Detalhe da pesquisa
1.
The Metabolic Map into the Pathomechanism and Treatment of PGM1-CDG.
Am J Hum Genet
; 104(5): 835-846, 2019 05 02.
Artigo
Inglês
| MEDLINE | ID: mdl-30982613
2.
A novel homozygous YARS2 mutation causes severe myopathy, lactic acidosis, and sideroblastic anemia 2.
J Hum Genet
; 59(4): 229-32, 2014 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-24430573
3.
Quality of life in children treated with restrictive diet for inherited metabolic disease.
Pediatr Int
; 55(4): 428-33, 2013 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-23461789
4.
Lipid apheresis applications in childhood: experience in the University Hospital of Gazi.
Transfus Apher Sci
; 39(3): 235-40, 2008 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-18955012
5.
Very long-chain acyl CoA dehydrogenase deficiency which was accepted as infanticide.
Forensic Sci Int
; 210(1-3): e1-3, 2011 Jul 15.
Artigo
Inglês
| MEDLINE | ID: mdl-21531094
6.
Factors related to non-alcoholic fatty liver disease in obese children.
Turk J Gastroenterol
; 19(2): 85-91, 2008 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-19110662