Zobrazeno 1 - 3
of 3
pro vyhledávání: '"in collaboration with the Canadian Inherited Metabolic Diseases Research Network (CIMDRN)"'
Autor:
Maria D. Karaceper, Sara D. Khangura, Kumanan Wilson, Doug Coyle, Marni Brownell, Christine Davies, Linda Dodds, Annette Feigenbaum, Deshayne B. Fell, Scott D. Grosse, Astrid Guttmann, Steven Hawken, Robin Z. Hayeems, Jonathan B. Kronick, Anne-Marie Laberge, Julian Little, Aizeddin Mhanni, John J. Mitchell, Meranda Nakhla, Murray Potter, Chitra Prasad, Cheryl Rockman-Greenberg, Rebecca Sparkes, Sylvia Stockler, Keiko Ueda, Hilary Vallance, Brenda J. Wilson, Pranesh Chakraborty, Beth K. Potter, in collaboration with the Canadian Inherited Metabolic Diseases Research Network (CIMDRN)
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-10 (2019)
Abstract Background We describe early health services utilization for children diagnosed with medium-chain acyl-CoA dehydrogenase (MCAD) deficiency through newborn screening in Ontario, Canada, relative to a screen negative comparison cohort. Methods
Externí odkaz:
https://doaj.org/article/a72bcbf99e054f53a45cf6d8dba004cf
Autor:
Nataliya Yuskiv, Beth K. Potter, Sylvia Stockler, Keiko Ueda, Alette Giezen, Barbara Cheng, Erica Langley, Suzanne Ratko, Valerie Austin, Maggie Chapman, Pranesh Chakraborty, Jean Paul Collet, Amy Pender, In collaboration with the Canadian Inherited Metabolic Diseases Research Network (CIMDRN)
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-13 (2019)
Abstract Background Phenylalanine hydroxylase (PAH) deficiency is one of 31 targeted inherited metabolic diseases (IMD) for the Canadian Inherited Metabolic Diseases Research Network (CIMDRN). Early diagnosis and initiation of treatment through newbo
Externí odkaz:
https://doaj.org/article/1b98183cdc9642988c4908da010160cd
Autor:
Deshayne B. Fell, Scott D. Grosse, Kumanan Wilson, Beth K. Potter, Hilary Vallance, John J. Mitchell, Steven Hawken, Annette Feigenbaum, Robin Z. Hayeems, Cheryl Rockman-Greenberg, Chitra Prasad, Doug Coyle, Astrid Guttmann, Brenda Wilson, Keiko Ueda, Anne-Marie Laberge, Jonathan B. Kronick, Sylvia Stockler, Christine Davies, Sara D. Khangura, Meranda Nakhla, Rebecca Sparkes, Maria D. Karaceper, Aizeddin A. Mhanni, Murray A. Potter, Pranesh Chakraborty, Julian Little, Marni Brownell, Linda Dodds
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-10 (2019)
Paediatrics Publications
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-10 (2019)
Paediatrics Publications
Copyright: The Authors in collaboration with the Canadian Inherited Metabolic Diseases Research Network (CIMDRN). Background: We describe early health services utilization for children diagnosed with medium-chain acyl-CoA dehydrogenase (MCAD) deficie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::53fab8f7a363293fccb2430ac74c1f22
https://pubmed.ncbi.nlm.nih.gov/30902101
https://pubmed.ncbi.nlm.nih.gov/30902101