The dietary challenge of propionicacidaemia in an Asian girl.
作者信息
Laing S C
出版信息
Hum Nutr Appl Nutr. 1985 Aug;39(4):273-6.
PMID:3930435
Abstract
An Asian girl with propionicacidaemia, now aged 2 1/2 years, is presented. The low protein regime required to treat this condition, along with the cultural differences and communication problems involved in dealing with this Moslem family are described.
摘要
相似文献
1
The dietary challenge of propionicacidaemia in an Asian girl.
Hum Nutr Appl Nutr. 1985 Aug;39(4):273-6.
2
L-carnitine therapy in propionicacidaemia.左旋肉碱治疗丙酸血症。
Lancet. 1982 Jun 19;1(8286):1411-2. doi: 10.1016/s0140-6736(82)92524-7.
3
Normal growth and development with unrestricted protein intake after severe infantile propionic acidaemia.严重婴儿丙酸血症后蛋白质摄入不受限情况下的正常生长发育。
J Inherit Metab Dis. 1989;12(3):307-11. doi: 10.1007/BF01799222.
4
[Blood propionic acid with hyperammonemic coma].
Klin Padiatr. 1987 Sep-Oct;199(5):348-50. doi: 10.1055/s-2008-1026817.
5
Propionic acidemia: a clinical update.丙酸血症：临床最新进展
J Pediatr. 1981 Dec;99(6):835-46. doi: 10.1016/s0022-3476(81)80004-2.
6
Propionic acidaemia presenting with pancytopaenia in infancy.婴儿期丙酸血症伴全血细胞减少症
J Inherit Metab Dis. 1980;2(3):65-9. doi: 10.1007/BF01801721.
7
A simple isotopic technique for assessing vitamin responsiveness in vivo in propionic acidaemia.
J Inherit Metab Dis. 1990;13(3):349-51. doi: 10.1007/BF01799392.
8
Neurologic outcome of propionic acidemia.
Pediatr Neurol. 1992 Sep-Oct;8(5):333-7. doi: 10.1016/0887-8994(92)90085-d.
9
Pyroglutamic aciduria in propionyl CoA carboxylase deficiency.
J Inherit Metab Dis. 1984;7(3):139-40. doi: 10.1007/BF01801776.
10
Dietary treatment and biochemical studies on a neonatal case of propionyl-CoA carboxylase deficiency.
J Inherit Metab Dis. 1982;5(2):121-4. doi: 10.1007/BF01800005.
Zotero 插件