ReP USP - Resultado da busca

Artigo de periodico
Obesity as a Thrombogenic and Cardiovascular Risk Factor in Children (2022)
Cominato, Louise; Franco, Ruth Rocha; Ybarra, Marina; Frascino, Alexandre Viana; Steinmetz, Leandra; Ferraro, Alexandre Archanjo ; Carneiro, Jorge David Aivazoglou; Damiani, Durval
Source: Hormone research in paediatrics. Unidade: FM
Subjects: CRIANÇAS, OBESIDADE, FATORES DE RISCO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
COMINATO, Louise et al. Obesity as a Thrombogenic and Cardiovascular Risk Factor in Children. Hormone research in paediatrics, v. 94, n. 11-12, p. 410-415, 2022Tradução . . Disponível em: https://doi.org/10.1159/000519264. Acesso em: 05 nov. 2024.
APA
Cominato, L., Franco, R. R., Ybarra, M., Frascino, A. V., Steinmetz, L., Ferraro, A. A., et al. (2022). Obesity as a Thrombogenic and Cardiovascular Risk Factor in Children. Hormone research in paediatrics, 94( 11-12), 410-415. doi:10.1159/000519264
NLM
Cominato L, Franco RR, Ybarra M, Frascino AV, Steinmetz L, Ferraro AA, Carneiro JDA, Damiani D. Obesity as a Thrombogenic and Cardiovascular Risk Factor in Children [Internet]. Hormone research in paediatrics. 2022 ; 94( 11-12): 410-415.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1159/000519264
Vancouver
Cominato L, Franco RR, Ybarra M, Frascino AV, Steinmetz L, Ferraro AA, Carneiro JDA, Damiani D. Obesity as a Thrombogenic and Cardiovascular Risk Factor in Children [Internet]. Hormone research in paediatrics. 2022 ; 94( 11-12): 410-415.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1159/000519264
Artigo de periodico
Growth and Clinical Characteristics of Children with Floating-Harbor Syndrome: Analysis of Current Original Data and a Review of the Literature (2020)
Homma, Thais K; Freire, Bruna L; Honjo, Rachel; Dauber, Andrew; Funari, Mariana F. A; Lerario, Antonio M; Albuquerque, Edoarda V. A; Vasques, Gabriela A; Bertola, Debora R; Kim, Chong Ae ; Jorge, Alexander Augusto de Lima
Source: Hormone research in paediatrics. Unidade: FM
Subjects: EXONS, TERAPÊUTICA, CRESCIMENTO, HORMÔNIO DO CRESCIMENTO, MUTAÇÃO, FENÓTIPOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
HOMMA, Thais K et al. Growth and Clinical Characteristics of Children with Floating-Harbor Syndrome: Analysis of Current Original Data and a Review of the Literature. Hormone research in paediatrics, v. 92, n. 2, p. 115-123, 2020Tradução . . Disponível em: https://doi.org/10.1159/000503782. Acesso em: 05 nov. 2024.
APA
Homma, T. K., Freire, B. L., Honjo, R., Dauber, A., Funari, M. F. A., Lerario, A. M., et al. (2020). Growth and Clinical Characteristics of Children with Floating-Harbor Syndrome: Analysis of Current Original Data and a Review of the Literature. Hormone research in paediatrics, 92( 2), 115-123. doi:10.1159/000503782
NLM
Homma TK, Freire BL, Honjo R, Dauber A, Funari MFA, Lerario AM, Albuquerque EVA, Vasques GA, Bertola DR, Kim CA, Jorge AA de L. Growth and Clinical Characteristics of Children with Floating-Harbor Syndrome: Analysis of Current Original Data and a Review of the Literature [Internet]. Hormone research in paediatrics. 2020 ; 92( 2): 115-123.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1159/000503782
Vancouver
Homma TK, Freire BL, Honjo R, Dauber A, Funari MFA, Lerario AM, Albuquerque EVA, Vasques GA, Bertola DR, Kim CA, Jorge AA de L. Growth and Clinical Characteristics of Children with Floating-Harbor Syndrome: Analysis of Current Original Data and a Review of the Literature [Internet]. Hormone research in paediatrics. 2020 ; 92( 2): 115-123.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1159/000503782
Artigo de periodico
A Bayesian approach to diagnose growth hormone deficiency in children: insulin-like growth factor type 1 is valuable for screening and IGF-binding protein type 3 for confirmation (2020)
Inoue-lima, Thais H; Vasques, Gabriela A; Nakaguma, Marilena; Brito, Luciana Pinto; Mendonca, Berenice Bilharinho de ; Arnhold, Ivo J. P; Jorge, Alexander Augusto de Lima
Source: Hormone research in paediatrics. Unidade: FM
Subjects: HORMÔNIO DO CRESCIMENTO, ESTUDOS RETROSPECTIVOS, PROTEÍNA 3 DE LIGAÇÃO AOS FATORES DE CRESCIMENTO INSULIN-LIKE, CRIANÇAS EM IDADE PRÉ-ESCOLAR, FATOR DE CRESCIMENTO INSULIN-LIKE I
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
INOUE-LIMA, Thais H et al. A Bayesian approach to diagnose growth hormone deficiency in children: insulin-like growth factor type 1 is valuable for screening and IGF-binding protein type 3 for confirmation. Hormone research in paediatrics, v. 93, n. 3, p. 197-205, 2020Tradução . . Disponível em: https://doi.org/10.1159/000509840. Acesso em: 05 nov. 2024.
