|1.||Biery, B J: 1 article (06/2000)|
|2.||Geisbrecht, B V: 1 article (06/2000)|
|3.||Gould, S J: 1 article (06/2000)|
|4.||Cox, R P: 1 article (06/2000)|
|5.||Morrell, J C: 1 article (06/2000)|
|6.||Geraghty, M T: 1 article (06/2000)|
|7.||Goodman, B K: 1 article (06/2000)|
|8.||Sacksteder, K A: 1 article (06/2000)|
06/01/2000 - "Defects in one or both of these activities result in familial hyperlysinemia, an autosomal recessive condition characterized by hyperlysinemia, lysinuria, and variable saccharopinuria. "
01/01/1998 - "[Saccharopinuria (a variant form of familial hyperlysinemia)]."
01/01/1991 - "These inborn errors are associated with a wide variety of clinical symptoms and biochemical profiles as persistent hyperlysinemia, saccharopinuria, "amino and ketoadipic aciduria, and glutaric aciduria."
05/01/1979 - "The relation of the two genetic entities involving lysine degradation, familial hyperlysinemia and saccharopinuria, is discussed. "
01/01/1983 - "This would explain the excretion of homocritrulline in the HHH-syndrome, saccharopinuria, citrullinemia and hyperlysinemia. "
|3.||Saccharopine Dehydrogenases (Saccharopine Dehydrogenase (NAD+, L-Glutamate Forming))