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Trabalho de evento-resumo
Mutational analysis in brazilian patients with familial glucocorticoid deficiency (2007)
Collares, Cristhiana V. A.; Franca, Suzana N.; Drummond, Juliana; Pereira, Luis A.; Moreira, Ayrton Custódio; Clark, Adrian; Castro, Margaret de; Antunes-Rodrigues, José; Elias, Lucila Leico Kagohara
Fonte: Program and Abstracts. Nome do evento: The Endocrine Society's Annual Meeting (ENDO). Unidade: FMRP
Assuntos: RECEPTORES DE GLICOCORTICOIDES, MUTAÇÃO GENÉTICA, HORMÔNIOS
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ABNT
COLLARES, Cristhiana V. A. et al. Mutational analysis in brazilian patients with familial glucocorticoid deficiency. 2007, Anais.. Toronto: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, 2007. . Acesso em: 28 nov. 2025.
APA
Collares, C. V. A., Franca, S. N., Drummond, J., Pereira, L. A., Moreira, A. C., Clark, A., et al. (2007). Mutational analysis in brazilian patients with familial glucocorticoid deficiency. In Program and Abstracts. Toronto: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Collares CVA, Franca SN, Drummond J, Pereira LA, Moreira AC, Clark A, Castro M de, Antunes-Rodrigues J, Elias LLK. Mutational analysis in brazilian patients with familial glucocorticoid deficiency. Program and Abstracts. 2007 ;[citado 2025 nov. 28 ]
Vancouver
Collares CVA, Franca SN, Drummond J, Pereira LA, Moreira AC, Clark A, Castro M de, Antunes-Rodrigues J, Elias LLK. Mutational analysis in brazilian patients with familial glucocorticoid deficiency. Program and Abstracts. 2007 ;[citado 2025 nov. 28 ]
Trabalho de evento-resumo
A homozigous 25 Bp duplication (Nt 4157-4181) at exon 5 in the CYP17 resulting in a premature stop codon as a new cause of combined 17alpha-hydroxylase/17,20-lyase deficiency (2005)
Martin, Regina M.; Costa, Elaine F.; Arnhold, Ivo J. P.; Mendonça, Berenice B.
Fonte: Program and Abstracts. Nome do evento: The Endocrine Society's Annual Meeting. Unidade: FM
Assuntos: HIPERTENSÃO (ETIOLOGIA), MUTAÇÃO GENÉTICA, BRASILEIROS, HORMÔNIOS SEXUAIS (ANORMALIDADES)
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ABNT
MARTIN, Regina M. et al. A homozigous 25 Bp duplication (Nt 4157-4181) at exon 5 in the CYP17 resulting in a premature stop codon as a new cause of combined 17alpha-hydroxylase/17,20-lyase deficiency. 2005, Anais.. San Diego: Faculdade de Medicina, Universidade de São Paulo, 2005. . Acesso em: 28 nov. 2025.
APA
Martin, R. M., Costa, E. F., Arnhold, I. J. P., & Mendonça, B. B. (2005). A homozigous 25 Bp duplication (Nt 4157-4181) at exon 5 in the CYP17 resulting in a premature stop codon as a new cause of combined 17alpha-hydroxylase/17,20-lyase deficiency. In Program and Abstracts. San Diego: Faculdade de Medicina, Universidade de São Paulo.
NLM
Martin RM, Costa EF, Arnhold IJP, Mendonça BB. A homozigous 25 Bp duplication (Nt 4157-4181) at exon 5 in the CYP17 resulting in a premature stop codon as a new cause of combined 17alpha-hydroxylase/17,20-lyase deficiency. Program and Abstracts. 2005 ;[citado 2025 nov. 28 ]
Vancouver
Martin RM, Costa EF, Arnhold IJP, Mendonça BB. A homozigous 25 Bp duplication (Nt 4157-4181) at exon 5 in the CYP17 resulting in a premature stop codon as a new cause of combined 17alpha-hydroxylase/17,20-lyase deficiency. Program and Abstracts. 2005 ;[citado 2025 nov. 28 ]
Trabalho de evento-resumo
Prevalence of a genetic variant of luteinizing hormone (Tr8Arg and lle 15Thr) in a brazilian population of healthy subjects and in patients with hypogonadotropic hypogonadism (2005)
Berger, Karina; Billerbeck, Ana Elisa C.; Costa, Elaine M. F.; Cavalho, Luciani R.; Arnhold, Ivo J. P.; Mendonça, Berenice B.
Fonte: Program and Abstracts. Nome do evento: The Endocrine Society's Annual Meeting. Unidade: FM
Assuntos: POLIMORFISMO, TÉCNICAS CITOLÓGICAS, BRASILEIROS, MUTAÇÃO GENÉTICA
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ABNT
BERGER, Karina et al. Prevalence of a genetic variant of luteinizing hormone (Tr8Arg and lle 15Thr) in a brazilian population of healthy subjects and in patients with hypogonadotropic hypogonadism. 2005, Anais.. San Diego: Faculdade de Medicina, Universidade de São Paulo, 2005. . Acesso em: 28 nov. 2025.
