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Trabalho de evento-resumo
Analysis of the promoter region of HESX1 in patients with combined pituitary hormone deficiency (CPHD) without mutations in the HESX1 coding sequence (2005)
Carvalho, Luciani R.; Antonini, Sonir Roberto Rauber; Castro, Margaret de; Arnhold, Ivo Jorge Prado; Mendonça, Berenice Bilharinho de
Source: Program and Abstracts. Conference titles: The Endocrine Society's Annual Meeting. Unidades: FMRP, FM
Assunto: ENDOCRINOLOGIA
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ABNT
CARVALHO, Luciani R. et al. Analysis of the promoter region of HESX1 in patients with combined pituitary hormone deficiency (CPHD) without mutations in the HESX1 coding sequence. 2005, Anais.. San Diego: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, 2005. . Acesso em: 10 ago. 2024.
APA
Carvalho, L. R., Antonini, S. R. R., Castro, M. de, Arnhold, I. J. P., & Mendonça, B. B. de. (2005). Analysis of the promoter region of HESX1 in patients with combined pituitary hormone deficiency (CPHD) without mutations in the HESX1 coding sequence. In Program and Abstracts. San Diego: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Carvalho LR, Antonini SRR, Castro M de, Arnhold IJP, Mendonça BB de. Analysis of the promoter region of HESX1 in patients with combined pituitary hormone deficiency (CPHD) without mutations in the HESX1 coding sequence. Program and Abstracts. 2005 ;[citado 2024 ago. 10 ]
Vancouver
Carvalho LR, Antonini SRR, Castro M de, Arnhold IJP, Mendonça BB de. Analysis of the promoter region of HESX1 in patients with combined pituitary hormone deficiency (CPHD) without mutations in the HESX1 coding sequence. Program and Abstracts. 2005 ;[citado 2024 ago. 10 ]
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.
Source: Program and Abstracts. Conference titles: The Endocrine Society's Annual Meeting. Unidade: FM
Subjects: 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: 10 ago. 2024.
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 2024 ago. 10 ]
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 2024 ago. 10 ]
Trabalho de evento-resumo
Molecular analysis of the GABA-A receptor alpha-1 subunit gene (GABRA1) and electroencephalographic findings in girls with idiopathic gonadotropin-dependent precocious puberty (2005)
Brito, Vinicius N.; Arnhold, Ivo J. P.; Mendonça, Berenice B.; Guilhoto, Laura M.; Freitas, Karina M.; Latronico, Ana C.
Source: Program and Abstracts. Conference titles: The Endocrine Society's Annual Meeting. Unidade: FM
Subjects: PUBERDADE PRECOCE (ETIOLOGIA), CRIANÇAS, GONADOTROFINAS, HORMÔNIOS HIPOFISÁRIOS (ANORMALIDADES)
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BRITO, Vinicius N. et al. Molecular analysis of the GABA-A receptor alpha-1 subunit gene (GABRA1) and electroencephalographic findings in girls with idiopathic gonadotropin-dependent precocious puberty. 2005, Anais.. San Diego: Faculdade de Medicina, Universidade de São Paulo, 2005. . Acesso em: 10 ago. 2024.
APA
Brito, V. N., Arnhold, I. J. P., Mendonça, B. B., Guilhoto, L. M., Freitas, K. M., & Latronico, A. C. (2005). Molecular analysis of the GABA-A receptor alpha-1 subunit gene (GABRA1) and electroencephalographic findings in girls with idiopathic gonadotropin-dependent precocious puberty. In Program and Abstracts. San Diego: Faculdade de Medicina, Universidade de São Paulo.
