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Pediatric Research
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March 1, 1990
Guanidino compound analysis as a complementary diagnostic parameter for hyperargininemia: follow-up of guanidino compound levels during therapy
B Marescau, P P De Deyn, A Lowenthal, et al.
Metabolism: Clinical and Experimental
|
September 1, 1992
The pathobiochemistry of uremia and hyperargininemia further demonstrates a metabolic relationship between urea and guanidinosuccinic acid
B Marescau, P P De Deyn, I A Qureshi, et al.
Journal of Inherited Metabolic Disease
|
January 25, 2007
The pathogenesis of the white matter abnormalities in phenylketonuria. A multimodal 3.0 tesla MRI and magnetic resonance spectroscopy (1H MRS) study
V Leuzzi, M Tosetti, D Montanaro, et al.
Journal of Endocrinological Investigation
|
February 14, 2013
The Italian screening program for primary congenital hypothyroidism: actions to improve screening, diagnosis, follow-up, and surveillance
A Cassio, C Corbetta, I Antonozzi, et al.
Clinical Genetics
|
January 12, 2010
Phenotypic variability, neurological outcome and genetics background of 6-pyruvoyl-tetrahydropterin synthase deficiency
V Leuzzi, C A Carducci, C L Carducci, et al.
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of 6
Search research articles
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Showing results (51-60 of 55) with videos related to
Sort By:
Page
of 6
You have reached the last page of results.
This site can display upto 55 results.
Pediatric Research
|
March 1, 1990
Guanidino compound analysis as a complementary diagnostic parameter for hyperargininemia: follow-up of guanidino compound levels during therapy
B Marescau, P P De Deyn, A Lowenthal, et al.
Metabolism: Clinical and Experimental
|
September 1, 1992
The pathobiochemistry of uremia and hyperargininemia further demonstrates a metabolic relationship between urea and guanidinosuccinic acid
B Marescau, P P De Deyn, I A Qureshi, et al.
Journal of Inherited Metabolic Disease
|
January 25, 2007
The pathogenesis of the white matter abnormalities in phenylketonuria. A multimodal 3.0 tesla MRI and magnetic resonance spectroscopy (1H MRS) study
V Leuzzi, M Tosetti, D Montanaro, et al.
Journal of Endocrinological Investigation
|
February 14, 2013
The Italian screening program for primary congenital hypothyroidism: actions to improve screening, diagnosis, follow-up, and surveillance
A Cassio, C Corbetta, I Antonozzi, et al.
Clinical Genetics
|
January 12, 2010
Phenotypic variability, neurological outcome and genetics background of 6-pyruvoyl-tetrahydropterin synthase deficiency
V Leuzzi, C A Carducci, C L Carducci, et al.
Page
of 6