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Artigo de periodico
Histopathological Characterization and Whole Exome Sequencing of Ectopic Thyroid: Fetal Architecture in a Functional Ectopic Gland from Adult Patient (2018)
Camargo, Rosalinda Yasato; Medeiros Neto, Geraldo Antônio
Source: International journal of endocrinology. Unidade: FM
Subjects: HIPOTIREOIDISMO, DOENÇAS CONGÊNITAS, IMUNOHISTOQUÍMICA, DIAGNÓSTICO PRÉ-NATAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CAMARGO, Rosalinda Yasato e MEDEIROS NETO, Geraldo Antônio. Histopathological Characterization and Whole Exome Sequencing of Ectopic Thyroid: Fetal Architecture in a Functional Ectopic Gland from Adult Patient. International journal of endocrinology, 2018Tradução . . Disponível em: https://doi.org/10.1155/2018/4682876. Acesso em: 18 out. 2024.
APA
Camargo, R. Y., & Medeiros Neto, G. A. (2018). Histopathological Characterization and Whole Exome Sequencing of Ectopic Thyroid: Fetal Architecture in a Functional Ectopic Gland from Adult Patient. International journal of endocrinology. doi:10.1155/2018/4682876
NLM
Camargo RY, Medeiros Neto GA. Histopathological Characterization and Whole Exome Sequencing of Ectopic Thyroid: Fetal Architecture in a Functional Ectopic Gland from Adult Patient [Internet]. International journal of endocrinology. 2018 ;[citado 2024 out. 18 ] Available from: https://doi.org/10.1155/2018/4682876
Vancouver
Camargo RY, Medeiros Neto GA. Histopathological Characterization and Whole Exome Sequencing of Ectopic Thyroid: Fetal Architecture in a Functional Ectopic Gland from Adult Patient [Internet]. International journal of endocrinology. 2018 ;[citado 2024 out. 18 ] Available from: https://doi.org/10.1155/2018/4682876
Artigo de periodico
Prevalence and characteristics of postpartum thyroid dysfunction in São Paulo, Brazil (2000)
Barca, Maria Fernanda; Knobel, Meyer; Tomimori, Eduardo; Cardia, Maria Silvia; Medeiros Neto, Geraldo Antônio
Source: Clinical Endocrinology. Unidade: FM
Assunto: ENDOCRINOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BARCA, Maria Fernanda et al. Prevalence and characteristics of postpartum thyroid dysfunction in São Paulo, Brazil. Clinical Endocrinology, v. 53, p. 21-31, 2000Tradução . . Disponível em: https://doi.org/10.1046/j.1365-2265.2000.01034.x. Acesso em: 18 out. 2024.
APA
Barca, M. F., Knobel, M., Tomimori, E., Cardia, M. S., & Medeiros Neto, G. A. (2000). Prevalence and characteristics of postpartum thyroid dysfunction in São Paulo, Brazil. Clinical Endocrinology, 53, 21-31. doi:10.1046/j.1365-2265.2000.01034.x
NLM
Barca MF, Knobel M, Tomimori E, Cardia MS, Medeiros Neto GA. Prevalence and characteristics of postpartum thyroid dysfunction in São Paulo, Brazil [Internet]. Clinical Endocrinology. 2000 ; 53 21-31.[citado 2024 out. 18 ] Available from: https://doi.org/10.1046/j.1365-2265.2000.01034.x
Vancouver
Barca MF, Knobel M, Tomimori E, Cardia MS, Medeiros Neto GA. Prevalence and characteristics of postpartum thyroid dysfunction in São Paulo, Brazil [Internet]. Clinical Endocrinology. 2000 ; 53 21-31.[citado 2024 out. 18 ] Available from: https://doi.org/10.1046/j.1365-2265.2000.01034.x
Artigo de periodico
A novel mutation in the TPO gene in goitrous hypothyroid patients with iodide organification defect (1999)
Santos, Cecilia L. S.; Bikker, Hennie; Rego, Katia G. M.; Nascimento, Antonio C.; Tambascia, Marcos; Vijlder, Jan J. M. de; Medeiros Neto, Geraldo Antônio
Source: Clinical Endocrinology. Unidade: FM
Subjects: ENDOCRINOLOGIA, HORMÔNIOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SANTOS, Cecilia L. S. et al. A novel mutation in the TPO gene in goitrous hypothyroid patients with iodide organification defect. Clinical Endocrinology, v. 51, n. 2, p. 165-172, 1999Tradução . . Disponível em: https://doi.org/10.1046/j.1365-2265.1999.00746.x. Acesso em: 18 out. 2024.
