • Vancouver

      Sugawara M, Summer CN, Kobayashi A, Murakami S, Kuma K, Medeiros Neto GA. Thyroid peroxidase in endemic goiter tissue [Internet]. Journal of Endocrinological Investigation. 1990 ;13 893-9.[citado 2024 out. 18 ] Available from: https://doi.org/10.1007/bf03349648
  • Source: Journal of Endocrinological Investigation. Unidade: FM

    Assunto: ENDOCRINOLOGIA

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    • ABNT

      ROSENTHAL, D et al. Dyshormonogenetic goiter: presence of an inhibitor of normal human thyroid peroxidase. Journal of Endocrinological Investigation, v. 13, p. 901-4, 1990Tradução . . Disponível em: https://doi.org/10.1007/bf03349651. Acesso em: 18 out. 2024.
    • APA

      Rosenthal, D., Carvalho Guimaraes, D. P., Knobel, M., & Medeiros Neto, G. A. (1990). Dyshormonogenetic goiter: presence of an inhibitor of normal human thyroid peroxidase. Journal of Endocrinological Investigation, 13, 901-4. doi:10.1007/bf03349651
    • NLM

      Rosenthal D, Carvalho Guimaraes DP, Knobel M, Medeiros Neto GA. Dyshormonogenetic goiter: presence of an inhibitor of normal human thyroid peroxidase [Internet]. Journal of Endocrinological Investigation. 1990 ;13 901-4.[citado 2024 out. 18 ] Available from: https://doi.org/10.1007/bf03349651
    • Vancouver

      Rosenthal D, Carvalho Guimaraes DP, Knobel M, Medeiros Neto GA. Dyshormonogenetic goiter: presence of an inhibitor of normal human thyroid peroxidase [Internet]. Journal of Endocrinological Investigation. 1990 ;13 901-4.[citado 2024 out. 18 ] Available from: https://doi.org/10.1007/bf03349651
  • Source: Journal of Endocrinological Investigation. Unidade: FM

    Subjects: GLOBULINAS, BÓCIO, SEQUENCIAMENTO GENÉTICO

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    • ABNT

      MEDEIROS NETO, Geraldo Antônio et al. Qualitative and quantitative defects of thyroglobulin resulting in congenital goiter . Absence of gross gene deletion of coding sequences in the tg gene structure. Journal of Endocrinological Investigation, v. 12, p. 805-13, 1989Tradução . . Disponível em: https://doi.org/10.1007/bf03350067. Acesso em: 18 out. 2024.
    • APA

      Medeiros Neto, G. A., Targovnik, H., Knobel, M., Propato, F., Varela, V., Alkmin, M., et al. (1989). Qualitative and quantitative defects of thyroglobulin resulting in congenital goiter . Absence of gross gene deletion of coding sequences in the tg gene structure. Journal of Endocrinological Investigation, 12, 805-13. doi:10.1007/bf03350067
    • NLM

      Medeiros Neto GA, Targovnik H, Knobel M, Propato F, Varela V, Alkmin M, Barbosa S, Wajchenberg BL. Qualitative and quantitative defects of thyroglobulin resulting in congenital goiter . Absence of gross gene deletion of coding sequences in the tg gene structure [Internet]. Journal of Endocrinological Investigation. 1989 ;12 805-13.[citado 2024 out. 18 ] Available from: https://doi.org/10.1007/bf03350067
    • Vancouver

      Medeiros Neto GA, Targovnik H, Knobel M, Propato F, Varela V, Alkmin M, Barbosa S, Wajchenberg BL. Qualitative and quantitative defects of thyroglobulin resulting in congenital goiter . Absence of gross gene deletion of coding sequences in the tg gene structure [Internet]. Journal of Endocrinological Investigation. 1989 ;12 805-13.[citado 2024 out. 18 ] Available from: https://doi.org/10.1007/bf03350067

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