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Pediatric Research|February 1, 1993
Catalytic activity of tetrahydrobiopterin in dihydropteridine reductase deficiency and indications for treatmentA Ponzone, O Guardamagna, I Dianzani, et al.Human Mutation|January 1, 1997
Identification of mutations causing 6-pyruvoyl-tetrahydropterin synthase deficiency in four Italian familiesT Oppliger, B Thöny, C Kluge, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|July 16, 1993
Hyperphenylalaninemia and pterin metabolism in serum and erythrocytesA Ponzone, O Guardamagna, M Spada, et al.Clinical Nephrology|January 5, 2002
Cystinuria phenotyping by oral lysine and arginine loadingL de Sanctis, G Bonetti, M Bruno, et al.Journal of Inherited Metabolic Disease|January 1, 1989
RFLPs of the phenylalanine hydroxylase gene in the Italian populationI Dianzani, L Farinasso, P Fortina, et al.Helvetica Paediatrica Acta|December 1, 1985
Bethanechol versus antiacids in the treatment of gastroesophageal refluxP Levi, F Marmo, C Saluzzo, et al.European Journal of Soil Science|June 26, 2018
The effect of microbial activity on soil water diffusivityB U Choudhury, S Ferraris, R W Ashton, et al.Analytical Biochemistry|February 15, 1989
Determination of physostigmine in plasma by high-performance liquid chromatography and fluorescence detectionN M Elsayed, J R Ryabik, S Ferraris, et al.Human Heredity|October 6, 2001
Genetic heterogeneity in five Italian regions: analysis of PAH mutations and minihaplotypesS Giannattasio, I Dianzani, P Lattanzio, 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.Pageof 7