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  • Source: Journal of Clinical Endocrinology and Metabolism. Unidade: FM

    Subject: ENDOCRINOLOGIA

    DOIHow to cite
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    • ABNT

      TARGOVNIK, H M et al. 138- nucleotid deletion in the thyroglobulin ribunocleic acid messenger in a congenital goiter with defective thyroglobulin synthesis. Journal of Clinical Endocrinology and Metabolism, v. no 1995, n. 11, p. 3356-60, 1995Tradução . . Acesso em: 27 set. 2022.
    • APA

      Targovnik, H. M., Vono, J., Billerbeck, A. E. C., Cerrone, G. E., Varela, V., Mendive, F., et al. (1995). 138- nucleotid deletion in the thyroglobulin ribunocleic acid messenger in a congenital goiter with defective thyroglobulin synthesis. Journal of Clinical Endocrinology and Metabolism, no 1995( 11), 3356-60. doi:10.1210/jcem.80.11.7593451
    • NLM

      Targovnik HM, Vono J, Billerbeck AEC, Cerrone GE, Varela V, Mendive F, Wajchenberg BL, Medeiros Neto GA. 138- nucleotid deletion in the thyroglobulin ribunocleic acid messenger in a congenital goiter with defective thyroglobulin synthesis. Journal of Clinical Endocrinology and Metabolism. 1995 ; no 1995( 11): 3356-60.[citado 2022 set. 27 ]
    • Vancouver

      Targovnik HM, Vono J, Billerbeck AEC, Cerrone GE, Varela V, Mendive F, Wajchenberg BL, Medeiros Neto GA. 138- nucleotid deletion in the thyroglobulin ribunocleic acid messenger in a congenital goiter with defective thyroglobulin synthesis. Journal of Clinical Endocrinology and Metabolism. 1995 ; no 1995( 11): 3356-60.[citado 2022 set. 27 ]
  • Source: Journal of Clinical Endocrinology and Metabolism. Unidade: FM

    Subject: ENDOCRINOLOGIA

    DOIHow to cite
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    • ABNT

      TARGOVNIK, H M et al. Nonsense mutation causes human hereditary congenital goiter with preferential production of a 171 nucleotide-deleted thyroglobulin ribunocleic acid messenger. Journal of Clinical Endocrinology and Metabolism, v. 77, n. 1 , p. 210-5, 1993Tradução . . Acesso em: 27 set. 2022.
    • APA

      Targovnik, H. M., Medeiros Neto, G. A., Varela, V., Cochaux, P., Wajchenberg, B. L., & Vassart, G. (1993). Nonsense mutation causes human hereditary congenital goiter with preferential production of a 171 nucleotide-deleted thyroglobulin ribunocleic acid messenger. Journal of Clinical Endocrinology and Metabolism, 77( 1 ), 210-5. doi:10.1210/jcem.77.1.8325944
    • NLM

      Targovnik HM, Medeiros Neto GA, Varela V, Cochaux P, Wajchenberg BL, Vassart G. Nonsense mutation causes human hereditary congenital goiter with preferential production of a 171 nucleotide-deleted thyroglobulin ribunocleic acid messenger. Journal of Clinical Endocrinology and Metabolism. 1993 ;77( 1 ): 210-5.[citado 2022 set. 27 ]
    • Vancouver

      Targovnik HM, Medeiros Neto GA, Varela V, Cochaux P, Wajchenberg BL, Vassart G. Nonsense mutation causes human hereditary congenital goiter with preferential production of a 171 nucleotide-deleted thyroglobulin ribunocleic acid messenger. Journal of Clinical Endocrinology and Metabolism. 1993 ;77( 1 ): 210-5.[citado 2022 set. 27 ]
  • Source: Journal of Endocrinological Investigation. Unidade: FM

    Subject: ENDOCRINOLOGIA

    DOIHow to cite
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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 . . Acesso em: 27 set. 2022.
    • 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. Journal of Endocrinological Investigation. 1993 ;16 415-9.[citado 2022 set. 27 ]
    • Vancouver

      Targovnik HM, Frechtel GD, Varela V, Wajchenberg BL, Vassart G, Dumont J, Medeiros Neto GA. Human thyroid tissue do not express thyroalbumin. Journal of Endocrinological Investigation. 1993 ;16 415-9.[citado 2022 set. 27 ]
  • Source: Journal of Endocrinological Investigation. Conference title: Annual Meeting of the European Thyroid Association. Unidade: FM

    Subject: 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: 27 set. 2022. , 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 2022 set. 27 ]
    • 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 2022 set. 27 ]
  • Source: Thyroid. Unidade: FM

    Subject: ENDOCRINOLOGIA

    How to cite
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    • ABNT

      TARGOVNIK, H M et al. Normal thyroglobulin and thyroperoxidase gene expression in thyroid congenital defective thyroglobulin synthesis. Thyroid, v. 1 , n. 4 , p. 339-45, 1991Tradução . . Acesso em: 27 set. 2022.
    • APA

      Targovnik, H. M., Varela, V., Abatangelo, C., Wajchenberg, B. L., & Medeiros Neto, G. A. (1991). Normal thyroglobulin and thyroperoxidase gene expression in thyroid congenital defective thyroglobulin synthesis. Thyroid, 1 ( 4 ), 339-45.
    • NLM

      Targovnik HM, Varela V, Abatangelo C, Wajchenberg BL, Medeiros Neto GA. Normal thyroglobulin and thyroperoxidase gene expression in thyroid congenital defective thyroglobulin synthesis. Thyroid. 1991 ;1 ( 4 ): 339-45.[citado 2022 set. 27 ]
    • Vancouver

