1 rowth, low molecular weight proteinuria, and aminoaciduria.

2 at include low molecular weight proteinuria, aminoaciduria and glycosuria, together with rickets in s

3 nconi syndrome, characterized by glycosuria, aminoaciduria, calciuria, and albuminuria.

4 y fetal growth retardation, lactic acidosis, aminoaciduria, cholestasis, and abnormalities in iron me

5                 GRACILE (growth retardation, aminoaciduria, cholestasis, iron overload, lactacidosis,

6 phosphate synthase (CPS), as well as dibasic aminoacidurias hyperammonemia-hyperornithinemia-homocitr

7 oni syndrome with glucosuria and generalized aminoaciduria in addition to diabetes.

8               We investigated glucosuria and aminoaciduria in patients with HNF-1alpha mutations.

9 i-like syndrome of glucosuria, phosphaturia, aminoaciduria, low molecular weight proteinuria, and alb

10                 In contrast, the generalized aminoaciduria seen in patients with HNF-1alpha mutations

11 ar weight (<70 kDa) proteinuria, generalized aminoaciduria that was more pronounced for neutral and p

12                                  Generalized aminoaciduria was also present in type 1 diabetic (Z sco

13                                              Aminoaciduria was not associated with microalbuminuria o

14 en on the same day showed significantly more aminoaciduria when glucosuria was present compared with

15    The HNF-1alpha patients had a generalized aminoaciduria with elevated levels of 14 of 16 amino aci