Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Délia Braz"'
Autor:
Renata Oliveira, Délia Braz, Nayla Samia Silva Pacheco, Luiz Claudio Castro, Fernanda Sousa Cardoso Lopes
Publikováno v:
Journal of the Endocrine Society
Introduction: Congenital central nervous system tumors are seldomly seen, with just few reported cases of neonatal craniopharyngioma (NCP). Albeit being a benign tumor arising from epithelial vestiges along the adenohypophysis migration, NCP may have
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2ab98bf085e51fd59293aba334397ea
http://europepmc.org/articles/PMC7207470
http://europepmc.org/articles/PMC7207470
Autor:
Luiz Claudio Castro, Lara Pereira, Alessandra Domingues, Renata Oliveira, Délia Braz, Fernanda Sousa Cardoso Lopes
Publikováno v:
Journal of the Endocrine Society
Background: Hypophosphatemic rickets (HR) is usually an inherited disorder, but it may also occur in several clinical settings as an acquired condition due to phosphate absorption and internal distribution issues. Recently it was described the associ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::435537d413a6cf7a6f2e42057292e414
https://doi.org/10.1210/jendso/bvaa046.1804
https://doi.org/10.1210/jendso/bvaa046.1804
Autor:
Délia Braz, Luiz Claudio Castro, Dyrlanne Bastos, Lenora Gandolfi, Lais Pereira de Oliveira, Naiara Nóbrega, Fernanda Jaqueline Lopes, Renata Oliveira
Publikováno v:
Journal of the Endocrine Society
Background: Celiac Disease (CD) is an autoimmune intestinal disorder triggered by gluten exposure in genetically predisposed individuals. It is well described its association with other autoimmune diseases (AIDs), mainly type 1 diabetes mellitus (T1D
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ffb4958b93d194d7f6138d8d45f32a39
https://doi.org/10.1210/js.2019-mon-581
https://doi.org/10.1210/js.2019-mon-581
Autor:
Alessandra Pfeilsticker, Délia Braz, Adriana Lofrano-Porto, Stela Lmr Rodrigues, Olivia Laquis de Moraes, Renata Oliveira
Publikováno v:
Journal of the Endocrine Society
Background: Paragangliomas (PGLs) are rare neuroendocrine cell tumors and due to its rarity, there is no current standardized treatment and optimal long-term follow-up for metastatic disease. We report two cases of SDHB-related malignant PGL in boys
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f50b7a81dd88987ac586a35d9ea6ba2d
https://doi.org/10.1210/js.2019-sat-319
https://doi.org/10.1210/js.2019-sat-319
Autor:
Adriana Lofrano-Porto, Renata Santarem de Oliveira, Délia Braz, Stela Lmr Rodrigues, Beatriz R. Versiani, Alessandra Pfeilsticker
Publikováno v:
Journal of the Endocrine Society
Background: 48,XXYY syndrome is a rare chromosomal anomaly that causes infertility, developmental and behavioral disorders, among other health problems, in males. Affected patients are often taller than other males of their age. This condition is not
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad82e4d7a44f5641b5ffc56a8f4d336f
https://doi.org/10.1210/js.2019-sat-299
https://doi.org/10.1210/js.2019-sat-299
Autor:
Matos Rezek Rodrigues S, Délia Braz, Adriana Lofrano-Porto, Fernanda Sousa Cardoso Lopes, Nobrega N, Bastos D, Florencio A, Mota G, Renata Santarem de Oliveira, Luiz Claudio Castro, Lais Pereira de Oliveira
Publikováno v:
Journal of the Endocrine Society
Background: Pathologic pituitary hyperplasia (PH) in Pediatrics may be observed in several clinical settings. In PH secondary to primary hypothyroidism the increased TRH levels, due to a long-standing hypothyroidism state and loss of negative thyroxi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::277fbb37521fc3386dff51e125752935
https://doi.org/10.1210/js.2019-sun-580
https://doi.org/10.1210/js.2019-sun-580