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Issue Date | Title | Author(s) |
---|---|---|
2013 | The benign spectrum of hypothalamic hamartomas: Infrequent epilepsy and normal cognition in patients presenting with central precocious puberty | CUKIER, Priscilla; CASTRO, Luiz Henrique Martins; BANASKIWITZ, Natalie; TELES, Leandro Roberto; FERREIRA, Luiz Roberto Kobuti; ADDA, Carla Cristina; LEITE, Claudia da Costa; ARNHOLD, Ivo J. P.; MENDONCA, Berenice Bilharinho; LATRONICO, Ana Claudia; BRITO, Vinicius Nahime |
2013 | Obesity and Familial Predisposition Are Significant Determining Factors of an Adverse Metabolic Profile in Young Patients with Congenital Adrenal Hyperplasia | MOREIRA, Ricardo P. P.; VILLARES, Sandra M.; MADUREIRA, Guiomar; MENDONCA, Berenice B.; BACHEGA, Tania A. S. S. |
2011 | Novel inactivating mutations in the GH secretagogue receptor gene in patients with constitutional delay of growth and puberty | PUGLIESE-PIRES, Patricia N.; FORTIN, Jean-Philippe; ARTHUR, Thais; LATRONICO, Ana Claudia; MENDONCA, Berenice B.; VILLARES, Sandra Mara F.; PARNHOLD, Ivo J.; KOPIN, Alan S.; JORGE, Alexander A. L. |
2021 | Management of functioning pediatric adrenal tumors | LOPES, Roberto Iglesias; SUARTZ, Caio Vinicius; PEDRENHO NETO, Rubens; BERJEAUT, Ricardo Haidar; MENDONCA, Berenice; ALMEIDA, Madson Q.; FRAGOSO, Maria Candida Villares; DENES, Francisco Tibor |
2013 | Relatively high frequency of non-synonymous GLI2 variants in patients with congenital hypopituitarism without holoprosencephaly | FRANCA, Marcela M.; JORGE, Alexander A. L.; CARVALHO, Luciani R. S.; COSTALONGA, Everlayny F.; OTTO, Aline P.; CORREA, Fernanda A.; MENDONCA, Berenice B.; ARNHOLD, Ivo J. P. |
2020 | Adverse Outcomes and Economic Burden of Congenital Adrenal Hyperplasia Late Diagnosis in the Newborn Screening Absence | MIRANDA, Mirela Costa de; HADDAD, Luciana Bertocco de Paiva; MADUREIRA, Guiomar; MENDONCA, Berenice Bilharinho de; BACHEGA, Tania A. S. S. |
2019 | Impact of Growth Hormone Therapy on Adult Height in Patients with PTPN11 Mutations Related to Noonan Syndrome | MALAQUIAS, Alexsandra C.; NORONHA, Renata M.; SOUZA, Thaiana T. O.; HOMMA, Thais K.; FUNARI, Mariana F. A.; YAMAMOTO, Guilherme L.; SILVA, Fernanda Viana; MORAES, Michelle B.; HONJO, Rachel S.; KIM, Chong A.; NESI-FRANCA, Suzana; CARVALHO, Julienne A. R.; QUEDAS, Elisangela P. S.; BERTOLA, Debora R.; JORGE, Alexander A. L. |
2012 | The Interactive Effect of GHR-Exon 3 and -202 A/C IGFBP3 Polymorphisms on rhGH Responsiveness and Treatment Outcomes in Patients with Turner Syndrome | BRAZ, Adriana F.; COSTALONGA, Everlayny F.; MONTENEGRO, Luciana R.; TRARBACH, Ericka B.; ANTONINI, Sonir R. R.; MALAQUIAS, Alexsandra C.; RAMOS, Ester S.; MENDONCA, Berenice B.; ARNHOLD, Ivo J. P.; JORGE, Alexander A. L. |
2012 | Growth standards of patients with Noonan and Noonan-like syndromes with mutations in the RAS/MAPK pathway | MALAQUIAS, Alexsandra C.; BRASIL, Amanda S.; PEREIRA, Alexandre C.; ARNHOLD, Ivo J. P.; MENDONCA, Berenice B.; BERTOLA, Debora R.; JORGE, Alexander A. L. |
2011 | Pharmacogenetics of glucocorticoid replacement could optimize the treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency | MOREIRA, Ricardo P. P.; JORGE, Alexander A. L.; GOMES, Larissa G.; KAUPERT, Laura C.; MASSUD FILHO, Joao; MENDONCA, Berenice B.; BACHEGA, Tania A. S. S. |