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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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ABNT
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: 26 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. 26 ] 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. 26 ] 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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ABNT
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: 26 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. 26 ] 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. 26 ] 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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ABNT
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: 26 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. 26 ] 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. 26 ] 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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ABNT
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: 26 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. 26 ] 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. 26 ] 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: 26 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. 26 ] 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. 26 ] 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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ABNT
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: 26 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. 26 ] 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. 26 ] 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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ABNT
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: 26 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. 26 ] 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. 26 ] Available from: https://doi.org/10.1159/000442289
Trabalho de evento-resumo periodico
LRP5 mutation in a boy with osteopetrosis and normal stature despite low IGF1 levels (2015)
Milani, Soraya Sader; Silva Júnior, Wilson Araújo da; Molfetta, Greice Andreotti de; Zanette, Dalila; Hirose, Thiago; Garcia, Bruna; Liberatore Junior, Raphael Del Roio; Paula, Francisco Jose Albuquerque de; Martinelli Junior, Carlos Eduardo
Fonte: Hormone Research in Paediatrics. Nome do evento: Annual Meeting of the European Society for Paediatric Endocrinology (ESPE). Unidade: FMRP
Assuntos: ENDOCRINOLOGIA PEDIÁTRICA, OSTEOPATIAS ENDRÓCRINAS
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ABNT
MILANI, Soraya Sader et al. LRP5 mutation in a boy with osteopetrosis and normal stature despite low IGF1 levels. Hormone Research in Paediatrics. Basel: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 26 out. 2025. , 2015
APA
Milani, S. S., Silva Júnior, W. A. da, Molfetta, G. A. de, Zanette, D., Hirose, T., Garcia, B., et al. (2015). LRP5 mutation in a boy with osteopetrosis and normal stature despite low IGF1 levels. Hormone Research in Paediatrics. Basel: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Milani SS, Silva Júnior WA da, Molfetta GA de, Zanette D, Hirose T, Garcia B, Liberatore Junior RDR, Paula FJA de, Martinelli Junior CE. LRP5 mutation in a boy with osteopetrosis and normal stature despite low IGF1 levels. Hormone Research in Paediatrics. 2015 ; 84 343-344.[citado 2025 out. 26 ]
Vancouver
Milani SS, Silva Júnior WA da, Molfetta GA de, Zanette D, Hirose T, Garcia B, Liberatore Junior RDR, Paula FJA de, Martinelli Junior CE. LRP5 mutation in a boy with osteopetrosis and normal stature despite low IGF1 levels. Hormone Research in Paediatrics. 2015 ; 84 343-344.[citado 2025 out. 26 ]
Trabalho de evento-resumo periodico
Regulation of IGF1R mRNA expression by GnRH agonist may be involved in the decrease of height velocity during central precocious puberty therapy (2015)