APA
Santos, C. L. S., Bikker, H., Rego, K. G. M., Nascimento, A. C., Tambascia, M., Vijlder, J. J. M. de, & Medeiros Neto, G. A. (1999). A novel mutation in the TPO gene in goitrous hypothyroid patients with iodide organification defect. Clinical Endocrinology, 51( 2), 165-172. doi:10.1046/j.1365-2265.1999.00746.x
NLM
Santos CLS, Bikker H, Rego KGM, Nascimento AC, Tambascia M, Vijlder JJM de, Medeiros Neto GA. A novel mutation in the TPO gene in goitrous hypothyroid patients with iodide organification defect [Internet]. Clinical Endocrinology. 1999 ; 51( 2): 165-172.[citado 2024 out. 18 ] Available from: https://doi.org/10.1046/j.1365-2265.1999.00746.x
Vancouver
Santos CLS, Bikker H, Rego KGM, Nascimento AC, Tambascia M, Vijlder JJM de, Medeiros Neto GA. A novel mutation in the TPO gene in goitrous hypothyroid patients with iodide organification defect [Internet]. Clinical Endocrinology. 1999 ; 51( 2): 165-172.[citado 2024 out. 18 ] Available from: https://doi.org/10.1046/j.1365-2265.1999.00746.x
Artigo de periodico
Dyshormonogenetic goiter: a morphological and immunohistochemical study (1994)
Matos, P. S.; Bisi, Hélio; Medeiros Neto, Geraldo Antônio
Source: Endocrine Pathology. Unidade: FM
Assunto: ENDOCRINOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MATOS, P. S. e BISI, Hélio e MEDEIROS NETO, Geraldo Antônio. Dyshormonogenetic goiter: a morphological and immunohistochemical study. Endocrine Pathology, v. 5, n. 1, p. 49-58, 1994Tradução . . Disponível em: https://doi.org/10.1007/bf02921370. Acesso em: 18 out. 2024.
APA
Matos, P. S., Bisi, H., & Medeiros Neto, G. A. (1994). Dyshormonogenetic goiter: a morphological and immunohistochemical study. Endocrine Pathology, 5( 1), 49-58. doi:10.1007/bf02921370
NLM
Matos PS, Bisi H, Medeiros Neto GA. Dyshormonogenetic goiter: a morphological and immunohistochemical study [Internet]. Endocrine Pathology. 1994 ; 5( 1): 49-58.[citado 2024 out. 18 ] Available from: https://doi.org/10.1007/bf02921370
Vancouver
Matos PS, Bisi H, Medeiros Neto GA. Dyshormonogenetic goiter: a morphological and immunohistochemical study [Internet]. Endocrine Pathology. 1994 ; 5( 1): 49-58.[citado 2024 out. 18 ] Available from: https://doi.org/10.1007/bf02921370
Artigo de periodico
Letters to the editors (1994)
Medeiros Neto, Geraldo Antônio
Source: Clinical Endocrinology. Unidade: FM
Assunto: ENDOCRINOLOGIA
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ABNT
MEDEIROS NETO, Geraldo Antônio. Letters to the editors. Clinical Endocrinology, v. 40, n. 3 , p. 435, 1994Tradução . . Acesso em: 18 out. 2024.
APA
Medeiros Neto, G. A. (1994). Letters to the editors. Clinical Endocrinology, 40( 3 ), 435.
NLM
Medeiros Neto GA. Letters to the editors. Clinical Endocrinology. 1994 ;40( 3 ): 435.[citado 2024 out. 18 ]
Vancouver
Medeiros Neto GA. Letters to the editors. Clinical Endocrinology. 1994 ;40( 3 ): 435.[citado 2024 out. 18 ]
Artigo de periodico
Nonsense mutation causes human hereditary congenital goiter with preferential production of a 171 nucleotide-deleted thyroglobulin ribunocleic acid messenger (1993)
Targovnik, H M; Medeiros Neto, Geraldo Antônio; Varela, V; Cochaux, P; Wajchenberg, B L; Vassart, G
Source: Journal of Clinical Endocrinology and Metabolism. Unidade: FM
Assunto: ENDOCRINOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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 . . Disponível em: https://doi.org/10.1210/jcem.77.1.8325944. Acesso em: 18 out. 2024.
