Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Mariana Del Pino"'
Autor:
Juan Llerena, Jr, Pablo Rosselli, Amanda Aragão, Cristina Valenzuela, Debora Bertola, Yaneth Mendez, Mariana del Pino, Nicolette Calvacanti, Paula Thomazinho, Jeanne M. Pimenta, Shelda Cohen, Tom Butt, José C. Thomaz, Jr, Renée Shediac, Richard Rowell, Tatiana S.P.C. Magalhães, Chong Kim, Virginia Fano
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 100843- (2024)
Purpose: The multisystem clinical manifestations and complications of achondroplasia, the most common form of disproportionate short stature, can cause functional impairment and psychosocial burden. The Lifetime Impact Study for Achondroplasia (LISA)
Externí odkaz:
https://doaj.org/article/eeb761d8dbb64f3f8ada3e518aeb0303
Publikováno v:
Journal of Plant Protection Research, Vol vol. 62, Iss No 4, Pp 393-402 (2023)
The excessive use of chemical products to control thrips and the tomato spotted wilt virus (TSWV) is not only harmful to human health, the environment, and biodiversity, but also the resistance these generate in insects turns them inefficient in the
Externí odkaz:
https://doaj.org/article/8ff2ea0518e54367ac91fee88e38352f
Autor:
Juan Llerena, Chong Ae Kim, Virginia Fano, Pablo Rosselli, Paulo Ferrez Collett-Solberg, Paula Frassinetti Vasconcelos de Medeiros, Mariana del Pino, Débora Bertola, Charles Marques Lourenço, Denise Pontes Cavalcanti, Têmis Maria Félix, Antonio Rosa-Bellas, Norma Teresa Rossi, Fanny Cortes, Flávia Abreu, Nicolette Cavalcanti, Maria Cecilia Hervias Ruz, Wagner Baratela
Publikováno v:
BMC Pediatrics, Vol 22, Iss 1, Pp 1-13 (2022)
Abstract Background Achondroplasia is the most common bone dysplasia associated with disproportionate short stature, and other comorbidities, such as foramen magnum stenosis, thoracolumbar kyphosis, lumbar hyperlordosis, genu varum and spinal compres
Externí odkaz:
https://doaj.org/article/6cb774ce002b42298b2e3017d9bdf78b
Autor:
Juan Llerena, Jr, Virginia Fano, Pablo Rosselli, Mariana del Pino, Cristina Valenzuela, Janeth Méndez, Nicolette Cavalcanti, Paula Thomazinho, Amanda Aragão, José Thomaz, Tom Butt, Richard Rowell, Jeanne Pimenta, Shelda Cohen, Renée Shediac, Tatiana Magalhães, Debora Bertola, Chong Kim
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100261- (2023)
Externí odkaz:
https://doaj.org/article/b35af266ef1c40f58dfe076e08253473
Autor:
Carlos Grandi, Mariana del Pino, Davi Casale Aragon, Livia dos Santos Rodrigues, Viviane Cunha Cardoso
Publikováno v:
Revista de la Facultad de Ciencias Médicas de Córdoba, Vol 77, Iss 2, Pp 86-93 (2020)
Introduction The use of local references or standard for neonatal studies still requires their validation through indicators of morbidity and mortality. Objective: evaluate the performance of the INTERGROWTH-21st Project (IG-21) standard and a com
Externí odkaz:
https://doaj.org/article/77896bd00db14693a84c96388993e3de
Publikováno v:
CIC Digital (CICBA)
Comisión de Investigaciones Científicas de la Provincia de Buenos Aires
instacron:CICBA
Comisión de Investigaciones Científicas de la Provincia de Buenos Aires
instacron:CICBA
To respond to increasing demands for good agricultural practices (GAP) and food safety, governments globally are introducing stringent regulations to govern agricultural compliance that affect production, storage, and sales activities. New legislatio
Autor:
Mariana del Pino, Victoria Huckstadt, Francisca Diaz‐Gonzalez, Maria Gabriela Obregon, Karen E. Heath, Virginia Fano
Publikováno v:
American Journal of Medical Genetics Part A.
Autor:
Sebastián Jaimovich, M. Arenas, Gisela Viterbo, Mariana del Pino, Roxana Marino, Natalia Perez Garrido, Virginia Fano
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism. 34:1105-1113
BackgroundCraniosynostosis is an underdiagnosed complication associated with hypophosphatemic rickets. The study aims to describe the clinical and auxological characteristic of children with hypophosphatemic rickets and craniosynostosis, describe the
Autor:
Viviane Cunha Cardoso, Lívia dos Santos Rodrigues, Carlos Grandi, Davi Casale Aragon, Mariana Del Pino
Publikováno v:
Revista de la Facultad de Ciencias Médicas de Córdoba, Vol 77, Iss 2, Pp 86-93 (2020)
The use of local references or standard for neonatal studies still requires their validation through indicators of morbidity and mortality.evaluate the performance of the INTERGROWTH-21st Project (IG-21) standard and a commonly used Argentinian refer
Autor:
Virginia Fano, Martyn T. Cobourne, Patricia Carl-Innig, Michael B. Bober, Melita Irving, Fabio Mazzoleni, Jeffrey W. Campbell, Brigitte Fauroux, Dominic Thompson, Judith P Rossiter, Jenna W. Briddell, Yosha Prasad, Mary C. Theroux, Geert Mortier, Antonio Leiva-Gea, Amaka C. Offiah, Klaus Mohnike, Penny Ireland, James A. Betts, Juan Llerena, Steven Powell, Heather Elphick, Pablo Rosselli, Wagner A.R. Baratela, Therese Hannon, Kenneth W. Martin, Marco Sessa, Natsuo Yasui, Michael Wright, Moira Cheung, Matthew Thomas, Inês Alves, Jonathan Gibbins, Cathleen L. Raggio, Muriel Deladure-Molla, Angelo Selicorni, Lars Hagenäs, Sharon McDonnell, William G. Mackenzie, Morrys Kaisermann, Maria Costanza Meazzini, Svein O. Fredwall, Laura Trespedi, Ravi Savarirayan, Philippe M. Campeau, Mari L. Groves, Valérie Cormier-Daire, Keiichi Ozono, Julie Hoover-Fong, David E. Tunkel, John A. Phillips, Josef Milerad, Silvio Boero, C Wallis, Mariana del Pino
Publikováno v:
Nature reviews : endocrinology
Savarirayan, R, Fredwall, S, Ireland, P, Irving, M D, Thompson, D, Alves, I, Baratela, W A R & Betts, J 2022, ' International Consensus Statement on the diagnosis, multidisciplinary management and lifelong care of individuals with achondroplasia ', Nature Reviews Endocrinology, vol. 18, no. 3, pp. 173-189 . https://doi.org/10.1038/s41574-021-00595-x
Savarirayan, R, Fredwall, S, Ireland, P, Irving, M D, Thompson, D, Alves, I, Baratela, W A R & Betts, J 2022, ' International Consensus Statement on the diagnosis, multidisciplinary management and lifelong care of individuals with achondroplasia ', Nature Reviews Endocrinology, vol. 18, no. 3, pp. 173-189 . https://doi.org/10.1038/s41574-021-00595-x
Achondroplasia, the most common skeletal dysplasia, is characterized by a variety of medical, functional and psychosocial challenges across the lifespan. The condition is caused by a common, recurring, gain-of-function mutation in FGFR3, the gene tha