APA
Inoue-lima, T. H., Vasques, G. A., Nakaguma, M., Brito, L. P., Mendonca, B. B. de, Arnhold, I. J. P., & Jorge, A. A. de L. (2020). A Bayesian approach to diagnose growth hormone deficiency in children: insulin-like growth factor type 1 is valuable for screening and IGF-binding protein type 3 for confirmation. Hormone research in paediatrics, 93( 3), 197-205. doi:10.1159/000509840
NLM
Inoue-lima TH, Vasques GA, Nakaguma M, Brito LP, Mendonca BB de, Arnhold IJP, Jorge AA de L. A Bayesian approach to diagnose growth hormone deficiency in children: insulin-like growth factor type 1 is valuable for screening and IGF-binding protein type 3 for confirmation [Internet]. Hormone research in paediatrics. 2020 ; 93( 3): 197-205.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1159/000509840
Vancouver
Inoue-lima TH, Vasques GA, Nakaguma M, Brito LP, Mendonca BB de, Arnhold IJP, Jorge AA de L. A Bayesian approach to diagnose growth hormone deficiency in children: insulin-like growth factor type 1 is valuable for screening and IGF-binding protein type 3 for confirmation [Internet]. Hormone research in paediatrics. 2020 ; 93( 3): 197-205.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1159/000509840
Artigo de periodico
Diagnosis, Genetics, and Therapy of Short Stature in Children: A Growth Hormone Research Society International Perspective (2019)
Collett-solberg, Paulo F; Ambler, Geoffrey; Backeljauw, Philippe F; Bidlingmaier, Martin; Biller, Beverly M. K; Boguszewski, Margaret C. S; Cheung, Pik To; Choong, Catherine Seut Yhoke; Cohen, Laurie E; Jorge, Alexander Augusto de Lima
Source: Hormone research in paediatrics. Unidade: FM
Subjects: TRANSTORNOS DO CRESCIMENTO, HORMÔNIO DO CRESCIMENTO, CRIANÇAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
COLLETT-SOLBERG, Paulo F et al. Diagnosis, Genetics, and Therapy of Short Stature in Children: A Growth Hormone Research Society International Perspective. Hormone research in paediatrics, v. 92, n. 1, p. 1-14, 2019Tradução . . Disponível em: https://doi.org/10.1159/000502231. Acesso em: 05 nov. 2024.
APA
Collett-solberg, P. F., Ambler, G., Backeljauw, P. F., Bidlingmaier, M., Biller, B. M. K., Boguszewski, M. C. S., et al. (2019). Diagnosis, Genetics, and Therapy of Short Stature in Children: A Growth Hormone Research Society International Perspective. Hormone research in paediatrics, 92( 1), 1-14. doi:10.1159/000502231
NLM
Collett-solberg PF, Ambler G, Backeljauw PF, Bidlingmaier M, Biller BMK, Boguszewski MCS, Cheung PT, Choong CSY, Cohen LE, Jorge AA de L. Diagnosis, Genetics, and Therapy of Short Stature in Children: A Growth Hormone Research Society International Perspective [Internet]. Hormone research in paediatrics. 2019 ; 92( 1): 1-14.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1159/000502231
Vancouver
Collett-solberg PF, Ambler G, Backeljauw PF, Bidlingmaier M, Biller BMK, Boguszewski MCS, Cheung PT, Choong CSY, Cohen LE, Jorge AA de L. Diagnosis, Genetics, and Therapy of Short Stature in Children: A Growth Hormone Research Society International Perspective [Internet]. Hormone research in paediatrics. 2019 ; 92( 1): 1-14.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1159/000502231
Artigo de periodico
Impact of growth hormone therapy on adult height in patients with PTPN11 mutations related to Noonan Syndrome (2019)
Malaquias, Alexsandra C; Noronha, Renata M; Souza, Thaiana T. O; Homma, Thais K; Funari, Mariana F. A; Yamamoto, Guilherme L; Silva, Fernanda Viana; Moraes, Michelle B; Kim, Chong Ae ; Jorge, Alexander Augusto de Lima
Source: Hormone research in paediatrics. Unidade: FM
Subjects: SÍNDROME DE NOONAN, HORMÔNIO DO CRESCIMENTO, PROTEÍNAS TIROSINA FOSFATASES, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MALAQUIAS, Alexsandra C et al. Impact of growth hormone therapy on adult height in patients with PTPN11 mutations related to Noonan Syndrome. Hormone research in paediatrics, v. 91, n. 4, p. 252-261, 2019Tradução . . Disponível em: https://doi.org/10.1159/000500264. Acesso em: 05 nov. 2024.