APA
Berger, K., Billerbeck, A. E. C., Costa, E. M. F., Cavalho, L. R., Arnhold, I. J. P., & Mendonça, B. B. (2005). Prevalence of a genetic variant of luteinizing hormone (Tr8Arg and lle 15Thr) in a brazilian population of healthy subjects and in patients with hypogonadotropic hypogonadism. In Program and Abstracts. San Diego: Faculdade de Medicina, Universidade de São Paulo.
NLM
Berger K, Billerbeck AEC, Costa EMF, Cavalho LR, Arnhold IJP, Mendonça BB. Prevalence of a genetic variant of luteinizing hormone (Tr8Arg and lle 15Thr) in a brazilian population of healthy subjects and in patients with hypogonadotropic hypogonadism. Program and Abstracts. 2005 ;[citado 2025 nov. 28 ]
Vancouver
Berger K, Billerbeck AEC, Costa EMF, Cavalho LR, Arnhold IJP, Mendonça BB. Prevalence of a genetic variant of luteinizing hormone (Tr8Arg and lle 15Thr) in a brazilian population of healthy subjects and in patients with hypogonadotropic hypogonadism. Program and Abstracts. 2005 ;[citado 2025 nov. 28 ]
Trabalho de evento-resumo
The effects of pamindronate treatment in girls with polyostotic fibrous dysplasia in McCune Albrigth syndrome (2005)
Bezerra, Milena G. T.; Brito, Vinicius N.; Arnhold, Ivo J. P.; Mendonça, Berenice B.; Latronico, Ana C.
Fonte: Program and Abstracts. Nome do evento: The Endocrine Society's Annual Meeting. Unidade: FM
Assuntos: DOENÇA RARA, MUTAÇÃO GENÉTICA, FÁRMACOS (SISTEMA REPRODUTOR;EFEITOS ADVERSOS)
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ABNT
BEZERRA, Milena G. T. et al. The effects of pamindronate treatment in girls with polyostotic fibrous dysplasia in McCune Albrigth syndrome. 2005, Anais.. San Diego: Faculdade de Medicina, Universidade de São Paulo, 2005. . Acesso em: 28 nov. 2025.
APA
Bezerra, M. G. T., Brito, V. N., Arnhold, I. J. P., Mendonça, B. B., & Latronico, A. C. (2005). The effects of pamindronate treatment in girls with polyostotic fibrous dysplasia in McCune Albrigth syndrome. In Program and Abstracts. San Diego: Faculdade de Medicina, Universidade de São Paulo.
NLM
Bezerra MGT, Brito VN, Arnhold IJP, Mendonça BB, Latronico AC. The effects of pamindronate treatment in girls with polyostotic fibrous dysplasia in McCune Albrigth syndrome. Program and Abstracts. 2005 ;[citado 2025 nov. 28 ]
Vancouver
Bezerra MGT, Brito VN, Arnhold IJP, Mendonça BB, Latronico AC. The effects of pamindronate treatment in girls with polyostotic fibrous dysplasia in McCune Albrigth syndrome. Program and Abstracts. 2005 ;[citado 2025 nov. 28 ]
Trabalho de evento-resumo
Patients with Noonan syndrome without mutation in PTPN11repond better to GH treatment than patients with PTPN11 mutations (2005)
Jorge. Alexandre A. L.; Ferreira, Lize V.; Souza, Silvia A. L.; Arnhold, Ivo J. P.; Mendonça, Berenice B.
Fonte: Program and Abstracts. Nome do evento: The Endocrine Society's Annual Meeting. Unidade: FM
Assuntos: CRIANÇAS, SEGUIMENTOS, HORMÔNIO DO CRESCIMENTO (TERAPIA), MUTAÇÃO GENÉTICA
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ABNT
JORGE. ALEXANDRE A. L., et al. Patients with Noonan syndrome without mutation in PTPN11repond better to GH treatment than patients with PTPN11 mutations. 2005, Anais.. San Diego: Faculdade de Medicina, Universidade de São Paulo, 2005. . Acesso em: 28 nov. 2025.
APA
Jorge. Alexandre A. L.,, Ferreira, L. V., Souza, S. A. L., Arnhold, I. J. P., & Mendonça, B. B. (2005). Patients with Noonan syndrome without mutation in PTPN11repond better to GH treatment than patients with PTPN11 mutations. In Program and Abstracts. San Diego: Faculdade de Medicina, Universidade de São Paulo.
