Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Helaine Charchar"'
Autor:
Beatriz Marinho de Paula Mariani, Mirian Yumie Nishi, Ingrid Quevedo Wanichi, Vania Balderrama Brondani, Amanda Meneses Ferreira Lacombe, Helaine Charchar, Maria Adelaide Albergaria Pereira, Victor Srougi, Fabio Yoshiaki Tanno, Filippo Ceccato, Daniela Regazzo, Mattia Barbot, Gianluca Occhi, Nora Maria Elvira Albiger, Marcelo Vieira-Corrêa, Claudio Elias Kater, Carla Scaroni, José Luis Chambô, Maria Claudia Nogueira Zerbini, Berenice B. Mendonca, Madson Q. Almeida, Maria Candida Barisson Villares Fragoso
Publikováno v:
Frontiers in Endocrinology, Vol 11 (2020)
Objective: Germline ARMC5 mutations are considered to be the main genetic cause of primary macronodular adrenal hyperplasia (PMAH). PMAH is associated with high variability of cortisol secretion caused from subclinical hypercortisolism to overt Cushi
Externí odkaz:
https://doaj.org/article/d26e5bf5debf46b8b1a8f741ad6b4046
Autor:
Marina Rocha Rolim, Berenice Bilharinho Mendonça, Felipe Ledesma, Helaine Charchar, Victor Srougi, Fabio Tanno, José Luis Chambo, Madson Queiroz Almeida, Ana Claudia Latronico, Maria Candida Villares Fragoso
Publikováno v:
Journal of the Endocrine Society. 6:A71-A71
Female patient, 37 years old, coming from China, with a history of resistant arterial hypertension since the age of 25 years old associated with spontaneous hypokalemia and classic ACTH-independent Cushing's syndrome. Radiological imaging exams showe
Autor:
Maria Claudia Nogueira Zerbini, Vanessa Petry Helena, Madson Q. Almeida, Maria Del Pilar Estevez Diz, Vania Balderrama Brondani, Ana O. Hoff, Amanda Meneses Ferreira, Ana Claudia Latronico, Berenice B. Mendonca, Helaine Charchar, Maria Candida Barisson Villares Fragoso, Luiz Antonio Senna Leite
Publikováno v:
The Journal of Steroid Biochemistry and Molecular Biology. 190:250-255
Background The TP53 p.R337H germline mutation is highly prevalent among children with adrenocortical tumors (ACTs) from South and Southeast Brazil. However, the prevalence of other tumors of the Li-Fraumeni syndrome (LFS) and Li-Fraumeni-like syndrom
Autor:
Fernando Morbeck Almeida Coelho, Fabio Y Tanno, Miguel Srougi, Maria Adelaide Albergaria Pereira, Victor Srougi, Helaine Charchar, Maria Claudia Nogueira Zerbini, Maria Candida Barisson Villares Fragoso, Berenice B. Mendonca, Mirian Yumie Nishi, Jose Luis Chambo, Madson Q. Almeida, Iracy Silvia Corrêa Soares, Amanda Meneses Ferreira Lacombe, Fernando Ide Yamauchi, Willian Nahas, Vania Balderrama Brondani
Publikováno v:
Journal of the Endocrine Society
Purpose This prospective study presents the results of a new approach in the treatment of primary macronodular adrenal hyperplasia (PMAH), with simultaneous total adrenalectomy of the larger adrenal gland and partial adrenalectomy of the contralatera
Autor:
Helaine Charchar, Madson Q. Almeida, Sandro S Fenelon, Maria Adelaide Albergaria Pereira, Maria Candida Barisson Villares Fragoso, Vânia Balderrama Brondani, Fabio Y Tanno, Victor Srougi, Ricardo Miguel Costa de Freitas, Jose Luis Chambo, Berenice B. Mendonca
Publikováno v:
Journal of the Endocrine Society
