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Artigo de periodico
MKRN3 inhibits the reproductive axis through actions in kisspeptin-expressing neurons (2020)
Abreu, Ana Paula; Toro, Carlos A; Song, Yong Bhum; Navarro, Victor M; Bosch, Martha A; Eren, Aysegul; Liang, Joy N; Carroll, Rona S; Xavier, Ana Claudia Latronico ; Ronnekleiv, Oline K
Fonte: Journal of clinical investigation. Unidade: FM
Assuntos: HORMÔNIO LIBERADOR DE GONADOTROFINAS, CAMUNDONGOS, NEURÔNIOS, PUBERDADE PRECOCE, TRANSCRIÇÃO GÊNICA
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ABNT
ABREU, Ana Paula et al. MKRN3 inhibits the reproductive axis through actions in kisspeptin-expressing neurons. Journal of clinical investigation, v. 130, n. 8, p. 4486-4500, 2020Tradução . . Disponível em: https://doi.org/10.1172/JCI136564. Acesso em: 20 jul. 2024.
APA
Abreu, A. P., Toro, C. A., Song, Y. B., Navarro, V. M., Bosch, M. A., Eren, A., et al. (2020). MKRN3 inhibits the reproductive axis through actions in kisspeptin-expressing neurons. Journal of clinical investigation, 130( 8), 4486-4500. doi:10.1172/JCI136564
NLM
Abreu AP, Toro CA, Song YB, Navarro VM, Bosch MA, Eren A, Liang JN, Carroll RS, Xavier ACL, Ronnekleiv OK. MKRN3 inhibits the reproductive axis through actions in kisspeptin-expressing neurons [Internet]. Journal of clinical investigation. 2020 ; 130( 8): 4486-4500.[citado 2024 jul. 20 ] Available from: https://doi.org/10.1172/JCI136564
Vancouver
Abreu AP, Toro CA, Song YB, Navarro VM, Bosch MA, Eren A, Liang JN, Carroll RS, Xavier ACL, Ronnekleiv OK. MKRN3 inhibits the reproductive axis through actions in kisspeptin-expressing neurons [Internet]. Journal of clinical investigation. 2020 ; 130( 8): 4486-4500.[citado 2024 jul. 20 ] Available from: https://doi.org/10.1172/JCI136564
Artigo de periodico
MKRN3 mutations in central precocious puberty: a systematic review and meta-analysis (2019)
Valadares, Luciana Pinto; Meireles, Cinthia Gabriel; Toledo, Isabela Porto De; Oliveira, Renata Santarem de; Castro, Luiz Claudio Goncalves de; Abreu, Ana Paula; Carroll, Rona S; Xavier, Ana Claudia Latronico ; Kaiser, Ursula B; Guerra, Eliete Neves Silva
Fonte: Journal of the endocrine society. Unidade: FM
Assuntos: PUBERDADE PRECOCE, MUTAÇÃO GENÉTICA, GENÓTIPOS, FENÓTIPOS, REVISÃO SISTEMÁTICA, METANÁLISE, CROMOSSOMOS HUMANOS
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ABNT
VALADARES, Luciana Pinto et al. MKRN3 mutations in central precocious puberty: a systematic review and meta-analysis. Journal of the endocrine society, v. 3, n. 5, p. 979-995, 2019Tradução . . Disponível em: https://doi.org/10.1210/js.2019-00041. Acesso em: 20 jul. 2024.
APA
Valadares, L. P., Meireles, C. G., Toledo, I. P. D., Oliveira, R. S. de, Castro, L. C. G. de, Abreu, A. P., et al. (2019). MKRN3 mutations in central precocious puberty: a systematic review and meta-analysis. Journal of the endocrine society, 3( 5), 979-995. doi:10.1210/js.2019-00041
NLM
Valadares LP, Meireles CG, Toledo IPD, Oliveira RS de, Castro LCG de, Abreu AP, Carroll RS, Xavier ACL, Kaiser UB, Guerra ENS. MKRN3 mutations in central precocious puberty: a systematic review and meta-analysis [Internet]. Journal of the endocrine society. 2019 ; 3( 5): 979-995.[citado 2024 jul. 20 ] Available from: https://doi.org/10.1210/js.2019-00041
Vancouver
Valadares LP, Meireles CG, Toledo IPD, Oliveira RS de, Castro LCG de, Abreu AP, Carroll RS, Xavier ACL, Kaiser UB, Guerra ENS. MKRN3 mutations in central precocious puberty: a systematic review and meta-analysis [Internet]. Journal of the endocrine society. 2019 ; 3( 5): 979-995.[citado 2024 jul. 20 ] Available from: https://doi.org/10.1210/js.2019-00041
Artigo de periodico
Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious Puberty (2017)
Dauber, Andrew; Cunha-Silva, Marina; Macedo, Delanie B.; Brito, Vinicius N.; Abreu, Ana Paula; Roberts, Stephanie A.; Montenegro, Luciana R.; Andrew, Melissa; Kirby, Andrew; Weirauch, Matthew T.; Labilloy, Guillaume; Bessa, Danielle S.; Carroll, Rona S.; Jacobs, Dakota C.; Chappell, Patrick E.; Mendonca, Berenice B.; Haig, David; Kaiser, Ursula B.; Latronico, Ana Claudia
Fonte: Journal of clinical endocrinology and metabolism. Unidade: FM
Assuntos: PUBERDADE PRECOCE, REAÇÃO EM CADEIA POR POLIMERASE, HIPOTÁLAMO, MUTAÇÃO GENÉTICA
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ABNT
DAUBER, Andrew et al. Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious Puberty. Journal of clinical endocrinology and metabolism, v. 102, n. 5, p. 1557-1567, 2017Tradução . . Disponível em: https://doi.org/10.1210/jc.2016-3677. Acesso em: 20 jul. 2024.