APA
Malaquias, A. C., Noronha, R. M., Souza, T. T. O., Homma, T. K., Funari, M. F. A., Yamamoto, G. L., et al. (2019). Impact of growth hormone therapy on adult height in patients with PTPN11 mutations related to Noonan Syndrome. Hormone research in paediatrics, 91( 4), 252-261. doi:10.1159/000500264
NLM
Malaquias AC, Noronha RM, Souza TTO, Homma TK, Funari MFA, Yamamoto GL, Silva FV, Moraes MB, Kim CA, Jorge AA de L. Impact of growth hormone therapy on adult height in patients with PTPN11 mutations related to Noonan Syndrome [Internet]. Hormone research in paediatrics. 2019 ; 91( 4): 252-261.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1159/000500264
Vancouver
Malaquias AC, Noronha RM, Souza TTO, Homma TK, Funari MFA, Yamamoto GL, Silva FV, Moraes MB, Kim CA, Jorge AA de L. Impact of growth hormone therapy on adult height in patients with PTPN11 mutations related to Noonan Syndrome [Internet]. Hormone research in paediatrics. 2019 ; 91( 4): 252-261.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1159/000500264
Artigo de periodico
Premature pubarche due to exogenous testosterone gel or intense diaper rash prevention cream use: a case series (2019)
Ramos, Carolina de Oliveira; Macedo, Delanie Bulcao; Bachega, Tania Aparecida Sartori Sanchez ; Nascimento, Marilza Leal; Madureira, Guiomar; Xavier, Ana Claudia Latronico ; Brito, Vinicius Nahime; Mendonça, Berenice Bilharinho de
Source: Hormone research in paediatrics. Unidade: FM
Subjects: PUBERDADE PRECOCE, TESTOSTERONA, MEDICAMENTO TÓPICO, DERMATITE DE CONTATO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RAMOS, Carolina de Oliveira et al. Premature pubarche due to exogenous testosterone gel or intense diaper rash prevention cream use: a case series. Hormone research in paediatrics, v. 91, n. 6, p. 411-415, 2019Tradução . . Disponível em: https://doi.org/10.1159/000495664. Acesso em: 05 nov. 2024.
APA
Ramos, C. de O., Macedo, D. B., Bachega, T. A. S. S., Nascimento, M. L., Madureira, G., Xavier, A. C. L., et al. (2019). Premature pubarche due to exogenous testosterone gel or intense diaper rash prevention cream use: a case series. Hormone research in paediatrics, 91( 6), 411-415. doi:10.1159/000495664
NLM
Ramos C de O, Macedo DB, Bachega TASS, Nascimento ML, Madureira G, Xavier ACL, Brito VN, Mendonça BB de. Premature pubarche due to exogenous testosterone gel or intense diaper rash prevention cream use: a case series [Internet]. Hormone research in paediatrics. 2019 ; 91( 6): 411-415.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1159/000495664
Vancouver
Ramos C de O, Macedo DB, Bachega TASS, Nascimento ML, Madureira G, Xavier ACL, Brito VN, Mendonça BB de. Premature pubarche due to exogenous testosterone gel or intense diaper rash prevention cream use: a case series [Internet]. Hormone research in paediatrics. 2019 ; 91( 6): 411-415.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1159/000495664
Trabalho de evento-resumo periodico
Paternally inherited DLK1 deletion as novel cause of familial central precocious puberty (2017)
Dauber, Andrew; Montenegro, Luciana Ribeiro; Mendonça, Berenice Bilharinho de; Xavier, Ana Claudia Latronico
Source: Hormone research in paediatrics. Conference titles: Joint meeting of paediatric endocrinology. Unidade: FM
Subjects: PUBERDADE PRECOCE, MUTAÇÃO GENÉTICA, ANORMALIDADES CROMOSSÔMICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DAUBER, Andrew et al. Paternally inherited DLK1 deletion as novel cause of familial central precocious puberty. Hormone research in paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 05 nov. 2024. , 2017
APA
Dauber, A., Montenegro, L. R., Mendonça, B. B. de, & Xavier, A. C. L. (2017). Paternally inherited DLK1 deletion as novel cause of familial central precocious puberty. Hormone research in paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo.
