Artigos e Materiais de Revistas Científicas - LIM/25
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Collection's Items (Sorted by Submit Date in Descending order): 1 to 20 of 412
Issue Date | Title | Author(s) |
---|---|---|
2022 | Contribution of Clinical and Genetic Approaches for Diagnosing 209 Index Cases With 46,XY Differences of Sex Development | GOMES, Nathalia Lisboa; BATISTA, Rafael Loch; NISHI, Mirian Y.; LERARIO, Antonio Marcondes; SILVA, Thatiana E.; NARCIZO, Amanda de Moraes; BENEDETTI, Anna Flavia Figueredo; FUNARI, Mariana Ferreira de Assis; FARIA JUNIOR, Jose Antonio; MORAES, Daniela Rodrigues, et al |
2022 | Cushing disease due to a somatic USP8 mutation in a patient with evolving pituitary hormone deficiencies due to a germline GH1 splicing variant | LABELLO, Julia Haddad; BENEDETTI, Anna Flavia Figueredo; AZEVEDO, Bruna Viscardi; JORGE, Alexander Augusto de Lima; CESCATO, Valter Angelo Sperling; ROSEMBERG, Sergio; FRASSETO, Fernando Pereira; ARNHOLD, Ivo Jorge Prado; CARVALHO, Luciani Renata Silveira de |
2021 | Resolution of Cyclicity After Pasireotide LAR in a Patient With Cushing Disease | MACHADO, M. C.; CESCATO, V. A. S.; FRAGOSO, M. C. B. V.; BRONSTEIN, M. D. |
2020 | Does autoimmune thyroid disorder act as a predisposing factor in the development of oral lichen planus? | HIROTA, Silvio; MARUI, Suemi; MIGLIARI, Dante |
2021 | International Multicenter Validation Study of the SAGIT (R) Instrument in Acromegaly | GIUSTINA, Andrea; BRONSTEIN, Marcello D.; CHANSON, Philippe; PETERSENN, Stephan; CASANUEVA, Felipe F.; SERT, Caroline; HOUCHARD, Aude; MELMED, Shlomo |
2021 | A year of great achievements | BRONSTEIN, Marcello D. |
2020 | Comprehensive Genetic Analysis of 128 Candidate Genes in a Cohort With Idiopathic, Severe, or Familial Osteoporosis | ROCHA-BRAZ, Manuela G. M.; FRANCA, Monica M.; FERNANDES, Adriana M.; LERARIO, Antonio M.; ZANARDO, Evelin A.; SANTANA, Lucas S. de; KULIKOWSKI, Leslie D.; MARTIN, Regina M.; MENDONCA, Berenice B.; FERRAZ-DE-SOUZA, Bruno |
2021 | Machine Learning-based Prediction Model for Treatment of Acromegaly With First-generation Somatostatin Receptor Ligands | WILDEMBERG, Luiz Eduardo; CAMACHO, Aline Helen da Silva; MIRANDA, Renan Lyra; ELIAS, Paula C. L.; MUSOLINO, Nina R. de Castro; NAZATO, Debora; JALLAD, Raquel; HUAYLLAS, Martha K. P.; MOTA, Jose Italo S.; ALMEIDA, Tobias, et al |
2021 | Cabergoline should be attempted in progressing non-functioning pituitary macroadenoma | GREENMAN, Yona; BRONSTEIN, Marcello D. |
2021 | Thyroid collision tumor containing oncocytic carcinoma, classical and hobnail variants of papillary carcinoma and areas of poorly differentiated carcinoma | TOYOSHIMA, Marcos Tadashi Kakitani; DOMINGUES, Regina Barros; SOARES, Ibere Cauduro; DANILOVIC, Debora Lucia Seguro; AMORIM, Larissa Costa; CAVALCANTE, Edla R. C.; ANTONACIO, Fernanda F.; ROITBERG, Felipe Santa Rosa; HOFF, Ana Oliveira |