APA
Dauber, A., Cunha-Silva, M., Macedo, D. B., Brito, V. N., Abreu, A. P., Roberts, S. A., et al. (2017). Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious Puberty. Journal of clinical endocrinology and metabolism, 102( 5), 1557-1567. doi:10.1210/jc.2016-3677
NLM
Dauber A, Cunha-Silva M, Macedo DB, Brito VN, Abreu AP, Roberts SA, Montenegro LR, Andrew M, Kirby A, Weirauch MT, Labilloy G, Bessa DS, Carroll RS, Jacobs DC, Chappell PE, Mendonca BB, Haig D, Kaiser UB, Latronico AC. Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious Puberty [Internet]. Journal of clinical endocrinology and metabolism. 2017 ; 102( 5): 1557-1567.[citado 2024 jul. 20 ] Available from: https://doi.org/10.1210/jc.2016-3677
Vancouver
Dauber A, Cunha-Silva M, Macedo DB, Brito VN, Abreu AP, Roberts SA, Montenegro LR, Andrew M, Kirby A, Weirauch MT, Labilloy G, Bessa DS, Carroll RS, Jacobs DC, Chappell PE, Mendonca BB, Haig D, Kaiser UB, Latronico AC. Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious Puberty [Internet]. Journal of clinical endocrinology and metabolism. 2017 ; 102( 5): 1557-1567.[citado 2024 jul. 20 ] Available from: https://doi.org/10.1210/jc.2016-3677
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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ABNT
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: 20 jul. 2024.
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 2024 jul. 20 ] 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 2024 jul. 20 ] Available from: https://doi.org/10.1159/000447515
Trabalho de evento-resumo
Idiopathic central precocious puberty in boys: clinical, hormonal and genetic findings (2015)
Bessa, Daniele de Souza; Macedo, Delanie B.; Abreu, Ana Paula; Dauber, Andrew; Silveira, Leticia Gontijo; Zegher, Francis de; Gagliardi, Priscila C.; Demir, Korcan; Longhi, Carlos Alberto; Rosenberg, Carla ; Krepischi, Ana Cristina Victorino ; Mendonca, Berenice B; Brito, Vinicius N.; Antonini, Sonir Roberto; Kaiser, Ursula B.; Latronico, Ana Claudia
Fonte: Abstracts. Nome do evento: Annual Meeting and Expo of the Endocrine Society. Unidades: IB, FM, FMRP
Assuntos: GENÉTICA MÉDICA, MENINOS, PUBERDADE PRECOCE
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ABNT
BESSA, Daniele de Souza et al. Idiopathic central precocious puberty in boys: clinical, hormonal and genetic findings. 2015, Anais.. San Diego: Instituto de Biociências, Universidade de São Paulo, 2015. Disponível em: https://endo.confex.com/endo/2015endo/webprogram/Paper21402.html. Acesso em: 20 jul. 2024.