NLM
Dauber A, Montenegro LR, Mendonça BB de, Xavier ACL. Paternally inherited DLK1 deletion as novel cause of familial central precocious puberty. Hormone research in paediatrics. 2017 ; 88[citado 2024 nov. 05 ]
Vancouver
Dauber A, Montenegro LR, Mendonça BB de, Xavier ACL. Paternally inherited DLK1 deletion as novel cause of familial central precocious puberty. Hormone research in paediatrics. 2017 ; 88[citado 2024 nov. 05 ]
Trabalho de evento-resumo periodico
Defining the dose, type and timing of glucocorticoid and mineralocorticoid replacement in 256 children and adults with congenital adrenal hyperplasia (CAH) in the I-CAH registry (2017)
Daniel, Eleni; Mendonça, Berenice Bilharinho de; Bachega, Tânia Aparecida Sartori Sanchez
Source: Hormone research in paediatrics. Conference titles: Joint meeting of paediatric endocrinology. Unidade: FM
Subjects: HIPERPLASIA SUPRARRENAL CONGÊNITA, HORMÔNIOS GLICOCORTICOIDES, CRIANÇAS, ADULTOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DANIEL, Eleni e MENDONÇA, Berenice Bilharinho de e BACHEGA, Tânia Aparecida Sartori Sanchez. Defining the dose, type and timing of glucocorticoid and mineralocorticoid replacement in 256 children and adults with congenital adrenal hyperplasia (CAH) in the I-CAH registry. Hormone research in paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 05 nov. 2024. , 2017
APA
Daniel, E., Mendonça, B. B. de, & Bachega, T. A. S. S. (2017). Defining the dose, type and timing of glucocorticoid and mineralocorticoid replacement in 256 children and adults with congenital adrenal hyperplasia (CAH) in the I-CAH registry. Hormone research in paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo.
NLM
Daniel E, Mendonça BB de, Bachega TASS. Defining the dose, type and timing of glucocorticoid and mineralocorticoid replacement in 256 children and adults with congenital adrenal hyperplasia (CAH) in the I-CAH registry. Hormone research in paediatrics. 2017 ; 88 358. res. P2-1503.[citado 2024 nov. 05 ]
Vancouver
Daniel E, Mendonça BB de, Bachega TASS. Defining the dose, type and timing of glucocorticoid and mineralocorticoid replacement in 256 children and adults with congenital adrenal hyperplasia (CAH) in the I-CAH registry. Hormone research in paediatrics. 2017 ; 88 358. res. P2-1503.[citado 2024 nov. 05 ]
Trabalho de evento-resumo periodico
Molecular analysis of brazilian patients with combined pituitary hormone deficiency (CPHD) and orthotopic posterior pituitary lobe (OPP) reveals 8 different PROP1 alterations with three novel mutations (2017)
Madeira, Joao L. O.; Jorge, Alexander Augusto de Lima; Mendonça, Berenice Bilharinho de
Source: Hormone research in paediatrics. Conference titles: Joint meeting of paediatric endocrinology. Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, HORMÔNIOS HIPOFISÁRIOS, SEQUENCIAMENTO GENÉTICO, ESTUDOS DE COORTES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MADEIRA, Joao L. O. e JORGE, Alexander Augusto de Lima e MENDONÇA, Berenice Bilharinho de. Molecular analysis of brazilian patients with combined pituitary hormone deficiency (CPHD) and orthotopic posterior pituitary lobe (OPP) reveals 8 different PROP1 alterations with three novel mutations. Hormone research in paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 05 nov. 2024. , 2017
APA
Madeira, J. L. O., Jorge, A. A. de L., & Mendonça, B. B. de. (2017). Molecular analysis of brazilian patients with combined pituitary hormone deficiency (CPHD) and orthotopic posterior pituitary lobe (OPP) reveals 8 different PROP1 alterations with three novel mutations. Hormone research in paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo.
NLM
Madeira JLO, Jorge AA de L, Mendonça BB de. Molecular analysis of brazilian patients with combined pituitary hormone deficiency (CPHD) and orthotopic posterior pituitary lobe (OPP) reveals 8 different PROP1 alterations with three novel mutations. Hormone research in paediatrics. 2017 ; 88 43-44.[citado 2024 nov. 05 ]
Vancouver
Madeira JLO, Jorge AA de L, Mendonça BB de. Molecular analysis of brazilian patients with combined pituitary hormone deficiency (CPHD) and orthotopic posterior pituitary lobe (OPP) reveals 8 different PROP1 alterations with three novel mutations. Hormone research in paediatrics. 2017 ; 88 43-44.[citado 2024 nov. 05 ]
Trabalho de evento-resumo periodico
Aromatase excess syndrome (AES) in a 10-year old girl with gigantomastia (2017)
Madeira, João L. O; Mendonça, Berenice Bilharinho de
Source: Hormone research in paediatrics. Conference titles: Joint meeting of paediatric endocrinology. Unidade: FM
Subjects: MAMOPLASTIA, MAMA, EXPRESSÃO GÊNICA, HIPOTÁLAMO, ADOLESCENTES, MENINAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MADEIRA, João L. O e MENDONÇA, Berenice Bilharinho de. Aromatase excess syndrome (AES) in a 10-year old girl with gigantomastia. Hormone research in paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 05 nov. 2024. , 2017
APA
Madeira, J. L. O., & Mendonça, B. B. de. (2017). Aromatase excess syndrome (AES) in a 10-year old girl with gigantomastia. Hormone research in paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo.
