Zobrazeno 1 - 10
of 507
pro vyhledávání: '"S. Kunii"'
Autor:
Michelle Cerutti C. Vargas, Felipe Scipião Moura, Cecília P. Elias, Sara R. Carvalho, Nelson Rassi, Ilda S. Kunii, Magnus R. Dias-da-Silva, Flavia Amanda Costa-Barbosa
Publikováno v:
BMC Endocrine Disorders, Vol 20, Iss 1, Pp 1-7 (2020)
Abstract Background Adrenal hypoplasia congenita (AHC) is an X-linked disorder that affects the adrenal cortex and hypothalamus-pituitary-gonadal axis (HPG), leading to primary adrenocortical insufficiency (PAI) and hypogonadotropic hypogonadism. AHC
Externí odkaz:
https://doaj.org/article/82085d1044cc4aaab002f6985a5c818c
Autor:
Luciane Simonetti, Lucas G. A. Ferreira, Angela Cristina Vidi, Janaina Sena de Souza, Ilda S. Kunii, Maria Isabel Melaragno, Claudia Berlim de Mello, Gianna Carvalheira, Magnus R. Dias da Silva
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Klinefelter syndrome (KS) displays a broad dysmorphological, endocrinological, and neuropsychological clinical spectrum. We hypothesized that the neurocognitive dysfunction present in KS relies on an imbalance in X-chromosome gene expression. Thus, t
Externí odkaz:
https://doaj.org/article/1e3a1c159dc34caab5ee074aede09c92
Genotype and phenotype landscape of MEN2 in 554 medullary thyroid cancer patients: the BrasMEN study
Autor:
Rui M B Maciel, Cleber P Camacho, Lígia V M Assumpção, Natassia E Bufalo, André L Carvalho, Gisah A de Carvalho, Luciana A Castroneves, Francisco M de Castro Jr, Lucieli Ceolin, Janete M Cerutti, Rossana Corbo, Tânia M B L Ferraz, Carla V Ferreira, M Inez C França, Henrique C R Galvão, Fausto Germano-Neto, Hans Graf, Alexander A L Jorge, Ilda S Kunii, Márcio W Lauria, Vera L G Leal, Susan C Lindsey, Delmar M Lourenço Jr, Léa M Z Maciel, Patrícia K R Magalhães, João R M Martins, M Cecília Martins-Costa, Gláucia M F S Mazeto, Anelise I Impellizzeri, Célia R Nogueira, Edenir I Palmero, Cencita H C N Pessoa, Bibiana Prada, Débora R Siqueira, Maria Sharmila A Sousa, Rodrigo A Toledo, Flávia O F Valente, Fernanda Vaisman, Laura S Ward, Shana S Weber, Rita V Weiss, Ji H Yang, Magnus R Dias-da-Silva, Ana O Hoff, Sergio P A Toledo, Ana L Maia
Publikováno v:
Endocrine Connections, Vol 8, Iss 3, Pp 289-298 (2019)
Multiple endocrine neoplasia type 2 (MEN2) is an autosomal dominant genetic disease caused by RET gene germline mutations that is characterized by medullary thyroid carcinoma (MTC) associated with other endocrine tumors. Several reports have demonstr
Externí odkaz:
https://doaj.org/article/37d0d78e06b24b48bb6c7725c95f14cc
Autor:
Ilda S. Kunii, Lívia Marcela Santos, Marise Lazaretti-Castro, Isabela Ohki Nacaguma, Monique Nakayama Ohe, Renata Elen Costa Silva, José Gilberto H. Vieira, Sthefanie Giovanna Pallone
Publikováno v:
Journal of Clinical Densitometry. 24:563-570
Primary Hyperparathyroidism (PHPT) often leads to bone loss, even in its asymptomatic presentations. Trabecular Bone Score (TBS) is a method to assess the trabecular bone structure of the spine. This study aimed to evaluate TBS measurements combined
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cda0739ac7a96b2f7af8b5ff94b956ae
https://doi.org/10.1016/j.jocd.2021.04.001
https://doi.org/10.1016/j.jocd.2021.04.001
Autor:
