Browsing "LIM/42 - Laboratório de Hormônios e Genética Molecular" by Issue Date

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Issue DateTitleAuthor(s)
201146,XY DSD due to 17 beta-HSD3 Deficiency and 5 alpha-Reductase Type 2 DeficiencyINACIO, Marlene; SIRCILI, Maria Helena P.; BRITO, Vinicius N.; DOMENICE, Sorahia; OLIVEIRA-JUNIOR, Ari Alves; ARNHOLD, Ivo J. P.; TIBOR, Francisco D.; COSTA, Elaine M. F.; MENDONCA, Berenice B.
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.
2011MAMLD1 (Mastermind-Like Domain Containing 1) Homozygous Gain-of-Function Missense Mutation Causing 46,XX Disorder of Sex Development in a Virilized FemaleBRANDAO, Maira Pontual; COSTA, Elaine Maria Frade; FUKAMI, Maki; GERDULO, Mariza; PEREIRA, Natalia P.; DOMENICE, Sorahia; OGATA, Tsutomu; MENDONCA, Berenice B.
2011BUPROPION/NALTREXONE FIXED-DOSE COMBINATION FOR THE TREATMENT OF OBESITYHALPERN, B.; FARIA, A. M.; HALPERN, A.
2011Zona fasciculata 21-hydroxysteroids and precursor-to-product ratios in 21-hydroxylase deficiency: Further characterization of classic and non-classic patients and heterozygote carriersCOSTA-BARBOSA, F. A.; CARVALHO, V. M.; NAKAMURA, O. H.; BACHEGA, T. A. S. S.; VIEIRA, J. G. H.; KATER, C. E.
2011Pharmacogenetics of glucocorticoid replacement could optimize the treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiencyMOREIRA, Ricardo P. P.; JORGE, Alexander A. L.; GOMES, Larissa G.; KAUPERT, Laura C.; MASSUD FILHO, Joao; MENDONCA, Berenice B.; BACHEGA, Tania A. S. S.
2011Glucose-dependent insulinotropic peptide receptor overexpression in adrenocortical hyperplasia in MEN1 syndrome without loss of heterozygosity at the 11q13 locusCOSTA, Marcia Helena Soares; DOMENICE, Sorahia; TOLEDO, Rodrigo Almeida; JUNIOR, Delmar Muniz L.; LATRONICO, Ana Claudia; PINTO, Emilia Modolo; TOLEDO, Sergio Pereira Almeida; MENDONCA, Berenice Bilharinho; FRAGOSO, Maria Candida Barisson Villares
2011Frequency of genetic polymorphisms of PXR gene in the Brazilian populationMOREIRA, Ricardo P. P.; JORGE, Alexander A. L.; MENDONCA, Berenice B.; BACHEGA, Tania A. S. S.
2011New mutation in the CASR gene in a family with familial hypocalciuric hypercalcemia (FHH) and neonatal severe hyperparathyroidism (NSHPT)RODRIGUES, Luiza Souza; CAU, Ana Carolina Arias; BUSSMANN, Luciane Zgoda; BASTIDA, Gabriela; BRUNETTO, Oscar H.; CORREA, Pedro Henrique Silveira; MARTIN, Regina Matsunaga
2011Transitory increase in creatinine levels after parathyroidectomy: evidence of another action of the parathyroid glands?MONTENEGRO, Fabio M.; BRANDAO, Lenine G.; FERREIRA, Gustavo F.; LOURENCO JR., Delmar M.; MARTIN, Regina M.; CUNHA-NETO, Malebranche B.; HELOU, Claudia B.; TOLEDO, Sergio A.; CORDEIRO, Anoi C.; IANHEZ, Luiz E.
2011Os interferentes endócrinos ambientais precisam receber a atenção dos endocrinologistas brasileirosBACHEGA, Tania A. S. Sanchez; VERRESCHI, Ieda T.; FRADE, Elaine M. Costa; D'ABRONZO, Francisco Homero; LAZARETTI-CASTRO, Marise
2011A novel WT1 heterozygous nonsense mutation (p.K248X) causing a mild and slightly progressive nephropathy in a 46,XY patient with Denys-Drash syndromeSILVA, Thatiana Evilen da; NISHI, Mirian Yumie; COSTA, Elaine Maria Frade; MARTIN, Regina Matsunaga; CARVALHO, Filomena Marino; MENDONCA, Berenice Bilharinho; DOMENICE, Sorahia
2011KISS1R Intracellular Trafficking and Degradation: Effect of the Arg386Pro Disease-Associated MutationBIANCO, Suzy D. C.; VANDEPAS, Lauren; CORREA-MEDINA, Mayrin; GEREBEN, Balazs; MUKHERJEE, Abir; KUOHUNG, Wendy; CARROLL, Rona; TELES, Milena G.; LATRONICO, Ana Claudia; KAISER, Ursula B.
2011Mutational analysis of the necdin gene in patients with congenital isolated hypogonadotropic hypogonadismBENEDUZZI, Daiane; IYER, Anita K.; TRARBACH, Ericka Barbosa; SILVEIRA-NETO, Acacio P.; SILVEIRA, Leticia G.; TUSSET, Cintia; YIP, Kathleen; MENDONCA, Berenice B.; MELLON, Pamela L.; LATRONICO, Ana Claudia
2011PROP1 and CTNNB1 expression in adamantinomatous craniopharyngiomas with or without beta-catenin mutationsCANI, Carolina M. G.; MATUSHITA, Hamilton; CARVALHO, Luciani R. S.; SOARES, Ibere C.; BRITO, Luciana P.; ALMEIDA, Madson Q.; MENDONCA, Berenice B.
2011Clinical and molecular aspects of congenital isolated hypogonadotropic hypogonadismTUSSET, Cintia; TRARBACH, Ericka B.; SILVEIRA, Leticia Ferreira Gontijo; BENEDUZZI, Daiane; MONTENEGRO, Luciana; LATRONICO, Ana Claudia
2011A premenopausal woman with virilization secondary to an ovarian Leydig cell tumorFARIA, Andre M.; PEREZ, Ricardo V.; MARCONDES, Jose A. M.; FREIRE, Daniel S.; BLASBALG, Roberto; SOARES JR., Jose; SIMOES, Kleber; HAYASHIDA, Sylvia A. Y.; PEREIRA, Maria A. A.
2011Thymic hyperplasia in Graves' diseaseDANILOVIC, Debora Lucia Seguro; MARTIN, Regina Matsunaga; CARUSO, Pedro; MARUI, Suemi
2011Clinical and molecular aspects of a pediatric metachronous adrenocortical tumorLIMA, Lorena de Oliveira; LERARIO, Antonio Marcondes; ALENCAR, Guilherme Asmar; BRITO, Luciana Pinto; ALMEIDA, Madson Queiroz; DOMENICE, Sorahia; LATRONICO, Ana Claudia; MENDONCA, Berenice Bilharinho; FRAGOSO, Maria Candida Barrison Villares
2011Mutations in insulin-like growth factor receptor 1 gene (IGF1R) resulting in intrauterine and postnatal growth retardationLEAL, Andrea de Castro; CANTON, Ana Pinheiro Machado; MONTENEGRO, Luciana Ribeiro; COUTINHO, Debora Cabral; ARNHOLD, Ivo Jorge Prado; JORGE, Alexander Augusto de Lima