NLM
Madeira JLO, Mendonça BB de. Aromatase excess syndrome (AES) in a 10-year old girl with gigantomastia. Hormone research in paediatrics. 2017 ; 88 369-370.[citado 2024 nov. 05 ]
Vancouver
Madeira JLO, Mendonça BB de. Aromatase excess syndrome (AES) in a 10-year old girl with gigantomastia. Hormone research in paediatrics. 2017 ; 88 369-370.[citado 2024 nov. 05 ]
Trabalho de evento-resumo periodico
Premature pubarche can be caused by exogenous testosterone gel or diaper rash prevention cream (2017)
Ramos, Carolina O; Macedo, Delainie; Bachega, Tânia Aparecida Sartori Sanchez; Lee, Juliana C; Nascimento, Marilza L; Madureira, Guiomar; Brito, Vinicius N; Xavier, Ana Claudia Latronico; Mendonça, Berenice Bilharinho de
Source: Hormone research in paediatrics. Conference titles: Joint meeting of paediatric endocrinology. Unidade: FM
Subjects: TESTOSTERONA, PUBERDADE PRECOCE, ENDOCRINOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RAMOS, Carolina O et al. Premature pubarche can be caused by exogenous testosterone gel or diaper rash prevention cream. Hormone research in paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 05 nov. 2024. , 2017
APA
Ramos, C. O., Macedo, D., Bachega, T. A. S. S., Lee, J. C., Nascimento, M. L., Madureira, G., et al. (2017). Premature pubarche can be caused by exogenous testosterone gel or diaper rash prevention cream. Hormone research in paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo.
NLM
Ramos CO, Macedo D, Bachega TASS, Lee JC, Nascimento ML, Madureira G, Brito VN, Xavier ACL, Mendonça BB de. Premature pubarche can be caused by exogenous testosterone gel or diaper rash prevention cream. Hormone research in paediatrics. 2017 ; 88[citado 2024 nov. 05 ]
Vancouver
Ramos CO, Macedo D, Bachega TASS, Lee JC, Nascimento ML, Madureira G, Brito VN, Xavier ACL, Mendonça BB de. Premature pubarche can be caused by exogenous testosterone gel or diaper rash prevention cream. Hormone research in paediatrics. 2017 ; 88[citado 2024 nov. 05 ]
Trabalho de evento-resumo periodico
Outcomes of girls with idiopathic central precocious puberty treated with 1-and 3-month gonadotropin-releasing hormone analog formulations (2017)
Ramos, Carolina O; Silva, Marina C; Salles, Priscila; Mendonça, Berenice Bilharinho de; Xavier, Ana Claudia Latronico; Brito, Vinicius N
Source: Hormone research in paediatrics. Conference titles: Joint meeting of paediatric endocrinology. Unidade: FM
Subjects: PUBERDADE PRECOCE, ADOLESCENTES, MENINAS, HORMÔNIO LIBERADOR DE GONADOTROFINAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RAMOS, Carolina O et al. Outcomes of girls with idiopathic central precocious puberty treated with 1-and 3-month gonadotropin-releasing hormone analog formulations. Hormone research in paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 05 nov. 2024. , 2017
APA
Ramos, C. O., Silva, M. C., Salles, P., Mendonça, B. B. de, Xavier, A. C. L., & Brito, V. N. (2017). Outcomes of girls with idiopathic central precocious puberty treated with 1-and 3-month gonadotropin-releasing hormone analog formulations. Hormone research in paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo.
NLM
Ramos CO, Silva MC, Salles P, Mendonça BB de, Xavier ACL, Brito VN. Outcomes of girls with idiopathic central precocious puberty treated with 1-and 3-month gonadotropin-releasing hormone analog formulations. Hormone research in paediatrics. 2017 ; 88 543-544.[citado 2024 nov. 05 ]
Vancouver
Ramos CO, Silva MC, Salles P, Mendonça BB de, Xavier ACL, Brito VN. Outcomes of girls with idiopathic central precocious puberty treated with 1-and 3-month gonadotropin-releasing hormone analog formulations. Hormone research in paediatrics. 2017 ; 88 543-544.[citado 2024 nov. 05 ]
Artigo de periodico
Global Application of the Assessment of Communication Skills of Paediatric Endocrinology Fellows in the Management of Differences in Sex Development Using the ESPE E-Learning.Org Portal (2017)
Kranenburg, Laura J. C.; Mendonça, Berenice Bilharinho de
Source: Hormone research in paediatrics. Unidade: FM
Subjects: DESENVOLVIMENTO SEXUAL, EDUCAÇÃO A DISTÂNCIA, ENDOCRINOLOGIA PEDIÁTRICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KRANENBURG, Laura J. C. e MENDONÇA, Berenice Bilharinho de. Global Application of the Assessment of Communication Skills of Paediatric Endocrinology Fellows in the Management of Differences in Sex Development Using the ESPE E-Learning.Org Portal. Hormone research in paediatrics, v. 88, n. 2, p. 127-139, 2017Tradução . . Disponível em: https://doi.org/10.1159/000475992. Acesso em: 05 nov. 2024.