NLM
Brito VN, Arnhold IJP, Mendonça BB, Guilhoto LM, Freitas KM, Latronico AC. Molecular analysis of the GABA-A receptor alpha-1 subunit gene (GABRA1) and electroencephalographic findings in girls with idiopathic gonadotropin-dependent precocious puberty. Program and Abstracts. 2005 ;[citado 2024 ago. 10 ]
Vancouver
Brito VN, Arnhold IJP, Mendonça BB, Guilhoto LM, Freitas KM, Latronico AC. Molecular analysis of the GABA-A receptor alpha-1 subunit gene (GABRA1) and electroencephalographic findings in girls with idiopathic gonadotropin-dependent precocious puberty. Program and Abstracts. 2005 ;[citado 2024 ago. 10 ]
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.
Source: Program and Abstracts. Conference titles: The Endocrine Society's Annual Meeting. Unidade: FM
Subjects: 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: 10 ago. 2024.
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 2024 ago. 10 ]
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 2024 ago. 10 ]
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.
Source: Program and Abstracts. Conference titles: The Endocrine Society's Annual Meeting. Unidade: FM
Subjects: 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: 10 ago. 2024.
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 2024 ago. 10 ]
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 2024 ago. 10 ]
Trabalho de evento-resumo
Quality of life (QoL) in GH deficient adults of childhood onset (GHDA-CO) with and without long-term GH replacement therapy (2005)
Marquezini, Guilherme F.; Oliveira, Camila M.; Rodrigues, Alina C.; Bastos, Maria O.; Melo, Maria E.; Knoepfelmacher, Mirta; Mendonça, Berenice B.
Source: Program and Abstracts. Conference titles: The Endocrine Society's Annual Meeting. Unidade: FM
Subjects: QUESTIONÁRIOS, FADIGA (ETIOLOGIA), QUALIDADE DE VIDA
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ABNT
MARQUEZINI, Guilherme F. et al. Quality of life (QoL) in GH deficient adults of childhood onset (GHDA-CO) with and without long-term GH replacement therapy. 2005, Anais.. San Diego: Faculdade de Medicina, Universidade de São Paulo, 2005. . Acesso em: 10 ago. 2024.
APA
Marquezini, G. F., Oliveira, C. M., Rodrigues, A. C., Bastos, M. O., Melo, M. E., Knoepfelmacher, M., & Mendonça, B. B. (2005). Quality of life (QoL) in GH deficient adults of childhood onset (GHDA-CO) with and without long-term GH replacement therapy. In Program and Abstracts. San Diego: Faculdade de Medicina, Universidade de São Paulo.
NLM
Marquezini GF, Oliveira CM, Rodrigues AC, Bastos MO, Melo ME, Knoepfelmacher M, Mendonça BB. Quality of life (QoL) in GH deficient adults of childhood onset (GHDA-CO) with and without long-term GH replacement therapy. Program and Abstracts. 2005 ;[citado 2024 ago. 10 ]
Vancouver
Marquezini GF, Oliveira CM, Rodrigues AC, Bastos MO, Melo ME, Knoepfelmacher M, Mendonça BB. Quality of life (QoL) in GH deficient adults of childhood onset (GHDA-CO) with and without long-term GH replacement therapy. Program and Abstracts. 2005 ;[citado 2024 ago. 10 ]
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.
Source: Program and Abstracts. Conference titles: The Endocrine Society's Annual Meeting. Unidade: FM
Subjects: 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: 10 ago. 2024.
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 2024 ago. 10 ]
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 2024 ago. 10 ]
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.
Source: Program and Abstracts. Conference titles: The Endocrine Society's Annual Meeting. Unidade: FM
Subjects: 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: 10 ago. 2024.
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 2024 ago. 10 ]
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 2024 ago. 10 ]
Trabalho de evento-resumo
Analisys of the distribuition of class I and II VNTR alleles of the insulin gene linked minisatellite locus in type 1 diabetes mellitus in Brazil (2005)
Davini, E.; Silva, Maria Elizabeth Rossi; Alves, Lais Isidoro; Latronico, Ana Claudia; Rocha, Dalva Marreiro; Ursich, Mileni J.; Correia, Marcia Regina Santos; Fukui, Rosa T.