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 [Internet]. Journal of Clinical Endocrinology and Metabolism. 1993 ;77( 1 ): 210-5.[citado 2024 out. 18 ] Available from: https://doi.org/10.1210/jcem.77.1.8325944
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 [Internet]. Journal of Clinical Endocrinology and Metabolism. 1993 ;77( 1 ): 210-5.[citado 2024 out. 18 ] Available from: https://doi.org/10.1210/jcem.77.1.8325944
Trabalho de evento
Genetic and molecular biological studies in defective iodide organification causing hereditary goiter and hypothyroidism (1993)
Medeiros Neto, Geraldo Antônio; Billerbeck, A E C; Wajchenberg, B L
Source: Progress in Endocrinology. Conference titles: International Congress of the Endocrinology. Unidade: FM
Assunto: ENDOCRINOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MEDEIROS NETO, Geraldo Antônio e BILLERBECK, A E C e WAJCHENBERG, B L. Genetic and molecular biological studies in defective iodide organification causing hereditary goiter and hypothyroidism. 1993, Anais.. Carnforth: Parthenon, 1993. . Acesso em: 18 out. 2024.
APA
Medeiros Neto, G. A., Billerbeck, A. E. C., & Wajchenberg, B. L. (1993). Genetic and molecular biological studies in defective iodide organification causing hereditary goiter and hypothyroidism. In Progress in Endocrinology. Carnforth: Parthenon.
NLM
Medeiros Neto GA, Billerbeck AEC, Wajchenberg BL. Genetic and molecular biological studies in defective iodide organification causing hereditary goiter and hypothyroidism. Progress in Endocrinology. 1993 ;[citado 2024 out. 18 ]
Vancouver
Medeiros Neto GA, Billerbeck AEC, Wajchenberg BL. Genetic and molecular biological studies in defective iodide organification causing hereditary goiter and hypothyroidism. Progress in Endocrinology. 1993 ;[citado 2024 out. 18 ]
Trabalho de evento-resumo
Genetic and molecular biological studies in defective iodide organification causing hereditary goiter and hypothyroidism (1992)
Medeiros Neto, Geraldo Antônio; Billerbeck, A E C; Wajchenberg, B L
Source: Progress in Endocrinology. Conference titles: International Congress of Endocrinology. Unidade: FM
Assunto: ENDOCRINOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MEDEIROS NETO, Geraldo Antônio e BILLERBECK, A E C e WAJCHENBERG, B L. Genetic and molecular biological studies in defective iodide organification causing hereditary goiter and hypothyroidism. 1992, Anais.. Carnforth: Parthenon Publishing Group, 1992. . Acesso em: 18 out. 2024.
APA
Medeiros Neto, G. A., Billerbeck, A. E. C., & Wajchenberg, B. L. (1992). Genetic and molecular biological studies in defective iodide organification causing hereditary goiter and hypothyroidism. In Progress in Endocrinology. Carnforth: Parthenon Publishing Group.
NLM
Medeiros Neto GA, Billerbeck AEC, Wajchenberg BL. Genetic and molecular biological studies in defective iodide organification causing hereditary goiter and hypothyroidism. Progress in Endocrinology. 1992 ;[citado 2024 out. 18 ]
Vancouver
Medeiros Neto GA, Billerbeck AEC, Wajchenberg BL. Genetic and molecular biological studies in defective iodide organification causing hereditary goiter and hypothyroidism. Progress in Endocrinology. 1992 ;[citado 2024 out. 18 ]
Artigo de periodico
Thyroid atrophy in myxoedematous endemic cretinism: possible role for growth-blocking immunoglobulins (1991)
Tsuboi, K; Lima, N; Ingbar, S H; Medeiros Neto, Geraldo Antônio
Source: Autoimmunity. Unidade: FM
Assunto: ENDOCRINOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TSUBOI, K et al. Thyroid atrophy in myxoedematous endemic cretinism: possible role for growth-blocking immunoglobulins. Autoimmunity, v. 9 , n. 4 , p. 201-6, 1991Tradução . . Acesso em: 18 out. 2024.
APA
Tsuboi, K., Lima, N., Ingbar, S. H., & Medeiros Neto, G. A. (1991). Thyroid atrophy in myxoedematous endemic cretinism: possible role for growth-blocking immunoglobulins. Autoimmunity, 9 ( 4 ), 201-6.
