Detalhe da pesquisa
1.
Assessing the quality and value of metabolic chart data for capturing core outcomes for pediatric medium-chain acyl-CoA dehydrogenase (MCAD) deficiency.
BMC Pediatr
; 24(1): 37, 2024 Jan 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-38216926
2.
Evaluation of the quality of clinical data collection for a pan-Canadian cohort of children affected by inherited metabolic diseases: lessons learned from the Canadian Inherited Metabolic Diseases Research Network.
Orphanet J Rare Dis
; 15(1): 89, 2020 04 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32276663
3.
Homozygous TRAP1 sequence variant in a child with Leigh syndrome and normal kidneys.
Kidney Int
; 86(4): 860, 2014 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-25265962
4.
Subcutaneous fat necrosis of the newborn and lactic acidosis.
Pediatr Dermatol
; 24(4): 435-6, 2007.
Artigo
em Inglês
| MEDLINE | ID: mdl-17845182
5.
Metabolic Clinic Atlas: Organization of Care for Children with Inherited Metabolic Disease in Canada.
JIMD Rep
; 21: 15-22, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25716610
6.
Influenza B acute necrotizing encephalopathy: a case report and literature review.
Pediatr Neurol
; 28(5): 396-9, 2003 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-12878304
7.
Familial recurrence of cerebral palsy with multiple risk factors.
Case Rep Pediatr
; 2011: 307857, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-22606510