Zobrazeno 1 - 10
of 92
pro vyhledávání: '"Maria Adelaide A. Pereira"'
Autor:
Delmar Muniz Lourenço, Maria Lucia Corrêa-Giannella, Sheila Aparecida Coelho Siqueira, Marcia Nery, Flavio Galvão Ribeiro, Elizangela Pereira de Souza Quedas, Manoel de Souza Rocha, Ramon Marcelino do Nascimento, Maria Adelaide Albergaria Pereira
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2024)
The best-known etiologies of hyperinsulinemic hypoglycemia are insulinoma, non-insulinoma pancreatogenous hypoglycemic syndrome, autoimmune processes, and factitious hypoglycemia. In 2009, a disease not associated with classic genetic syndromes and c
Externí odkaz:
https://doaj.org/article/c4bff7e8323245fbb077be2b075027fe
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:
Katia Regina Marchetti, Maria Adelaide Albergaria Pereira, Arnaldo Lichtenstein, Edison Ferreira Paiva
Publikováno v:
Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-4 (2016)
Adrenacarcinomas are rare, and hypoglycemic syndrome resulting from the secretion of insulin-like growth factor II (IGF-II) by these tumors have been described infrequently. This study describes the case of a young woman with severe persistent hypogl
Externí odkaz:
https://doaj.org/article/05399db9e03b4659b4f4fdd5ed1d5290
Autor:
Gustavo F C Fagundes, Felipe Freitas-Castro, Lucas S Santana, Ana Caroline F Afonso, Janaina Petenuci, Mariana F A Funari, Augusto G Guimaraes, Felipe L Ledesma, Maria Adelaide A Pereira, Carolina R Victor, Marcela S M Ferrari, Fernando M A Coelho, Victor Srougi, Fabio Y Tanno, Jose L Chambo, Ana Claudia Latronico, Berenice B Mendonca, Maria Candida B V Fragoso, Ana O Hoff, Madson Q Almeida
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism.
ContextLimited information is available concerning the genetic spectrum of pheochromocytoma and paraganglioma (PPGL) patients in South America. Germline SDHB large deletions are very rare worldwide, but most of the individuals harboring the SDHB exon
Autor:
Maria Candida Barisson Villares Fragoso, Fernando Ide Yamauchi, Madson Q. Almeida, Berenice B. Mendonca, Ana Claudia Latronico, Sheila Aparecida Coelho Siqueira, Jose Luis Chambo, Ana O. Hoff, Silvia C Soares, Francisco Tibor Dénes, Augusto G Guimaraes, Janaina Petenuci, Roberto Iglesias Lopes, Anna Flavia Figueredo Benedetti, Maria Adelaide Albergaria Pereira, Gustavo F C Fagundes, Fabio Y Tanno, Victor Srougi, Maria Claudia Nogueira Zerbini, Ana Caroline F Afonso
Publikováno v:
Clinical Endocrinology. 95:117-124
Objective Few and conflicting reports have characterized the genetics of paediatric pheochromocytomas and paragangliomas (PPGLs). This study aimed to investigate the clinical and genetic features of Brazilian children with PPGL. Patients and methods
Autor:
Bruna Pilan, Ana Claudia Latronico, Antonio Lerario, Anna Flavia Figueredo Benedetti, Victor Srougi, Luciano F. Drager, Leticia A P Vilela, Tatiana S Goldbaum, Luiz Aparecido Bortolotto, Berenice B. Mendonca, Marcela Rassi-Cruz, Maria Adelaide Albergaria Pereira, Fabio R. Faucz, Lucas Santos de Santana, Aline C B S Cavalcante, Fabio Y Tanno, Jose Luis Chambo, Andrea Gutierrez Maria, Maria Candida Barisson Villares Fragoso, Francisco Cesar Carnevale, Maria Claudia Nogueira Zerbini, Edra London, Madson Q. Almeida, Constantine A. Stratakis