NLM
Jorge. Alexandre A. L., Ferreira LV, Souza SAL, Arnhold IJP, Mendonça BB. Patients with Noonan syndrome without mutation in PTPN11repond better to GH treatment than patients with PTPN11 mutations. Program and Abstracts. 2005 ;[citado 2025 nov. 28 ]
Vancouver
Jorge. Alexandre A. L., Ferreira LV, Souza SAL, Arnhold IJP, Mendonça BB. Patients with Noonan syndrome without mutation in PTPN11repond better to GH treatment than patients with PTPN11 mutations. Program and Abstracts. 2005 ;[citado 2025 nov. 28 ]
Trabalho de evento-resumo
Prevalence of mutations in gonadotropin-releasing hormone receptor (GnRH) gene in brazilian patients with hypogonadotropic hypogonadism and no olfaction (2005)
Costa, Elaine F.; Latronico, Ana Claudia; Arnhold, Ivo P.; Mendonça, Berenice B.
Fonte: Program and Abstracts. Nome do evento: The Endocrine Society's Annual Meeting. Unidade: FM
Assuntos: OLFATO, SÍNDROME DE KALLMANN, BRASILEIROS, HORMÔNIO LIBERADOR DE GONADOTROFINAS (ANORMALIDADES), MUTAÇÃO GENÉTICA
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ABNT
COSTA, Elaine F. et al. Prevalence of mutations in gonadotropin-releasing hormone receptor (GnRH) gene in brazilian patients with hypogonadotropic hypogonadism and no olfaction. 2005, Anais.. San Diego: Faculdade de Medicina, Universidade de São Paulo, 2005. . Acesso em: 28 nov. 2025.
APA
Costa, E. F., Latronico, A. C., Arnhold, I. P., & Mendonça, B. B. (2005). Prevalence of mutations in gonadotropin-releasing hormone receptor (GnRH) gene in brazilian patients with hypogonadotropic hypogonadism and no olfaction. In Program and Abstracts. San Diego: Faculdade de Medicina, Universidade de São Paulo.
NLM
Costa EF, Latronico AC, Arnhold IP, Mendonça BB. Prevalence of mutations in gonadotropin-releasing hormone receptor (GnRH) gene in brazilian patients with hypogonadotropic hypogonadism and no olfaction. Program and Abstracts. 2005 ;[citado 2025 nov. 28 ]
Vancouver
Costa EF, Latronico AC, Arnhold IP, Mendonça BB. Prevalence of mutations in gonadotropin-releasing hormone receptor (GnRH) gene in brazilian patients with hypogonadotropic hypogonadism and no olfaction. Program and Abstracts. 2005 ;[citado 2025 nov. 28 ]
Trabalho de evento-resumo
Absence of mutations in the entire coding region of FSH receptor in patients with latrogenic ovarian hyperstimulation syndrome (2005)
Alva, Catarina B. d; Serafini, Paulo; Motta, Eduardo; Kohek, Maria F.; Latronico, Ana C.; Mendonça, Berenice B.
Fonte: Program and Abstracts. Nome do evento: The Endocrine Society's Annual Meeting. Unidade: FM
Assuntos: OVÁRIO (FISIOPATOLOGIA), POLIMORFISMO, FERTILIDADE, MUTAÇÃO GENÉTICA
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ABNT
ALVA, Catarina B. d et al. Absence of mutations in the entire coding region of FSH receptor in patients with latrogenic ovarian hyperstimulation syndrome. 2005, Anais.. San Diego: Faculdade de Medicina, Universidade de São Paulo, 2005. . Acesso em: 28 nov. 2025.
APA
Alva, C. B. d, Serafini, P., Motta, E., Kohek, M. F., Latronico, A. C., & Mendonça, B. B. (2005). Absence of mutations in the entire coding region of FSH receptor in patients with latrogenic ovarian hyperstimulation syndrome. In Program and Abstracts. San Diego: Faculdade de Medicina, Universidade de São Paulo.
NLM
Alva CB d, Serafini P, Motta E, Kohek MF, Latronico AC, Mendonça BB. Absence of mutations in the entire coding region of FSH receptor in patients with latrogenic ovarian hyperstimulation syndrome. Program and Abstracts. 2005 ;[citado 2025 nov. 28 ]
Vancouver
Alva CB d, Serafini P, Motta E, Kohek MF, Latronico AC, Mendonça BB. Absence of mutations in the entire coding region of FSH receptor in patients with latrogenic ovarian hyperstimulation syndrome. Program and Abstracts. 2005 ;[citado 2025 nov. 28 ]
Trabalho de evento-resumo
A novel germline mutation (Y21X) in the PRKAR1A gene in a Brazilian family with Carney complex (2005)
Costa, Marcia H. S.; Almeida, Madson Q.; Domenice, Sorahia; Mendonça, Berenice B.; Fragoso, Maria Candida B. V.