APA
Kranenburg, L. J. C., & Mendonça, B. B. de. (2017). Global Application of the Assessment of Communication Skills of Paediatric Endocrinology Fellows in the Management of Differences in Sex Development Using the ESPE E-Learning.Org Portal. Hormone research in paediatrics, 88( 2), 127-139. doi:10.1159/000475992
NLM
Kranenburg LJC, Mendonça BB de. Global Application of the Assessment of Communication Skills of Paediatric Endocrinology Fellows in the Management of Differences in Sex Development Using the ESPE E-Learning.Org Portal [Internet]. Hormone research in paediatrics. 2017 ; 88( 2): 127-139.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1159/000475992
Vancouver
Kranenburg LJC, Mendonça BB de. Global Application of the Assessment of Communication Skills of Paediatric Endocrinology Fellows in the Management of Differences in Sex Development Using the ESPE E-Learning.Org Portal [Internet]. Hormone research in paediatrics. 2017 ; 88( 2): 127-139.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1159/000475992
Trabalho de evento-resumo periodico
Partial recovery of pituitary function linear growth in patients with congenital combined pituitary hormone deficiency (CPHD) (2017)
Madeira, Joao L. O.; Jorge, Alexander Augusto de Lima; Mendonça, Berenice Bilharinho de
Source: Hormone research in paediatrics. Conference titles: Joint meeting of paediatric endocrinology. Unidade: FM
Subjects: HORMÔNIOS HIPOFISÁRIOS, GLÂNDULA PITUITÁRIA, HORMÔNIOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MADEIRA, Joao L. O. e JORGE, Alexander Augusto de Lima e MENDONÇA, Berenice Bilharinho de. Partial recovery of pituitary function linear growth in patients with congenital combined pituitary hormone deficiency (CPHD). Hormone research in paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 05 nov. 2024. , 2017
APA
Madeira, J. L. O., Jorge, A. A. de L., & Mendonça, B. B. de. (2017). Partial recovery of pituitary function linear growth in patients with congenital combined pituitary hormone deficiency (CPHD). Hormone research in paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo.
NLM
Madeira JLO, Jorge AA de L, Mendonça BB de. Partial recovery of pituitary function linear growth in patients with congenital combined pituitary hormone deficiency (CPHD). Hormone research in paediatrics. 2017 ; 88 461. res. P3-301.[citado 2024 nov. 05 ]
Vancouver
Madeira JLO, Jorge AA de L, Mendonça BB de. Partial recovery of pituitary function linear growth in patients with congenital combined pituitary hormone deficiency (CPHD). Hormone research in paediatrics. 2017 ; 88 461. res. P3-301.[citado 2024 nov. 05 ]
Trabalho de evento-resumo periodico
Anthropometric, metabolic and reproductive outcome of patients with central precocious puberty due to hypothalamic hamartoma in adult life (2017)
Ramos, Carolina O; Xavier, Ana Claudia Latronico; Cukier, Priscila; Cukier, Priscila; Macedo, Delaine; Bessa, Danielle S; Silva, Marina C; Arnhold, Ivo J; Mendonça, Berenice Bilharinho de; Brito, Vinicius N
Source: Hormone research in paediatrics. Conference titles: Joint meeting of paediatric endocrinology. Unidade: FM
Subjects: PUBERDADE PRECOCE, NEOPLASIAS, HIPOTÁLAMO, HORMÔNIO LIBERADOR DE GONADOTROFINAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RAMOS, Carolina O et al. Anthropometric, metabolic and reproductive outcome of patients with central precocious puberty due to hypothalamic hamartoma in adult life. Hormone research in paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 05 nov. 2024. , 2017
APA
Ramos, C. O., Xavier, A. C. L., Cukier, P., Cukier, P., Macedo, D., Bessa, D. S., et al. (2017). Anthropometric, metabolic and reproductive outcome of patients with central precocious puberty due to hypothalamic hamartoma in adult life. Hormone research in paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo.