NLM
Tsuboi K, Lima N, Ingbar SH, Medeiros Neto GA. Thyroid atrophy in myxoedematous endemic cretinism: possible role for growth-blocking immunoglobulins. Autoimmunity. 1991 ;9 ( 4 ): 201-6.[citado 2024 out. 18 ]
Vancouver
Tsuboi K, Lima N, Ingbar SH, Medeiros Neto GA. Thyroid atrophy in myxoedematous endemic cretinism: possible role for growth-blocking immunoglobulins. Autoimmunity. 1991 ;9 ( 4 ): 201-6.[citado 2024 out. 18 ]
Artigo de periodico
Immunologically mediated cytotoxicity against human eye muscle and thyroid cells in enthyroid and thyrotoxic graves' ophthalmopathy (1991)
Medeiros Neto, Geraldo Antônio; Zhang, Z G; Lima, N; Iacona, A; Liberman, A; Salvi, M; Wall, J R
Source: Autoimmunity. Unidade: FM
Assunto: ENDOCRINOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MEDEIROS NETO, Geraldo Antônio et al. Immunologically mediated cytotoxicity against human eye muscle and thyroid cells in enthyroid and thyrotoxic graves' ophthalmopathy. Autoimmunity, v. 9 , p. 293-300, 1991Tradução . . Acesso em: 18 out. 2024.
APA
Medeiros Neto, G. A., Zhang, Z. G., Lima, N., Iacona, A., Liberman, A., Salvi, M., & Wall, J. R. (1991). Immunologically mediated cytotoxicity against human eye muscle and thyroid cells in enthyroid and thyrotoxic graves' ophthalmopathy. Autoimmunity, 9 , 293-300.
NLM
Medeiros Neto GA, Zhang ZG, Lima N, Iacona A, Liberman A, Salvi M, Wall JR. Immunologically mediated cytotoxicity against human eye muscle and thyroid cells in enthyroid and thyrotoxic graves' ophthalmopathy. Autoimmunity. 1991 ;9 293-300.[citado 2024 out. 18 ]
Vancouver
Medeiros Neto GA, Zhang ZG, Lima N, Iacona A, Liberman A, Salvi M, Wall JR. Immunologically mediated cytotoxicity against human eye muscle and thyroid cells in enthyroid and thyrotoxic graves' ophthalmopathy. Autoimmunity. 1991 ;9 293-300.[citado 2024 out. 18 ]
Artigo de periodico
Thyroid peroxidase in endemic goiter tissue (1990)
Sugawara, M; Summer, C N; Kobayashi, A; Murakami, S; Kuma, K; Medeiros Neto, Geraldo Antônio
Source: Journal of Endocrinological Investigation. Unidade: FM
Assunto: ENDOCRINOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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
Artigo de periodico
Dyshormonogenetic goiter: presence of an inhibitor of normal human thyroid peroxidase (1990)
Rosenthal, D; Carvalho Guimaraes, D P; Knobel, M; Medeiros Neto, Geraldo Antônio
Source: Journal of Endocrinological Investigation. Unidade: FM
Assunto: ENDOCRINOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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
Artigo de periodico
Alternative diagnosis for thyrotoxicosis associated with aeromegaly: primary thyroid hyperplasia due to elevated plasma levels of insulin-like growth factors (1990)
Mendonça, B. B.; Aguirre, A; Barca, M F; Madureira, G; Bloise, W; Liberman, Bernardo; Semer, M; Salgado, L R; Medeiros Neto, Geraldo Antônio
Source: Medical Science Research. Unidade: FM
Assunto: ENDOCRINOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MENDONÇA, B. B. et al. Alternative diagnosis for thyrotoxicosis associated with aeromegaly: primary thyroid hyperplasia due to elevated plasma levels of insulin-like growth factors. Medical Science Research, v. 18, p. 11-3, 1990Tradução . . Acesso em: 18 out. 2024.
APA
Mendonça, B. B., Aguirre, A., Barca, M. F., Madureira, G., Bloise, W., Liberman, B., et al. (1990). Alternative diagnosis for thyrotoxicosis associated with aeromegaly: primary thyroid hyperplasia due to elevated plasma levels of insulin-like growth factors. Medical Science Research, 18, 11-3.
NLM
Mendonça BB, Aguirre A, Barca MF, Madureira G, Bloise W, Liberman B, Semer M, Salgado LR, Medeiros Neto GA. Alternative diagnosis for thyrotoxicosis associated with aeromegaly: primary thyroid hyperplasia due to elevated plasma levels of insulin-like growth factors. Medical Science Research. 1990 ;18 11-3.[citado 2024 out. 18 ]
Vancouver
Mendonça BB, Aguirre A, Barca MF, Madureira G, Bloise W, Liberman B, Semer M, Salgado LR, Medeiros Neto GA. Alternative diagnosis for thyrotoxicosis associated with aeromegaly: primary thyroid hyperplasia due to elevated plasma levels of insulin-like growth factors. Medical Science Research. 1990 ;18 11-3.[citado 2024 out. 18 ]

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