Source: Program and Abstracts. Conference titles: The Endocrine Society's Annual Meeting. Unidade: FM
Subjects: DOENÇAS AUTOIMUNES, DIABETES MELLITUS, AUTOANTICORPOS, GENÓTIPOS
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ABNT
DAVINI, E. et al. Analisys of the distribuition of class I and II VNTR alleles of the insulin gene linked minisatellite locus in type 1 diabetes mellitus in Brazil. 2005, Anais.. San Diego: Faculdade de Medicina, Universidade de São Paulo, 2005. . Acesso em: 10 ago. 2024.
APA
Davini, E., Silva, M. E. R., Alves, L. I., Latronico, A. C., Rocha, D. M., Ursich, M. J., et al. (2005). Analisys of the distribuition of class I and II VNTR alleles of the insulin gene linked minisatellite locus in type 1 diabetes mellitus in Brazil. In Program and Abstracts. San Diego: Faculdade de Medicina, Universidade de São Paulo.
NLM
Davini E, Silva MER, Alves LI, Latronico AC, Rocha DM, Ursich MJ, Correia MRS, Fukui RT. Analisys of the distribuition of class I and II VNTR alleles of the insulin gene linked minisatellite locus in type 1 diabetes mellitus in Brazil. Program and Abstracts. 2005 ;[citado 2024 ago. 10 ]
Vancouver
Davini E, Silva MER, Alves LI, Latronico AC, Rocha DM, Ursich MJ, Correia MRS, Fukui RT. Analisys of the distribuition of class I and II VNTR alleles of the insulin gene linked minisatellite locus in type 1 diabetes mellitus in Brazil. Program and Abstracts. 2005 ;[citado 2024 ago. 10 ]
Trabalho de evento-resumo
Absence of mutations in the follicle-stimulating hormone receptor gene in children with primary hypothyroidism and gonadal hyperstimulation (2005)
Alva, Catarina B. d; Suarez, Elizabeth; Latronico, Ana C.; Mendonça, Berenice B.
Source: Program and Abstracts. Conference titles: The Endocrine Society's Annual Meeting. Unidade: FM
Subjects: CRIANÇAS, POLIMORFISMO, HIPOTIROIDISMO (ETIOLOGIA)
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ABNT
ALVA, Catarina B. d et al. Absence of mutations in the follicle-stimulating hormone receptor gene in children with primary hypothyroidism and gonadal hyperstimulation. 2005, Anais.. San Diego: Faculdade de Medicina, Universidade de São Paulo, 2005. . Acesso em: 10 ago. 2024.
APA
Alva, C. B. d, Suarez, E., Latronico, A. C., & Mendonça, B. B. (2005). Absence of mutations in the follicle-stimulating hormone receptor gene in children with primary hypothyroidism and gonadal hyperstimulation. In Program and Abstracts. San Diego: Faculdade de Medicina, Universidade de São Paulo.
NLM
Alva CB d, Suarez E, Latronico AC, Mendonça BB. Absence of mutations in the follicle-stimulating hormone receptor gene in children with primary hypothyroidism and gonadal hyperstimulation. Program and Abstracts. 2005 ;[citado 2024 ago. 10 ]
Vancouver
Alva CB d, Suarez E, Latronico AC, Mendonça BB. Absence of mutations in the follicle-stimulating hormone receptor gene in children with primary hypothyroidism and gonadal hyperstimulation. Program and Abstracts. 2005 ;[citado 2024 ago. 10 ]
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.
Source: Program and Abstracts. Conference titles: The Endocrine Society's Annual Meeting. Unidade: FM
Subjects: 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: 10 ago. 2024.
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 2024 ago. 10 ]
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 2024 ago. 10 ]
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.
Source: Program and Abstracts. Conference titles: The Endocrine Society's Annual Meeting. Unidade: FM
Subjects: 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: 10 ago. 2024.
