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Artigo de periodico
Histopathological criteria for paediatric adrenocortical carcinoma (2022)
Paschoalin, Victor Pereira; Tucci Júnior, Silvio ; Estevanato, Andrey Garcia; Tiraboschi, Ricardo Brianezi; Antonini, Sonir Roberto Rauber ; Muglia, Valdair Francisco ; Chahud, Fernando ; Mermejo, Lívia Mara; Bessa Junior, José de; Molina, Carlos Augusto Fernandes
Fonte: Hormone Research in Paediatrics. Unidade: FMRP
Assuntos: CARCINOMA, NEOPLASIAS, CRIANÇAS, CÓRTEX ADRENAL, PROGNÓSTICO, ESTUDOS RETROSPECTIVOS
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PASCHOALIN, Victor Pereira et al. Histopathological criteria for paediatric adrenocortical carcinoma. Hormone Research in Paediatrics, v. 95, n. 4, p. 347-353, 2022Tradução . . Disponível em: https://doi.org/10.1159/000524892. Acesso em: 22 out. 2025.
APA
Paschoalin, V. P., Tucci Júnior, S., Estevanato, A. G., Tiraboschi, R. B., Antonini, S. R. R., Muglia, V. F., et al. (2022). Histopathological criteria for paediatric adrenocortical carcinoma. Hormone Research in Paediatrics, 95( 4), 347-353. doi:10.1159/000524892
NLM
Paschoalin VP, Tucci Júnior S, Estevanato AG, Tiraboschi RB, Antonini SRR, Muglia VF, Chahud F, Mermejo LM, Bessa Junior J de, Molina CAF. Histopathological criteria for paediatric adrenocortical carcinoma [Internet]. Hormone Research in Paediatrics. 2022 ; 95( 4): 347-353.[citado 2025 out. 22 ] Available from: https://doi.org/10.1159/000524892
Vancouver
Paschoalin VP, Tucci Júnior S, Estevanato AG, Tiraboschi RB, Antonini SRR, Muglia VF, Chahud F, Mermejo LM, Bessa Junior J de, Molina CAF. Histopathological criteria for paediatric adrenocortical carcinoma [Internet]. Hormone Research in Paediatrics. 2022 ; 95( 4): 347-353.[citado 2025 out. 22 ] Available from: https://doi.org/10.1159/000524892
Artigo de periodico
Adult height in 299 patients with Turner syndrome with or without growth hormone therapy: results and literature review (2021)
Dantas, Naiara Castelo Branco; Braz, Adriana F.; Malaquias, Alexsandra; Lemos-Marini, Sofia; Arnhold, Ivo Jorge Prado ; Ramos, Ester Silveira; Antonini, Sonir Roberto Rauber ; Guerra-Junior, Gil; Mendonça, Berenice Bilharinho de; Jorge, Alexander Augusto de Lima ; Scalco, Renata C.
Fonte: Hormone Research in Paediatrics. Unidades: FM, FMRP
Assuntos: HORMÔNIO DO CRESCIMENTO, ADULTOS, HORMÔNIOS
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DANTAS, Naiara Castelo Branco et al. Adult height in 299 patients with Turner syndrome with or without growth hormone therapy: results and literature review. Hormone Research in Paediatrics, v. 94, n. 1-2, p. 63-70, 2021Tradução . . Disponível em: https://doi.org/10.1159/000516869. Acesso em: 22 out. 2025.
APA
Dantas, N. C. B., Braz, A. F., Malaquias, A., Lemos-Marini, S., Arnhold, I. J. P., Ramos, E. S., et al. (2021). Adult height in 299 patients with Turner syndrome with or without growth hormone therapy: results and literature review. Hormone Research in Paediatrics, 94( 1-2), 63-70. doi:10.1159/000516869
NLM
Dantas NCB, Braz AF, Malaquias A, Lemos-Marini S, Arnhold IJP, Ramos ES, Antonini SRR, Guerra-Junior G, Mendonça BB de, Jorge AA de L, Scalco RC. Adult height in 299 patients with Turner syndrome with or without growth hormone therapy: results and literature review [Internet]. Hormone Research in Paediatrics. 2021 ; 94( 1-2): 63-70.[citado 2025 out. 22 ] Available from: https://doi.org/10.1159/000516869
Vancouver
Dantas NCB, Braz AF, Malaquias A, Lemos-Marini S, Arnhold IJP, Ramos ES, Antonini SRR, Guerra-Junior G, Mendonça BB de, Jorge AA de L, Scalco RC. Adult height in 299 patients with Turner syndrome with or without growth hormone therapy: results and literature review [Internet]. Hormone Research in Paediatrics. 2021 ; 94( 1-2): 63-70.[citado 2025 out. 22 ] Available from: https://doi.org/10.1159/000516869
Trabalho de evento-resumo periodico
Loss-of-function NNT mutations impair antioxidantes mechanisms and decreases cortisol secretion in patients with famililar glucocorticoid deficiency (2019)
Bodoni, Aline F. ; Coeli-Lacchini, Fernanda Borchers ; Gebenlian, Juliana Lourenço; Sobral, Lays Martin ; Moreira, Ayrton Custódio; Elias, Lucila Leico Kagohara ; Silva Junior, Wilson Araújo da ; Castro, Margaret de ; Leopoldino, Andréia Machado ; Antonini, Sonir Roberto Rauber
