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O Guardamagna

Showing results (31-40 of 36) with videos related to

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Helvetica Paediatrica Acta|December 1, 1985
Bethanechol versus antiacids in the treatment of gastroesophageal refluxP Levi, F Marmo, C Saluzzo, et al.
The Journal of Pediatrics|December 1, 1984
DHPR deficiency in ItalyA Ponzone, V Ricca, S Ferraris, et al.
The Journal of Pediatrics|August 1, 1994
Recurrent episodes of bizarre behavior in a boy with ornithine transcarbamylase deficiency: diagnostic failure of protein loading and allopurinol challenge testsM Spada, O Guardamagna, D Rabier, et al.
European Journal of Clinical Investigation|November 3, 2007
Beta-sitosterolaemia: a new nonsense mutation in the ABCG5 geneL Mannucci, O Guardamagna, P Bertucci, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Maple syrup urine disease (MSUD): screening for known mutations in Italian patientsT Parrella, S Surrey, A Iolascon, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Prenatal diagnosis of atypical phenylketonuriaN Blau, A Niederwieser, H C Curtius, et al.
Pageof 4

Showing results (31-40 of 36) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 36 results.
Helvetica Paediatrica Acta|December 1, 1985
Bethanechol versus antiacids in the treatment of gastroesophageal refluxP Levi, F Marmo, C Saluzzo, et al.
The Journal of Pediatrics|December 1, 1984
DHPR deficiency in ItalyA Ponzone, V Ricca, S Ferraris, et al.
The Journal of Pediatrics|August 1, 1994
Recurrent episodes of bizarre behavior in a boy with ornithine transcarbamylase deficiency: diagnostic failure of protein loading and allopurinol challenge testsM Spada, O Guardamagna, D Rabier, et al.
European Journal of Clinical Investigation|November 3, 2007
Beta-sitosterolaemia: a new nonsense mutation in the ABCG5 geneL Mannucci, O Guardamagna, P Bertucci, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Maple syrup urine disease (MSUD): screening for known mutations in Italian patientsT Parrella, S Surrey, A Iolascon, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Prenatal diagnosis of atypical phenylketonuriaN Blau, A Niederwieser, H C Curtius, et al.
Pageof 4