APA
Bessa, D. de S., Macedo, D. B., Abreu, A. P., Dauber, A., Silveira, L. G., Zegher, F. de, et al. (2015). Idiopathic central precocious puberty in boys: clinical, hormonal and genetic findings. In Abstracts. San Diego: Instituto de Biociências, Universidade de São Paulo. Recuperado de https://endo.confex.com/endo/2015endo/webprogram/Paper21402.html
NLM
Bessa D de S, Macedo DB, Abreu AP, Dauber A, Silveira LG, Zegher F de, Gagliardi PC, Demir K, Longhi CA, Rosenberg C, Krepischi ACV, Mendonca BB, Brito VN, Antonini SR, Kaiser UB, Latronico AC. Idiopathic central precocious puberty in boys: clinical, hormonal and genetic findings [Internet]. Abstracts. 2015 ;[citado 2024 jul. 20 ] Available from: https://endo.confex.com/endo/2015endo/webprogram/Paper21402.html
Vancouver
Bessa D de S, Macedo DB, Abreu AP, Dauber A, Silveira LG, Zegher F de, Gagliardi PC, Demir K, Longhi CA, Rosenberg C, Krepischi ACV, Mendonca BB, Brito VN, Antonini SR, Kaiser UB, Latronico AC. Idiopathic central precocious puberty in boys: clinical, hormonal and genetic findings [Internet]. Abstracts. 2015 ;[citado 2024 jul. 20 ] Available from: https://endo.confex.com/endo/2015endo/webprogram/Paper21402.html
Artigo de periodico
A new pathway in the control of the initiation of puberty: the MKRN3 gene (2015)
Abreu, Ana Paula; Macedo, Delanie B.; Brito, Vinicius N.; Kaiser, Ursula B.; Latronico, Ana Claudia
Fonte: Journal of Molecular Endocrinology. Unidade: FM
Assuntos: SECREÇÃO, PUBERDADE, HIPOTÁLAMO, GONADOTROFINAS, ESTÁGIOS DE DESENVOLVIMENTO, NEUROENDOCRINOLOGIA, MUTAÇÃO
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ABNT
ABREU, Ana Paula et al. A new pathway in the control of the initiation of puberty: the MKRN3 gene. Journal of Molecular Endocrinology, v. 54, n. 3, p. R131-R139, 2015Tradução . . Disponível em: https://doi.org/10.1530/JME-14-0315. Acesso em: 20 jul. 2024.
APA
Abreu, A. P., Macedo, D. B., Brito, V. N., Kaiser, U. B., & Latronico, A. C. (2015). A new pathway in the control of the initiation of puberty: the MKRN3 gene. Journal of Molecular Endocrinology, 54( 3), R131-R139. doi:10.1530/JME-14-0315
NLM
Abreu AP, Macedo DB, Brito VN, Kaiser UB, Latronico AC. A new pathway in the control of the initiation of puberty: the MKRN3 gene [Internet]. Journal of Molecular Endocrinology. 2015 ; 54( 3): R131-R139.[citado 2024 jul. 20 ] Available from: https://doi.org/10.1530/JME-14-0315
Vancouver
Abreu AP, Macedo DB, Brito VN, Kaiser UB, Latronico AC. A new pathway in the control of the initiation of puberty: the MKRN3 gene [Internet]. Journal of Molecular Endocrinology. 2015 ; 54( 3): R131-R139.[citado 2024 jul. 20 ] Available from: https://doi.org/10.1530/JME-14-0315
Artigo de periodico
Central Precocious Puberty That Appears to Be Sporadic Caused by Paternally Inherited Mutations in the Imprinted Gene Makorin Ring Finger 3 (2014)
Macedo, Delanie B.; Abreu, Ana Paula; Reis, Ana Claudia S.; Montenegro, Luciana R.; Dauber, Andrew; Beneduzzi, Daiane; Cukier, Priscilla; Silveira, Leticia F. G.; Teles, Milena G.; Carroll, Rona S.; Guerra Junior, Gil; Guaragna Filho, Guilherme; Gucev, Zoran; Arnhold, Ivo J. P.; Castro, Margaret de; Moreira, Ayrton C.; Martinelli Jr., Carlos Eduardo; Hirschhorn, Joel N.; Mendonca, Berenice B.; Brito, Vinicius N.; Antonini, Sonir R.; Kaiser, Ursula B.; Latronico, Ana Claudia
Fonte: Journal of Clinical Endocrinology and Metabolism. Unidades: FM, FMRP
Assuntos: CRIANÇAS, TÉCNICAS GENÉTICAS, PUBERDADE PRECOCE, MUTAÇÃO GENÉTICA
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ABNT
MACEDO, Delanie B. et al. Central Precocious Puberty That Appears to Be Sporadic Caused by Paternally Inherited Mutations in the Imprinted Gene Makorin Ring Finger 3. Journal of Clinical Endocrinology and Metabolism, v. 99, n. 6, p. E1097-E1103, 2014Tradução . . Disponível em: https://doi.org/10.1210/jc.2013-3126. Acesso em: 20 jul. 2024.