Fonte: Hormone Research in Paediatrics. Nome do evento: Annual Meeting European Society for Paediatric Endocrinology - ESPE. Unidades: FMRP, FCFRP
Assuntos: CORTISOL, HORMÔNIOS GLICOCORTICOIDES
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BODONI, Aline F. et al. Loss-of-function NNT mutations impair antioxidantes mechanisms and decreases cortisol secretion in patients with famililar glucocorticoid deficiency. Hormone Research in Paediatrics. Basel: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. Disponível em: https://doi.org/10.1159/000501868. Acesso em: 22 out. 2025. , 2019
APA
Bodoni, A. F., Coeli-Lacchini, F. B., Gebenlian, J. L., Sobral, L. M., Moreira, A. C., Elias, L. L. K., et al. (2019). Loss-of-function NNT mutations impair antioxidantes mechanisms and decreases cortisol secretion in patients with famililar glucocorticoid deficiency. Hormone Research in Paediatrics. Basel: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. doi:10.1159/000501868
NLM
Bodoni AF, Coeli-Lacchini FB, Gebenlian JL, Sobral LM, Moreira AC, Elias LLK, Silva Junior WA da, Castro M de, Leopoldino AM, Antonini SRR. Loss-of-function NNT mutations impair antioxidantes mechanisms and decreases cortisol secretion in patients with famililar glucocorticoid deficiency [Internet]. Hormone Research in Paediatrics. 2019 ; 91 108.[citado 2025 out. 22 ] Available from: https://doi.org/10.1159/000501868
Vancouver
Bodoni AF, Coeli-Lacchini FB, Gebenlian JL, Sobral LM, Moreira AC, Elias LLK, Silva Junior WA da, Castro M de, Leopoldino AM, Antonini SRR. Loss-of-function NNT mutations impair antioxidantes mechanisms and decreases cortisol secretion in patients with famililar glucocorticoid deficiency [Internet]. Hormone Research in Paediatrics. 2019 ; 91 108.[citado 2025 out. 22 ] Available from: https://doi.org/10.1159/000501868
Artigo de periodico
Recurrent Copy Number Variants Associated with Syndromic Short Stature of Unknown Cause (2018)
Homma, Thais K; Krepischi, Ana Cristina Victorino ; Furuya, Tatiane K; Honjo, Rachel S; Malaquias, Alexsandra C; Bertola, Débora R; Costa, Sílvia S; Canton, Ana P; Roela, Rosimeire A; Freire, Bruna L.; Kim, Chong A; Rosenberg, Carla ; Jorge, Alexander A L
Fonte: Hormone Research in Paediatrics. Unidades: IB, FM
Assuntos: GENÉTICA, TRANSTORNOS DO CRESCIMENTO, DESENVOLVIMENTO HUMANO, ESTATURA, CROMOSSOMOS, ENDOCRINOLOGIA
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HOMMA, Thais K et al. Recurrent Copy Number Variants Associated with Syndromic Short Stature of Unknown Cause. Hormone Research in Paediatrics, v. 89, p. 13-21, 2018Tradução . . Disponível em: https://doi.org/10.1159/000481777. Acesso em: 22 out. 2025.
APA
Homma, T. K., Krepischi, A. C. V., Furuya, T. K., Honjo, R. S., Malaquias, A. C., Bertola, D. R., et al. (2018). Recurrent Copy Number Variants Associated with Syndromic Short Stature of Unknown Cause. Hormone Research in Paediatrics, 89, 13-21. doi:10.1159/000481777
NLM
Homma TK, Krepischi ACV, Furuya TK, Honjo RS, Malaquias AC, Bertola DR, Costa SS, Canton AP, Roela RA, Freire BL, Kim CA, Rosenberg C, Jorge AAL. Recurrent Copy Number Variants Associated with Syndromic Short Stature of Unknown Cause [Internet]. Hormone Research in Paediatrics. 2018 ; 89 13-21.[citado 2025 out. 22 ] Available from: https://doi.org/10.1159/000481777
Vancouver
Homma TK, Krepischi ACV, Furuya TK, Honjo RS, Malaquias AC, Bertola DR, Costa SS, Canton AP, Roela RA, Freire BL, Kim CA, Rosenberg C, Jorge AAL. Recurrent Copy Number Variants Associated with Syndromic Short Stature of Unknown Cause [Internet]. Hormone Research in Paediatrics. 2018 ; 89 13-21.[citado 2025 out. 22 ] Available from: https://doi.org/10.1159/000481777
Artigo de periodico
Time course of central precocious puberty development caused by an MKRN3 gene mutation: a prismatic care (2016)
Stecchini, Monica F.; Macedo, Delanie B.; Reis, Ana Claudia S.; Abreu, Ana Paula; Moreira, Ayrton Custódio; Castro, Margaret de; Kaiser, Ursula B.; Latronico, Ana Claudia; Antonini, Sonir Roberto Rauber
Fonte: Hormone Research in Paediatrics. Unidade: FMRP
Assuntos: PUBERDADE PRECOCE, MUTAÇÃO GENÉTICA, AMINOÁCIDOS
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STECCHINI, Monica F. et al. Time course of central precocious puberty development caused by an MKRN3 gene mutation: a prismatic care. Hormone Research in Paediatrics, v. 86, n. 2, p. 126-130, 2016Tradução . . Disponível em: https://doi.org/10.1159/000447515. Acesso em: 22 out. 2025.