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 2024 ago. 10 ]
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 2024 ago. 10 ]
Trabalho de evento-resumo
Glucose metabolism and body composition during long-term growth hormone replacement therapy in adults with growth hormone deficiency of childhood-onset (GHDA-CO) (2005)
Bastos, Maria socorro C. B. O.; Marquezine, Guilherme F.; Oliveira, Camila M.; Rodrigues, Alina C.; Melo, Maria Edna; Fragoso, Maria Candida B. V.; Mendonça, Berenice B.; Knoepfelmacher, Mirta
Source: Program and Abstracts. Conference titles: The Endocrine Society's Annual Meeting. Unidade: FM
Subjects: HIPERLIPIDEMIA (ETIOLOGIA), TERAPIA DE REPOSIÇÃO HORMONAL, GANHO DE PESO (ETIOLOGIA), HORMÔNIO DO CRESCIMENTO
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ABNT
BASTOS, Maria socorro C. B. O. et al. Glucose metabolism and body composition during long-term growth hormone replacement therapy in adults with growth hormone deficiency of childhood-onset (GHDA-CO). 2005, Anais.. San Diego: Faculdade de Medicina, Universidade de São Paulo, 2005. . Acesso em: 10 ago. 2024.
APA
Bastos, M. socorro C. B. O., Marquezine, G. F., Oliveira, C. M., Rodrigues, A. C., Melo, M. E., Fragoso, M. C. B. V., et al. (2005). Glucose metabolism and body composition during long-term growth hormone replacement therapy in adults with growth hormone deficiency of childhood-onset (GHDA-CO). In Program and Abstracts. San Diego: Faculdade de Medicina, Universidade de São Paulo.
NLM
Bastos M socorro CBO, Marquezine GF, Oliveira CM, Rodrigues AC, Melo ME, Fragoso MCBV, Mendonça BB, Knoepfelmacher M. Glucose metabolism and body composition during long-term growth hormone replacement therapy in adults with growth hormone deficiency of childhood-onset (GHDA-CO). Program and Abstracts. 2005 ;[citado 2024 ago. 10 ]
Vancouver
Bastos M socorro CBO, Marquezine GF, Oliveira CM, Rodrigues AC, Melo ME, Fragoso MCBV, Mendonça BB, Knoepfelmacher M. Glucose metabolism and body composition during long-term growth hormone replacement therapy in adults with growth hormone deficiency of childhood-onset (GHDA-CO). Program and Abstracts. 2005 ;[citado 2024 ago. 10 ]
Trabalho de evento-resumo
Expression of type-2 matrix metalloproteinase (MMP2) by metastatic and non-metastatic adrenocortical tumours (2005)
Lerario, Antonio M.; Mendonça, Berenice B.; Domenice, Sorahia; Costa, Marcia H.; Lin, Chin J.
Source: Program and Abstracts. Conference titles: The Endocrine Society's Annual Meeting. Unidade: FM
Subjects: BIOMARCADORES, NEOPLASIAS (HISTOLOGIA), PROGNÓSTICO, METÁSTASE NEOPLÁSICA
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ABNT
LERARIO, Antonio M. et al. Expression of type-2 matrix metalloproteinase (MMP2) by metastatic and non-metastatic adrenocortical tumours. 2005, Anais.. San Diego: Faculdade de Medicina, Universidade de São Paulo, 2005. . Acesso em: 10 ago. 2024.
APA
Lerario, A. M., Mendonça, B. B., Domenice, S., Costa, M. H., & Lin, C. J. (2005). Expression of type-2 matrix metalloproteinase (MMP2) by metastatic and non-metastatic adrenocortical tumours. In Program and Abstracts. San Diego: Faculdade de Medicina, Universidade de São Paulo.