APA
Macedo, D. B., Abreu, A. P., Reis, A. C. S., Montenegro, L. R., Dauber, A., Beneduzzi, D., et al. (2014). Central Precocious Puberty That Appears to Be Sporadic Caused by Paternally Inherited Mutations in the Imprinted Gene Makorin Ring Finger 3. Journal of Clinical Endocrinology and Metabolism, 99( 6), E1097-E1103. doi:10.1210/jc.2013-3126
NLM
Macedo DB, Abreu AP, Reis ACS, Montenegro LR, Dauber A, Beneduzzi D, Cukier P, Silveira LFG, Teles MG, Carroll RS, Guerra Junior G, Guaragna Filho G, Gucev Z, Arnhold IJP, Castro M de, Moreira AC, Martinelli Jr. CE, Hirschhorn JN, Mendonca BB, Brito VN, Antonini SR, Kaiser UB, Latronico AC. Central Precocious Puberty That Appears to Be Sporadic Caused by Paternally Inherited Mutations in the Imprinted Gene Makorin Ring Finger 3 [Internet]. Journal of Clinical Endocrinology and Metabolism. 2014 ; 99( 6): E1097-E1103.[citado 2024 jul. 20 ] Available from: https://doi.org/10.1210/jc.2013-3126
Vancouver
Macedo DB, Abreu AP, Reis ACS, Montenegro LR, Dauber A, Beneduzzi D, Cukier P, Silveira LFG, Teles MG, Carroll RS, Guerra Junior G, Guaragna Filho G, Gucev Z, Arnhold IJP, Castro M de, Moreira AC, Martinelli Jr. CE, Hirschhorn JN, Mendonca BB, Brito VN, Antonini SR, Kaiser UB, Latronico AC. Central Precocious Puberty That Appears to Be Sporadic Caused by Paternally Inherited Mutations in the Imprinted Gene Makorin Ring Finger 3 [Internet]. Journal of Clinical Endocrinology and Metabolism. 2014 ; 99( 6): E1097-E1103.[citado 2024 jul. 20 ] Available from: https://doi.org/10.1210/jc.2013-3126
Artigo de periodico
A PROKR2 Mutant Exerts Dominant Negative Effects on Wild-Type PROKR2: New Insights into the Effects of PROKR2 Heterozygous Mutations (2012)
Abreu, Ana Paula; Xu, Shuvun; Noel, Sekomi D.; Carroll, Rona S.; Kaiser, Ursula B.; Latronico, Ana C.
Fonte: Endocrine Reviews. Nome do evento: ENDO 2012: The Endocrine Society's 94th Annual Meeting & Expo. Unidade: FM
Assuntos: PUBERDADE PRECOSE, WESTERN BLOTTING, HIPOGONADISMO, MUTAÇÃO GENÉTICA, RESUMOS (EVENTOS)
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ABNT
ABREU, Ana Paula et al. A PROKR2 Mutant Exerts Dominant Negative Effects on Wild-Type PROKR2: New Insights into the Effects of PROKR2 Heterozygous Mutations. Endocrine Reviews, v. 33, 2012Tradução . . Disponível em: http://edrv.endojournals.org/cgi/content/meeting_abstract/33/03_MeetingAbstracts/SUN-620. Acesso em: 20 jul. 2024.
APA
Abreu, A. P., Xu, S., Noel, S. D., Carroll, R. S., Kaiser, U. B., & Latronico, A. C. (2012). A PROKR2 Mutant Exerts Dominant Negative Effects on Wild-Type PROKR2: New Insights into the Effects of PROKR2 Heterozygous Mutations. Endocrine Reviews, 33. Recuperado de http://edrv.endojournals.org/cgi/content/meeting_abstract/33/03_MeetingAbstracts/SUN-620
NLM
Abreu AP, Xu S, Noel SD, Carroll RS, Kaiser UB, Latronico AC. A PROKR2 Mutant Exerts Dominant Negative Effects on Wild-Type PROKR2: New Insights into the Effects of PROKR2 Heterozygous Mutations [Internet]. Endocrine Reviews. 2012 ; 33[citado 2024 jul. 20 ] Available from: http://edrv.endojournals.org/cgi/content/meeting_abstract/33/03_MeetingAbstracts/SUN-620
Vancouver
Abreu AP, Xu S, Noel SD, Carroll RS, Kaiser UB, Latronico AC. A PROKR2 Mutant Exerts Dominant Negative Effects on Wild-Type PROKR2: New Insights into the Effects of PROKR2 Heterozygous Mutations [Internet]. Endocrine Reviews. 2012 ; 33[citado 2024 jul. 20 ] Available from: http://edrv.endojournals.org/cgi/content/meeting_abstract/33/03_MeetingAbstracts/SUN-620
Artigo de periodico
An ancient founder mutation in PROKR2 impairs human reproduction (2012)
Stefanija, Magdalena Avbelj; Jeanpierre, Marc; Sykiotis, Gerasimos P.; Young, Jacques; Quinton, Richard; Abreu, Ana Paula; Plummer, Lacey; Au, Margaret G.; Balasubramanian, Ravikumar; Dwyer, Andrew A.; Florez, Jose C.; Cheetham, Timothy; Pearce, Simon H.; Purushothaman, Radhika; Schinzel, Albert; Pugeat, Michel; Jacobson-Dickman, Elka E.; Ten, Svetlana; Latronico, Ana Claudia; Gusella, James F.; Dode, Catherine; Crowley Jr, William F.; Pitteloud, Nelly
Fonte: Human Molecular Genetics. Unidade: FM
Assuntos: FENÓTIPOS, GENÓTIPOS, INFLAMAÇÃO, MUTAÇÃO GENÉTICA, POLIMORFISMO, HIPOGANADISMO (DIAGNÓSTICO), GONADOTROFINAS HIPOFISÁRIAS (DEFICIÊNCIA)
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ABNT
STEFANIJA, Magdalena Avbelj et al. An ancient founder mutation in PROKR2 impairs human reproduction. Human Molecular Genetics, v. 21, n. 19, p. 4314-4324, 2012Tradução . . Disponível em: https://doi.org/10.1093/hmg/dds264. Acesso em: 20 jul. 2024.