APA
Stecchini, M. F., Macedo, D. B., Reis, A. C. S., Abreu, A. P., Moreira, A. C., Castro, M. de, et al. (2016). Time course of central precocious puberty development caused by an MKRN3 gene mutation: a prismatic care. Hormone Research in Paediatrics, 86( 2), 126-130. doi:10.1159/000447515
NLM
Stecchini MF, Macedo DB, Reis ACS, Abreu AP, Moreira AC, Castro M de, Kaiser UB, Latronico AC, Antonini SRR. Time course of central precocious puberty development caused by an MKRN3 gene mutation: a prismatic care [Internet]. Hormone Research in Paediatrics. 2016 ; 86( 2): 126-130.[citado 2025 out. 22 ] Available from: https://doi.org/10.1159/000447515
Vancouver
Stecchini MF, Macedo DB, Reis ACS, Abreu AP, Moreira AC, Castro M de, Kaiser UB, Latronico AC, Antonini SRR. Time course of central precocious puberty development caused by an MKRN3 gene mutation: a prismatic care [Internet]. Hormone Research in Paediatrics. 2016 ; 86( 2): 126-130.[citado 2025 out. 22 ] Available from: https://doi.org/10.1159/000447515
Artigo de periodico
A Single Nucleotide Variant in the Promoter Region of 17β-HSD Type 5 Gene Influences External Genitalia Virilization in Females with 21-Hydroxylase Deficiency (2016)
Kaupert, Laura C. ; Gomes, Larissa G. ; Brito, Vinícius N. ; Lemos-Marini, Sofia H. V. ; Mello, Maricilda P. de ; Longui, Carlos A. ; Kochi, Cristiane ; Castro, Margaret de; Guerra Jr., Gil ; Mendonca, Berenice B. ; Bachega, Tânia A. S. S.
Fonte: Hormone Research in Paediatrics. Unidades: FM, FMRP
Assuntos: MUTAÇÃO GENÉTICA, ALELOS, HIDROXILIASE, HORMÔNIOS SEXUAIS FEMININOS
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KAUPERT, Laura C. et al. A Single Nucleotide Variant in the Promoter Region of 17β-HSD Type 5 Gene Influences External Genitalia Virilization in Females with 21-Hydroxylase Deficiency. Hormone Research in Paediatrics, v. 85, n. 5, p. 333-338, 2016Tradução . . Disponível em: https://doi.org/10.1159/000445684. Acesso em: 22 out. 2025.
APA
Kaupert, L. C. , Gomes, L. G. , Brito, V. N. , Lemos-Marini, S. H. V. , Mello, M. P. de , Longui, C. A. , et al. (2016). A Single Nucleotide Variant in the Promoter Region of 17β-HSD Type 5 Gene Influences External Genitalia Virilization in Females with 21-Hydroxylase Deficiency. Hormone Research in Paediatrics, 85( 5), 333-338. doi:10.1159/000445684
NLM
Kaupert L C , Gomes L G , Brito V N , Lemos-Marini S HV , Mello M P de , Longui C A , Kochi C , Castro M de, Guerra Jr. G , Mendonca B B , Bachega T ASS . A Single Nucleotide Variant in the Promoter Region of 17β-HSD Type 5 Gene Influences External Genitalia Virilization in Females with 21-Hydroxylase Deficiency [Internet]. Hormone Research in Paediatrics. 2016 ; 85( 5): 333-338.[citado 2025 out. 22 ] Available from: https://doi.org/10.1159/000445684
Vancouver
Kaupert L C , Gomes L G , Brito V N , Lemos-Marini S HV , Mello M P de , Longui C A , Kochi C , Castro M de, Guerra Jr. G , Mendonca B B , Bachega T ASS . A Single Nucleotide Variant in the Promoter Region of 17β-HSD Type 5 Gene Influences External Genitalia Virilization in Females with 21-Hydroxylase Deficiency [Internet]. Hormone Research in Paediatrics. 2016 ; 85( 5): 333-338.[citado 2025 out. 22 ] Available from: https://doi.org/10.1159/000445684
Artigo de periodico
Clinical and Hormonal Features of a Male Adolescent with Congenital Isolated Follicle-Stimulating Hormone Deficiency (2016)
Şimşek, Enver ; Montenegro, Luciana R. ; Binay, Cigdem ; Demiral, Meliha ; Acıkalin, Mustafa Fuat ; Latronico, Ana Claudia
Fonte: Hormone Research in Paediatrics. Unidade: FM
Assuntos: ADOLESCENTES, PUBERDADE PRECOCE, INFERTILIDADE, HORMÔNIO DO CRESCIMENTO
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ŞIMŞEK, Enver et al. Clinical and Hormonal Features of a Male Adolescent with Congenital Isolated Follicle-Stimulating Hormone Deficiency. Hormone Research in Paediatrics, v. 85, n. 3, p. 207-212, 2016Tradução . . Disponível em: https://doi.org/10.1159/000442289. Acesso em: 22 out. 2025.
APA
Şimşek, E. , Montenegro, L. R. , Binay, C. , Demiral, M. , Acıkalin, M. F. , & Latronico, A. C. . (2016). Clinical and Hormonal Features of a Male Adolescent with Congenital Isolated Follicle-Stimulating Hormone Deficiency. Hormone Research in Paediatrics, 85( 3), 207-212. doi:10.1159/000442289
NLM
Şimşek E , Montenegro L R , Binay C , Demiral M , Acıkalin M F , Latronico A C . Clinical and Hormonal Features of a Male Adolescent with Congenital Isolated Follicle-Stimulating Hormone Deficiency [Internet]. Hormone Research in Paediatrics. 2016 ; 85( 3): 207-212.[citado 2025 out. 22 ] Available from: https://doi.org/10.1159/000442289
Vancouver
Şimşek E , Montenegro L R , Binay C , Demiral M , Acıkalin M F , Latronico A C . Clinical and Hormonal Features of a Male Adolescent with Congenital Isolated Follicle-Stimulating Hormone Deficiency [Internet]. Hormone Research in Paediatrics. 2016 ; 85( 3): 207-212.[citado 2025 out. 22 ] Available from: https://doi.org/10.1159/000442289
Artigo de periodico
Association Study of GWAS-Derived Loci with Height in Brazilian Children: Importance of MAP3K3, MMP24 and IGF1R Polymorphisms for Height Variation (2015)
Fontenele, Eveline Gadelha Pereira ; Moraes, Maria Elisabete Amaral de; d’Alva, Catarina Brasil; Pinheiro, Daniel Pascoalino; Landim, Sara Aguiar Sales Pinheiro; Trarbach, Ericka Barbosa; Mendonca, Berenice Bilharinho de; Jorge, Alexander Augusto Lima
Fonte: Hormone Research in Paediatrics. Unidade: FM
Assuntos: CRIANÇAS, BRASILEIROS, VARIAÇÃO GENÉTICA, POLIMORFISMO
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FONTENELE, Eveline Gadelha Pereira et al. Association Study of GWAS-Derived Loci with Height in Brazilian Children: Importance of MAP3K3, MMP24 and IGF1R Polymorphisms for Height Variation. Hormone Research in Paediatrics, v. 84, n. 4, p. 248-253, 2015Tradução . . Disponível em: https://doi.org/10.1159/000437324. Acesso em: 22 out. 2025.