Fonte: Program and Abstracts. Nome do evento: The Endocrine Society's Annual Meeting. Unidade: FM
Assuntos: IMAGEM POR RESSONÂNCIA MAGNÉTICA, MANIFESTAÇÕES CUTÂNEAS, BRASILEIROS, MUTAÇÃO GENÉTICA, FENÓTIPOS
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ABNT
COSTA, Marcia H. S. et al. A novel germline mutation (Y21X) in the PRKAR1A gene in a Brazilian family with Carney complex. 2005, Anais.. San Diego: Faculdade de Medicina, Universidade de São Paulo, 2005. . Acesso em: 28 nov. 2025.
APA
Costa, M. H. S., Almeida, M. Q., Domenice, S., Mendonça, B. B., & Fragoso, M. C. B. V. (2005). A novel germline mutation (Y21X) in the PRKAR1A gene in a Brazilian family with Carney complex. In Program and Abstracts. San Diego: Faculdade de Medicina, Universidade de São Paulo.
NLM
Costa MHS, Almeida MQ, Domenice S, Mendonça BB, Fragoso MCBV. A novel germline mutation (Y21X) in the PRKAR1A gene in a Brazilian family with Carney complex. Program and Abstracts. 2005 ;[citado 2025 nov. 28 ]
Vancouver
Costa MHS, Almeida MQ, Domenice S, Mendonça BB, Fragoso MCBV. A novel germline mutation (Y21X) in the PRKAR1A gene in a Brazilian family with Carney complex. Program and Abstracts. 2005 ;[citado 2025 nov. 28 ]
Trabalho de evento-resumo
Growth and bone mineral density in patients with androgem insensitivity syndrome with mutations in the androgen receptor gene (2005)
Danilovic, Debora L. S.; Costa, Elaine M. F.; Melo, Karla; Correa, Rafaela V.; Correa, Pedro H. S.; Mendonça, Berenice B.; Arnhold, Ivo J. P.; Fragoso, Maria Candida B. V.
Fonte: Program and Abstracts. Nome do evento: The Endocrine Society's Annual Meeting. Unidade: FM
Assuntos: ESTRÓGENOS (TERAPIA), DENSIDADE ÓSSEA, MUTAÇÃO GENÉTICA
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ABNT
DANILOVIC, Debora L. S. et al. Growth and bone mineral density in patients with androgem insensitivity syndrome with mutations in the androgen receptor gene. 2005, Anais.. San Diego: Faculdade de Medicina, Universidade de São Paulo, 2005. . Acesso em: 28 nov. 2025.
APA
Danilovic, D. L. S., Costa, E. M. F., Melo, K., Correa, R. V., Correa, P. H. S., Mendonça, B. B., et al. (2005). Growth and bone mineral density in patients with androgem insensitivity syndrome with mutations in the androgen receptor gene. In Program and Abstracts. San Diego: Faculdade de Medicina, Universidade de São Paulo.
NLM
Danilovic DLS, Costa EMF, Melo K, Correa RV, Correa PHS, Mendonça BB, Arnhold IJP, Fragoso MCBV. Growth and bone mineral density in patients with androgem insensitivity syndrome with mutations in the androgen receptor gene. Program and Abstracts. 2005 ;[citado 2025 nov. 28 ]
Vancouver
Danilovic DLS, Costa EMF, Melo K, Correa RV, Correa PHS, Mendonça BB, Arnhold IJP, Fragoso MCBV. Growth and bone mineral density in patients with androgem insensitivity syndrome with mutations in the androgen receptor gene. Program and Abstracts. 2005 ;[citado 2025 nov. 28 ]
Trabalho de evento-resumo
Allelic variantions of the LHX4 gene in patients with hypopituitarism and ectopic neurohypophysis (2004)
Melo, Maria E; Marui, Suemi; Gomes, Miriam C; Arnhold, Ivo J; Mendonça, Berenice Bilharinho de; Knopfelmacher, Mirta
Fonte: Program and Abstracts. Nome do evento: ENDO 2004: The Endocrine Society's Annual Meeting. Unidade: FM
Assuntos: DIFERENCIAÇÃO CELULCAR, MUTAÇÃO GENÉTICA, POLIMORFISMO, HIPÓFISE (ANORMALIDADES)
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ABNT
MELO, Maria E et al. Allelic variantions of the LHX4 gene in patients with hypopituitarism and ectopic neurohypophysis. 2004, Anais.. New Orleans: Faculdade de Medicina, Universidade de São Paulo, 2004. . Acesso em: 28 nov. 2025.
APA
Melo, M. E., Marui, S., Gomes, M. C., Arnhold, I. J., Mendonça, B. B. de, & Knopfelmacher, M. (2004). Allelic variantions of the LHX4 gene in patients with hypopituitarism and ectopic neurohypophysis. In Program and Abstracts. New Orleans: Faculdade de Medicina, Universidade de São Paulo.
