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Showing results (41-50 of 55) with videos related to

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Human Mutation|April 1, 1998
Eight new mutations of the phenylalanine hydroxylase gene in Italian patients with hyperphenylalaninemiaP Bosco, F Cali, C Meli, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|December 3, 2003
Physical activity modulates effects of some genetic polymorphisms affecting cardiovascular risk in men aged over 40 yearsL Pisciotta, A Cantafora, A Piana, et al.
Clinical Genetics|November 1, 1983
Incidence of classic PKU in Italy estimated from consanguineous marriages and from neonatal screeningG Romeo, P Menozzi, A Ferlini, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
Haplotype distribution and molecular defects of PKU in ItalyI Dianzani, C Camaschella, G Saglio, et al.
Human Genetics|November 1, 1990
Haplotype distribution and molecular defects at the phenylalanine hydroxylase locus in ItalyI Dianzani, M Devoto, C Camaschella, 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.
Cephalalgia : an International Journal of Headache|May 12, 2006
Metabolic and genetic risk factors for migraine in childrenF Bottini, M E Celle, M G Calevo, et al.
Human Genetics|January 1, 1982
Duplication of the short arm of chromosome 9. Analysis of five casesC Cuoco, G Gimelli, F Pasquali, et al.
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.
Journal of Inherited Metabolic Disease|July 15, 2000
Genotype-phenotype correlation in dihydropteridine reductase deficiencyL de Sanctis, C Alliaudi, M Spada, et al.
Pageof 6

Showing results (41-50 of 55) with videos related to

Sort By:
Pageof 6
Human Mutation|April 1, 1998
Eight new mutations of the phenylalanine hydroxylase gene in Italian patients with hyperphenylalaninemiaP Bosco, F Cali, C Meli, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|December 3, 2003
Physical activity modulates effects of some genetic polymorphisms affecting cardiovascular risk in men aged over 40 yearsL Pisciotta, A Cantafora, A Piana, et al.
Clinical Genetics|November 1, 1983
Incidence of classic PKU in Italy estimated from consanguineous marriages and from neonatal screeningG Romeo, P Menozzi, A Ferlini, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
Haplotype distribution and molecular defects of PKU in ItalyI Dianzani, C Camaschella, G Saglio, et al.
Human Genetics|November 1, 1990
Haplotype distribution and molecular defects at the phenylalanine hydroxylase locus in ItalyI Dianzani, M Devoto, C Camaschella, 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.
Cephalalgia : an International Journal of Headache|May 12, 2006
Metabolic and genetic risk factors for migraine in childrenF Bottini, M E Celle, M G Calevo, et al.
Human Genetics|January 1, 1982
Duplication of the short arm of chromosome 9. Analysis of five casesC Cuoco, G Gimelli, F Pasquali, et al.
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.
Journal of Inherited Metabolic Disease|July 15, 2000
Genotype-phenotype correlation in dihydropteridine reductase deficiencyL de Sanctis, C Alliaudi, M Spada, et al.
Pageof 6