APA
Stefanija, M. A., Jeanpierre, M., Sykiotis, G. P., Young, J., Quinton, R., Abreu, A. P., et al. (2012). An ancient founder mutation in PROKR2 impairs human reproduction. Human Molecular Genetics, 21( 19), 4314-4324. doi:10.1093/hmg/dds264
NLM
Stefanija MA, Jeanpierre M, Sykiotis GP, Young J, Quinton R, Abreu AP, Plummer L, Au MG, Balasubramanian R, Dwyer AA, Florez JC, Cheetham T, Pearce SH, Purushothaman R, Schinzel A, Pugeat M, Jacobson-Dickman EE, Ten S, Latronico AC, Gusella JF, Dode C, Crowley Jr WF, Pitteloud N. An ancient founder mutation in PROKR2 impairs human reproduction [Internet]. Human Molecular Genetics. 2012 ; 21( 19): 4314-4324.[citado 2024 jul. 20 ] Available from: https://doi.org/10.1093/hmg/dds264
Vancouver
Stefanija MA, Jeanpierre M, Sykiotis GP, Young J, Quinton R, Abreu AP, Plummer L, Au MG, Balasubramanian R, Dwyer AA, Florez JC, Cheetham T, Pearce SH, Purushothaman R, Schinzel A, Pugeat M, Jacobson-Dickman EE, Ten S, Latronico AC, Gusella JF, Dode C, Crowley Jr WF, Pitteloud N. An ancient founder mutation in PROKR2 impairs human reproduction [Internet]. Human Molecular Genetics. 2012 ; 21( 19): 4314-4324.[citado 2024 jul. 20 ] Available from: https://doi.org/10.1093/hmg/dds264
Trabalho de evento-resumo periodico
Phenotype-genotype correlations in patients with inactivating gonadotropin hormone receptor mutations (2012)
Beneduzzi, Daiane; Costa, Elaine M. F.; Abreu, Ana Paula; Lofrano-Porto, Adriana; Silveira, Leticia G. F.; Mendonça, Berenice B.; Trarbach, Ericka B.; Latronico, Ana Claudia
Fonte: Hormone research in paediatrics. Nome do evento: 51th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE). Unidade: FM
Assuntos: GENÓTIPOS, RECEPTORES HORMONAIS, GONADOTROFINAS HIPOFISÁRIAS, FENÓTIPOS, HIPOGONADISMO, HORMÔNOS (USO TERAPÊUTICO), RESUMOS (EVENTOS)
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ABNT
BENEDUZZI, Daiane et al. Phenotype-genotype correlations in patients with inactivating gonadotropin hormone receptor mutations. Hormone research in paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. Disponível em: https://doi.org/10.1159/000343181. Acesso em: 20 jul. 2024. , 2012
APA
Beneduzzi, D., Costa, E. M. F., Abreu, A. P., Lofrano-Porto, A., Silveira, L. G. F., Mendonça, B. B., et al. (2012). Phenotype-genotype correlations in patients with inactivating gonadotropin hormone receptor mutations. Hormone research in paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. doi:10.1159/000343181
NLM
Beneduzzi D, Costa EMF, Abreu AP, Lofrano-Porto A, Silveira LGF, Mendonça BB, Trarbach EB, Latronico AC. Phenotype-genotype correlations in patients with inactivating gonadotropin hormone receptor mutations [Internet]. Hormone research in paediatrics. 2012 ;78( suppl. 1): 42.[citado 2024 jul. 20 ] Available from: https://doi.org/10.1159/000343181
Vancouver
Beneduzzi D, Costa EMF, Abreu AP, Lofrano-Porto A, Silveira LGF, Mendonça BB, Trarbach EB, Latronico AC. Phenotype-genotype correlations in patients with inactivating gonadotropin hormone receptor mutations [Internet]. Hormone research in paediatrics. 2012 ;78( suppl. 1): 42.[citado 2024 jul. 20 ] Available from: https://doi.org/10.1159/000343181
Artigo de periodico
Phenotype–Genotype Correlations in Patients with Inactivating Gonadotropin Hormone Receptor Mutations (2012)
Beneduzzi, Daiane; Costa, Elaine M. F.; Silveira, Leticia; Trarbach, Ericka; Abreu, Ana Paula; Porto, Adriana Lofrano; Latronico, Ana C.; Mendonca, Berenice B.
