Last Posted: Jul 25, 2019
- How an AI expert took on his toughest project ever: writing code to save his son’s life,
by Casey Ross, Stats News, July 25, 2019 - National platform for Rare Diseases Data Registry of Japan.
Furusawa Yoshihiko et al. Learning health systems 2019 Jul 3(3) e10080 - The Era of the Genome and Dental Medicine.
Divaris K et al. Journal of dental research 2019 Aug 98(9) 949-955 - Quantitative analysis of a rare disease network's international contact database and E-repository provides insights into biobanking in the electronic consent era.
Suarez Alexander et al. Orphanet journal of rare diseases 2019 Jul 14(1) 173 - Precision Medicines' Impact on Orphan Drug Designation.
Mueller Christine M et al. Clinical and translational science 2019 Jul - Critical Trio Exome Benefits In-Time Decision-Making for Pediatric Patients With Severe Illnesses.
Wu En-Ting et al. Pediatric critical care medicine : a journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies 2019 Jul - Secondary findings from next generation sequencing: Psychological and ethical issues. Family and patient perspectives.
Houdayer F et al. European journal of medical genetics 2019 Jun 103711 - To treat their baby’s rare disorder, the only case of its kind in Canada, a family risks all for a gene-therapy breakthrough
M Devlin, Globe and Mail, July 9, 2019 - Family fights for genetic screening to save others from muscle-wasting disease afflicting their toddler
C Thorbecke, Good Morning America, July 9, 2019 - Australian Genomics: A Federated Model for Integrating Genomics into Healthcare.
Stark Zornitza et al. American journal of human genetics 2019 Jul 105(1) 7-14
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