NLM
Ramos CO, Xavier ACL, Cukier P, Cukier P, Macedo D, Bessa DS, Silva MC, Arnhold IJ, Mendonça BB de, Brito VN. Anthropometric, metabolic and reproductive outcome of patients with central precocious puberty due to hypothalamic hamartoma in adult life. Hormone research in paediatrics. 2017 ; 88 351-352.[citado 2024 nov. 05 ]
Vancouver
Ramos CO, Xavier ACL, Cukier P, Cukier P, Macedo D, Bessa DS, Silva MC, Arnhold IJ, Mendonça BB de, Brito VN. Anthropometric, metabolic and reproductive outcome of patients with central precocious puberty due to hypothalamic hamartoma in adult life. Hormone research in paediatrics. 2017 ; 88 351-352.[citado 2024 nov. 05 ]
Trabalho de evento-resumo periodico
E74 like ETS transcription factor 4 (ELF4) is a candidate gene for X-linked by whole exome sequencing (2017)
Correa, Fernanda A; Jorge, Alexander Augusto de Lima; Mendonça, Berenice Bilharinho de
Source: Hormone research in paediatrics. Conference titles: Joint meeting of paediatric endocrinology. Unidade: FM
Subjects: HORMÔNIO DO CRESCIMENTO, GENES, MUTAÇÃO GENÉTICA, IMUNOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CORREA, Fernanda A e JORGE, Alexander Augusto de Lima e MENDONÇA, Berenice Bilharinho de. E74 like ETS transcription factor 4 (ELF4) is a candidate gene for X-linked by whole exome sequencing. Hormone research in paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 05 nov. 2024. , 2017
APA
Correa, F. A., Jorge, A. A. de L., & Mendonça, B. B. de. (2017). E74 like ETS transcription factor 4 (ELF4) is a candidate gene for X-linked by whole exome sequencing. Hormone research in paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo.
NLM
Correa FA, Jorge AA de L, Mendonça BB de. E74 like ETS transcription factor 4 (ELF4) is a candidate gene for X-linked by whole exome sequencing. Hormone research in paediatrics. 2017 ; 88 290-291.[citado 2024 nov. 05 ]
Vancouver
Correa FA, Jorge AA de L, Mendonça BB de. E74 like ETS transcription factor 4 (ELF4) is a candidate gene for X-linked by whole exome sequencing. Hormone research in paediatrics. 2017 ; 88 290-291.[citado 2024 nov. 05 ]
Trabalho de evento-resumo periodico
Novel LZTR1 variants associated to noonan syndrome and growth hormone deficiency (2017)
Nakaguma, Marilena; Jorge, Alexander Augusto de Lima; Mendonça, Berenice Bilharinho de
Source: Hormone research in paediatrics. Conference titles: Joint meeting of paediatric endocrinology. Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, ANORMALIDADES CRANIOFACIAIS, HORMÔNIO DO CRESCIMENTO, GLÂNDULA PITUITÁRIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NAKAGUMA, Marilena e JORGE, Alexander Augusto de Lima e MENDONÇA, Berenice Bilharinho de. Novel LZTR1 variants associated to noonan syndrome and growth hormone deficiency. Hormone research in paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 05 nov. 2024. , 2017
APA
Nakaguma, M., Jorge, A. A. de L., & Mendonça, B. B. de. (2017). Novel LZTR1 variants associated to noonan syndrome and growth hormone deficiency. Hormone research in paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo.
NLM
Nakaguma M, Jorge AA de L, Mendonça BB de. Novel LZTR1 variants associated to noonan syndrome and growth hormone deficiency. Hormone research in paediatrics. 2017 ; 88[citado 2024 nov. 05 ]
Vancouver
Nakaguma M, Jorge AA de L, Mendonça BB de. Novel LZTR1 variants associated to noonan syndrome and growth hormone deficiency. Hormone research in paediatrics. 2017 ; 88[citado 2024 nov. 05 ]
Trabalho de evento-resumo periodico
Clinical and molecular analysis of pubertal control in a cohort of silver-russel and temple syndromes patients (2017)
Canton, Ana; Jorge, Alexander A. L.