NLM
Lerario AM, Mendonça BB, Domenice S, Costa MH, Lin CJ. Expression of type-2 matrix metalloproteinase (MMP2) by metastatic and non-metastatic adrenocortical tumours. Program and Abstracts. 2005 ;[citado 2024 ago. 10 ]
Vancouver
Lerario AM, Mendonça BB, Domenice S, Costa MH, Lin CJ. Expression of type-2 matrix metalloproteinase (MMP2) by metastatic and non-metastatic adrenocortical tumours. Program and Abstracts. 2005 ;[citado 2024 ago. 10 ]
Trabalho de evento-resumo
Rearrangement between CYP19 and MAPK6 genes as cause of aromatase excess syndrome in a brazilian family (2005)
Martin, Regina M.; Nishi, Mirian Y.; Demura, Masashi; Lin, Chin J.; Mendonça, Berenice B.; Bulun, Serdar E.
Source: Program and Abstracts. Conference titles: The Endocrine Society's Annual Meeting. Unidade: FM
Subjects: REAÇÃO EM CADEIA POR POLIMERASE, DOENÇAS HEREDITÁRIAS, HORMÔNIOS SEXUAIS (ANORMALIDADES), ESTRÓGENOS
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ABNT
MARTIN, Regina M. et al. Rearrangement between CYP19 and MAPK6 genes as cause of aromatase excess syndrome in a brazilian family. 2005, Anais.. San Diego: Faculdade de Medicina, Universidade de São Paulo, 2005. . Acesso em: 10 ago. 2024.
APA
Martin, R. M., Nishi, M. Y., Demura, M., Lin, C. J., Mendonça, B. B., & Bulun, S. E. (2005). Rearrangement between CYP19 and MAPK6 genes as cause of aromatase excess syndrome in a brazilian family. In Program and Abstracts. San Diego: Faculdade de Medicina, Universidade de São Paulo.
NLM
Martin RM, Nishi MY, Demura M, Lin CJ, Mendonça BB, Bulun SE. Rearrangement between CYP19 and MAPK6 genes as cause of aromatase excess syndrome in a brazilian family. Program and Abstracts. 2005 ;[citado 2024 ago. 10 ]
Vancouver
Martin RM, Nishi MY, Demura M, Lin CJ, Mendonça BB, Bulun SE. Rearrangement between CYP19 and MAPK6 genes as cause of aromatase excess syndrome in a brazilian family. Program and Abstracts. 2005 ;[citado 2024 ago. 10 ]
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.
Source: Program and Abstracts. Conference titles: The Endocrine Society's Annual Meeting. Unidade: FM
Subjects: ESTRÓGENOS (TERAPIA), DENSIDADE ÓSSEA, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 10 ago. 2024.
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 2024 ago. 10 ]
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 2024 ago. 10 ]
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
Source: Program and Abstracts. Conference titles: ENDO 2004: The Endocrine Society's Annual Meeting. Unidade: FM
Subjects: DIFERENCIAÇÃO CELULCAR, MUTAÇÃO GENÉTICA, POLIMORFISMO, HIPÓFISE (ANORMALIDADES)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 10 ago. 2024.
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 2024 ago. 10 ]
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 2024 ago. 10 ]
Trabalho de evento-resumo
LH receptor mutations (2004)
Mendonca, B. B.; Arnhold, I. J.; Latronico, A. C.; Mendonca, B. B.
Source: Program and Abstracts. Conference titles: International Congress of Endocrinology. Unidade: FM
Subjects: RECEPTORES CELULARES, RECEPTORES DO FSH, RECEPTORES HORMONAIS, MUTAÇÃO GENÉTICA, GENES SUPRESSORES DE TUMOR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MENDONCA, B. B. et al. LH receptor mutations. 2004, Anais.. Lisboa: International Society of Endocrinology, 2004. . Acesso em: 10 ago. 2024.
