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

M A Vilaseca

Showing results (41-50 of 118) with videos related to

Pageof 12
Sort By:
European Journal of Clinical Nutrition|July 25, 2003
Plasma thiols and their determinants in phenylketonuriaC Colomé, R Artuch, C Sierra, et al.
Pediatric Emergency Care|January 4, 2001
Diagnostic approach to inborn errors of metabolism in an emergency unitM Calvo, R Artuch, E Macià, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
A new case of holocarboxylase synthetase deficiencyP Briones, A Ribes, M A Vilaseca, et al.
Clinical Genetics|October 30, 2009
Analysis of the CTNS gene in 32 cystinosis patients from SpainJ Macías-Vidal, M Rodés, J M Hernández-Pérez, et al.
Brain & Development|December 12, 2001
Oxidative stress in Rett syndromeC Sierra, M A Vilaseca, N Brandi, et al.
Journal of Child Neurology|June 1, 2000
Children with stroke: polymorphism of the MTHFR gene, mild hyperhomocysteinemia, and vitamin statusE Cardo, E Monrós, C Colomé, et al.
Revista De Neurologia|November 6, 2008
[Late-onset presentation of carbamoyl phosphate synthetase 1 deficiency in a 6-year-old boy]L Gómez-López, R Artuch, M A Vilaseca, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
Controlled diet in phenylketonuria may cause serum carnitine deficiencyM A Vilaseca, P Briones, I Ferrer, et al.
Developmental Medicine and Child Neurology|March 13, 1999
Fatal haemorrhagic infarct in an infant with homocystinuriaE Cardo, J Campistol, J Caritg, et al.
Anales Espanoles De Pediatria|September 27, 2000
[Proposed protocol for the study of cerebrovascular disease in childhood]E Cardo Jalón, M Pineda Marfà, R Artuch Iriberri, et al.
Pageof 12

Showing results (41-50 of 118) with videos related to

Sort By:
Pageof 12
European Journal of Clinical Nutrition|July 25, 2003
Plasma thiols and their determinants in phenylketonuriaC Colomé, R Artuch, C Sierra, et al.
Pediatric Emergency Care|January 4, 2001
Diagnostic approach to inborn errors of metabolism in an emergency unitM Calvo, R Artuch, E Macià, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
A new case of holocarboxylase synthetase deficiencyP Briones, A Ribes, M A Vilaseca, et al.
Clinical Genetics|October 30, 2009
Analysis of the CTNS gene in 32 cystinosis patients from SpainJ Macías-Vidal, M Rodés, J M Hernández-Pérez, et al.
Brain & Development|December 12, 2001
Oxidative stress in Rett syndromeC Sierra, M A Vilaseca, N Brandi, et al.
Journal of Child Neurology|June 1, 2000
Children with stroke: polymorphism of the MTHFR gene, mild hyperhomocysteinemia, and vitamin statusE Cardo, E Monrós, C Colomé, et al.
Revista De Neurologia|November 6, 2008
[Late-onset presentation of carbamoyl phosphate synthetase 1 deficiency in a 6-year-old boy]L Gómez-López, R Artuch, M A Vilaseca, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
Controlled diet in phenylketonuria may cause serum carnitine deficiencyM A Vilaseca, P Briones, I Ferrer, et al.
Developmental Medicine and Child Neurology|March 13, 1999
Fatal haemorrhagic infarct in an infant with homocystinuriaE Cardo, J Campistol, J Caritg, et al.
Anales Espanoles De Pediatria|September 27, 2000
[Proposed protocol for the study of cerebrovascular disease in childhood]E Cardo Jalón, M Pineda Marfà, R Artuch Iriberri, et al.
Pageof 12