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Cancers|March 12, 2020
High Prevalence of Alterations in DNA Mismatch Repair Genes of Lynch Syndrome in Pediatric Patients with Adrenocortical Tumors Carrying a Germline Mutation on <i>TP53</i>Vania Balderrama Brondani, Luciana Montenegro, Amanda Meneses Ferreira Lacombe, et al.Archives of Endocrinology and Metabolism|May 14, 2025
Peripheral precocious puberty in girls with McCune-Albright syndrome: a case seriesAline Guimarães Faria, Luciana R Montenegro, Alexander Augusto Lima Jorge, et al.Clinical Endocrinology|September 10, 2014
Expression of LIN28 and its regulatory microRNAs in adult adrenocortical cancerAndré M Faria, Silviu Sbiera, Tamaya C Ribeiro, et al.Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|December 1, 2023
Renal Function Evolution and Hypoaldosteronism Risk After Unilateral Adrenalectomy for Primary AldosteronismNara L Queiroz, Matheo A M Stumpf, Victor C M Souza, et al.Journal of the Endocrine Society|September 19, 2019
New Insights Into Pheochromocytoma Surveillance of Young Patients With <i>VHL</i> Missense MutationsGustavo F C Fagundes, Janaina Petenuci, Delmar M Lourenco, et al.The Journal of Clinical Endocrinology and Metabolism|August 14, 2025
A Global Approach to the Long-Term Follow-up of 17 Families with Bilateral Macronodular Adrenal DiseaseHelaine Laiz Silva Charchar, Guilherme Asmar Alencar, Beatriz Marinho de Paula Mariani, et al.Journal of the Endocrine Society|May 27, 2024
Identification of Predictors of Metastatic Potential in Paragangliomas to Develop a Prognostic Score (PSPGL)Daniela Yone Veiga Iguchi, Sebastião Nunes Martins Filho, Iberê Cauduro Soares, et al.Cancers|January 23, 2020
Sterol O-Acyl Transferase 1 as a Prognostic Marker of Adrenocortical CarcinomaAmanda Meneses Ferreira Lacombe, Iberê Cauduro Soares, Beatriz Marinho de Paula Mariani, et al.Clinical Endocrinology|March 21, 2021
Genetic and clinical aspects of paediatric pheochromocytomas and paragangliomasJanaina Petenuci, Augusto G Guimaraes, Gustavo F C Fagundes, et al.Epilepsia|February 2, 2026
Characterizing early behavioral and social-emotional problems in young children with SCN1A+ Dravet syndrome: Findings from the ENVISION prospective natural history studyIngrid E Scheffer, M Scott Perry, Joseph Sullivan, et al.Pageof 22