      Targovnik HM, Varela V, Abatangelo C, Wajchenberg BL, Medeiros Neto GA. Normal thyroglobulin and thyroperoxidase gene expression in thyroid congenital defective thyroglobulin synthesis. Thyroid. 1991 ;1 ( 4 ): 339-45.[citado 2022 set. 27 ]
  • Source: Program and Abstracts. Conference title: Annual Meeting of the Endocrine Society. Unidade: FM

    Subject: ENDOCRINOLOGIA

    How to cite
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    • ABNT

      TARGOVNIK, H M et al. Normal thyroglobulin and thyroperoxidase gene expression in thyroid congenital goiter with defective thyroglobulin. 1991, Anais.. Washington: Endocrine Society, 1991. . Acesso em: 27 set. 2022.
    • APA

      Targovnik, H. M., Varela, V., Abatangelo, C., Wajchenberg, B. L., & Medeiros Neto, G. A. (1991). Normal thyroglobulin and thyroperoxidase gene expression in thyroid congenital goiter with defective thyroglobulin. In Program and Abstracts. Washington: Endocrine Society.
    • NLM

      Targovnik HM, Varela V, Abatangelo C, Wajchenberg BL, Medeiros Neto GA. Normal thyroglobulin and thyroperoxidase gene expression in thyroid congenital goiter with defective thyroglobulin. Program and Abstracts. 1991 ;[citado 2022 set. 27 ]
    • Vancouver

      Targovnik HM, Varela V, Abatangelo C, Wajchenberg BL, Medeiros Neto GA. Normal thyroglobulin and thyroperoxidase gene expression in thyroid congenital goiter with defective thyroglobulin. Program and Abstracts. 1991 ;[citado 2022 set. 27 ]
  • Source: Program and Abstracts. Conference title: Latin-American Thyroid Congress. Unidade: FM

    Subject: ENDOCRINOLOGIA

    How to cite
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    • ABNT

      TARGOVNIK, H M et al. Searching for restriction fragment length polymorphisms in congenital goiter with defective thyroglobulin. 1991, Anais.. São Paulo: Faculdade de Medicina, Universidade de São Paulo, 1991. . Acesso em: 27 set. 2022.
    • APA

      Targovnik, H. M., Varela, V., Abatangelo, C., Billerbeck, A. E., & Wajchenberg, B. L. (1991). Searching for restriction fragment length polymorphisms in congenital goiter with defective thyroglobulin. In Program and Abstracts. São Paulo: Faculdade de Medicina, Universidade de São Paulo.
    • NLM

      Targovnik HM, Varela V, Abatangelo C, Billerbeck AE, Wajchenberg BL. Searching for restriction fragment length polymorphisms in congenital goiter with defective thyroglobulin. Program and Abstracts. 1991 ;[citado 2022 set. 27 ]
    • Vancouver

      Targovnik HM, Varela V, Abatangelo C, Billerbeck AE, Wajchenberg BL. Searching for restriction fragment length polymorphisms in congenital goiter with defective thyroglobulin. Program and Abstracts. 1991 ;[citado 2022 set. 27 ]
  • Source: Journal of Clinical Endocrinology and Metabolism. Unidade: FM

    Subjects: RNA MENSAGEIRO, IMUNOGLOBULINAS, BÓCIO (FISIOPATOLOGIA)

    How to cite
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    • ABNT

      TARGOVNIK, H et al. Low levels of thyroglobulin messenger ribonucleic acid in congenital goitrous hypothyroidism with defective thyroglobulin synthesis. Journal of Clinical Endocrinology and Metabolism, v. 69, n. 6 , p. 1137-47, 1989Tradução . . Acesso em: 27 set. 2022.
    • APA

      Targovnik, H., Propato, F., Varela, V., Wajchenberg, B. L., Knobel, M., D'abronzo, H. F., & Medeiros Neto, S. A. (1989). Low levels of thyroglobulin messenger ribonucleic acid in congenital goitrous hypothyroidism with defective thyroglobulin synthesis. Journal of Clinical Endocrinology and Metabolism, 69( 6 ), 1137-47.
    • NLM

      Targovnik H, Propato F, Varela V, Wajchenberg BL, Knobel M, D'abronzo HF, Medeiros Neto SA. Low levels of thyroglobulin messenger ribonucleic acid in congenital goitrous hypothyroidism with defective thyroglobulin synthesis. Journal of Clinical Endocrinology and Metabolism. 1989 ;69( 6 ): 1137-47.[citado 2022 set. 27 ]
    • Vancouver

      Targovnik H, Propato F, Varela V, Wajchenberg BL, Knobel M, D'abronzo HF, Medeiros Neto SA. Low levels of thyroglobulin messenger ribonucleic acid in congenital goitrous hypothyroidism with defective thyroglobulin synthesis. Journal of Clinical Endocrinology and Metabolism. 1989 ;69( 6 ): 1137-47.[citado 2022 set. 27 ]
  • Source: Journal of Endocrinological Investigation. Unidade: FM

    Subjects: GLOBULINAS, BÓCIO, SEQUENCIAMENTO GENÉTICO

    DOIHow to cite
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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 . . Acesso em: 27 set. 2022.
    • 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. Journal of Endocrinological Investigation. 1989 ;12 805-13.[citado 2022 set. 27 ]
    • 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. Journal of Endocrinological Investigation. 1989 ;12 805-13.[citado 2022 set. 27 ]

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