Publikováno v:
Endocr Relat Cancer
Familial primary aldosteronism (PA) is rare and mostly diagnosed in early-onset hypertension (HT). However, ‘sporadic’ bilateral adrenal hyperplasia (BAH) is the most frequent cause of PA and remains without genetic etiology in most cases. Our ai
Autor:
Andreas Ebbehoj, Eleonora P M Corssmit, Jan Calissendorff, Thera P. Links, Özer Makay, Maximilien Rappaport, Petr Vlĕek, Tushar Bandgar, Catharina Larsson, Elena N. Grineva, Luigi Petramala, Ravinder Kaur, Viacheslav I. Egorov, Hartmut P. H. Neumann, Heather Wachtel, Tobias Else, Francesca Boaretto, Xiao-Ping Qi, Henri J L M Timmers, Anna Roslyakova, M. Umit Ugurlu, Ronald M. Lechan, Anand Vaidya, Kornelia Hasse-Lazar, Claudio E. Kater, Esben Søndergaard, Zhi-xian Yu, Rene Eduardo Diaz, Mohammad Hassan Murad, Ruth T Casey, Debbie L. Cohen, Roman Petrov, Lucinda Gruber, C Christofer Juhlin, Claudio Letizia, Maria Adelaide Albergaria Pereira, Inna Stepanovna Kudlai, Bernadette Jenner, Sergiy Cherenko, Lauren Fishbein, William F. Young, Ya-Sheng Huang, Marina Y. Yukina, Scott A Akker, Andrey Y Kovalenko, Uma Kaimal Saikia, Minghao Li, Silvia Rizzati, Stefania Zovato, Xu-dong Fang, Nelson Wohllk, Charis Eng, Mariola Pęczkowska, Martin Fassnacht, Sanjeet Kumar Jaiswal, Oliver Gimm, Gianluca Donatini, Milan Jovanovic, Robin P.F Dullaart, Ilgin Yildirim Simsir, Helen Simpson, Maciej Robaczyk, Marcin Barczyński, Steven G. Waguespack, Katharina Langton, Martin K. Walz, Paul Skierczynski, Alfonso Massimiliano Ferrara, Dipti Sarma, Irina Bancos, Vishnu Garla, Birke Bausch, Maria João Bugalho, Merav Fraenkel, Joanne Ngeow Yuen Yie, Flavia A Costa-Barbosa, Giuseppe Opocher, Camilo Jimenez, Tada Kunavisarut, Larry J. Prokop, Lawrence S Kirschner, Longfei Liu, Feyza Erenler, Elisa Taschin, Valentina Morelli, Per Løgstrup Poulsen, Marcus Quinkler, Natalia Valeryevna Khudiakova, Åse Krogh Rasmussen, Volha Vasilkova, Nicola Tufton, Nikita V. Ivanov, William Drake, Maryna Bobryk, Eric Jonasch, Swati Ramteke-Jadhav, Aviva Cohn, Diane Donegan, Sarka Dvorakova, Elizabeth J. Atkinson, Dmitry Beltsevich, Emma Hodson, Uliana Tsoy, Nino Zavrashvili, Jochen Seufert, Zulfiya Shafigullina, Xin He, Utku E Soyaltin, Nicole M. Iñiguez-Ariza, Timo Deutschbein, Francesca Schiavi, Mark Sherlock, Stefan Zschiedrich, Jes Sloth Mathiesen, Bonita Bennett, Anna Riester, Nalini S. Shah, Giovanni Barbon, Julie A Miller
Publikováno v:
Bancos, I, Atkinson, E J, Eng, C, Young, W F, Neumann, H P H & International Pheochromocytoma and Pregnancy Study Group 2021, ' Maternal and fetal outcomes in phaeochromocytoma and pregnancy : a multicentre retrospective cohort study and systematic review of literature ', The Lancet Diabetes & Endocrinology, vol. 9, no. 1, pp. 13-21 . https://doi.org/10.1016/S2213-8587(20)30363-6
Lancet Diabetes & Endocrinology, 9, 1, pp. 13-21
Bancos, I, Atkinson, E, Eng, C, Young, W F, Neumann, H P H, International Pheochromocytoma and Pregnancy Study Group & Robaczyk, M G 2021, ' Maternal and fetal outcomes in phaeochromocytoma and pregnancy : a multicentre retrospective cohort study and systematic review of literature ', The Lancet Diabetes and Endocrinology, vol. 9, no. 1, pp. 13-21 . https://doi.org/10.1016/S2213-8587(20)30363-6
