Showing results (11-20 of 389) with videos related to
Sort By:
Pageof 39
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.Human Heredity|November 1, 1993
Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency: the prevalent mutation G985 (K304E) is subject to a strong founder effect from northwestern EuropeN Gregersen, V Winter, D Curtis, 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.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.Biomedicine / [Publiee Pour L'A.A.I.C.I.G.]|July 1, 1976
Casein phenotyping in witch's milkA Ponzone, G F VoglinoActa Paediatrica Scandinavica|September 1, 1977
Cellular and humoral factors involvement in the enhanced NBT reduction by neutrophil leucocytes of newborn infantsP A Tovo, A PonzoneThe International Journal of Biological Markers|February 12, 2000
Student report--the fight against cancer and angiogenesis inhibitors: are we entering a new era?M SpadaMaterials Science & Engineering. C, Materials for Biological Applications|February 4, 2016
Antibacterial titanium surfaces for medical implantsS Ferraris, S SprianoPageof 39