Paula, Mariana Sarti de; Ricco, Rafaela; Custodio, Rodrigo; Milani, Soraya Sader; Atique, Patricia; Moreira, Ayrton Custódio; Antonini, Sonir Roberto Rauber; Liberatore Junior, Raphael Del Roio; Martinelli Junior, Carlos Eduardo
Fonte: Hormone Research in Paediatrics. Nome do evento: Annual Meeting of the European Society for Paediatric Endocrinology (ESPE). Unidade: FMRP
Assuntos: ENDOCRINOLOGIA PEDIÁTRICA, EXPRESSÃO GÊNICA
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ABNT
PAULA, Mariana Sarti de et al. Regulation of IGF1R mRNA expression by GnRH agonist may be involved in the decrease of height velocity during central precocious puberty therapy. Hormone Research in Paediatrics. Basel: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 26 out. 2025. , 2015
APA
Paula, M. S. de, Ricco, R., Custodio, R., Milani, S. S., Atique, P., Moreira, A. C., et al. (2015). Regulation of IGF1R mRNA expression by GnRH agonist may be involved in the decrease of height velocity during central precocious puberty therapy. Hormone Research in Paediatrics. Basel: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Paula MS de, Ricco R, Custodio R, Milani SS, Atique P, Moreira AC, Antonini SRR, Liberatore Junior RDR, Martinelli Junior CE. Regulation of IGF1R mRNA expression by GnRH agonist may be involved in the decrease of height velocity during central precocious puberty therapy. Hormone Research in Paediatrics. 2015 ; 84 236-237.[citado 2025 out. 26 ]
Vancouver
Paula MS de, Ricco R, Custodio R, Milani SS, Atique P, Moreira AC, Antonini SRR, Liberatore Junior RDR, Martinelli Junior CE. Regulation of IGF1R mRNA expression by GnRH agonist may be involved in the decrease of height velocity during central precocious puberty therapy. Hormone Research in Paediatrics. 2015 ; 84 236-237.[citado 2025 out. 26 ]
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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ABNT
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: 26 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. 26 ] 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. 26 ] 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: 26 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. 26 ]
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. 26 ]
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: 26 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. 26 ]
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. 26 ]
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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 26 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. 26 ] 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. 26 ] Available from: http://www.karger.com/Article/Pdf/365049
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: 26 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. 26 ] 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. 26 ] Available from: https://doi.org/10.1159/000351942
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: 26 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. 26 ] 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. 26 ] Available from: http://www.karger.com/Article/FullText/354643
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: 26 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. 26 ] 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. 26 ] Available from: http://www.karger.com/Article/Pdf/353762
Artigo de periodico
The Sitting Height/Height Ratio for Age in Healthy and Short Individuals and Its Potential Role in Selecting Short Children for SHOX Analysis (2013)
Malaquias, A. C.; Scalco, R. C.; Fontenele, E. G. P.; Costalonga, E. F.; Baldin, A. D.; Braz, A. F.; Funari, M. F. A.; Nishi, M. Y.; Guerra-Junior, G.; Mendonca, B. B.; Arnhold, I. J. P.; Jorge, A. A. L.
Fonte: Hormone Research in Paediatrics. Unidade: FM