APA
Fontenele, E. G. P., Moraes, M. E. A. de, d’Alva, C. B., Pinheiro, D. P., Landim, S. A. S. P., Trarbach, E. B., et al. (2015). Association Study of GWAS-Derived Loci with Height in Brazilian Children: Importance of MAP3K3, MMP24 and IGF1R Polymorphisms for Height Variation. Hormone Research in Paediatrics, 84( 4), 248-253. doi:10.1159/000437324
NLM
Fontenele EGP, Moraes MEA de, d’Alva CB, Pinheiro DP, Landim SASP, Trarbach EB, Mendonca BB de, Jorge AAL. Association Study of GWAS-Derived Loci with Height in Brazilian Children: Importance of MAP3K3, MMP24 and IGF1R Polymorphisms for Height Variation [Internet]. Hormone Research in Paediatrics. 2015 ; 84( 4): 248-253.[citado 2025 out. 22 ] Available from: https://doi.org/10.1159/000437324
Vancouver
Fontenele EGP, Moraes MEA de, d’Alva CB, Pinheiro DP, Landim SASP, Trarbach EB, Mendonca BB de, Jorge AAL. Association Study of GWAS-Derived Loci with Height in Brazilian Children: Importance of MAP3K3, MMP24 and IGF1R Polymorphisms for Height Variation [Internet]. Hormone Research in Paediatrics. 2015 ; 84( 4): 248-253.[citado 2025 out. 22 ] Available from: https://doi.org/10.1159/000437324
Trabalho de evento-resumo periodico
Analysis of DAX1 and SF1 genes and their interaction with genes involved in stem cell maintenance in adrenocortical tumors (2015)
Cavalcanti, M.; Leal, L.; Lacchini, F.; Martinelli Junior, Carlos Eduardo; Scrideli, Carlos Alberto; Tucci Júnior, Silvio; Molina, C; Yunes, J.; Mastellaro. M.; Brandalise, S.; Cardinalli, I.; Moreira, Ayrton Custódio; Ramalho, Leandra Naíra Zambelli; Castro, Margaret de; Antonini, Sonir Roberto Rauber
Fonte: Hormone Research in Paediatrics. Nome do evento: Congress of the Latin American Society of Pediatric Endocrinology. Unidade: FMRP
Assuntos: CÉLULAS-TRONCO, EXPRESSÃO GÊNICA, ENDOCRINOLOGIA
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ABNT
CAVALCANTI, M. et al. Analysis of DAX1 and SF1 genes and their interaction with genes involved in stem cell maintenance in adrenocortical tumors. Hormone Research in Paediatrics. Basel: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 22 out. 2025. , 2015
APA
Cavalcanti, M., Leal, L., Lacchini, F., Martinelli Junior, C. E., Scrideli, C. A., Tucci Júnior, S., et al. (2015). Analysis of DAX1 and SF1 genes and their interaction with genes involved in stem cell maintenance in adrenocortical tumors. Hormone Research in Paediatrics. Basel: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Cavalcanti M, Leal L, Lacchini F, Martinelli Junior CE, Scrideli CA, Tucci Júnior S, Molina C, Yunes J, Mastellaro. M., Brandalise S, Cardinalli I, Moreira AC, Ramalho LNZ, Castro M de, Antonini SRR. Analysis of DAX1 and SF1 genes and their interaction with genes involved in stem cell maintenance in adrenocortical tumors. Hormone Research in Paediatrics. 2015 ; 84 15.[citado 2025 out. 22 ]
Vancouver
Cavalcanti M, Leal L, Lacchini F, Martinelli Junior CE, Scrideli CA, Tucci Júnior S, Molina C, Yunes J, Mastellaro. M., Brandalise S, Cardinalli I, Moreira AC, Ramalho LNZ, Castro M de, Antonini SRR. Analysis of DAX1 and SF1 genes and their interaction with genes involved in stem cell maintenance in adrenocortical tumors. Hormone Research in Paediatrics. 2015 ; 84 15.[citado 2025 out. 22 ]
Trabalho de evento-resumo periodico
A homozygous NNT gene mutation identified by whole exoma sequencing (WES) in a boy with familial glucocorticoid deficiency (FGD) impairs mitochondrial oxidative stress (2015)
Bodoni, A.; Coeli-Lacchini, F.; Sobral, L.; Moreira, Ayrton Custódio; Elias, Lucila Leico Kagohara; Silva Júnior, Wilson Araújo da; Leopoldino, Andréia Machado; Castro, Margaret de; Antonini, Sonir Roberto Rauber
Fonte: Hormone Research in Paediatrics. Nome do evento: Congress of the Latin American Society of Pediatric Endocrinology. Unidades: FMRP, FCFRP
Assuntos: ESTRESSE OXIDATIVO, MUTAÇÃO GENÉTICA, MITOCÔNDRIAS
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ABNT
BODONI, A. et al. A homozygous NNT gene mutation identified by whole exoma sequencing (WES) in a boy with familial glucocorticoid deficiency (FGD) impairs mitochondrial oxidative stress. Hormone Research in Paediatrics. Basel: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 22 out. 2025. , 2015
APA
