ReP USP - Resultado da busca

Artigo de periodico
Long-term response to growth hormone therapy in a patient with short stature caused by a novel heterozygous mutation in NPR2 (2017)
Vasques, Gabriela A.; Hisado-Oliva, Alfonso; Funari, Mariana F. A.; Lerario, Antonio M.; Quedas, Elisangela P. S.; Solberg, Paulo; Heath, Karen E.; Jorge, Alexander A. L.
Source: Journal of pediatric endocrinology & metabolism. Unidade: FM
Subjects: HORMÔNIO DO CRESCIMENTO, MUTAÇÃO GENÉTICA, ESTATUTO DA CRIANÇA E DO ADOLESCENTE, IMAGEM POR RESSONÂNCIA MAGNÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VASQUES, Gabriela A. et al. Long-term response to growth hormone therapy in a patient with short stature caused by a novel heterozygous mutation in NPR2. Journal of pediatric endocrinology & metabolism, v. 30, n. 1, p. 111-116, 2017Tradução . . Disponível em: https://doi.org/10.1515/jpem-2016-0280. Acesso em: 01 nov. 2024.
APA
Vasques, G. A., Hisado-Oliva, A., Funari, M. F. A., Lerario, A. M., Quedas, E. P. S., Solberg, P., et al. (2017). Long-term response to growth hormone therapy in a patient with short stature caused by a novel heterozygous mutation in NPR2. Journal of pediatric endocrinology & metabolism, 30( 1), 111-116. doi:10.1515/jpem-2016-0280
NLM
Vasques GA, Hisado-Oliva A, Funari MFA, Lerario AM, Quedas EPS, Solberg P, Heath KE, Jorge AAL. Long-term response to growth hormone therapy in a patient with short stature caused by a novel heterozygous mutation in NPR2 [Internet]. Journal of pediatric endocrinology & metabolism. 2017 ; 30( 1): 111-116.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1515/jpem-2016-0280
Vancouver
Vasques GA, Hisado-Oliva A, Funari MFA, Lerario AM, Quedas EPS, Solberg P, Heath KE, Jorge AAL. Long-term response to growth hormone therapy in a patient with short stature caused by a novel heterozygous mutation in NPR2 [Internet]. Journal of pediatric endocrinology & metabolism. 2017 ; 30( 1): 111-116.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1515/jpem-2016-0280
Artigo de periodico
Autosomal recessive form of isolated growth hormone deficiency is more frequent than the autosomal dominant form in a Brazilian cohort (2014)
Lido, Andria C. V.; França, Marcela M.; Correa, Fernanda A.; Otto, Aline P.; Carvalho, Luciani R.; Quedas, Elisangela P. S.; Nishi, Mirian Y.; Mendonça, Berenice B.; Arnhold, Ivo J. P.; Jorge, Alexander A. L.
Source: Growth Hormone and IGF Research. Unidade: FM
Subjects: HORMÔNIO DO CRESCIMENTO (ANORMALIDADES), GENES RECESSIVOS, ESTUDOS DE COORTES, BRASILEIROS, MUTAÇÃO GENÉTICA, BIOMETRIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LIDO, Andria C. V. et al. Autosomal recessive form of isolated growth hormone deficiency is more frequent than the autosomal dominant form in a Brazilian cohort. Growth Hormone and IGF Research, v. 24, n. 5, p. 180-186, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.ghir.2014.07.001. Acesso em: 01 nov. 2024.
APA
Lido, A. C. V., França, M. M., Correa, F. A., Otto, A. P., Carvalho, L. R., Quedas, E. P. S., et al. (2014). Autosomal recessive form of isolated growth hormone deficiency is more frequent than the autosomal dominant form in a Brazilian cohort. Growth Hormone and IGF Research, 24( 5), 180-186. doi:10.1016/j.ghir.2014.07.001
NLM
Lido ACV, França MM, Correa FA, Otto AP, Carvalho LR, Quedas EPS, Nishi MY, Mendonça BB, Arnhold IJP, Jorge AAL. Autosomal recessive form of isolated growth hormone deficiency is more frequent than the autosomal dominant form in a Brazilian cohort [Internet]. Growth Hormone and IGF Research. 2014 ; 24( 5): 180-186.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.ghir.2014.07.001
Vancouver
Lido ACV, França MM, Correa FA, Otto AP, Carvalho LR, Quedas EPS, Nishi MY, Mendonça BB, Arnhold IJP, Jorge AAL. Autosomal recessive form of isolated growth hormone deficiency is more frequent than the autosomal dominant form in a Brazilian cohort [Internet]. Growth Hormone and IGF Research. 2014 ; 24( 5): 180-186.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.ghir.2014.07.001
Artigo de periodico
Heterozygous Mutations in Natriuretic Peptide Receptor-B (NPR2) Gene as a Cause of Short Stature in Patients Initially Classified as Idiopathic Short Stature (2013)
Vasques, Gabriela A.; Amano, Naoko; ADocko, na J.; Funari, Mariana F. A.; Quedas, Elisangela P. S.; Nishi, Mirian Y.; Arnhold, Ivo J. P.; Hasegawa, Tomonobu; Jorge, Alexander A. L.