Fonte: Endocrine Reviews. Nome do evento: ENDO 2012: The Endocrine Society's 94th Annual Meeting & Expo. Unidade: FM
Assuntos: GENÓTIPOS, MUTAÇÃO GENÉTICA, FENÓTIPOS, HIPOGONADISMO, RESUMOS (EVENTOS)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BENEDUZZI, Daiane et al. Phenotype–Genotype Correlations in Patients with Inactivating Gonadotropin Hormone Receptor Mutations. Endocrine Reviews, v. 33, 2012Tradução . . Disponível em: http://edrv.endojournals.org/cgi/content/meeting_abstract/33/03_MeetingAbstracts/SUN-618. Acesso em: 20 jul. 2024.
APA
Beneduzzi, D., Costa, E. M. F., Silveira, L., Trarbach, E., Abreu, A. P., Porto, A. L., et al. (2012). Phenotype–Genotype Correlations in Patients with Inactivating Gonadotropin Hormone Receptor Mutations. Endocrine Reviews, 33. Recuperado de http://edrv.endojournals.org/cgi/content/meeting_abstract/33/03_MeetingAbstracts/SUN-618
NLM
Beneduzzi D, Costa EMF, Silveira L, Trarbach E, Abreu AP, Porto AL, Latronico AC, Mendonca BB. Phenotype–Genotype Correlations in Patients with Inactivating Gonadotropin Hormone Receptor Mutations [Internet]. Endocrine Reviews. 2012 ; 33[citado 2024 jul. 20 ] Available from: http://edrv.endojournals.org/cgi/content/meeting_abstract/33/03_MeetingAbstracts/SUN-618
Vancouver
Beneduzzi D, Costa EMF, Silveira L, Trarbach E, Abreu AP, Porto AL, Latronico AC, Mendonca BB. Phenotype–Genotype Correlations in Patients with Inactivating Gonadotropin Hormone Receptor Mutations [Internet]. Endocrine Reviews. 2012 ; 33[citado 2024 jul. 20 ] Available from: http://edrv.endojournals.org/cgi/content/meeting_abstract/33/03_MeetingAbstracts/SUN-618
Artigo de periodico
Nonsense Mutations in FGF8 Gene Causing Different Degrees of Human Gonadotropin-Releasing Deficiency (2010)
Trarbach, Ericka B.; Abreu, Ana Paula; Silveira, Leticia Ferreira Gontijo; Garmes, Heraldo Mendes; Baptista, Maria Tereza M.; Teles, Milena Gurgel; Costa, Elaine M. F.; Mohammadi, Moosa; Pitteloud, Nelly; Mendonça, Berenice Bilharinho; Latronico, Ana Claudia
Fonte: Journal of Clinical Endocrinology and Metabolism. Unidade: FM
Assuntos: MUTAÇÃO GÊNICA, GONADOTROFINAS (DEFICIÊNCIA), REAÇÃO EM CADEIA POR POLIMERASE, ENDOCRINOPATIAS (GENÉTICA)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TRARBACH, Ericka B. et al. Nonsense Mutations in FGF8 Gene Causing Different Degrees of Human Gonadotropin-Releasing Deficiency. Journal of Clinical Endocrinology and Metabolism, v. 95, n. 7, p. 3491-3496, 2010Tradução . . Disponível em: https://doi.org/10.1210/jc.2010-0176. Acesso em: 20 jul. 2024.