Bodoni, A., Coeli-Lacchini, F., Sobral, L., Moreira, A. C., Elias, L. L. K., Silva Júnior, W. A. da, et al. (2015). A homozygous NNT gene mutation identified by whole exoma sequencing (WES) in a boy with familial glucocorticoid deficiency (FGD) impairs mitochondrial oxidative stress. Hormone Research in Paediatrics. Basel: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Bodoni A, Coeli-Lacchini F, Sobral L, Moreira AC, Elias LLK, Silva Júnior WA da, Leopoldino AM, Castro M de, Antonini SRR. A homozygous NNT gene mutation identified by whole exoma sequencing (WES) in a boy with familial glucocorticoid deficiency (FGD) impairs mitochondrial oxidative stress. Hormone Research in Paediatrics. 2015 ; 84 6.[citado 2025 out. 22 ]
Vancouver
Bodoni A, Coeli-Lacchini F, Sobral L, Moreira AC, Elias LLK, Silva Júnior WA da, Leopoldino AM, Castro M de, Antonini SRR. A homozygous NNT gene mutation identified by whole exoma sequencing (WES) in a boy with familial glucocorticoid deficiency (FGD) impairs mitochondrial oxidative stress. Hormone Research in Paediatrics. 2015 ; 84 6.[citado 2025 out. 22 ]
Artigo de periodico
Role of the Natriuretic Peptide System in Normal Growth and Growth Disorders (2014)
Vasques, G. A.; Arnhold, I. J. P.; Jorge, A. A. L.
Fonte: Hormone Research in Paediatrics. Unidade: FM
Assuntos: FATORES DE RISCO, MODELOS ANIMAIS, PEPTÍDEOS, PEPTÍDEO NATRIURÉTICO ATRIAL
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ABNT
VASQUES, G. A. e ARNHOLD, I. J. P. e JORGE, A. A. L. Role of the Natriuretic Peptide System in Normal Growth and Growth Disorders. Hormone Research in Paediatrics, v. 82, n. 4, p. 222-229, 2014Tradução . . Disponível em: http://www.karger.com/Article/Pdf/365049. Acesso em: 22 out. 2025.
APA
Vasques, G. A., Arnhold, I. J. P., & Jorge, A. A. L. (2014). Role of the Natriuretic Peptide System in Normal Growth and Growth Disorders. Hormone Research in Paediatrics, 82( 4), 222-229. doi:10.1159/000365049
NLM
Vasques GA, Arnhold IJP, Jorge AAL. Role of the Natriuretic Peptide System in Normal Growth and Growth Disorders [Internet]. Hormone Research in Paediatrics. 2014 ; 82( 4): 222-229.[citado 2025 out. 22 ] Available from: http://www.karger.com/Article/Pdf/365049
Vancouver
Vasques GA, Arnhold IJP, Jorge AAL. Role of the Natriuretic Peptide System in Normal Growth and Growth Disorders [Internet]. Hormone Research in Paediatrics. 2014 ; 82( 4): 222-229.[citado 2025 out. 22 ] Available from: http://www.karger.com/Article/Pdf/365049
Trabalho de evento-resumo periodico
Analysis of Sox9 gene expression regulatory region in 46,XY DSD patients without campomelic dysplasia (2013)
Fanelli, Marina; Silva, Rosana B. Silva; Domenice, Sorahia.; Mendonça, Berenice Bilharinho de; Costa, Elaine M. F.
Fonte: Hormone Research in Paediatrics. Nome do evento: European Society for Paediatric Endocrinology (ESPE)/ Joint Meeting. Unidade: FM
Assuntos: GENES (ANÁLISE), TRANSTORNOS GONADAIS, ENDOCRINOPATIAS
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ABNT
FANELLI, Marina et al. Analysis of Sox9 gene expression regulatory region in 46,XY DSD patients without campomelic dysplasia. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. Disponível em: https://doi.org/10.1159/000353762. Acesso em: 22 out. 2025. , 2013
APA
Fanelli, M., Silva, R. B. S., Domenice, S., Mendonça, B. B. de, & Costa, E. M. F. (2013). Analysis of Sox9 gene expression regulatory region in 46,XY DSD patients without campomelic dysplasia. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. doi:10.1159/000353762
NLM
Fanelli M, Silva RBS, Domenice S, Mendonça BB de, Costa EMF. Analysis of Sox9 gene expression regulatory region in 46,XY DSD patients without campomelic dysplasia [Internet]. Hormone Research in Paediatrics. 2013 ; 80 185.[citado 2025 out. 22 ] Available from: https://doi.org/10.1159/000353762
Vancouver
Fanelli M, Silva RBS, Domenice S, Mendonça BB de, Costa EMF. Analysis of Sox9 gene expression regulatory region in 46,XY DSD patients without campomelic dysplasia [Internet]. Hormone Research in Paediatrics. 2013 ; 80 185.[citado 2025 out. 22 ] Available from: https://doi.org/10.1159/000353762
Artigo de periodico
Measurement of salivary cortisol as a marker of stress in newborns in a neonatal intensive care unit (2013)
Cabral, Débora Macedo; Antonini, Sonir Roberto Rauber; Custódio, Rodrigo José; Martinelli Junior, Carlos Eduardo; Silva, Carlos Antonio Bruno da
Fonte: Hormone Research in Paediatrics. Unidade: FMRP
Assuntos: CORTISOL, RECÉM-NASCIDO, ENDOCRINOLOGIA PEDIÁTRICA, ESTRESSE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CABRAL, Débora Macedo et al. Measurement of salivary cortisol as a marker of stress in newborns in a neonatal intensive care unit. Hormone Research in Paediatrics, v. 79, n. 6, p. 373-378, 2013Tradução . . Disponível em: https://doi.org/10.1159/000351942. Acesso em: 22 out. 2025.
