Zobrazeno 1 - 10
of 2 132
pro vyhledávání: '"Wilson MA"'
Publikováno v:
Pharmacy Practice, Vol 5, Iss 2, Pp 95-98 (2007)
During patient care rounds with the medical team, pharmacy students have made positive contributions for the benefit of the patient. However, very little has been documented regarding the impact these future healthcare professionals are making while
Externí odkaz:
https://doaj.org/article/14ed1a57bb654983a3eb2d3d1bcac1d5
Autor:
Lea, AJ, Caldas, IV, Garske, KM, Echwa, J, Gurven, M, Handley, C, Kahumbu, J, Kamau, Kinyua, P, Lotukoi, F, Lopurudoi, A, Lowasa, S, Mallarino, R, Martins, D, Messer, PW, Miano, C, Muhoya, B, Peng, J, Phung, T, Rabinowitz, JD, Roichman, A, Siford, R, Stone, A, Oill, AM Taravella, Mathew, S, Wilson, MA, Ayroles, JF
Publikováno v:
bioRxiv
The Turkana people inhabit arid regions of east Africa—where temperatures are high and water is scarce—and they practice subsistence pastoralism, such that their diet is primarily composed of animal products. Working with Turkana communities, we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2db1e1ade742571dcd20c2f1e276d60d
https://doi.org/10.1101/2023.01.17.524066
https://doi.org/10.1101/2023.01.17.524066
Autor:
Fábio Fernandes, Georgina del Cisne Jadán Luzuriaga, Guilherme Wesley Peixoto da Fonseca, Edileide Barros Correia, Alzira Alves Siqueira Carvalho, Ariane Vieira Scarlatelli Macedo, Otavio Rizzi Coelho-Filho, Phillip Scheinberg, Murillo Oliveira Antunes, Pedro Vellosa Schwartzmann, Sandrigo Mangini, Wilson Marques, Marcus Vinicius Simões
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-10 (2024)
Abstract Background Transthyretin amyloidosis (ATTR) is a multisystem disease caused by the deposition of fibrillar protein in organs and tissues. ATTR genotypes and phenotypes are highly heterogeneous. We present data on physical signs and symptoms,
Externí odkaz:
https://doaj.org/article/13652cdb50a54f85899e744d9db684ce
Publikováno v:
Diá-logos, Vol 16, Iss 28, Pp 57-84 (2024)
La educación en tecnología en la escuela básica permite al estudiante adquirir destrezas que le faciliten relacionarse con un entorno equipado de artefactos de uso diario; cuando un niño con discapacidad intelectual llega al aula regular por medi
Externí odkaz:
https://doaj.org/article/534ffa31d82d41129603bf9c9390b8ae
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 82, Iss 06, Pp 001-010 (2024)
Neuromuscular diseases (NMD) include a broad group of medical conditions with both acquired and genetic causes. In recent years, important advances have been made in the treatment of genetically caused NMD, and most of these advances are due to the i
Externí odkaz:
https://doaj.org/article/e28f903fa4774e919921309e93bc562f
Autor:
Schneegass Christina, Wilson Max L., Shaban Jwan, Niess Jasmin, Chiossi Francesco, Mitrevska Teodora, Woźniak Paweł W.
Publikováno v:
i-com, Vol 23, Iss 2, Pp 165-177 (2024)
People are increasingly eager to know more about themselves through technology. To date, technology has primarily provided information on our physiology. Yet, with advances in wearable technology and artificial intelligence, the current advent of con
Externí odkaz:
https://doaj.org/article/9ace4cc599434ff5bf69784483421aca
Publikováno v:
Proceedings of the 4th Workshop on NLP for Conversational AI.