NLM
Melo ME, Marui S, Gomes MC, Arnhold IJ, Mendonça BB de, Knopfelmacher M. Allelic variantions of the LHX4 gene in patients with hypopituitarism and ectopic neurohypophysis. Program and Abstracts. 2004 ;[citado 2025 nov. 28 ]
Vancouver
Melo ME, Marui S, Gomes MC, Arnhold IJ, Mendonça BB de, Knopfelmacher M. Allelic variantions of the LHX4 gene in patients with hypopituitarism and ectopic neurohypophysis. Program and Abstracts. 2004 ;[citado 2025 nov. 28 ]
Trabalho de evento-resumo
LH receptor mutations (2004)
Mendonca, B. B.; Arnhold, I. J.; Latronico, A. C.; Mendonca, B. B.
Fonte: Program and Abstracts. Nome do evento: International Congress of Endocrinology. Unidade: FM
Assuntos: RECEPTORES CELULARES, RECEPTORES DO FSH, RECEPTORES HORMONAIS, MUTAÇÃO GENÉTICA, GENES SUPRESSORES DE TUMOR
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ABNT
MENDONCA, B. B. et al. LH receptor mutations. 2004, Anais.. Lisboa: International Society of Endocrinology, 2004. . Acesso em: 28 nov. 2025.
APA
Mendonca, B. B., Arnhold, I. J., Latronico, A. C., & Mendonca, B. B. (2004). LH receptor mutations. In Program and Abstracts. Lisboa: International Society of Endocrinology.
NLM
Mendonca BB, Arnhold IJ, Latronico AC, Mendonca BB. LH receptor mutations. Program and Abstracts. 2004 ;[citado 2025 nov. 28 ]
Vancouver
Mendonca BB, Arnhold IJ, Latronico AC, Mendonca BB. LH receptor mutations. Program and Abstracts. 2004 ;[citado 2025 nov. 28 ]
Trabalho de evento-resumo
Low levels of GH andPRL release are responsive to hypothalamic factors in PROP-1 deficient, patients (2004)
Katakami, Hideki; Tojo, Katsuyoshi; Kikuchi, Kiyoshi; Nose, Osamu; Fujimoto, Shigehiro; Hayashida, Cesar Y; Toledo, Sergio P. A.; Hashida, Seiichi
Fonte: Program and Abstracts. Nome do evento: ENDO 2004: The Endocrine Society's Annual Meeting. Unidade: FM
Assuntos: HORMÔNIODO CRESCIMENTO ( DEFICIÊNCIA), MUTAÇÃO GENÉTICA, PROLACTINA, TESTES IMUNOLÓGICOS (MÉTODOS)
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ABNT
KATAKAMI, Hideki et al. Low levels of GH andPRL release are responsive to hypothalamic factors in PROP-1 deficient, patients. 2004, Anais.. New Orleans: Faculdade de Medicina, Universidade de São Paulo, 2004. . Acesso em: 28 nov. 2025.
APA
Katakami, H., Tojo, K., Kikuchi, K., Nose, O., Fujimoto, S., Hayashida, C. Y., et al. (2004). Low levels of GH andPRL release are responsive to hypothalamic factors in PROP-1 deficient, patients. In Program and Abstracts. New Orleans: Faculdade de Medicina, Universidade de São Paulo.
NLM
Katakami H, Tojo K, Kikuchi K, Nose O, Fujimoto S, Hayashida CY, Toledo SPA, Hashida S. Low levels of GH andPRL release are responsive to hypothalamic factors in PROP-1 deficient, patients. Program and Abstracts. 2004 ;[citado 2025 nov. 28 ]
Vancouver
Katakami H, Tojo K, Kikuchi K, Nose O, Fujimoto S, Hayashida CY, Toledo SPA, Hashida S. Low levels of GH andPRL release are responsive to hypothalamic factors in PROP-1 deficient, patients. Program and Abstracts. 2004 ;[citado 2025 nov. 28 ]
Trabalho de evento-resumo
High frequency of allelic variants in SF-1 (Steroidogenic Factor 1) gene in 46,XY sex-reversed patients (2004)
Correa, R. V.; Domenice, S.; Billerberck, A. E. C.; Mendonca, B. B.
Fonte: Program and Abstracts. Nome do evento: International Congress of Endocrinology. Unidade: FM
Assuntos: ANORMALIDADES CROMOSSÔMICAS, AGENESIA, GÔNADAS ANIMAL (ANORMALIDADES), MUTAÇÃO GENÉTICA, CROMOSSOMOS (ANORMALIDADES)
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ABNT
CORREA, R. V. et al. High frequency of allelic variants in SF-1 (Steroidogenic Factor 1) gene in 46,XY sex-reversed patients. 2004, Anais.. Lisboa: International Society of Endocrinology, 2004. . Acesso em: 28 nov. 2025.
