A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MEDEIROS NETO, Geraldo Antônio e CAMARGO, R. Multinodular goiter and thyroid cancer. 1999, Anais.. Pisa: Faculdade de Medicina, Universidade de São Paulo, 1999. . Acesso em: 14 maio 2024.
APA
Medeiros Neto, G. A., & Camargo, R. (1999). Multinodular goiter and thyroid cancer. In . Pisa: Faculdade de Medicina, Universidade de São Paulo.
NLM
Medeiros Neto GA, Camargo R. Multinodular goiter and thyroid cancer. 1999 ;[citado 2024 maio 14 ]
Vancouver
Medeiros Neto GA, Camargo R. Multinodular goiter and thyroid cancer. 1999 ;[citado 2024 maio 14 ]
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 14 maio 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 maio 14 ] 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 maio 14 ] Available from: https://doi.org/10.1007/bf03346922
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 14 maio 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 maio 14 ]
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 maio 14 ]
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 14 maio 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 maio 14 ]
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 maio 14 ]
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 14 maio 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 maio 14 ] 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 maio 14 ] Available from: https://doi.org/10.1007/bf03347788
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 14 maio 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 maio 14 ] 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 maio 14 ] Available from: https://doi.org/10.1007/bf03348869
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 14 maio 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 maio 14 ]
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 maio 14 ]
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 14 maio 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 maio 14 ] 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 maio 14 ] Available from: https://doi.org/10.1007/bf03350067