Autor:
Fabio Fernandes, Marcus V. Simões, Edileide de Barros Correia, Fabiana Goulart Marcondes-Braga, Otavio Rizzi Coelho-Filho, Cláudio Tinoco Mesquita, Wilson Mathias Junior, Murillo de Oliveira Antunes, Edmundo Arteaga-Fernández, Carlos Eduardo Rochitte, Felix José Alvarez Ramires, Silvia Marinho Martins Alves, Marcelo Westerlund Montera, Renato Delascio Lopes, Mucio Tavares de Oliveira Junior, Fernando Luis Scolari, Walkiria Samuel Avila, Manoel Fernandes Canesin, Edimar Alcides Bocchi, Fernando Bacal, Lidia Zytynski Moura, Eduardo Benchimol Saad, Mauricio Ibrahim Scanavacca, Bruno Pereira Valdigem, Manuel Nicolas Cano, Alexandre Antonio Cunha Abizaid, Henrique Barbosa Ribeiro, Pedro Alves Lemos Neto, Gustavo Calado de Aguiar Ribeiro, Fabio Biscegli Jatene, Ricardo Ribeiro Dias, Luis Beck-da-Silva, Luis Eduardo Paim Rohde, Marcelo Imbroinise Bittencourt, Alexandre da Costa Pereira, José Eduardo Krieger, Humberto Villacorta Junior, Wolney de Andrade Martins, José Albuquerque de Figueiredo Neto, Juliano Novaes Cardoso, Carlos Alberto Pastore, Ieda Biscegli Jatene, Ana Cristina Sayuri Tanaka, Viviane Tiemi Hotta, Minna Moreira Dias Romano, Denilson Campos de Albuquerque, Ricardo Mourilhe-Rocha, Ludhmila Abrahão Hajjar, Fabio Sandoli de Brito Junior, Bruno Caramelli, Daniela Calderaro, Pedro Silvio Farsky, Alexandre Siciliano Colafranceschi, Ibraim Masciarelli Francisco Pinto, Marcelo Luiz Campos Vieira, Luiz Claudio Danzmann, Silvio Henrique Barberato, Charles Mady, Martino Martinelli Filho, Ana Flavia Malheiros Torbey, Pedro Vellosa Schwartzmann, Ariane Vieira Scarlatelli Macedo, Silvia Moreira Ayub Ferreira, Andre Schmidt, Marcelo Dantas Tavares de Melo, Moysés Oliveira Lima Filho, Andrei C. Sposito, Flávio de Souza Brito, Andreia Biolo, Vagner Madrini Junior, Stephanie Itala Rizk, Evandro Tinoco Mesquita
Publikováno v:
Arquivos Brasileiros de Cardiologia, Vol 121, Iss 7 (2024)
Externí odkaz:
https://doaj.org/article/0ed2ece57751488fa1a9fef364f0c809
Autor:
Wilson Max Almeida Monteiro de Moraes, Ronaldo Ferreira Moura, Ragami Alves, José de Oliveira Vilar Neto, Bruno Magalhães de Castro, Douglas Leão, Jonato Prestes
Publikováno v:
Dietetics, Vol 3, Iss 1, Pp 52-62 (2024)
Lean bodybuilder athletes may encounter challenges in adapting their eating habits during ad libitum refeed, either intuitively or consciously. Aims: This paper investigates whether there is a relationship between adaptive eating and energy intake co
Externí odkaz:
https://doaj.org/article/daa696e6012948bdb301089e3820fb29
Autor:
Edmar Zanoteli, Alexandra Prufer de Queiróz Campos Araujo, Michele Michelin Becker, Clarisse Pereira Dias Drumond Fortes, Marcondes Cavalcante França, Marcela Camara Machado-Costa, Wilson Marques, Ciro Matsui Jr, Rodrigo Holanda Mendonça, Flávia Nardes, Acary Souza Bulle Oliveira, Andre Luis Santos Pessoa, Jonas Alex Morales Saute, Paulo Sgobbi, Hélio Van der Linden, Juliana Gurgel-Giannetti
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 82, Iss 01, Pp 001-018 (2024)
Spinal muscular atrophy linked to chromosome 5 (SMA-5q) is an autosomal recessive genetic disease caused by mutations in the SMN1. SMA-5q is characterized by progressive degeneration of the spinal cord and bulbar motor neurons, causing severe motor a
Externí odkaz:
https://doaj.org/article/d5abdbdbc3fe4b4b985d20f677267041