APA
Correa, R. V., Domenice, S., Billerberck, A. E. C., & Mendonca, B. B. (2004). High frequency of allelic variants in SF-1 (Steroidogenic Factor 1) gene in 46,XY sex-reversed patients. In Program and Abstracts. Lisboa: International Society of Endocrinology.
NLM
Correa RV, Domenice S, Billerberck AEC, Mendonca BB. High frequency of allelic variants in SF-1 (Steroidogenic Factor 1) gene in 46,XY sex-reversed patients. Program and Abstracts. 2004 ;[citado 2025 nov. 28 ]
Vancouver
Correa RV, Domenice S, Billerberck AEC, Mendonca BB. High frequency of allelic variants in SF-1 (Steroidogenic Factor 1) gene in 46,XY sex-reversed patients. Program and Abstracts. 2004 ;[citado 2025 nov. 28 ]
Trabalho de evento-resumo
The unusually high incidence of germline Arg337His mutation in the p53 tumor suppressor gene among brazilian with adrenocortical tumors can be attributed to founder effect (2004)
Pinto, E. M.; Billerbeck, A. E.; Mendonca, B. B.; Latronico, A. C.
Fonte: Program and Abstracts. Nome do evento: International Congress of Endocrinology. Unidade: FM
Assuntos: BIOMARCADORES, MUTAÇÃO GENÉTICA, POLIMORFISMO, GENES SUPRESSORES DE TUMOR, BRASILEIROS
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ABNT
PINTO, E. M. et al. The unusually high incidence of germline Arg337His mutation in the p53 tumor suppressor gene among brazilian with adrenocortical tumors can be attributed to founder effect. 2004, Anais.. Lisboa: International Society of Endocrinology, 2004. . Acesso em: 28 nov. 2025.
APA
Pinto, E. M., Billerbeck, A. E., Mendonca, B. B., & Latronico, A. C. (2004). The unusually high incidence of germline Arg337His mutation in the p53 tumor suppressor gene among brazilian with adrenocortical tumors can be attributed to founder effect. In Program and Abstracts. Lisboa: International Society of Endocrinology.
NLM
Pinto EM, Billerbeck AE, Mendonca BB, Latronico AC. The unusually high incidence of germline Arg337His mutation in the p53 tumor suppressor gene among brazilian with adrenocortical tumors can be attributed to founder effect. Program and Abstracts. 2004 ;[citado 2025 nov. 28 ]
Vancouver
Pinto EM, Billerbeck AE, Mendonca BB, Latronico AC. The unusually high incidence of germline Arg337His mutation in the p53 tumor suppressor gene among brazilian with adrenocortical tumors can be attributed to founder effect. Program and Abstracts. 2004 ;[citado 2025 nov. 28 ]
Trabalho de evento-resumo
Evidence for a founder effect of the R337H mutation of p53 in brazilian patients with adrenocortical tumors (2004)
Pinto, Emilia M; Billerbeck, Ana Elisa C; Fragoso, Maria Candida B. V; Domenice, Sorahia; Mendonça, Berenice Bilharinho de; Latronico, Ana Claudia
Fonte: Program and Abstracts. Nome do evento: ENDO 2004: The Endocrine Society's Annual Meeting. Unidade: FM
Assuntos: BIOMARCADORES, MUTAÇÃO GENÉTICA, POLIMORFISMO, BRASILEIROS
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ABNT
PINTO, Emilia M et al. Evidence for a founder effect of the R337H mutation of p53 in brazilian patients with adrenocortical tumors. 2004, Anais.. New Orleans: Faculdade de Medicina, Universidade de São Paulo, 2004. . Acesso em: 28 nov. 2025.
APA
Pinto, E. M., Billerbeck, A. E. C., Fragoso, M. C. B. V., Domenice, S., Mendonça, B. B. de, & Latronico, A. C. (2004). Evidence for a founder effect of the R337H mutation of p53 in brazilian patients with adrenocortical tumors. In Program and Abstracts. New Orleans: Faculdade de Medicina, Universidade de São Paulo.
NLM
Pinto EM, Billerbeck AEC, Fragoso MCBV, Domenice S, Mendonça BB de, Latronico AC. Evidence for a founder effect of the R337H mutation of p53 in brazilian patients with adrenocortical tumors. Program and Abstracts. 2004 ;[citado 2025 nov. 28 ]
Vancouver
Pinto EM, Billerbeck AEC, Fragoso MCBV, Domenice S, Mendonça BB de, Latronico AC. Evidence for a founder effect of the R337H mutation of p53 in brazilian patients with adrenocortical tumors. Program and Abstracts. 2004 ;[citado 2025 nov. 28 ]
Trabalho de evento-resumo
No evidence of a role for activating mutations and polymorphisms of the FSH receptor in the pathogenesis of iatrogenic ovarian hyperstimulation syndrome (2004)
d'Alva, Catarina B; Serafini, Paulo; Motta, Eduardo; Koherk, Maria Beatriz F; Latronico, Ana Claudia; Mendonça, Berenice Bilharinho de
Fonte: Program and Abstracts. Nome do evento: ENDO 2004: The Endocrine Society's Annual Meeting. Unidade: FM
Assuntos: FERTILIZAÇÃO (TERAPIA), MUTAÇÃO GENÉTICA, POLIMORFISMO, OVÁRIO (FISIOPATOLOGIA)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
D'ALVA, Catarina B et al. No evidence of a role for activating mutations and polymorphisms of the FSH receptor in the pathogenesis of iatrogenic ovarian hyperstimulation syndrome. 2004, Anais.. New Orleans: Faculdade de Medicina, Universidade de São Paulo, 2004. . Acesso em: 28 nov. 2025.
