LE WE PMID CA
Urea cycle1104Harnstoffzyklus

Amino acids (Hereditary diseases)

Ammonia (Hyperammonemia)

Arginase

Arginine

Argininosuccinate lyase

Argininosuccinate synthetase

Azauridine

Carbamoyl phosphate

Carbamoylphosphate synthetase1

Carglumic acid

CNS (Stroke BASKET)

Hepatic encephalopathy

Homocystinuria

Liver (Transplantation)

Lysinuric protein intolerance

N Acetylglutamate synthase deficiency

Ornithine carbamoyltransferase deficiency

Orotic acid

Transporter (Ornithine adn citrulline)

Urea cycle

Urea

1977  
1
Urea biosynthesis I. The urea cycle and relationships to the citric acid cycle.
[337792] Am J Clin Nutr 30(12): 2083-7 (1977)
2004  
2
Clinical consequences of urea cycle enzyme deficiencies and potential links to arginine and nitric oxide metabolism.
[15465784] J Nutr 134(10 Suppl): 2775S-2782S; discussion 2796S-2797S (2004)
2004  
3
Clinical manifestations of inborn errors of the urea cycle and related metabolic disorders during childhood.
[15173438] J Nutr 134(6 Suppl): 1605S-1609S; discussion 1630S-1632S, 1667S-1672S (2004)
1993  
4
Hepatic glutaminase expression: relationship to kidney-type glutaminase and to the urea cycle.
[8262331] FASEB J 7(15): 1468-74 (1993)
2003  
5
Argininosuccinate synthetase from the urea cycle to the citrulline-NO cycle.
[12709047] Eur J Biochem 270(9): 1887-99 (2003)
2006  
6
Regulation of ornithine decarboxylase.
[16459331] J Biol Chem 281(21): 14529-32 (2006)
2005  
7
Current role of liver transplantation for the treatment of urea cycle disorders: a review of the worldwide English literature and 13 cases at Kyoto University.
[16237708] Liver Transpl 11(11): 1332-42 (2005)
2007  
8
Hyperammonemia in the ICU.
[17934124] Chest 132(4): 1368-78 (2007)
2007  
9
Orotic acid excretion and arginine metabolism.
[17513443] J Nutr 137(6 Suppl 2): 1656S-1661S (2007)
2010  
10
Inherited metabolic disorders and stroke part 2: homocystinuria, organic acidurias, and urea cycle disorders.
[20142522] Arch Neurol 67(2): 148-53 (2010)
2011  
11
Role of carglumic acid in the treatment of acute hyperammonemia due to N-acetylglutamate synthase deficiency.
[21941437] Ther Clin Risk Manag 7(-): 327-32 (2011)
2008  
12
Contrasting features of urea cycle disorders in human patients and knockout mouse models.
[17933574] Mol Genet Metab 93(1): 7-14 (2008)

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