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Journal of the Endocrine Society|December 11, 2023
Efficacy of Oral Furosemide Test for Primary Aldosteronism DiagnosisThais C Freitas, Ana Alice W Maciel, Gustavo F C Fagundes, et al.
Frontiers in Endocrinology|March 3, 2020
Allelic Variants of <i>ARMC5</i> in Patients With Adrenal Incidentalomas and in Patients With Cushing's Syndrome Associated With Bilateral Adrenal NodulesBeatriz Marinho de Paula Mariani, Mirian Yumie Nishi, Ingrid Quevedo Wanichi, et al.
European Journal of Endocrinology|December 17, 2024
Insights into the genetic landscape of pheochromocytomas and paragangliomas in a Brazilian cohortGustavo F C Fagundes, Felipe Freitas-Castro, Lucas S Santana, et al.
Epilepsia|November 18, 2025
Cognitive stagnation and executive function deficits in young children with SCN1A+ Dravet syndrome: Detailed characterization of onset, progression, and impact in the ENVISION natural history studyJoseph Sullivan, M Scott Perry, Ingrid E Scheffer, et al.
Epilepsia|December 4, 2023
Severe communication delays are independent of seizure burden and persist despite contemporary treatments in SCN1A+ Dravet syndrome: Insights from the ENVISION natural history studyM Scott Perry, Ingrid E Scheffer, Joseph Sullivan, et al.
The Journal of Clinical Endocrinology and Metabolism|January 18, 2023
Evidence for a Founder Effect of SDHB Exon 1 Deletion in Brazilian Patients With ParagangliomaGustavo F C Fagundes, Felipe Freitas-Castro, Lucas S Santana, et al.
European Journal of Endocrinology|June 20, 2025
Histopathological evaluation based on CYP11B2 staining predicts outcomes in unilateral primary aldosteronismTatiana S Goldbaum, Felipe L Ledesma, Augusto G Guimaraes, et al.
Endocrine-Related Cancer|February 18, 2014
p27 variant and corticotropinoma susceptibility: a genetic and in vitro studyTomoko Sekiya, Marcello D Bronstein, Katiuscia Benfini, et al.
European Journal of Endocrinology|February 8, 2025
KDM1A genetic alterations, a rare cause of primary bilateral macronodular adrenal hyperplasia, strongly associated with food-dependent Cushing's syndrome: results of its systematic germline screening in 301 index cases and genotype/phenotype correlationLucas Bouys, Patricia Vaduva, Anne Jouinot, et al.
American Journal of Respiratory Cell and Molecular Biology|March 27, 2020
Comparison of Human and Experimental Pulmonary Veno-Occlusive DiseaseGrégoire Manaud, Esther J Nossent, Mélanie Lambert, et al.
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