1 rowth, low molecular weight proteinuria, and aminoaciduria.

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

3 t proteinuria, renal tubular acidosis (RTA), aminoaciduria, and hypercalciuria.

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

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

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

7 c BCS1L variants include growth retardation, aminoaciduria, cholestasis, iron overload, lactic acidos

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

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

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

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

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

13 the first patient presented as an adult with aminoaciduria, seizures, bilateral sensorineural deafnes

14 x of Slc7a7Lbu/Lbu mice, which combined with aminoaciduria suggests proximal tubular dysfunction.

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

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

17                                              Aminoaciduria was not associated with microalbuminuria o

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

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