Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Nicola Longo

Showing results (1-10 of 501) with videos related to

Pageof 51
Sort By:
Annals of Nutrition & Metabolism|December 9, 2016
Primary Carnitine Deficiency and Newborn Screening for Disorders of the Carnitine CycleNicola Longo
Molecular Genetics and Metabolism|February 4, 2012
SIMD statement on investigational new drugs for rare disease therapiesNicola Longo
Journal of Inherited Metabolic Disease|February 24, 2009
Disorders of biopterin metabolismNicola Longo
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|April 8, 2006
Inborn errors of metabolism: new challenges with expanded newborn screening programsNicola Longo
Neurologic Clinics|January 28, 2004
Mitochondrial encephalopathyNicola Longo
Expert Opinion on Pharmacotherapy|February 10, 2015
Alternative therapies to address the unmet medical needs of patients with phenylketonuriaNenad Blau, Nicola Longo
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|February 22, 2011
Newborn screening and inborn errors of metabolismMarzia Pasquali, Nicola Longo
Molecular Genetics and Metabolism|April 27, 2023
Phenylketonuria and the brainValentina Rovelli, Nicola Longo
Human Mutation|March 23, 2013
Response to chen et Al.: carnitine uptake defect (primary carnitine deficiency): risk in genotype-phenotype correlationMarzia Pasquali, Nicola Longo
Molecular Genetics and Metabolism|April 22, 2014
National Institutes of Health (NIH) review of evidence in phenylalanine hydroxylase deficiency (phenylketonuria) and recommendations/guidelines for therapy from the American College of Medical Genetics (ACMG) and Genetics Metabolic Dietitians International (GMDI)Carol L Greene, Nicola Longo
Pageof 51

Showing results (1-10 of 501) with videos related to

Sort By:
Pageof 51
Annals of Nutrition & Metabolism|December 9, 2016
Primary Carnitine Deficiency and Newborn Screening for Disorders of the Carnitine CycleNicola Longo
Molecular Genetics and Metabolism|February 4, 2012
SIMD statement on investigational new drugs for rare disease therapiesNicola Longo
Journal of Inherited Metabolic Disease|February 24, 2009
Disorders of biopterin metabolismNicola Longo
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|April 8, 2006
Inborn errors of metabolism: new challenges with expanded newborn screening programsNicola Longo
Neurologic Clinics|January 28, 2004
Mitochondrial encephalopathyNicola Longo
Expert Opinion on Pharmacotherapy|February 10, 2015
Alternative therapies to address the unmet medical needs of patients with phenylketonuriaNenad Blau, Nicola Longo
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|February 22, 2011
Newborn screening and inborn errors of metabolismMarzia Pasquali, Nicola Longo
Molecular Genetics and Metabolism|April 27, 2023
Phenylketonuria and the brainValentina Rovelli, Nicola Longo
Human Mutation|March 23, 2013
Response to chen et Al.: carnitine uptake defect (primary carnitine deficiency): risk in genotype-phenotype correlationMarzia Pasquali, Nicola Longo
Molecular Genetics and Metabolism|April 22, 2014
National Institutes of Health (NIH) review of evidence in phenylalanine hydroxylase deficiency (phenylketonuria) and recommendations/guidelines for therapy from the American College of Medical Genetics (ACMG) and Genetics Metabolic Dietitians International (GMDI)Carol L Greene, Nicola Longo
Pageof 51