Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Hugo Gomes da Silva"'
Autor:
Karina Soboleva, Nirmal Kumar Shankar, Madhavi Yadavalli, Cátia Ferreira, Nadia Foskett, Kert Putsepp, Lisa Beth Ferstenberg, Magnus Nord, Hugo Gomes da Silva, Prakash Bhuyan
Publikováno v:
The Lancet Global Health, Vol 10, Iss 1, Pp e33-e34 (2022)
Externí odkaz:
https://doaj.org/article/525df1f110cb4dc6a15140f90e8b3fbf
Autor:
Wolfgang Högler, Craig Langman, Hugo Gomes da Silva, Shona Fang, Agnès Linglart, Keiichi Ozono, Anna Petryk, Cheryl Rockman-Greenberg, Lothar Seefried, Priya S. Kishnani
Publikováno v:
BMC Musculoskeletal Disorders, Vol 20, Iss 1, Pp 1-9 (2019)
Abstract Background Hypophosphatasia (HPP) is a rare, systemic disease caused by mutation(s) within the ALPL gene encoding tissue-nonspecific alkaline phosphatase (ALP). HPP has a heterogeneous presentation, which coupled with its rarity, often leads
Externí odkaz:
https://doaj.org/article/3ca8f22474df4533a9a737611ad11518
Autor:
Dawn Phillips, Ioannis C Tomazos, Scott Moseley, Gil L'Italien, Hugo Gomes da Silva, Sergio Lerma Lara
Publikováno v:
JBMR Plus, Vol 3, Iss 6, Pp n/a-n/a (2019)
ABSTRACT This investigation evaluated the reliability and validity of the 6‐Minute Walk Test (6MWT) in patients with pediatric hypophosphatasia (HPP). Children (aged 6 to 12 years; n = 11), adolescents (13 to 17 years; n = 4), and adults (18 to 65
Externí odkaz:
https://doaj.org/article/c01abcbd223a479086ae856f06803a45
Autor:
Sully Milena Mejia Quintero, Luiz Carlos Guedes Valente, Marcos Sebastião de Paula Gomes, Hugo Gomes da Silva, Bernardo Caroli de Souza, Sergio R. K. Morikawa
Publikováno v:
Sensors, Vol 18, Iss 12, p 4393 (2018)
A realistic implementation of an all-fiber CO2 sensor, using 74 cm of hollow core photonic crystal fiber (HC-PCF) as the cavity for light/gas interaction, has been implemented. It is based on CO2 absorbance in the 2 µm region. The working range is f
Externí odkaz:
https://doaj.org/article/ae11417c6ede442c9d5a4cc337de3406
Autor:
HUGO GOMES DA SILVA
[pt] Esta dissertação faz parte de um projeto mais abrangente que visa caracterizar os parâmetros ideais para perfuração e corte a laser em rochas, metais e cimentos tipicamente utilizados na indústria do petróleo. Este trabalho teve por objet
Autor:
HUGO GOMES DA SILVA
Publikováno v:
Repositório Institucional da PUC_RIOPontifícia Universidade Católica do Rio de JaneiroPUC_RIO.
PONTIFÍCIA UNIVERSIDADE CATÓLICA DO RIO DE JANEIRO
COORDENAÇÃO DE APERFEIÇOAMENTO DO PESSOAL DE ENSINO SUPERIOR
PROGRAMA DE EXCELENCIA ACADEMICA
Esta dissertação faz parte de um projeto mais abrangente que visa caracterizar os p
COORDENAÇÃO DE APERFEIÇOAMENTO DO PESSOAL DE ENSINO SUPERIOR
PROGRAMA DE EXCELENCIA ACADEMICA
Esta dissertação faz parte de um projeto mais abrangente que visa caracterizar os p
Autor:
Hana Müllerová, Jennie Medin, Matthew Arnold, Hugo Gomes da Silva, Supriya Kumar, Magnus Nord, Richard Hubbard, Simon de Lusignan
ObjectivesDuring COVID-19 vaccination programmes, new safety signals have emerged for vaccines, including extremely rare cases of thrombosis with thrombocytopaenia syndrome (TTS). Background event rates before and during the pandemic are essential fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14b698fe1c3c6b57300ae9a299bf8fbb
https://doi.org/10.1136/bmjopen-2022-063645
https://doi.org/10.1136/bmjopen-2022-063645
Autor:
Michael A Laffan, Sue Rees, Madhavi Yadavalli, Lisa Beth Ferstenberg, Nirmal Kumar Shankar, Jennie Medin, Nadia Foskett, Matthew Arnold, Hugo Gomes da Silva, Prakash Bhuyan, Magnus Nord
Publikováno v:
Vaccine. 40(38)
Post-marketing surveillance for COVID-19 vaccines during the pandemic identified an extremely rare thrombosis with thrombocytopenia syndrome (TTS) reported post-vaccination, requiring further characterisation to improve diagnosis and management.We se
Autor:
Jennie Medin, Magnus Nord, Nirmal Kumar Shankar, Hana Müllerová, Prakash Bhuyan, Madhavi Yadavalli, Hugo Gomes da Silva, M. Arnold
Publikováno v:
The Lancet. 398:577-578
Autor:
Hugo Gomes da Silva, Agnès Linglart, Cheryl Rockman-Greenberg, Wolfgang Högler, Priya S. Kishnani, Keiichi Ozono, Lothar Seefried, Anna Petryk, Shona Fang, Craig B. Langman
Publikováno v:
BMC Musculoskeletal Disorders
BMC Musculoskeletal Disorders, Vol 20, Iss 1, Pp 1-9 (2019)
BMC Musculoskeletal Disorders, Vol 20, Iss 1, Pp 1-9 (2019)
Background Hypophosphatasia (HPP) is a rare, systemic disease caused by mutation(s) within the ALPL gene encoding tissue-nonspecific alkaline phosphatase (ALP). HPP has a heterogeneous presentation, which coupled with its rarity, often leads to misse