about
Urea synthesis after oral protein ingestion in manSynthesis of urea after stimulation with amino acids: relation to liver function.Neonatal hyperammonaemia with complete absence of liver carbamyl phosphate synthetase activityAcute neonatal and benign citrullinaemia in one sibshipVariants of citrullinaemia.Hyperammonaemia in 20 families. Biochemical and genetical survey, including investigations in 3 new families.Plasma ammonia levels in newborn infants admitted to an intensive care baby unit.Citrulline synthesis in rat tissues and liver content of carbamoyl phosphate and ornithine.
P2860
Q34484188-AC490440-6FF6-45FB-B807-77CB16C43A40Q34493818-E2C26D1F-242D-4F7E-ADD4-E883B49991BAQ34986724-3C1D2E82-31F3-4172-8ACB-02537DE5EBA8Q34987231-94330969-33F6-407A-97BC-A79205DAF6F9Q35150827-BE06DC63-63F0-4B5E-BC4F-34FE4105FCADQ35151196-3CAB9D68-21EB-453B-A2EF-5B77090E0497Q38916503-BAB2D1AB-B137-4223-A379-96C89C7D1F75Q42561183-4E0664D1-B8F3-4C1D-8C8A-F8FBD2267A7A
P2860
description
1971 nî lūn-bûn
@nan
1971年の論文
@ja
1971年学术文章
@wuu
1971年学术文章
@zh-cn
1971年学术文章
@zh-hans
1971年学术文章
@zh-my
1971年学术文章
@zh-sg
1971年學術文章
@yue
1971年學術文章
@zh
1971年學術文章
@zh-hant
name
Hereditary metabolic disorders of the urea cycle.
@en
type
label
Hereditary metabolic disorders of the urea cycle.
@en
prefLabel
Hereditary metabolic disorders of the urea cycle.
@en
P1476
Hereditary metabolic disorders of the urea cycle.
@en
P2093
P304
P577
1971-01-01T00:00:00Z