2021 | Hormone resistance and short stature: A journey through the pathways of hormone signaling | SCALCO, Renata C.; CORREA, Fernanda A.; DANTAS, Naiara C. B.; VASQUES, Gabriela A.; JORGE, Alexander A. L. |
2021 | High-throughput splicing assays identify missense and silent splice-disruptive POU1F1 variants underlying pituitary hormone deficiency | GERGICS, Peter; SMITH, Cathy; BANDO, Hironori; JORGE, Alexander A. L.; ROCKSTROH-LIPPOLD, Denise; VISHNOPOLSKA, Sebastian A.; CASTINETTI, Frederic; MAKSUTOVA, Mariam; CARVALHO, Luciani Renata Silveira; HOPPMANN, Julia, et al |
2021 | Allelic Variants in Established Hypopituitarism Genes Expand Our Knowledge of the Phenotypic Spectrum | NAKAGUMA, Marilena; FERREIRA, Nathalia Garcia Bianchi Pereira; BENEDETTI, Anna Flavia Figueredo; MADI, Mariana Cotarelli; SILVA, Juliana Moreira; LI, Jun Z.; MA, Qianyi; OZEL, Ayse Bilge; FANG, Qing; NARCIZO, Amanda de Moraes, et al |
2021 | Impaired Bone Microarchitecture in Premenopausal Women With Acromegaly: The Possible Role of Wnt Signaling | SILVA, Paula P. B.; PEREIRA, Rosa M. R.; TAKAYAMA, Liliam; BORBA, Clarissa G.; DUARTE, Felipe H.; TRARBACH, Ericka B.; MARTIN, Regina Matsunaga; BRONSTEIN, Marcello D.; TRITOS, Nicholas A.; JALLAD, Raquel S. |
2021 | The phenotypic spectrum associated with OTX2 mutations in humans | GREGORY, Louise C.; GERGICS, Peter; NAKAGUMA, Marilena; BANDO, Hironori; PATTI, Giuseppa; MCCABE, Mark J.; FANG, Qing; MA, Qianyi; OZEL, Ayse Bilge; LI, Jun Z., et al |
2021 | Congenital chromoanagenesis in the routine postnatal chromosomal microarray analyses | VILLELA, Darine; MAZZONETTO, Patricia C.; MIGLIAVACCA, Michele P.; PERRONE, Eduardo; GUIDA, Gustavo; MILANEZI, Maria Fernanda G.; JORGE, Alexander A. L.; RIBEIRO-BICUDO, Lucilene A.; KOK, Fernando; CAMPAGNARI, Francine, et al |
2021 | Adult Height in 299 Patients with Turner Syndrome with or without Growth Hormone Therapy: Results and Literature Review | DANTAS, Naiara C. B.; BRAZ, Adriana F.; MALAQUIAS, Alexsandra; LEMOS-MARINI, Sofia; ARNHOLD, Ivo J. P.; SILVEIRA, Ester R.; ANTONINI, Sonir R.; GUERRA-JUNIOR, Gil; MENDONCA, Berenice; JORGE, Alexander, et al |
2020 | Pasireotide for acromegaly: long- term outcomes from an extension to the Phase III PAOLA study | COLAO, Annamaria; BRONSTEIN, Marcello D.; BRUE, Thierry; MARINIS, Laura De; FLESERIU, Maria; GUITELMAN, Mirtha; RAVEROT, Gerald; SHIMON, Ilan; FLECK, Juergen; GUPTA, Pritam, et al |
2021 | Pituitary Neoplasm Nomenclature Workshop: Does Adenoma Stand the Test of Time? | HO, Ken; FLESERIU, Maria; KAISER, Ursula; SALVATORI, Roberto; BRUE, Thierry; LOPES, M. Beatriz; KUNZ, Pamela; MOLITCH, Mark; CAMPER, Sally A.; GADELHA, Monica, et al |
2021 | Insights from the genetic characterization of central precocious puberty associated with multiple anomalies | CANTON, Ana Pinheiro Machado; KREPISCHI, Ana Cristina Victorino; MONTENEGRO, Luciana Ribeiro; COSTA, Silvia; ROSENBERG, Carla; STEUNOU, Virginie; SOBRIER, Marie-Laure; SANTANA, Lucas; HONJO, Rachel Sayuri; KIM, Chong Ae, et al |
Collection's Items (Sorted by Submit Date in Descending order): 1 to 20 of 412