Assuntos: GENES (ANÁLISE), ENDOCRINOPATIAS, INSUFICIÊNCIA DE CRESCIMENTO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MALAQUIAS, A. C. et al. The Sitting Height/Height Ratio for Age in Healthy and Short Individuals and Its Potential Role in Selecting Short Children for SHOX Analysis. Hormone Research in Paediatrics, v. 80, n. 6 p. 449-456, 2013Tradução . . Disponível em: https://doi.org/10.1159/000355411. Acesso em: 26 out. 2025.
APA
Malaquias, A. C., Scalco, R. C., Fontenele, E. G. P., Costalonga, E. F., Baldin, A. D., Braz, A. F., et al. (2013). The Sitting Height/Height Ratio for Age in Healthy and Short Individuals and Its Potential Role in Selecting Short Children for SHOX Analysis. Hormone Research in Paediatrics, 80( 6 p. 449-456). doi:10.1159/000355411
NLM
Malaquias AC, Scalco RC, Fontenele EGP, Costalonga EF, Baldin AD, Braz AF, Funari MFA, Nishi MY, Guerra-Junior G, Mendonca BB, Arnhold IJP, Jorge AAL. The Sitting Height/Height Ratio for Age in Healthy and Short Individuals and Its Potential Role in Selecting Short Children for SHOX Analysis [Internet]. Hormone Research in Paediatrics. 2013 ; 80( 6 p. 449-456):[citado 2025 out. 26 ] Available from: https://doi.org/10.1159/000355411
Vancouver
Malaquias AC, Scalco RC, Fontenele EGP, Costalonga EF, Baldin AD, Braz AF, Funari MFA, Nishi MY, Guerra-Junior G, Mendonca BB, Arnhold IJP, Jorge AAL. The Sitting Height/Height Ratio for Age in Healthy and Short Individuals and Its Potential Role in Selecting Short Children for SHOX Analysis [Internet]. Hormone Research in Paediatrics. 2013 ; 80( 6 p. 449-456):[citado 2025 out. 26 ] Available from: https://doi.org/10.1159/000355411
Artigo de periodico
Absence of Functional LIN28B Mutations in a Large Cohort of Patients with Idiopathic Central Precocious Puberty (2012)
Silveira-Neto, Acácio P.; Leal, Leticia Ferro; Emerman, Amy B.; Henderson, Katherine D.; Piskounova, Elena; Henderson, Brian E.; Gregory, Richard I.; Silveira, Letícia F. Gontijo; Hirschhorn, Joel N.; Nguyen, Thutrang T.; Beneduzzi, Daiane; Tusset, Cintia; Reis, Ana Claudia S.; Brito, Vinicius N.; Mendonca, Berenice B.; Palmert, Mark R.; Antonini, Sonir R.; Latronico, Ana Claudia
Fonte: Hormone Research in Paediatrics. Unidades: FM, FMRP
Assuntos: CRIANÇAS, MENINAS, PUBERDADE PRECOCE (TRATAMENTO), HORMÔNIO LIBERADOR DE GONADOTROFINAS
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ABNT
SILVEIRA-NETO, Acácio P. et al. Absence of Functional LIN28B Mutations in a Large Cohort of Patients with Idiopathic Central Precocious Puberty. Hormone Research in Paediatrics, v. 78, n. 3, p. 144-150, 2012Tradução . . Disponível em: http://content.karger.com/ProdukteDB/produkte.asp?doi=10.1159/000342212. Acesso em: 26 out. 2025.
APA
Silveira-Neto, A. P., Leal, L. F., Emerman, A. B., Henderson, K. D., Piskounova, E., Henderson, B. E., et al. (2012). Absence of Functional LIN28B Mutations in a Large Cohort of Patients with Idiopathic Central Precocious Puberty. Hormone Research in Paediatrics, 78( 3), 144-150. doi:10.1159/00034221272229
NLM
Silveira-Neto AP, Leal LF, Emerman AB, Henderson KD, Piskounova E, Henderson BE, Gregory RI, Silveira LFG, Hirschhorn JN, Nguyen TT, Beneduzzi D, Tusset C, Reis ACS, Brito VN, Mendonca BB, Palmert MR, Antonini SR, Latronico AC. Absence of Functional LIN28B Mutations in a Large Cohort of Patients with Idiopathic Central Precocious Puberty [Internet]. Hormone Research in Paediatrics. 2012 ;78( 3): 144-150.[citado 2025 out. 26 ] Available from: http://content.karger.com/ProdukteDB/produkte.asp?doi=10.1159/000342212
Vancouver
Silveira-Neto AP, Leal LF, Emerman AB, Henderson KD, Piskounova E, Henderson BE, Gregory RI, Silveira LFG, Hirschhorn JN, Nguyen TT, Beneduzzi D, Tusset C, Reis ACS, Brito VN, Mendonca BB, Palmert MR, Antonini SR, Latronico AC. Absence of Functional LIN28B Mutations in a Large Cohort of Patients with Idiopathic Central Precocious Puberty [Internet]. Hormone Research in Paediatrics. 2012 ;78( 3): 144-150.[citado 2025 out. 26 ] Available from: http://content.karger.com/ProdukteDB/produkte.asp?doi=10.1159/000342212
Trabalho de evento-resumo periodico
Underexpression of class II histocompatibility antigens (HLA) is related with poor prognosis in childhood adrenocortical tumors (ACT) (2012)