Lancet Diabetes & Endocrinology, 9, 13-21
Lancet Diabetes Endocrinol
Lancet Diabetes & Endocrinology, 9, 1, pp. 13-21
Bancos, I, Atkinson, E, Eng, C, Young, W F, Neumann, H P H, International Pheochromocytoma and Pregnancy Study Group & Robaczyk, M G 2021, ' Maternal and fetal outcomes in phaeochromocytoma and pregnancy : a multicentre retrospective cohort study and systematic review of literature ', The Lancet Diabetes and Endocrinology, vol. 9, no. 1, pp. 13-21 . https://doi.org/10.1016/S2213-8587(20)30363-6
Lancet Diabetes & Endocrinology, 9, 13-21
Lancet Diabetes Endocrinol
Contains fulltext : 245825.pdf (Publisher’s version ) (Closed access) BACKGROUND: Phaeochromocytoma or paraganglioma (collectively known as PPGL) in pregnant women can lead to severe complications and death due to associated catecholamine excess. W
Autor:
Ana Alice W Maciel, Thais C Freitas, Gustavo F C Fagundes, Janaina Petenuci, Leticia A P Vilela, Luciana P Brito, Tatiana S Goldbaum, Maria Claudia N Zerbini, Felipe L Ledesma, Fabio Y Tanno, Victor Srougi, Jose L Chambo, Maria Adelaide A Pereira, Fernando M A Coelho, Aline C B S Cavalcante, Francisco C Carnevale, Bruna Pilan, Andrea Pio-Abreu, João V Silveira, Fernanda M Consolim-Colombo, Luiz A Bortolotto, Ana Claudia Latronico, Maria Candida B V Fragoso, Luciano F Drager, Berenice B Mendonca, Madson Q Almeida
Publikováno v:
The Journal of clinical endocrinology and metabolism.
Context Primary aldosteronism (PA) screening relies on an elevated aldosterone to renin ratio with a minimum aldosterone level, which varies from 10 to 15 ng/dL (277-415.5 pmol/L) using immunoassay. Objective To evaluate intra-individual coefficient
Autor:
Beatriz Marinho de Paula Mariani, Ericka Barbosa Trarbach, Tamaya Castro Ribeiro, Maria Adelaide Albergaria Pereira, Berenice Bilharinho Mendonca, Maria Candida Barisson Villares Fragoso
Publikováno v:
Clinics, Vol 67, Iss 2, Pp 95-98 (2012)
OBJECTIVE: Endostatin is a potent endogenous inhibitor of angiogenesis. It is derived from the proteolytic cleavage of collagen XVIII, which is encoded by the COL18A1 gene. A polymorphic COL18A1 allele encoding the functional polymorphism p.D104N imp
Externí odkaz:
https://doaj.org/article/a3986f7a3a14466f9f0d4d55615dcee2
Autor:
Gustavo F Fagundes, Madson Q Almeida, Lucas Santana, Felipe Castro, Ana Caroline Afonso, Janaina Petenuci, Mariana Funari, Augusto G Guimarães, Elaine V Sales, Ana Vieites, Gabriela Sanso, Felipe L Ledesma, Sheila Siqueira, Maria Adelaide A Pereira, Fabio Y Tanno, Vitor Srougi, Jose L Chambo, Carolina R Victor, Marcela S Ferrari, Fernando M Coelho, Silvia C Soares, Ana Claudia Latronico, Berenice B Mendonca, Maria Candida BV Fragoso, Ana O Hoff
Publikováno v:
Journal of the Endocrine Society. 6:A134-A134
Background Pheochromocytomas and paragangliomas (PPGLs) have the highest degree of heritability among endocrine tumors. Currently, ∼40% of PPGL individuals have a genetic germline pathogenic variant and exist at least 12 different genetic syndromes