Detalles de la búsqueda
1.
Health services use by children identified as heterozygous hemoglobinopathy mutation carriers via newborn screening.
BMC Pediatr
; 21(1): 296, 2021 07 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-34210267
2.
Biotinidase deficiency: Spectrum of molecular, enzymatic and clinical information from newborn screening Ontario, Canada (2007-2014).
Mol Genet Metab
; 116(3): 146-51, 2015 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-26361991
3.
Scoping review of patient- and family-oriented outcomes and measures for chronic pediatric disease.
BMC Pediatr
; 15: 7, 2015 Feb 13.
Artículo
en Inglés
| MEDLINE | ID: mdl-25886474
4.
Achieving the "triple aim" for inborn errors of metabolism: a review of challenges to outcomes research and presentation of a new practice-based evidence framework.
Genet Med
; 15(6): 415-22, 2013 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-23222662
5.
An examination of sex differences in associations between cord blood adipokines and childhood adiposity.
Pediatr Obes
; 15(3): e12587, 2020 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-31845502
6.
Health services use among children diagnosed with medium-chain acyl-CoA dehydrogenase deficiency through newborn screening: a cohort study in Ontario, Canada.
Orphanet J Rare Dis
; 14(1): 70, 2019 03 22.
Artículo
en Inglés
| MEDLINE | ID: mdl-30902101
7.
The health system impact of false positive newborn screening results for medium-chain acyl-CoA dehydrogenase deficiency: a cohort study.
Orphanet J Rare Dis
; 11: 12, 2016 Feb 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-26841949
Resultados
1 -
7
de 7
1
Próxima >
>>