APA
d'Alva, C. B., Serafini, P., Motta, E., Koherk, M. B. F., Latronico, A. C., & Mendonça, B. B. de. (2004). No evidence of a role for activating mutations and polymorphisms of the FSH receptor in the pathogenesis of iatrogenic ovarian hyperstimulation syndrome. In Program and Abstracts. New Orleans: Faculdade de Medicina, Universidade de São Paulo.
NLM
d'Alva CB, Serafini P, Motta E, Koherk MBF, Latronico AC, Mendonça BB de. No evidence of a role for activating mutations and polymorphisms of the FSH receptor in the pathogenesis of iatrogenic ovarian hyperstimulation syndrome. Program and Abstracts. 2004 ;[citado 2025 nov. 28 ]
Vancouver
d'Alva CB, Serafini P, Motta E, Koherk MBF, Latronico AC, Mendonça BB de. No evidence of a role for activating mutations and polymorphisms of the FSH receptor in the pathogenesis of iatrogenic ovarian hyperstimulation syndrome. Program and Abstracts. 2004 ;[citado 2025 nov. 28 ]
Trabalho de evento-resumo
Cortical bone mineral loss in multiple endocrine neoplasia type 1 (2004)
Lourenço, Delmar M; Ding, Changlin; Mackowiak, Ivone; Montenegro, Fabio; Cordeiro, Anói Castro; Machado, Marcel Cerqueira César; Levine, Michael A; Toledo, Sergio P. A.
Fonte: Program and Abstracts. Nome do evento: ENDO 2004: The Endocrine Society's Annual Meeting. Unidade: FM
Assuntos: GLÂNDULAS ENDÓCRINAS(PATOLOGIA), MUTAÇÃO GENÉTICA, DENSITOMETRIA ÓSSEA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LOURENÇO, Delmar M et al. Cortical bone mineral loss in multiple endocrine neoplasia type 1. 2004, Anais.. New Orleans: Faculdade de Medicina, Universidade de São Paulo, 2004. . Acesso em: 28 nov. 2025.
APA
Lourenço, D. M., Ding, C., Mackowiak, I., Montenegro, F., Cordeiro, A. C., Machado, M. C. C., et al. (2004). Cortical bone mineral loss in multiple endocrine neoplasia type 1. In Program and Abstracts. New Orleans: Faculdade de Medicina, Universidade de São Paulo.
NLM
Lourenço DM, Ding C, Mackowiak I, Montenegro F, Cordeiro AC, Machado MCC, Levine MA, Toledo SPA. Cortical bone mineral loss in multiple endocrine neoplasia type 1. Program and Abstracts. 2004 ;[citado 2025 nov. 28 ]
Vancouver
Lourenço DM, Ding C, Mackowiak I, Montenegro F, Cordeiro AC, Machado MCC, Levine MA, Toledo SPA. Cortical bone mineral loss in multiple endocrine neoplasia type 1. Program and Abstracts. 2004 ;[citado 2025 nov. 28 ]
Trabalho de evento-resumo
Pattern of TSH and PRL response to TRH in patients presenting hypopituitarism with an identified hypothalamic or pituitary origin (2004)
Carvalho, L. R.; Berger, K.; Melo, M. E.; Abrao, M.; Nishi, M.; Marui, S.; Estefan, V.; Arnhold, I. J. P.; Mendonca, B. B.
Fonte: Program and Abstracts. Nome do evento: International Congress of Endocrinology. Unidade: FM
Assuntos: MUTAÇÃO GENÉTICA, GLÂNDULA PITUITÁRIA ANTERIOR (DEFICIÊNCIA), DIAGNÓSTICO DIFERENCIAL, HORMÔNIOS TIREOIDIANOS (DEFICIÊNCIA)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CARVALHO, L. R. et al. Pattern of TSH and PRL response to TRH in patients presenting hypopituitarism with an identified hypothalamic or pituitary origin. 2004, Anais.. Lisboa: International Society of Endocrinology, 2004. . Acesso em: 28 nov. 2025.
