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Results 1-10 of 39 (Search time: 0.041 seconds).
Issue DateTitleAuthor(s)
2013Angiotensin converting enzyme insertion/deletion polymorphism is associated with increased adiposity and blood pressure in obese children and adolescentsLEMES, Vinicius A. F.; NEVES, Ana Luisa; GUAZZELLI, Isabel C.; FRAZZATTO, Eliana; NICOLAU, Christiane; CORREA-GIANNELLA, Maria Lucia; VELHO, Gilberto; VILLARES, Sandra M. F.
201146,XY Disorders of Sex Development (46,XY DSD) due to Androgen Receptor Defects: Androgen Insensitivity SyndromeARNHOLD, Ivo J. P.; MELO, Karla; COSTA, Elaine M. F.; DANILOVIC, Debora; INACIO, Marlene; DOMENICE, Sorahia; MENDONCA, Berenice B.
2011Risk Profiles and Penetrance Estimations in Multiple Endocrine Neoplasia Type 2A Caused by Germline RET Mutations Located in Exon 10FRANK-RAUE, Karin; RYBICKI, Lisa A.; ERLIC, Zoran; SCHWEIZER, Heiko; WINTER, Aurelia; MILOS, Ioana; TOLEDO, Sergio P. A.; TOLEDO, Rodrigo A.; TAVARES, Marcos R.; ALEVIZAKI, Maria; MIAN, Caterina; SIGGELKOW, Heide; HUEFNER, Michael; WOHLLK, Nelson; OPOCHER, Giuseppe; DVORAKOVA, Sarka; BENDLOVA, Bela; CZETWERTYNSKA, Malgorzata; SKASKO, Elzbieta; BARONTINI, Marta; SANSO, Gabriela; VORLAENDER, Christian; MAIA, Ana Luiza; PATOCS, Attila; LINKS, Thera P.; GROOT, Jan Willem de; KERSTENS, Michiel N.; VALK, Gerlof D.; MIEHLE, Konstanze; MUSHOLT, Thomas J.; BIARNES, Josefina; DAMJANOVIC, Svetozar; MURESAN, Mihaela; WUESTER, Christian; FASSNACHT, Martin; PECZKOWSKA, Mariola; FAUTH, Christine; GOLCHER, Henriette; WALTER, Martin A.; PICHL, Josef; RAUE, Friedhelm; ENG, Charis; NEUMANN, Hartmut P. H.
2013Epoxiconazole-Induced Degeneration in Rat Placenta and the Effects of Estradiol SupplementationMORENO, Maria Cecilia Rey; FUSSELL, Karma C.; GROETERS, Sibylle; SCHNEIDER, Steffen; STRAUSS, Volker; STINCHCOMBE, Stefan; FEGERT, Ivana; VERAS, Mariana; RAVENZWAAY, Bennard van
2019Allelic variations in genes belonging to glutathione system increase proliferative retinopathy risk in type 1 diabetes individualsPEREZ, Ricardo Vessoni; MACHADO, Cleide Guimaraes; SANTOS-BEZERRA, Daniele Pereira; ADMONI, Sharon Nina; PATENTE, Thiago Andrade; MONTEIRO, Maria Beatriz; CAVALEIRO, Ana Mercedes; QUEIROZ, Marcia Silva; NERY, Marcia; CORREA-GIANNELLA, Maria Lucia
2019Targeted sequencing identifies novel variants in common and rare MODY genesSANTANA, Lucas S. de; CAETANO, Lilian A.; COSTA-RIQUETTO, Aline D.; FRANCO, Pedro C.; DOTTO, Renata P.; REIS, Andre F.; WEINERT, Leticia S.; SILVEIRO, Sandra P.; VENDRAMINI, Marcio F.; PRADO, Flaviene A. do; ABRAHAO, Giovanna C. P.; ALMEIDA, Ana Gregoria F. P. de; TAVARES, Maria da G. Rodrigues; GONCALVES, Wagner Rodrigo B.; SANTOMAURO JUNIOR, Augusto C.; HALPERN, Bruno; JORGE, Alexander A. L.; NERY, Marcia; TELES, Milena G.
2018Novel SUZ12 mutations in Weaver-like syndromeIMAGAWA, Eri; ALBUQUERQUE, Edoarda V. A.; ISIDOR, Bertrand; MITSUHASHI, Satomi; MIZUGUCHI, Takeshi; MIYATAKE, Satoko; TAKATA, Atsushi; MIYAKE, Noriko; BOGUSZEWSKI, Margaret C. S.; BOGUSZEWSKI, Cesar L.; LERARIO, Antonio M.; FUNARI, Mariana A.; JORGE, Alexander A. L.; MATSUMOTO, Naomichi
2012Growth hormone pharmacogenetics: the interactive effect of a microsatellite in the IGF1 promoter region with the GHR-exon 3 and-202 A/C IGFBP3 variants on treatment outcomes of children with severe GH deficiencyCOSTALONGA, E. F.; ANTONINI, S. R. R.; GUERRA-JUNIOR, G.; COLETTA, R. R. D.; FRANCA, M. M.; BRAZ, A. F.; MENDONCA, B. B.; ARNHOLD, I. J. P.; JORGE, A. A. L.
2012Autoimmune disease and multiple autoantibodies in 42 patients with RASopathiesQUAIO, Caio R. D. C.; CARVALHO, Jozelio F.; SILVA, Clovis A. da; BUENO, Cleonice; BRASIL, Amanda S.; PEREIRA, Alexandre C.; JORGE, Alexander A. L.; MALAQUIAS, Alexsandra C.; KIM, Chong A.; BERTOLA, Debora R.
2012Growth standards of patients with Noonan and Noonan-like syndromes with mutations in the RAS/MAPK pathwayMALAQUIAS, Alexsandra C.; BRASIL, Amanda S.; PEREIRA, Alexandre C.; ARNHOLD, Ivo J. P.; MENDONCA, Berenice B.; BERTOLA, Debora R.; JORGE, Alexander A. L.