Vanessa A. Santarosa, Denise M. Orlandi, Lia B. Fiorin, Teresa S. Kasamatsu, Gilberto K. Furuzawa, Ilda S. Kunii, Rosália P. Padovani, Marília M. S. Marone, Mário L. Castiglioni, José Gilberto H Vieira, Rui M. B. Maciel, Magnus R. Dias-da-Silva, João R. M. Martins
Publikováno v:
Archives of Endocrinology and Metabolism, Vol 59, Iss 6, Pp 501-506 (2015)
Objective Consuming a low-iodine diet (LID) is a widely accepted practice before administering radioiodine (131I) to evaluate and to treat thyroid disease. Although this procedure is well established for the management of patients with differentiated
Externí odkaz:
https://doaj.org/article/bb99c904bc8548bab2d66f9263facc1e
Autor:
Marlyn Zapata, Ilda S. Kunii, Rolf M. Paninka, Denise M. N. Simões, Víctor A. Castillo, Archivaldo Reche, Rui M. B. Maciel, Magnus R. Dias da Silva
Publikováno v:
Biology Open, Vol 3, Iss 9, Pp 785-793 (2014)
Neck ventroflexion in cats has different causes; however, the most common is the hypokalemia associated with flaccid paralysis secondary to chronic renal failure. In humans, the most common causes of acute flaccid paralysis are hypokalemia precipitat
Externí odkaz:
https://doaj.org/article/f456913f306d4d7e9c7b2300371cfbe5
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Magnus R. Dias-da-Silva, Nelson Rassi, Flávia A. Costa-Barbosa, Michelle Cerutti C. Vargas, Cecília Pacheco Elias, Sara R. Carvalho, Ilda S. Kunii, Felipe Scipião Moura
Publikováno v:
BMC Endocrine Disorders, Vol 20, Iss 1, Pp 1-7 (2020)
BMC Endocrine Disorders
BMC Endocrine Disorders
Background Adrenal hypoplasia congenita (AHC) is an X-linked disorder that affects the adrenal cortex and hypothalamus-pituitary-gonadal axis (HPG), leading to primary adrenocortical insufficiency (PAI) and hypogonadotropic hypogonadism. AHC is cause
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::681e25575997877c1d067bb8681aec1d
https://doaj.org/article/82085d1044cc4aaab002f6985a5c818c
https://doaj.org/article/82085d1044cc4aaab002f6985a5c818c
Autor:
Silvia Regina Correia-Silva, Lívia Almeida Dutra, Orlando Graziani Povoas Barsottini, Magnus R. Dias da Silva, Patrick A. Dion, Lilia Alves Maria, Pedro Braga-Neto, Ary Gadelha, Ilda S. Kunii, Helena Alessi, Guy A. Rouleau, José Luiz Pedroso, Bruno Bertolucci Ortiz, Marcondes C. França, Maria Thereza Drumond Gama
Publikováno v:
The Cerebellum. 18:731-737
SYNE1 gene mutations were identified as a cause of late-onset pure cerebellar syndrome. Non-cerebellar symptoms, including cognitive impairment, were already described in this condition. The aim of this study was to perform a detailed cognitive and p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::707a7caa79397d2a70f4254ce3f2427a
https://doi.org/10.1007/s12311-019-01033-5
https://doi.org/10.1007/s12311-019-01033-5
Autor:
Marise Lazaretti-Castro, Isabela Ohki Nacaguma, Sthefanie Giovanna Pallone, José Gilberto H. Vieira, Renata Elen Costa Silva, Lívia Marcela Santos, Ilda S. Kunii, Monique Nakayama Ohe, Bruno Gabriel Pereira
Publikováno v:
Journal of the Endocrine Society
Background: Vitamin D deficiency is common among PHP patients. While data are limited, some studies suggest that vitamin D deficiency may exacerbates skeletal disease in PHP. TBS is a software-based method for assessment of trabecular bone structure
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b49cd7e77808ae5d4c8eded1d8633f1
http://europepmc.org/articles/PMC7209552
http://europepmc.org/articles/PMC7209552