APA
Cabral, D. M., Antonini, S. R. R., Custódio, R. J., Martinelli Junior, C. E., & Silva, C. A. B. da. (2013). Measurement of salivary cortisol as a marker of stress in newborns in a neonatal intensive care unit. Hormone Research in Paediatrics, 79( 6), 373-378. doi:10.1159/000351942
NLM
Cabral DM, Antonini SRR, Custódio RJ, Martinelli Junior CE, Silva CAB da. Measurement of salivary cortisol as a marker of stress in newborns in a neonatal intensive care unit [Internet]. Hormone Research in Paediatrics. 2013 ; 79( 6): 373-378.[citado 2025 out. 22 ] Available from: https://doi.org/10.1159/000351942
Vancouver
Cabral DM, Antonini SRR, Custódio RJ, Martinelli Junior CE, Silva CAB da. Measurement of salivary cortisol as a marker of stress in newborns in a neonatal intensive care unit [Internet]. Hormone Research in Paediatrics. 2013 ; 79( 6): 373-378.[citado 2025 out. 22 ] Available from: https://doi.org/10.1159/000351942
Trabalho de evento-resumo periodico
Polymorphism rs8081612 in the mitogen-activated protein 3 kinase 3 (MAP3K3) gene is associated with children height ina brazilian cohort (2013)
Fontenele, Eveline Gadelha Pereira ; d'Alva, Catarina B.; Pinheiro, Daniel P.; Trarbach, Ericka Barbosa ; Mendonça, Berenice Bilharinho de; Moraes, Maria Elisabete A.; Jorge, Alexander Augusto de Lima
Fonte: Hormone Research in Paediatrics. Nome do evento: European Society for Paediatric Endocrinology (ESPE)/ Joint Meeting. Unidade: FM
Assuntos: GENES (ANÁLISE), PESOS E MEDIDAS CORPORAIS, POLIMORFISMO, CRIANÇAS, BRASIL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FONTENELE, Eveline Gadelha Pereira et al. Polymorphism rs8081612 in the mitogen-activated protein 3 kinase 3 (MAP3K3) gene is associated with children height ina brazilian cohort. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. Disponível em: https://doi.org/10.1159/000353762. Acesso em: 22 out. 2025. , 2013
APA
Fontenele, E. G. P., d'Alva, C. B., Pinheiro, D. P., Trarbach, E. B., Mendonça, B. B. de, Moraes, M. E. A., & Jorge, A. A. de L. (2013). Polymorphism rs8081612 in the mitogen-activated protein 3 kinase 3 (MAP3K3) gene is associated with children height ina brazilian cohort. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. doi:10.1159/000353762
NLM
Fontenele EGP, d'Alva CB, Pinheiro DP, Trarbach EB, Mendonça BB de, Moraes MEA, Jorge AA de L. Polymorphism rs8081612 in the mitogen-activated protein 3 kinase 3 (MAP3K3) gene is associated with children height ina brazilian cohort [Internet]. Hormone Research in Paediatrics. 2013 ; 80 295.[citado 2025 out. 22 ] Available from: https://doi.org/10.1159/000353762
Vancouver
Fontenele EGP, d'Alva CB, Pinheiro DP, Trarbach EB, Mendonça BB de, Moraes MEA, Jorge AA de L. Polymorphism rs8081612 in the mitogen-activated protein 3 kinase 3 (MAP3K3) gene is associated with children height ina brazilian cohort [Internet]. Hormone Research in Paediatrics. 2013 ; 80 295.[citado 2025 out. 22 ] Available from: https://doi.org/10.1159/000353762
Trabalho de evento-resumo periodico
A case of Leydig cell hypoplasia associated with two distinct homozygous mutations of the human luteinizing hormone/chorionic gonadotropin receptor that include a novel mutation with unusual functional properties (2013)
Charmandari, Evangelia; Zhang, Meilin; Silveira, Letícia Gontijo; Chrousos, Geiorge P.; Sertedaki, Amalia; Xavier, Ana Claudia Latronico; Segaloff, Deborah L.
Fonte: Hormone Research in Paediatrics. Nome do evento: European Society for Paediatric Endocrinology (ESPE)/ Joint Meeting. Unidade: FM
Assuntos: MUTAÇÃO GENÉTICA, RECEPTORES, GENÉTICA, ENDOCRINOPATIAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CHARMANDARI, Evangelia et al. A case of Leydig cell hypoplasia associated with two distinct homozygous mutations of the human luteinizing hormone/chorionic gonadotropin receptor that include a novel mutation with unusual functional properties. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 22 out. 2025. , 2013
APA
Charmandari, E., Zhang, M., Silveira, L. G., Chrousos, G. P., Sertedaki, A., Xavier, A. C. L., & Segaloff, D. L. (2013). A case of Leydig cell hypoplasia associated with two distinct homozygous mutations of the human luteinizing hormone/chorionic gonadotropin receptor that include a novel mutation with unusual functional properties. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo.