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 2024 ago. 10 ]
Vancouver
Mendonca BB, Arnhold IJ, Latronico AC, Mendonca BB. LH receptor mutations. Program and Abstracts. 2004 ;[citado 2024 ago. 10 ]
Trabalho de evento-resumo
Effect of severe long-standing hyperandrogenemia on pituitary-gonadal axis in females with virilizing tumors (2004)
Ferraz de Souza, B.; D' Alva, C. B.; Normando, A. P. C.; Hayashida, S.; Mendonca, B. B.; Marcondes, J. A. M.
Source: Program and Abstracts. Conference titles: International Congress of Endocrinology. Unidade: FM
Subjects: NEOPLASIAS OVARIANAS (ETIOLOGIA;CIRURGIA), HORMÔNIOS HIPOTALÂMICOS (ANÁLISE), HORMÔNIOS SEXUAIS (DEFICIÊNCIA;ANORMALIDADES)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FERRAZ DE SOUZA, B. et al. Effect of severe long-standing hyperandrogenemia on pituitary-gonadal axis in females with virilizing tumors. 2004, Anais.. Lisboa: International Society of Endocrinology, 2004. . Acesso em: 10 ago. 2024.
APA
Ferraz de Souza, B., D' Alva, C. B., Normando, A. P. C., Hayashida, S., Mendonca, B. B., & Marcondes, J. A. M. (2004). Effect of severe long-standing hyperandrogenemia on pituitary-gonadal axis in females with virilizing tumors. In Program and Abstracts. Lisboa: International Society of Endocrinology.
NLM
Ferraz de Souza B, D' Alva CB, Normando APC, Hayashida S, Mendonca BB, Marcondes JAM. Effect of severe long-standing hyperandrogenemia on pituitary-gonadal axis in females with virilizing tumors. Program and Abstracts. 2004 ;[citado 2024 ago. 10 ]
Vancouver
Ferraz de Souza B, D' Alva CB, Normando APC, Hayashida S, Mendonca BB, Marcondes JAM. Effect of severe long-standing hyperandrogenemia on pituitary-gonadal axis in females with virilizing tumors. Program and Abstracts. 2004 ;[citado 2024 ago. 10 ]
Trabalho de evento-resumo
Mutational analysis of neuropeptide y-y1 receptor gene (npy-y1) in human idiopathic pubertal disorders (2004)
Freitas, K.; Brito, V.; Costa, E.; Arnhold, I.; Mendonca, B. B.; Latronico, A. C.
Source: Program and Abstracts. Conference titles: International Congress of Endocrinology. Unidade: FM
Subjects: HORMÔNIO DO CRESCIMENTO (SECREÇÃO), PUBERDADE PRECOCE (ANORMALIDADES;GENÉTICAS), SEQUENCIAMENTO GENÉTICO, HORMÔNIOS SEXUAIS (GENÉTICA)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FREITAS, K. et al. Mutational analysis of neuropeptide y-y1 receptor gene (npy-y1) in human idiopathic pubertal disorders. 2004, Anais.. Lisboa: International Society of Endocrinology, 2004. . Acesso em: 10 ago. 2024.
APA
Freitas, K., Brito, V., Costa, E., Arnhold, I., Mendonca, B. B., & Latronico, A. C. (2004). Mutational analysis of neuropeptide y-y1 receptor gene (npy-y1) in human idiopathic pubertal disorders. In Program and Abstracts. Lisboa: International Society of Endocrinology.
NLM
Freitas K, Brito V, Costa E, Arnhold I, Mendonca BB, Latronico AC. Mutational analysis of neuropeptide y-y1 receptor gene (npy-y1) in human idiopathic pubertal disorders. Program and Abstracts. 2004 ;[citado 2024 ago. 10 ]
Vancouver
Freitas K, Brito V, Costa E, Arnhold I, Mendonca BB, Latronico AC. Mutational analysis of neuropeptide y-y1 receptor gene (npy-y1) in human idiopathic pubertal disorders. Program and Abstracts. 2004 ;[citado 2024 ago. 10 ]

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