APA
Trarbach, E. B., Abreu, A. P., Silveira, L. F. G., Garmes, H. M., Baptista, M. T. M., Teles, M. G., et al. (2010). Nonsense Mutations in FGF8 Gene Causing Different Degrees of Human Gonadotropin-Releasing Deficiency. Journal of Clinical Endocrinology and Metabolism, 95( 7), 3491-3496. doi:10.1210/jc.2010-0176
NLM
Trarbach EB, Abreu AP, Silveira LFG, Garmes HM, Baptista MTM, Teles MG, Costa EMF, Mohammadi M, Pitteloud N, Mendonça BB, Latronico AC. Nonsense Mutations in FGF8 Gene Causing Different Degrees of Human Gonadotropin-Releasing Deficiency [Internet]. Journal of Clinical Endocrinology and Metabolism. 2010 ; 95( 7): 3491-3496.[citado 2024 jul. 20 ] Available from: https://doi.org/10.1210/jc.2010-0176
Vancouver
Trarbach EB, Abreu AP, Silveira LFG, Garmes HM, Baptista MTM, Teles MG, Costa EMF, Mohammadi M, Pitteloud N, Mendonça BB, Latronico AC. Nonsense Mutations in FGF8 Gene Causing Different Degrees of Human Gonadotropin-Releasing Deficiency [Internet]. Journal of Clinical Endocrinology and Metabolism. 2010 ; 95( 7): 3491-3496.[citado 2024 jul. 20 ] Available from: https://doi.org/10.1210/jc.2010-0176
Artigo de periodico
The Role of Prokineticins in the Pathogenesis of Hypogonadotropic Hypogonadism (2010)
Abreu, Ana Paula; Kaiser, Ursukla B.; Xavier, Ana Claudia Latronico
Fonte: Neuroendocrinology. Unidade: FM
Assuntos: HIPOGONADISMO (PATOLOGIA), MODELOS ANIMAIS, DOENÇAS GENÉTICAS, CAMUNDONGOS, GENÓTIPOS, GONADOTROFINAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ABREU, Ana Paula e KAISER, Ursukla B. e XAVIER, Ana Claudia Latronico. The Role of Prokineticins in the Pathogenesis of Hypogonadotropic Hypogonadism. Neuroendocrinology, v. 91, n. 4, p. 283-290, 2010Tradução . . Disponível em: http://content.karger.com/ProdukteDB/produkte.asp?doi=10.1159/000308880. Acesso em: 20 jul. 2024.
APA
Abreu, A. P., Kaiser, U. B., & Xavier, A. C. L. (2010). The Role of Prokineticins in the Pathogenesis of Hypogonadotropic Hypogonadism. Neuroendocrinology, 91( 4), 283-290. doi:10.1159/000308880
NLM
Abreu AP, Kaiser UB, Xavier ACL. The Role of Prokineticins in the Pathogenesis of Hypogonadotropic Hypogonadism [Internet]. Neuroendocrinology. 2010 ; 91( 4): 283-290.[citado 2024 jul. 20 ] Available from: http://content.karger.com/ProdukteDB/produkte.asp?doi=10.1159/000308880
Vancouver
Abreu AP, Kaiser UB, Xavier ACL. The Role of Prokineticins in the Pathogenesis of Hypogonadotropic Hypogonadism [Internet]. Neuroendocrinology. 2010 ; 91( 4): 283-290.[citado 2024 jul. 20 ] Available from: http://content.karger.com/ProdukteDB/produkte.asp?doi=10.1159/000308880
Artigo de periodico
Screening of autosomal gene deletions in patients with hypogonadotropic hypogonadism using multiplex ligation-dependent probe amplification: detection of a hemizygosis for the fibroblast growth factor receptor 1 (2010)
Trarbach, Ericka Barbosa; Teles, Milena Gurgel; Costa, Elaine Maria Frade; Abreu, Ana Paula; Garmes, Heraldo Mendes; Guerra Junior, Gil; Baptista, Maria Tereza Matias; Castro, Margaret de; Mendonca, Berenice Bilharinho; Latronico, Ana Claudia
Fonte: Clinical endocrinology. Unidade: FM
Assuntos: FATORES DE CRESCIMENTO, DELEÇÃO DE GENES, RASTREAMENTO, FIBROBLASTOS, HIPOGONADISMO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TRARBACH, Ericka Barbosa et al. Screening of autosomal gene deletions in patients with hypogonadotropic hypogonadism using multiplex ligation-dependent probe amplification: detection of a hemizygosis for the fibroblast growth factor receptor 1. Clinical endocrinology, v. 72, n. 3, p. 371-376, 2010Tradução . . Disponível em: https://doi.org/10.1111/j.1365-2265.2009.03642.x. Acesso em: 20 jul. 2024.