NLM
Charmandari E, Zhang M, Silveira LG, Chrousos GP, Sertedaki A, Xavier ACL, Segaloff DL. A case of Leydig cell hypoplasia associated with two distinct homozygous mutations of the human luteinizing hormone/chorionic gonadotropin receptor that include a novel mutation with unusual functional properties. Hormone Research in Paediatrics. 2013 ; 80 44.[citado 2025 out. 22 ]
Vancouver
Charmandari E, Zhang M, Silveira LG, Chrousos GP, Sertedaki A, Xavier ACL, Segaloff DL. A case of Leydig cell hypoplasia associated with two distinct homozygous mutations of the human luteinizing hormone/chorionic gonadotropin receptor that include a novel mutation with unusual functional properties. Hormone Research in Paediatrics. 2013 ; 80 44.[citado 2025 out. 22 ]
Artigo de periodico
Molecular and gene network analysis of thyroid transcription factor 1(TFF1) and enhanced at puberty (EAP1) gene in patients with GnRH-dependent pubertal disorders (2013)
Cukier, Priscilla; Wright, Hollis; Rulfs, Tomke; Silveira, Leticia Ferreira Gontijo; Teles, Milena Gurgel; Mendonça, Berenice Bilharinho de; Arnhold, Ivo J. P.; Heger, Sabine; Xavier, Ana Claudia Latronico; Ojeba, Sergio R.; Brito, Vinicius Nahime
Fonte: Hormone Research in Paediatrics. Unidade: FM
Assuntos: PUBERDADE (ANORMALIDADES), GONADOTROFINAS, EXPRESSÃO GÊNICA, HIPOGONADISMO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CUKIER, Priscilla et al. Molecular and gene network analysis of thyroid transcription factor 1(TFF1) and enhanced at puberty (EAP1) gene in patients with GnRH-dependent pubertal disorders. Hormone Research in Paediatrics, v. 80, n. 2, p. 257-266, 2013Tradução . . Disponível em: http://www.karger.com/Article/FullText/354643. Acesso em: 22 out. 2025.
APA
Cukier, P., Wright, H., Rulfs, T., Silveira, L. F. G., Teles, M. G., Mendonça, B. B. de, et al. (2013). Molecular and gene network analysis of thyroid transcription factor 1(TFF1) and enhanced at puberty (EAP1) gene in patients with GnRH-dependent pubertal disorders. Hormone Research in Paediatrics, 80( 2), 257-266. Recuperado de http://www.karger.com/Article/FullText/354643
NLM
Cukier P, Wright H, Rulfs T, Silveira LFG, Teles MG, Mendonça BB de, Arnhold IJP, Heger S, Xavier ACL, Ojeba SR, Brito VN. Molecular and gene network analysis of thyroid transcription factor 1(TFF1) and enhanced at puberty (EAP1) gene in patients with GnRH-dependent pubertal disorders [Internet]. Hormone Research in Paediatrics. 2013 ; 80( 2): 257-266.[citado 2025 out. 22 ] Available from: http://www.karger.com/Article/FullText/354643
Vancouver
Cukier P, Wright H, Rulfs T, Silveira LFG, Teles MG, Mendonça BB de, Arnhold IJP, Heger S, Xavier ACL, Ojeba SR, Brito VN. Molecular and gene network analysis of thyroid transcription factor 1(TFF1) and enhanced at puberty (EAP1) gene in patients with GnRH-dependent pubertal disorders [Internet]. Hormone Research in Paediatrics. 2013 ; 80( 2): 257-266.[citado 2025 out. 22 ] Available from: http://www.karger.com/Article/FullText/354643
Trabalho de evento-resumo periodico
Genetic causes of central precocious puberty (2013)
Xavier, Ana Claudia Latronico
Fonte: Hormone Research in Paediatrics. Nome do evento: European Society for Paediatric Endocrinology (ESPE)/ Joint Meeting. Unidade: FM
Assuntos: PUBERDADE PRECOCE, TRANSTORNOS DO CRESCIMENTO, ENDOCRINOPATIAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
XAVIER, Ana Claudia Latronico. Genetic causes of central precocious puberty. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 22 out. 2025. , 2013
APA
Xavier, A. C. L. (2013). Genetic causes of central precocious puberty. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo.
NLM
Xavier ACL. Genetic causes of central precocious puberty. Hormone Research in Paediatrics. 2013 ; 80 11.[citado 2025 out. 22 ]
Vancouver
Xavier ACL. Genetic causes of central precocious puberty. Hormone Research in Paediatrics. 2013 ; 80 11.[citado 2025 out. 22 ]
Artigo de periodico
Obesity and Familial Predisposition Are Significant Determining Factors of an Adverse Metabolic Profile in Young Patients with Congenital Adrenal Hyperplasia (2013)
Moreira, Ricardo P. P.; Villares, Sandra M.; Madureira, Guiomar; Mendonca, Berenice B.; Bachega, Tânia A. S. S.
Fonte: Hormone Research in Paediatrics. Unidade: FM
Assuntos: HIPERPLASIA SUPRARRENAL CONGÊNITA, JOVENS, PACIENTES, OBESIDADE (MORTALIDADE), ÍNDICE DE MASSA CORPORAL, DOENÇAS HEREDITÁRIAS, HIDROXILASE (DEFICIÊNCIA)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MOREIRA, Ricardo P. P. et al. Obesity and Familial Predisposition Are Significant Determining Factors of an Adverse Metabolic Profile in Young Patients with Congenital Adrenal Hyperplasia. Hormone Research in Paediatrics, v. 80, n. 2, p. 111-118, 2013Tradução . . Disponível em: http://www.karger.com/Article/Pdf/353762. Acesso em: 22 out. 2025.
