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Results 61-70 of 81 (Search time: 0.027 seconds).
Issue Date | Title | Author(s) |
---|---|---|
2017 | PARTIAL RECOVERY OF PITUITARY FUNCTION AFTER LINEAR GROWTH IN PATIENTS WITH CONGENITAL COMBINED PITUITARY HORMONE DEFICIENCY (CPHD) | MADEIRA, Joao L. O.; BISCOTTO, Isabela P.; CORREA, Fernanda A.; OTTO, Aline P.; COSTALONGA, Everlayny F.; FRANCA, Marcela M.; JORGE, Alexander; ARNHOLD, Ivo J.; MENDONCA, Berenice B.; CARVALHO, Luciani R. |
2017 | NOVEL LZTR1 GENE VARIANTS ASSOCIATED TO NOONAN SYNDROME AND GROWTH HORMONE DEFICIENCY | NAKAGUMA, Marilena; JORGE, Alexander A. L.; MARIANA, Funari F. A.; ANTONIO, Lerario M.; FERNANDA, Correa A.; LUCIANI, Carvalho R. S.; BERENICE, Mendonca B.; ARNHOLD, Ivo J. |
2017 | CLINICAL AND MOLECULAR ANALYSIS OF PUBERTAL CONTROL IN A COHORT OF SILVER-RUSSELL AND TEMPLE SYNDROMES PATIENTS | CANTON, Ana; HARBISON, Madeleine D.; HABIB, Walid Abi; SALEM, Jennifer; BLAISE, Annick; GEOFFRON, Sophie; GIABICANI, Eloise; JORGE, Alexander A. L.; BRIOUDE, Frederic; NETCHINE, Irene |
2013 | Associations of genetic variants in thioredoxin (TXN) and mitochondrial thioredoxin reductase (TXNRD2) genes with kidney disease in type 1 diabetes | PATENTE, T. A.; MONTEIRO, M. B.; QUEIROZ, M.; NERY, M.; AZEVEDO, M. J.; CANANI, L. H.; PAVIN, E. J.; PARISI, M. C.; MACHADO, U. F.; PASSARELLI, M.; GIANNELLA-NETO, D.; CORREA-GIANNELLA, M. L. C. |
2022 | Usefulness of Next Generation Sequencing in the Molecular Diagnosis of McCune-Albright Syndrome in Peripheral Blood | FARIA, Aline Guimaraes; JORGE, Alexander Augusto Lima; MONTENEGRO, Luciana; CANTO, Ana Pinheiro Machado; SERAPHIM, Carlos Eduardo; TINANO, Flavia Rezende; JALLAD, Raquel Soares; MARTIN, Regina Matsunaga; FRAGOSO, Maria Candida Villares; PINTO, Nadja Christina Souza; MENDONCA, Berenice Bilharinho; LATRONICO, Ana Claudia; BRITO, Vinicius Nahime |
2014 | Glutathione peroxidase 1 (GPX1) variants, oxidative stress markers, and risk of kidney complications in patients with type 1 diabetes | MOHAMMEDI, K.; BELLILI-MUNOZ, N.; DRISS, F.; PATENTE, T.; HADJADJ, S.; FUMERON, F.; ROUSSEL, R.; CORREA-GIANNELLA, M.; MARRE, M.; VELHO, G. |
2021 | Characterization of puberty development in a large cohort of patients with Noonan syndrome with molecular diagnosis | REZENDE, Raissa; JORGE, Alexander; NORONHA, Renata; KESELMAN, Ana; ANDRADE, Nathalia; DANTAS, Naiara; BERTOLA, Debora; MALAQUIAS, Alexsandra |
2021 | Outcomes in growth hormone-treated Noonan syndrome children: impact of PTPN11 mutation status | JORGE, Alexander A. L.; PIETROPOLI, Alberto; KELEPOURIS, Nicky; HORIKAWA, Reiko |
2021 | POTENTIALLY PATHOGENIC VARIANTS IDENTIFIED BY NEXT- GENERATION SEQUENCING IN PATIENTS WITH SHORT STATURE OF UNKNOWN ORIGIN | SANGUINETI, Nora Maria; SCAGLIA, Paula; KESELMAN, Ana; CASALI, Barbara; BRASLAVSKY, Debora; GUTIERREZ, Mariana; RAMIREZ, Laura; LANDI, Estefania; ROPELATO, Maria Gabriela; BALLERINI, Maria Gabriela; PENNISI, Patricia; MARTIN, Ayelen; CASSINELLI, Hamilton; DOMENE, Sabina; BERENSTEIN, Ariel; IZQUIERDO, Agustin; REY, Graciela Del; VILLEGAS, Florencia; ARMANDO, Romina; FERNANDEZ, Maria Del Carmen; AZCOITI, Maria Esnaola; ARBERAS, Claudia; DOMENE, Horacio; JASPER, Hector; ARNHOLD, Ivo Jorge Prado; VASQUES, Gabriela A.; JORGE, Alexander A. L.; REY, Rodolfo; BERGADA, Ignacio |
2019 | Evaluation of Puberty in Patients with Noonan Syndrome and Mutations in the RAS/MAPK Genes | MALAQUIAS, A. C.; NORONHA, R. M.; HOMMA, T. K.; ALBUQUERQUE, E. V. A.; VASQUES, G. A.; BERTOLA, D. R.; JORGE, A. A. L. |
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