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Health services use among children diagnosed with medium-ch..:
in collaboration with the Canadian Inherited Metabolic Diseases Research Network (CIMDRN)
;
Karaceper, Maria D.
;
Khangura, Sara D.
...
Orphanet Journal of Rare Diseases. 14 (2019) 1 - p. , 2019
Link:
https://doi.org/10.1186/s13023-019-1001-0
RT Journal T1
Health services use among children diagnosed with medium-chain acyl-CoA dehydrogenase deficiency through newborn screening: a cohort study in Ontario, Canada
UL https://suche.suub.uni-bremen.de/peid=cr-10.1186_s13023-019-1001-0&Exemplar=1&LAN=DE A1 in collaboration with the Canadian Inherited Metabolic Diseases Research Network (CIMDRN) A1 Karaceper, Maria D. A1 Khangura, Sara D. A1 Wilson, Kumanan A1 Coyle, Doug A1 Brownell, Marni A1 Davies, Christine A1 Dodds, Linda A1 Feigenbaum, Annette A1 Fell, Deshayne B. A1 Grosse, Scott D. A1 Guttmann, Astrid A1 Hawken, Steven A1 Hayeems, Robin Z. A1 Kronick, Jonathan B. A1 Laberge, Anne-Marie A1 Little, Julian A1 Mhanni, Aizeddin A1 Mitchell, John J. A1 Nakhla, Meranda A1 Potter, Murray A1 Prasad, Chitra A1 Rockman-Greenberg, Cheryl A1 Sparkes, Rebecca A1 Stockler, Sylvia A1 Ueda, Keiko A1 Vallance, Hilary A1 Wilson, Brenda J. A1 Chakraborty, Pranesh A1 Potter, Beth K. PB Springer Science and Business Media LLC YR 2019 SN 1750-1172 JF Orphanet Journal of Rare Diseases VO 14 IS 1 LK http://dx.doi.org/https://doi.org/10.1186/s13023-019-1001-0 DO https://doi.org/10.1186/s13023-019-1001-0 SF ELIB - SuUB Bremen
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