APA
Moreira, R. P. P., Villares, S. M., Madureira, G., Mendonca, B. B., & Bachega, T. A. S. S. (2013). Obesity and Familial Predisposition Are Significant Determining Factors of an Adverse Metabolic Profile in Young Patients with Congenital Adrenal Hyperplasia. Hormone Research in Paediatrics, 80( 2), 111-118. doi:10.1159/000353762
NLM
Moreira RPP, Villares SM, Madureira G, Mendonca BB, Bachega TASS. Obesity and Familial Predisposition Are Significant Determining Factors of an Adverse Metabolic Profile in Young Patients with Congenital Adrenal Hyperplasia [Internet]. Hormone Research in Paediatrics. 2013 ; 80( 2): 111-118.[citado 2025 out. 22 ] Available from: http://www.karger.com/Article/Pdf/353762
Vancouver
Moreira RPP, Villares SM, Madureira G, Mendonca BB, Bachega TASS. Obesity and Familial Predisposition Are Significant Determining Factors of an Adverse Metabolic Profile in Young Patients with Congenital Adrenal Hyperplasia [Internet]. Hormone Research in Paediatrics. 2013 ; 80( 2): 111-118.[citado 2025 out. 22 ] Available from: http://www.karger.com/Article/Pdf/353762
Trabalho de evento-resumo periodico
Copy number variants in Brazilian patients with congenital hypopituirarism (2013)
Correa, Fernanda A.; Franca, Marcela M.; Canton, Ana P. M; Otto, Aline p.; Costalonga, Everlayne F.; Brito, Vinicius N.; Carvalho, Luciani R.; Costa, Silvia; Arnhold, Ivo J. P.; Jorge, Alexander Augusto de Lima; Rosenberg, Carla ; Mendonça, Berenice Bilharinho de
Fonte: Hormone Research in Paediatrics. Nome do evento: European Society for Paediatric Endocrinology (ESPE)/ Joint Meeting. Unidades: FM, IB
Assuntos: GLÂNDULA PITUITÁRIA, ENDOCRINOPATIAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CORREA, Fernanda A. et al. Copy number variants in Brazilian patients with congenital hypopituirarism. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. Disponível em: https://doi.org/10.1159/000353762. Acesso em: 22 out. 2025. , 2013
APA
Correa, F. A., Franca, M. M., Canton, A. P. M., Otto, A. p., Costalonga, E. F., Brito, V. N., et al. (2013). Copy number variants in Brazilian patients with congenital hypopituirarism. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. doi:10.1159/000353762
NLM
Correa FA, Franca MM, Canton APM, Otto A p., Costalonga EF, Brito VN, Carvalho LR, Costa S, Arnhold IJP, Jorge AA de L, Rosenberg C, Mendonça BB de. Copy number variants in Brazilian patients with congenital hypopituirarism [Internet]. Hormone Research in Paediatrics. 2013 ; 80 161.[citado 2025 out. 22 ] Available from: https://doi.org/10.1159/000353762
Vancouver
Correa FA, Franca MM, Canton APM, Otto A p., Costalonga EF, Brito VN, Carvalho LR, Costa S, Arnhold IJP, Jorge AA de L, Rosenberg C, Mendonça BB de. Copy number variants in Brazilian patients with congenital hypopituirarism [Internet]. Hormone Research in Paediatrics. 2013 ; 80 161.[citado 2025 out. 22 ] Available from: https://doi.org/10.1159/000353762
Trabalho de evento-resumo periodico
Autosomal recessive (type I) is more frequent than autosomal dominant (type II) isolated growth hormone deficiencyin acohort of Brazilian patients (2013)
Lido, Andria C. V.; França, Marcela M.; Otto, Aline P.; Carvalho, Luciani R.; Mendonça, Berenice Bilharinho de; Arnhold, Ivo J.P.; Jorge, Alexander Augusto de Lima
Fonte: Hormone Research in Paediatrics. Nome do evento: European Society for Paediatric Endocrinology (ESPE)/ Joint Meeting. Unidade: FM
Assuntos: ENDOCRINOPATIAS, HORMÔNIO DO CRESCIMENTO (DEFICIÊNCIA), TRANSTORNOS DO CRESCIMENTO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LIDO, Andria C. V. et al. Autosomal recessive (type I) is more frequent than autosomal dominant (type II) isolated growth hormone deficiencyin acohort of Brazilian patients. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. Disponível em: https://doi.org/10.1159/000353762. Acesso em: 22 out. 2025. , 2013
APA
Lido, A. C. V., França, M. M., Otto, A. P., Carvalho, L. R., Mendonça, B. B. de, Arnhold, I. J. P., & Jorge, A. A. de L. (2013). Autosomal recessive (type I) is more frequent than autosomal dominant (type II) isolated growth hormone deficiencyin acohort of Brazilian patients. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. doi:10.1159/000353762
NLM
Lido ACV, França MM, Otto AP, Carvalho LR, Mendonça BB de, Arnhold IJP, Jorge AA de L. Autosomal recessive (type I) is more frequent than autosomal dominant (type II) isolated growth hormone deficiencyin acohort of Brazilian patients [Internet]. Hormone Research in Paediatrics. 2013 ; 80 295.[citado 2025 out. 22 ] Available from: https://doi.org/10.1159/000353762
Vancouver
Lido ACV, França MM, Otto AP, Carvalho LR, Mendonça BB de, Arnhold IJP, Jorge AA de L. Autosomal recessive (type I) is more frequent than autosomal dominant (type II) isolated growth hormone deficiencyin acohort of Brazilian patients [Internet]. Hormone Research in Paediatrics. 2013 ; 80 295.[citado 2025 out. 22 ] Available from: https://doi.org/10.1159/000353762

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