APA
Carvalho, L. R., Berger, K., Melo, M. E., Abrao, M., Nishi, M., Marui, S., et al. (2004). Pattern of TSH and PRL response to TRH in patients presenting hypopituitarism with an identified hypothalamic or pituitary origin. In Program and Abstracts. Lisboa: International Society of Endocrinology.
NLM
Carvalho LR, Berger K, Melo ME, Abrao M, Nishi M, Marui S, Estefan V, Arnhold IJP, Mendonca BB. Pattern of TSH and PRL response to TRH in patients presenting hypopituitarism with an identified hypothalamic or pituitary origin. Program and Abstracts. 2004 ;[citado 2025 nov. 28 ]
Vancouver
Carvalho LR, Berger K, Melo ME, Abrao M, Nishi M, Marui S, Estefan V, Arnhold IJP, Mendonca BB. Pattern of TSH and PRL response to TRH in patients presenting hypopituitarism with an identified hypothalamic or pituitary origin. Program and Abstracts. 2004 ;[citado 2025 nov. 28 ]
Trabalho de evento-resumo
Long term primary hyperparathyroidism with severe bone disease, extremely high levels of serum PTH and a large single parathyroid adenoma (2004)
Freire, D. S; Alexandre, R. D; Camargo, R; Tomimori, E; Medeiros Neto, Geraldo Antônio
Fonte: Program and Abstracts. Nome do evento: ENDO 2004: The Endocrine Society's Annual Meeting. Unidade: FM
Assuntos: NEOPLASIA ENDÓCRINA MÚLTIPLA (GENÉTICA;COMPLICAÇÕES), MUTAÇÃO GENÉTICA, PERDA ÓSSEA, DENSITOMETRIA ÓSSEA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FREIRE, D. S et al. Long term primary hyperparathyroidism with severe bone disease, extremely high levels of serum PTH and a large single parathyroid adenoma. 2004, Anais.. New Orleans: Faculdade de Medicina, Universidade de São Paulo, 2004. . Acesso em: 28 nov. 2025.
APA
Freire, D. S., Alexandre, R. D., Camargo, R., Tomimori, E., & Medeiros Neto, G. A. (2004). Long term primary hyperparathyroidism with severe bone disease, extremely high levels of serum PTH and a large single parathyroid adenoma. In Program and Abstracts. New Orleans: Faculdade de Medicina, Universidade de São Paulo.
NLM
Freire DS, Alexandre RD, Camargo R, Tomimori E, Medeiros Neto GA. Long term primary hyperparathyroidism with severe bone disease, extremely high levels of serum PTH and a large single parathyroid adenoma. Program and Abstracts. 2004 ;[citado 2025 nov. 28 ]
Vancouver
Freire DS, Alexandre RD, Camargo R, Tomimori E, Medeiros Neto GA. Long term primary hyperparathyroidism with severe bone disease, extremely high levels of serum PTH and a large single parathyroid adenoma. Program and Abstracts. 2004 ;[citado 2025 nov. 28 ]
Trabalho de evento-resumo
Analysis of the LHX4 gene in patients with hypopituitarism and ectopic posterior pituitary lobe: Identification of four novel allelic variations (2004)
Melo, M. E.; Marui, S.; Leite, C. C.; Mendonca, B. B.; knoepfelmacher, M.
Fonte: Program and Abstracts. Nome do evento: International Congress of Endocrinology. Unidade: FM
Assuntos: MUTAÇÃO GENÉTICA, GLÂNDULA PITUITÁRIA (ANORMALIDADES;DEFICIÊNCIA), SEQUENCIAMENTO GENÉTICO, HORMÔNIO DO CRESCIMENTO (DEFICIÊNCIA)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MELO, M. E. et al. Analysis of the LHX4 gene in patients with hypopituitarism and ectopic posterior pituitary lobe: Identification of four novel allelic variations. 2004, Anais.. Lisboa: International Society of Endocrinology, 2004. . Acesso em: 28 nov. 2025.
APA
Melo, M. E., Marui, S., Leite, C. C., Mendonca, B. B., & knoepfelmacher, M. (2004). Analysis of the LHX4 gene in patients with hypopituitarism and ectopic posterior pituitary lobe: Identification of four novel allelic variations. In Program and Abstracts. Lisboa: International Society of Endocrinology.
NLM
Melo ME, Marui S, Leite CC, Mendonca BB, knoepfelmacher M. Analysis of the LHX4 gene in patients with hypopituitarism and ectopic posterior pituitary lobe: Identification of four novel allelic variations. Program and Abstracts. 2004 ;[citado 2025 nov. 28 ]
Vancouver
Melo ME, Marui S, Leite CC, Mendonca BB, knoepfelmacher M. Analysis of the LHX4 gene in patients with hypopituitarism and ectopic posterior pituitary lobe: Identification of four novel allelic variations. Program and Abstracts. 2004 ;[citado 2025 nov. 28 ]

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