Source: The Journal of Clinical Endocrinology & Metabolism. Unidade: FM
Subjects: MEDIDAS FÍSICAS, MUTAÇÃO GENÉTICA, DNA (ANÁLISE), TÉCNICAS CITOLÓGICAS (TENDÊNCIAS), PEPTÍDEOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VASQUES, Gabriela A. et al. Heterozygous Mutations in Natriuretic Peptide Receptor-B (NPR2) Gene as a Cause of Short Stature in Patients Initially Classified as Idiopathic Short Stature. The Journal of Clinical Endocrinology & Metabolism, v. 98, n. 10, p. E1636-E1644, 2013Tradução . . Disponível em: http://jcem.endojournals.org/content/98/10/E1636.full.pdf+html. Acesso em: 01 nov. 2024.
APA
Vasques, G. A., Amano, N., ADocko, na J., Funari, M. F. A., Quedas, E. P. S., Nishi, M. Y., et al. (2013). Heterozygous Mutations in Natriuretic Peptide Receptor-B (NPR2) Gene as a Cause of Short Stature in Patients Initially Classified as Idiopathic Short Stature. The Journal of Clinical Endocrinology & Metabolism, 98( 10), E1636-E1644. doi:10.1210/jc.2013-2142
NLM
Vasques GA, Amano N, ADocko na J, Funari MFA, Quedas EPS, Nishi MY, Arnhold IJP, Hasegawa T, Jorge AAL. Heterozygous Mutations in Natriuretic Peptide Receptor-B (NPR2) Gene as a Cause of Short Stature in Patients Initially Classified as Idiopathic Short Stature [Internet]. The Journal of Clinical Endocrinology & Metabolism. 2013 ; 98( 10): E1636-E1644.[citado 2024 nov. 01 ] Available from: http://jcem.endojournals.org/content/98/10/E1636.full.pdf+html
Vancouver
Vasques GA, Amano N, ADocko na J, Funari MFA, Quedas EPS, Nishi MY, Arnhold IJP, Hasegawa T, Jorge AAL. Heterozygous Mutations in Natriuretic Peptide Receptor-B (NPR2) Gene as a Cause of Short Stature in Patients Initially Classified as Idiopathic Short Stature [Internet]. The Journal of Clinical Endocrinology & Metabolism. 2013 ; 98( 10): E1636-E1644.[citado 2024 nov. 01 ] Available from: http://jcem.endojournals.org/content/98/10/E1636.full.pdf+html
Artigo de periodico
RET haplotype, not linked to the C620R activating mutation, associated with Hirschsprung disease in a novel MEN2 family (2012)
Quedas, Elisangela P. S.; Toledo, Rodrigo A.; Longuini, Viviane C.; Sekiya, Tomoko; Coutinho, Flavia L.; Toledo, Sergio P. A.; Tannuri, Uenis
Source: Clinics. Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, NEOPLASIA ENDÓCRINA MÚLTIPLA (GENÉTICA), DOENÇAS GENÉTICAS, CARCINOMA, MEGACOLON (GENÉTICA), NEOPLASIAS DA TIREOIDE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
QUEDAS, Elisangela P. S. et al. RET haplotype, not linked to the C620R activating mutation, associated with Hirschsprung disease in a novel MEN2 family. Clinics, v. 67, p. 57-61, 2012Tradução . . Disponível em: https://doi.org/10.6061/clinics/2012(Sup01)11. Acesso em: 01 nov. 2024.
APA
Quedas, E. P. S., Toledo, R. A., Longuini, V. C., Sekiya, T., Coutinho, F. L., Toledo, S. P. A., & Tannuri, U. (2012). RET haplotype, not linked to the C620R activating mutation, associated with Hirschsprung disease in a novel MEN2 family. Clinics, 67, 57-61. doi:10.6061/clinics/2012(Sup01)11
NLM
Quedas EPS, Toledo RA, Longuini VC, Sekiya T, Coutinho FL, Toledo SPA, Tannuri U. RET haplotype, not linked to the C620R activating mutation, associated with Hirschsprung disease in a novel MEN2 family [Internet]. Clinics. 2012 ; 67 57-61.[citado 2024 nov. 01 ] Available from: https://doi.org/10.6061/clinics/2012(Sup01)11
Vancouver
Quedas EPS, Toledo RA, Longuini VC, Sekiya T, Coutinho FL, Toledo SPA, Tannuri U. RET haplotype, not linked to the C620R activating mutation, associated with Hirschsprung disease in a novel MEN2 family [Internet]. Clinics. 2012 ; 67 57-61.[citado 2024 nov. 01 ] Available from: https://doi.org/10.6061/clinics/2012(Sup01)11

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