APA
Trarbach, E. B., Teles, M. G., Costa, E. M. F., Abreu, A. P., Garmes, H. M., Guerra Junior, G., et al. (2010). Screening of autosomal gene deletions in patients with hypogonadotropic hypogonadism using multiplex ligation-dependent probe amplification: detection of a hemizygosis for the fibroblast growth factor receptor 1. Clinical endocrinology, 72( 3), 371-376. doi:10.1111/j.1365-2265.2009.03642.x
NLM
Trarbach EB, Teles MG, Costa EMF, Abreu AP, Garmes HM, Guerra Junior G, Baptista MTM, Castro M de, Mendonca BB, Latronico AC. Screening of autosomal gene deletions in patients with hypogonadotropic hypogonadism using multiplex ligation-dependent probe amplification: detection of a hemizygosis for the fibroblast growth factor receptor 1 [Internet]. Clinical endocrinology. 2010 ; 72( 3): 371-376.[citado 2024 jul. 20 ] Available from: https://doi.org/10.1111/j.1365-2265.2009.03642.x
Vancouver
Trarbach EB, Teles MG, Costa EMF, Abreu AP, Garmes HM, Guerra Junior G, Baptista MTM, Castro M de, Mendonca BB, Latronico AC. Screening of autosomal gene deletions in patients with hypogonadotropic hypogonadism using multiplex ligation-dependent probe amplification: detection of a hemizygosis for the fibroblast growth factor receptor 1 [Internet]. Clinical endocrinology. 2010 ; 72( 3): 371-376.[citado 2024 jul. 20 ] Available from: https://doi.org/10.1111/j.1365-2265.2009.03642.x
Artigo de periodico
Loss-of-function mutations in the genes encoding prokineticin-2 or prokineticin receptor-2 cause autosomal recessive Kallmann syndrome (2008)
Abreu, Ana Paula; Trarbach, Ericka Barbosa; Castro, Margaret de; Costa, Elaine Maria Frade; Versiani, Beatriz; Baptista, Maria Tereza Matias; Garmes, Heraldo Mendes; Mendonça, Berenice Bilharinho; Latronico, Ana Claudia
Fonte: Journal of Clinical Endocrinology and Metabolism. Unidade: FMRP
Assuntos: SÍNDROME DE KALLMANN, ENDOCRINOLOGIA, METABOLISMO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ABREU, Ana Paula et al. Loss-of-function mutations in the genes encoding prokineticin-2 or prokineticin receptor-2 cause autosomal recessive Kallmann syndrome. Journal of Clinical Endocrinology and Metabolism, v. 93, n. 10, p. 4113-4118, 2008Tradução . . Acesso em: 20 jul. 2024.
APA
Abreu, A. P., Trarbach, E. B., Castro, M. de, Costa, E. M. F., Versiani, B., Baptista, M. T. M., et al. (2008). Loss-of-function mutations in the genes encoding prokineticin-2 or prokineticin receptor-2 cause autosomal recessive Kallmann syndrome. Journal of Clinical Endocrinology and Metabolism, 93( 10), 4113-4118.
NLM
Abreu AP, Trarbach EB, Castro M de, Costa EMF, Versiani B, Baptista MTM, Garmes HM, Mendonça BB, Latronico AC. Loss-of-function mutations in the genes encoding prokineticin-2 or prokineticin receptor-2 cause autosomal recessive Kallmann syndrome. Journal of Clinical Endocrinology and Metabolism. 2008 ; 93( 10): 4113-4118.[citado 2024 jul. 20 ]
Vancouver
Abreu AP, Trarbach EB, Castro M de, Costa EMF, Versiani B, Baptista MTM, Garmes HM, Mendonça BB, Latronico AC. Loss-of-function mutations in the genes encoding prokineticin-2 or prokineticin receptor-2 cause autosomal recessive Kallmann syndrome. Journal of Clinical Endocrinology and Metabolism. 2008 ; 93( 10): 4113-4118.[citado 2024 jul. 20 ]
Trabalho de evento-resumo
Mutations in the prokineticin receptor-2 gene in patients with Kallmann syndrome (2007)
Abreu, Ana Paula; Trarbach, Ericka; Castro, Margaret de; Costa, Elaine M. F.; Versiani, Beatriz; Baptista, Maria Tereza M.; Garmes, Heraldo M.; Mendonça, Berenice B.; Latronico, Ana Claudia
Fonte: Program and Abstracts. Nome do evento: The Endocrine Society's Annual Meeting (ENDO). Unidade: FMRP
Assunto: HIPOGONADISMO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ABREU, Ana Paula et al. Mutations in the prokineticin receptor-2 gene in patients with Kallmann syndrome. 2007, Anais.. Toronto: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, 2007. . Acesso em: 20 jul. 2024.
APA
Abreu, A. P., Trarbach, E., Castro, M. de, Costa, E. M. F., Versiani, B., Baptista, M. T. M., et al. (2007). Mutations in the prokineticin receptor-2 gene in patients with Kallmann syndrome. In Program and Abstracts. Toronto: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Abreu AP, Trarbach E, Castro M de, Costa EMF, Versiani B, Baptista MTM, Garmes HM, Mendonça BB, Latronico AC. Mutations in the prokineticin receptor-2 gene in patients with Kallmann syndrome. Program and Abstracts. 2007 ;[citado 2024 jul. 20 ]
Vancouver
Abreu AP, Trarbach E, Castro M de, Costa EMF, Versiani B, Baptista MTM, Garmes HM, Mendonça BB, Latronico AC. Mutations in the prokineticin receptor-2 gene in patients with Kallmann syndrome. Program and Abstracts. 2007 ;[citado 2024 jul. 20 ]

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