Introduction: Masses in adrenal topography are diagnosed frequently due to the increase in radiological imaging in clinical practice. Adrenal incidentalomas occur between 4% and 10% of the patients above 50 years undergoing abdominal imaging, and the
Autor:
Helaine Charchar, Vânia Balderrama Brondani, Rafael Fernandes de Oliveira, Bruna S Pessoa, Maria Candida Barisson Villares Fragoso, Madson Q. Almeida, Ronne Costa, Berenice B. Mendonca, Thamiris Freitas Maia, Natasha Scaranello Cartolano, Amanda Meneses Ferreira Lacombe
Publikováno v:
Journal of the Endocrine Society
Background: Hypermineralocorticism (hypertension, hypokalemia, and low plasma renin activity) due to deoxycorticosterone (DOC) excess associated with adrenocortical carcinoma is extremely rare. DOC-producing tumors cause primary aldosteronism-like sy
Autor:
Beatriz Marinho de Paula, Mariani, Mirian Yumie, Nishi, Ingrid Quevedo, Wanichi, Vania Balderrama, Brondani, Amanda Meneses Ferreira, Lacombe, Helaine, Charchar, Maria Adelaide Albergaria, Pereira, Victor, Srougi, Fabio Yoshiaki, Tanno, Filippo, Ceccato, Daniela, Regazzo, Mattia, Barbot, Gianluca, Occhi, Nora Maria Elvira, Albiger, Marcelo, Vieira-Corrêa, Claudio Elias, Kater, Carla, Scaroni, José Luis, Chambô, Maria Claudia Nogueira, Zerbini, Berenice B, Mendonca, Madson Q, Almeida, Maria Candida Barisson Villares, Fragoso
Publikováno v:
Frontiers in Endocrinology
Objective: Germline ARMC5 mutations are considered to be the main genetic cause of primary macronodular adrenal hyperplasia (PMAH). PMAH is associated with high variability of cortisol secretion caused from subclinical hypercortisolism to overt Cushi
Autor:
Larissa Costa Amorim, Helaine Charchar, Maria Claudia Nogueira Zerbini, Fabio Y Tanno, Madson Q. Almeida, Ricardo Miguel Costa de Freitas, Amanda Schenatto Ferreira, Maria Candida Barisson Villares Fragoso, Victor Srougi, Vânia Balderrama Brondani, Berenice B. Mendonca, Joao E. Bezerra, Ana O. Hoff, Jose Luis Chambo
Publikováno v:
Journal of the Endocrine Society
Background: Adrenocortical carcinoma (ACC) is a rare and, in the vast majority of cases, aggressive neoplasia. Even in cases of localized disease at the diagnosis in which complete surgical resection of the tumor is performed, rates of local and dist
Autor:
Elyse Ribeiro, Helaine Charchar, Elisa Del Rosario Ugarte Verduguez, Maria Candida Barisson Villares Fragoso, Vânia Balderrama Brondani, Amanda Schenatto Ferreira, Kenia Campanholo
Publikováno v:
Journal of the Endocrine Society
Background: The majority of patients with Cushing’s syndrome (CS) have physical and psychological symptoms that may lead to impaired quality of life (QoL). QoL improving with treatment but remaining significantly impaired compared with the general
Autor:
Helaine Charchar, Vânia Balderrama Brondani, Berenice B. Mendonca, Fabio Y Tanno, Jose Luis Chambo, Mirian Yumie Nishi, Maria Claudia Nogueira Zerbini, Maria Candida Barisson Villares Fragoso, Amanda Schenatto Ferreira, Madson Q. Almeida, Barbara Brito da Conceição, Claudimara Ferini Pacicco Lotfi, Victor Srougi
Publikováno v:
Journal of the Endocrine Society
Background: PMAH is a cause of adrenal hypercortisolism and it is a genetic disease linked to ARMC5 gene in most cases. Heterogenous phenotypes due to cortisol secretion and also due to different germline mutations in the ARMC5 have been described in