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I Antonozzi

Showing results (51-60 of 55) with videos related to

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Pediatric Research|March 1, 1990
Guanidino compound analysis as a complementary diagnostic parameter for hyperargininemia: follow-up of guanidino compound levels during therapyB 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 acidB 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) studyV 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 surveillanceA Cassio, C Corbetta, I Antonozzi, et al.
Clinical Genetics|January 12, 2010
Phenotypic variability, neurological outcome and genetics background of 6-pyruvoyl-tetrahydropterin synthase deficiencyV Leuzzi, C A Carducci, C L Carducci, et al.
Pageof 6

Showing results (51-60 of 55) with videos related to

Sort By:
Pageof 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 therapyB 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 acidB 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) studyV 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 surveillanceA Cassio, C Corbetta, I Antonozzi, et al.
Clinical Genetics|January 12, 2010
Phenotypic variability, neurological outcome and genetics background of 6-pyruvoyl-tetrahydropterin synthase deficiencyV Leuzzi, C A Carducci, C L Carducci, et al.
Pageof 6