Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Joshua Atienza"'
Autor:
Joshua Atienza, Anjalee Benedict, Lincoln D Stein, Kashif Pirzada, Cheryl White, Shraddha Pai
Publikováno v:
PLoS Computational Biology, Vol 19, Iss 9, p e1011285 (2023)
This article presents 14 quick tips to build a team to crowdsource data for public health advocacy. It includes tips around team building and logistics, infrastructure setup, media and industry outreach, and project wrap-up and archival for posterity
Externí odkaz:
https://doaj.org/article/64cef38b9acb4a22a091a288bdc8b8d7
Publikováno v:
Healthcare Management Forum. 32:202-207
The Living Kidney Donation Program at the Toronto General Hospital, University Health Network sought to develop a comprehensive, secure, accurate, and up-to-date information system for the purposes of quality improvement, research, and performance ev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d3c51e3fe05ed631765363d3e34441b
https://doi.org/10.1177/0840470419843672
https://doi.org/10.1177/0840470419843672
Autor:
Ilona Tkachyova, Madeleine Hall, Joshua Atienza, Haneen Ali, Jens Feugmann, Niko Guischard, Andreas Schulze
Publikováno v:
Molecular Genetics and Metabolism. 135:304
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d8485bb81ae8bf6ffe2a57ad9368cec4
https://doi.org/10.1016/j.ymgme.2022.01.095
https://doi.org/10.1016/j.ymgme.2022.01.095
Publikováno v:
Molecular Genetics and Metabolism. 135:259
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::66631a59073ba241eb9e02f905d9998c
https://doi.org/10.1016/j.ymgme.2022.01.018
https://doi.org/10.1016/j.ymgme.2022.01.018
Autor:
Jose G. Teodoro, Philippe M. Campeau, Sharon E. Plon, Linchao Lu, Joshua Atienza, Thomas J. Kucharski, Weidong Jin, Justine Rousseau, Brendan Lee, Thi Tuyet Mai Nguyen, Norbert F. Ajeawung, Sirinart Molidperee, Lisa L. Wang, Isabel Gamache
Publikováno v:
American journal of human genetics. 105(3)
Rothmund-Thomson syndrome (RTS) is an autosomal-recessive disorder characterized by poikiloderma, sparse hair, short stature, and skeletal anomalies. Type 2 RTS, which is defined by the presence of bi-allelic mutations in RECQL4, is characterized by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c4e4003bc3b9b19dc3a5709470fd0a7
https://pubmed.ncbi.nlm.nih.gov/31303264
https://pubmed.ncbi.nlm.nih.gov/31303264