Leite, Fabíola; Lira, Régia Caroline Peixoto; Fedatto, Paola Fernanda; Martinelli Junior, Carlos Eduardo; Antonini, Sonir Roberto Rauber; Custódio, Rodrigo José; Castro, Margaret de; Tucci Júnior, Silvio; Serafini, Luciano Neder; Ramalho, Leandra Naíra Zambelli; Seidinger, Ana; Cardinalli, Izilda; Mastellaro, Maria José; Yunes, José A.; Brandalise, Sílvia; Tone, Luiz Gonzaga; Scrideli, Carlos Alberto
Fonte: Hormone Research in Paediatrics. Nome do evento: Annual Meeting of the European Society for Paediatric Endocrinology (ESPE). Unidade: FMRP
Assuntos: NEOPLASIAS DAS GLÂNDULAS SUPRARRENAIS, CRIANÇAS, EXPRESSÃO GÊNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LEITE, Fabíola et al. Underexpression of class II histocompatibility antigens (HLA) is related with poor prognosis in childhood adrenocortical tumors (ACT). Hormone Research in Paediatrics. Basel: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 26 out. 2025. , 2012
APA
Leite, F., Lira, R. C. P., Fedatto, P. F., Martinelli Junior, C. E., Antonini, S. R. R., Custódio, R. J., et al. (2012). Underexpression of class II histocompatibility antigens (HLA) is related with poor prognosis in childhood adrenocortical tumors (ACT). Hormone Research in Paediatrics. Basel: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Leite F, Lira RCP, Fedatto PF, Martinelli Junior CE, Antonini SRR, Custódio RJ, Castro M de, Tucci Júnior S, Serafini LN, Ramalho LNZ, Seidinger A, Cardinalli I, Mastellaro MJ, Yunes JA, Brandalise S, Tone LG, Scrideli CA. Underexpression of class II histocompatibility antigens (HLA) is related with poor prognosis in childhood adrenocortical tumors (ACT). Hormone Research in Paediatrics. 2012 ; 78( suppl. 1): 20-21.[citado 2025 out. 26 ]
Vancouver
Leite F, Lira RCP, Fedatto PF, Martinelli Junior CE, Antonini SRR, Custódio RJ, Castro M de, Tucci Júnior S, Serafini LN, Ramalho LNZ, Seidinger A, Cardinalli I, Mastellaro MJ, Yunes JA, Brandalise S, Tone LG, Scrideli CA. Underexpression of class II histocompatibility antigens (HLA) is related with poor prognosis in childhood adrenocortical tumors (ACT). Hormone Research in Paediatrics. 2012 ; 78( suppl. 1): 20-21.[citado 2025 out. 26 ]
Artigo de periodico
The Role of SRY Mutations in the Etiology of Gonadal Dysgenesis in Patients with 45,X/46,XY Disorder of Sex Development and Variants (2011)
Nishi, Mirian Yumie; Costa, Elaine Maria Frade; Oliveira, Suely Beirão; Mendonca, Berenice Bilharinho; Domenice, Sorahia
Fonte: Hormone Research in Paediatrics. Unidade: FM
Assuntos: MUTAÇÃO GENÉTICA, TRANSTORNOS GONADAIS, CROMOSSOMOS SEXUAIS (FISIOPATOLOGIA)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NISHI, Mirian Yumie et al. The Role of SRY Mutations in the Etiology of Gonadal Dysgenesis in Patients with 45,X/46,XY Disorder of Sex Development and Variants. Hormone Research in Paediatrics, v. 75, n. 1, p. 26-31, 2011Tradução . . Disponível em: https://doi.org/10.1159/000316536. Acesso em: 26 out. 2025.
APA
Nishi, M. Y., Costa, E. M. F., Oliveira, S. B., Mendonca, B. B., & Domenice, S. (2011). The Role of SRY Mutations in the Etiology of Gonadal Dysgenesis in Patients with 45,X/46,XY Disorder of Sex Development and Variants. Hormone Research in Paediatrics, 75( 1), 26-31. doi:10.1159/000316536
NLM
Nishi MY, Costa EMF, Oliveira SB, Mendonca BB, Domenice S. The Role of SRY Mutations in the Etiology of Gonadal Dysgenesis in Patients with 45,X/46,XY Disorder of Sex Development and Variants [Internet]. Hormone Research in Paediatrics. 2011 ; 75( 1): 26-31.[citado 2025 out. 26 ] Available from: https://doi.org/10.1159/000316536
Vancouver
Nishi MY, Costa EMF, Oliveira SB, Mendonca BB, Domenice S. The Role of SRY Mutations in the Etiology of Gonadal Dysgenesis in Patients with 45,X/46,XY Disorder of Sex Development and Variants [Internet]. Hormone Research in Paediatrics. 2011 ; 75( 1): 26-31.[citado 2025 out. 26 ] Available from: https://doi.org/10.1159/000316536

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