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

K Michals-Matalon

Showing results (1-10 of 13) with videos related to

Pageof 2
Sort By:
Advances in Pediatrics|January 25, 2000
Recent advances in Canavan diseaseR Matalon, K Michals-Matalon
Prenatal Diagnosis|July 27, 1999
Prenatal diagnosis of Canavan diseaseR Matalon, K Michals-Matalon
Neurochemical Research|May 5, 1999
Biochemistry and molecular biology of Canavan diseaseR Matalon, K Michals-Matalon
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 21, 2000
Molecular basis of Canavan diseaseR Matalon, K Michals-Matalon
Frontiers in Bioscience : a Journal and Virtual Library|March 8, 2000
Spongy degeneration of the brain, Canavan disease: biochemical and molecular findingsR M Matalon, K Michals-Matalon
Neuroscience Letters|March 16, 2004
Mental retardation and hypotonia seen in the knock out mouse for Canavan disease is not due to succinate semialdehyde dehydrogenase deficiencyS Surendran, E L Ezell, M J Quast, et al.
International Journal of Immunopathology and Pharmacology|September 17, 2005
Abnormal expression of genes associated with development and inflammation in the heart of mouse maternal phenylketonuria offspringR Matalon, S Surendran, J D McDonald, et al.
The Journal of Pediatrics|September 1, 1994
Maternal mild hyperphenylalaninemia: results of treated and untreated pregnancies in two sistersH L Levy, B S Goss, D K Sullivan, et al.
Journal of Inherited Metabolic Disease|September 22, 2006
Large neutral amino acids in the treatment of phenylketonuria (PKU)R Matalon, K Michals-Matalon, G Bhatia, et al.
Annals of the New York Academy of Sciences|March 15, 1993
The effect of nutrient intake on pregnancy outcome in maternal phenylketonuriaR Koch, E Wenz, C Azen, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Advances in Pediatrics|January 25, 2000
Recent advances in Canavan diseaseR Matalon, K Michals-Matalon
Prenatal Diagnosis|July 27, 1999
Prenatal diagnosis of Canavan diseaseR Matalon, K Michals-Matalon
Neurochemical Research|May 5, 1999
Biochemistry and molecular biology of Canavan diseaseR Matalon, K Michals-Matalon
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 21, 2000
Molecular basis of Canavan diseaseR Matalon, K Michals-Matalon
Frontiers in Bioscience : a Journal and Virtual Library|March 8, 2000
Spongy degeneration of the brain, Canavan disease: biochemical and molecular findingsR M Matalon, K Michals-Matalon
Neuroscience Letters|March 16, 2004
Mental retardation and hypotonia seen in the knock out mouse for Canavan disease is not due to succinate semialdehyde dehydrogenase deficiencyS Surendran, E L Ezell, M J Quast, et al.
International Journal of Immunopathology and Pharmacology|September 17, 2005
Abnormal expression of genes associated with development and inflammation in the heart of mouse maternal phenylketonuria offspringR Matalon, S Surendran, J D McDonald, et al.
The Journal of Pediatrics|September 1, 1994
Maternal mild hyperphenylalaninemia: results of treated and untreated pregnancies in two sistersH L Levy, B S Goss, D K Sullivan, et al.
Journal of Inherited Metabolic Disease|September 22, 2006
Large neutral amino acids in the treatment of phenylketonuria (PKU)R Matalon, K Michals-Matalon, G Bhatia, et al.
Annals of the New York Academy of Sciences|March 15, 1993
The effect of nutrient intake on pregnancy outcome in maternal phenylketonuriaR Koch, E Wenz, C Azen, et al.
Pageof 2