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Arginine HCl, Cyanocobalamin, Folic Acid, L-Citrulline, L-ornithine HCl, Nicotinamide | ÀϹÝÀǾàǰ | ºñ±Þ¿© |
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Arginine HCl, Ascorbic Acid, Caffeine anhydrous, Gamma-oryzanol, Garlic extract, Nicotinamide, Pyridoxine HCl, Riboflavin, Thiamine nitrate, Tocopherol Calcium Succinate, Vitamin A oil | ÀϹÝÀǾàǰ | ºñ±Þ¿© |
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Arginine Tidiacicate, Ascorbic Acid, Riboflavin, Thiamine HCl | ÀϹÝÀǾàǰ | ¹Ì»ý»ê |
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A12954071 | Arginine Thiazolidine Carboxylate | ÀϹÝÀǾàǰ | ±Þ¿© |
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| argininosuccinic acid |
a compound formed by the condensation of aspartic acid and citrulline as a step in the urea cycle (q.v.).
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
|
|---|---|
| argininosuccinicacidemia |
the presence in the blood of argininosuccinic acid.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| argininosuccinicaciduria |
1. an autosomal recessive aminoacidopathy characterized by urinary excretion of argininosuccinic acid, owing to a deficiency of argininosuccinate lyase, with hyperammonemia, argininosuccinicacidemia, and citrullinemia. Neonatal and late onset forms exist, and clinical findings, which vary widely in severity, include mental retardation, seizures, ataxia, hepatomegaly, and friable hair (trichorrhexis nodosa). Called also argininosuccinase or argininosuccinate lyase deficiency. 2. excretion of argininosuccinic acid in the urine.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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