Source: Hormone research in paediatrics. Conference titles: Joint meeting of paediatric endocrinology. Unidade: FM
Subjects: PUBERDADE PRECOCE, CROMOSSOMOS, DOENÇAS GENÉTICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CANTON, Ana e JORGE, Alexander A. L. Clinical and molecular analysis of pubertal control in a cohort of silver-russel and temple syndromes patients. Hormone research in paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. Disponível em: https://www.karger.com/Journal/Issue/276809. Acesso em: 05 nov. 2024. , 2017
APA
Canton, A., & Jorge, A. A. L. (2017). Clinical and molecular analysis of pubertal control in a cohort of silver-russel and temple syndromes patients. Hormone research in paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. Recuperado de https://www.karger.com/Journal/Issue/276809
NLM
Canton A, Jorge AAL. Clinical and molecular analysis of pubertal control in a cohort of silver-russel and temple syndromes patients [Internet]. Hormone research in paediatrics. 2017 ; 88 8-9.[citado 2024 nov. 05 ] Available from: https://www.karger.com/Journal/Issue/276809
Vancouver
Canton A, Jorge AAL. Clinical and molecular analysis of pubertal control in a cohort of silver-russel and temple syndromes patients [Internet]. Hormone research in paediatrics. 2017 ; 88 8-9.[citado 2024 nov. 05 ] Available from: https://www.karger.com/Journal/Issue/276809
Artigo de periodico
Triple A Syndrome: Preliminary Response to the Antioxidant N-Acetylcysteine Treatment in a Child (2017)
Fragoso, Maria Candida Barisson Villares; Schimizu, Maria Heloisa Massola; Passarelli, Marisa; Xavier, Ana Claudia Latronico; Mendonca, Berenice Bilharinho
Source: Hormone research in paediatrics. Unidade: FM
Subjects: ANORMALIDADES CROMOSSÔMICAS, CROMOSSOMO X, CRIANÇAS, TERAPÊUTICA, CORTISOL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FRAGOSO, Maria Candida Barisson Villares et al. Triple A Syndrome: Preliminary Response to the Antioxidant N-Acetylcysteine Treatment in a Child. Hormone research in paediatrics, v. 88, n. 2, p. 167-171, 2017Tradução . . Disponível em: https://doi.org/10.1159/000465520. Acesso em: 05 nov. 2024.
APA
Fragoso, M. C. B. V., Schimizu, M. H. M., Passarelli, M., Xavier, A. C. L., & Mendonca, B. B. (2017). Triple A Syndrome: Preliminary Response to the Antioxidant N-Acetylcysteine Treatment in a Child. Hormone research in paediatrics, 88( 2), 167-171. doi:10.1159/000465520
NLM
Fragoso MCBV, Schimizu MHM, Passarelli M, Xavier ACL, Mendonca BB. Triple A Syndrome: Preliminary Response to the Antioxidant N-Acetylcysteine Treatment in a Child [Internet]. Hormone research in paediatrics. 2017 ; 88( 2): 167-171.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1159/000465520
Vancouver
Fragoso MCBV, Schimizu MHM, Passarelli M, Xavier ACL, Mendonca BB. Triple A Syndrome: Preliminary Response to the Antioxidant N-Acetylcysteine Treatment in a Child [Internet]. Hormone research in paediatrics. 2017 ; 88( 2): 167-171.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1159/000465520
Trabalho de evento-resumo periodico
Analysis of major causative hypogonadotropic hypogonadism genes in patients with constitutional delay of growth and puberty (2012)
Silveira, Leticia F. G.; Tusset, Cintia; Moura, Lucas; Beneduzzi, Daiane; Teles, Milena; Jorge, Alexander A. L.; Trarbach, Ericka B.; Latronico, Ana Claudia
Source: Hormone research in paediatrics. Conference titles: 51th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE). Unidade: FM
Subjects: HIPOGONADISMO (DIAGNÓSTICO), GENES, CRESCIMENTO (DEFICIÊNCIA), FENÓTIPOS, POLIMORFISMO, DOENÇAS GENÉTICAS (DIAGNÓSTICO), RESUMOS (EVENTOS)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVEIRA, Leticia F. G. et al. Analysis of major causative hypogonadotropic hypogonadism genes in patients with constitutional delay of growth and puberty. Hormone research in paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. Disponível em: https://doi.org/10.1159/000343182. Acesso em: 05 nov. 2024. , 2012
APA
Silveira, L. F. G., Tusset, C., Moura, L., Beneduzzi, D., Teles, M., Jorge, A. A. L., et al. (2012). Analysis of major causative hypogonadotropic hypogonadism genes in patients with constitutional delay of growth and puberty. Hormone research in paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. doi:10.1159/000343182
NLM
Silveira LFG, Tusset C, Moura L, Beneduzzi D, Teles M, Jorge AAL, Trarbach EB, Latronico AC. Analysis of major causative hypogonadotropic hypogonadism genes in patients with constitutional delay of growth and puberty [Internet]. Hormone research in paediatrics. 2012 ;78( suppl. 1): 119.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1159/000343182
Vancouver
Silveira LFG, Tusset C, Moura L, Beneduzzi D, Teles M, Jorge AAL, Trarbach EB, Latronico AC. Analysis of major causative hypogonadotropic hypogonadism genes in patients with constitutional delay of growth and puberty [Internet]. Hormone research in paediatrics. 2012 ;78( suppl. 1): 119.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1159/000343182

USP Schools

ReP

Filtros

Authors

USP affiliated authors

Date published

Subjects

Funding Agencies