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Issue DateTitleAuthor(s)
201625-Hydroxyvitamin D and TSH as Risk Factors or Prognostic Markers in Thyroid CarcinomaDANILOVIC, Debora Lucia Seguro; FERRAZ-DE-SOUZA, Bruno; FABRI, Amanda Wictky; SANTANA, Nathalie Oliveira; KULCSAR, Marco Aurelio; CERNEA, Claudio Roberto; MARUI, Suemi; HOFF, Ana Oliveira
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.
201865 YEARS OF THE DOUBLE HELIX Genetics informs precision practice in the diagnosis and management of pheochromocytomaNEUMANN, Hartmut P.; YOUNG JR., William F.; KRAUSS, Tobias; BAYLEY, Jean-Pierre; SCHIAVI, Francesca; OPOCHER, Giuseppe; BOEDEKER, Carsten C.; TIROSH, Amit; CASTINETTI, Frederic; RUF, Juri, et al
2013A consensus on the diagnosis and treatment of acromegaly complicationsMELMED, S.; CASANUEVA, F. F.; KLIBANSKI, A.; BRONSTEIN, M. D.; CHANSON, P.; LAMBERTS, S. W.; STRASBURGER, C. J.; WASS, J. A. H.; GIUSTINA, A.
2018A Consensus Statement on acromegaly therapeutic outcomesMELMED, Shlomo; BRONSTEIN, Marcello D.; CHANSON, Philippe; KLIBANSKI, Anne; CASANUEVA, Felipe F.; WASS, John A. H.; STRASBURGER, Christian J.; LUGER, Anton; CLEMMONS, David R.; GIUSTINA, Andrea
2013A differential diagnosis of inherited endocrine tumors and their tumor counterpartsTOLEDO, Sergio P. A.; LOURENCO JR., Delmar M.; TOLEDO, Rodrigo A.
2016A homozygous point mutation in the GH1 promoter (c.-223C > T) leads to reduced GH1 expression in siblings with isolated GH deficiency (IGHD)MADEIRA, Joao L. O.; JORGE, Alexander A. L.; MARTIN, Regina M.; MONTENEGRO, Luciana R.; FRANCA, Marcela M.; COSTALONGA, Everlayny F.; CORREA, Fernanda A.; OTTO, Aline P.; ARNHOLD, Ivo J. P.; FREITAS, Helayne S., et al
2018A Novel Generalized Lipodystrophy-Associated Progeroid Syndrome Due to Recurrent Heterozygous LMNA p.T10I MutationHUSSAIN, Iram; PATNI, Nivedita; UEDA, Masako; SORKINA, Ekaterina; VALERIO, Cynthia M.; COCHRAN, Elaine; BROWN, Rebecca J.; PEEDEN, Joseph; TIKHONOVICH, Yulia; TIULPAKOV, Anatoly, et al
2014A Novel Homologous Model for Gene Therapy of Dwarfism by Non-Viral Transfer of the Mouse Growth Hormone Gene into Immunocompetent Dwarf MiceCECCHI, Claudia R.; HIGUTI, Eliza; OLIVEIRA, Nelio A. J.; LIMA, Eliana R.; JAKOBSEN, Maria; DAGNAES-HANSEN, Frederick; GISSEL, Hanne; AAGAARD, Lars; JENSEN, Thomas G.; JORGE, Alexander A. L., et al
2016A promising first year: Happy birthday AE&M!BRONSTEIN, Marcello D.
2015A randomized-controlled, double-blind study of the impact of selenium supplementation on thyroid autoimmunity and inflammation with focus on the GPx1 genotypesFARIAS, C. R. de; CARDOSO, B. R.; OLIVEIRA, G. M. B. de; GUAZZELLI, I. C. de Mello; CATARINO, R. M.; CHAMMAS, M. C.; COZZOLINO, S. M. F.; KNOBEL, M.
2018A review of Cushing's disease treatment by the Department of Neuroendocrinology of the Brazilian Society of Endocrinology and MetabolismMACHADO, Marcio Carlos; FRAGOSO, Maria Candida Barisson Vilares; MOREIRA, Ayrton Custodio; BOGUSZEWSKI, Cesar Luiz; NETO, Leonardo Vieira; NAVES, Luciana A.; VILAR, Lucio; ARAUJO, Luiz Antonio de; MUSOLINO, Nina Rosa Castro; MIRANDA, Paulo Augusto C., et al
2016A review on the diagnosis and treatment of patients with clinically nonfunctioning pituitary adenoma by the Neuroendocrinology Department of the Brazilian Society of Endocrinology and MetabolismVIEIRA NETO, Leonardo; BOGUSZEWSKI, Cesar L.; ARAÚJO, Luiz Antônio de; BRONSTEIN, Marcello D.; MIRANDA, Paulo Augusto C.; MUSOLINO, Nina R. de C.; NAVES, Luciana A.; VILAR, Lucio; RIBEIRO-OLIVEIRA JÚNIOR, Antônio; GADELHA, Mônica R.
2011Abnormal chronotropic reserve and heart rate recovery in patients with SLE: a case-control studyPRADO, D. M. Leite do; GUALANO, B.; MIOSSI, R.; SA-PINTO, A. L.; LIMA, F. R.; ROSCHEL, H.; BORBA, E. F.; BONFA, E.
2011Absence of GH-Releasing Hormone (GHRH) Mutations in Selected Patients with Isolated GH DeficiencyFRANCA, Marcela M.; JORGE, Alexander A. L.; ALATZOGLOU, Kyriaki S.; CARVALHO, Luciani R. S.; MENDONCA, Berenice B.; AUDI, Laura; CARRASCOSA, Antonio; DATTANI, Mehul T.; ARNHOLD, Ivo J. P.
2012Absence of mutations in PAX8, NKX2.5, and TSH receptor genes in patients with thyroid dysgenesisBRUST, Ester S.; BELTRAO, Cristine B.; CHAMMAS, Maria C.; WATANABE, Tomoco; SAPIENZA, Marcelo T.; MARUI, Suemi
2019Acquired Lipodystrophy Associated With Nivolumab in a Patient With Advanced Renal Cell CarcinomaFALCAO, Camila Kruschewsky; CABRAL, Marina Campos Simoes; MOTA, Jose Mauricio; ARBACHE, Samia Trigo; COSTA-RIQUETTO, Aline Dantas; MUNIZ, David Queiroz Borges; CURY-MARTINS, Jade; ALMEIDA, Madson Q.; KACZEMORSKA, Priscilla Cukier; NERY, Marcia, et al
2017Acromegaly and pregnancy: a contemporary reviewABUCHAM, Julio; BRONSTEIN, Marcello D.; DIAS, Monike L.
2019Acromegaly in the elderly patientJALLAD, Raquel S.; BRONSTEIN, Marcello D.
2021Activation of the MAPK pathway (RASopathies) and partial growth hormone insensitivityMALAQUIAS, Alexsandra C.; JORGE, Alexander A. L.