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

R Matalon

Showing results (141-150 of 185) with videos related to

Pageof 19
Sort By:
Lancet (London, England)|June 14, 1975
Letter: Phenotypic variation in alpha-L-iduronidase deficiencyJ Leisti, D L Rimoin, M M Kaback, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 14, 2023
Clinical, technical, and environmental biases influencing equitable access to clinical genetics/genomics testing: A points to consider statement of the American College of Medical Genetics and Genomics (ACMG)Dena R Matalon, Cinthya J Zepeda-Mendoza, Mahmoud Aarabi, et al.
European Journal of Clinical Nutrition|August 3, 2017
Long-term treatment of phenylketonuria with a new medical food containing large neutral amino acidsD Concolino, I Mascaro, M T Moricca, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Maternal PKU collaborative study: the effect of nutrient intake on pregnancy outcomeR Matalon, K Michals, C Azen, et al.
European Journal of Pediatrics|July 1, 1996
The International Collaborative Study on maternal phenylketonuria: organization, study design and description of the sampleE G Friedman, R Koch, C Azen, et al.
European Journal of Clinical Nutrition|September 15, 2016
Long-term treatment of phenylketonuria with a new medical food containing large neutral amino acidsD Concolino, I Mascaro, M T Moricca, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Prenatal diagnosis for Canavan disease: the use of DNA markersR Matalon, R Kaul, G P Gao, 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.
American Journal of Human Genetics|July 1, 1996
Identification and expression of eight novel mutations among non-Jewish patients with Canavan diseaseR Kaul, G P Gao, R Matalon, et al.
Pageof 19

Showing results (141-150 of 185) with videos related to

Sort By:
Pageof 19
Lancet (London, England)|June 14, 1975
Letter: Phenotypic variation in alpha-L-iduronidase deficiencyJ Leisti, D L Rimoin, M M Kaback, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 14, 2023
Clinical, technical, and environmental biases influencing equitable access to clinical genetics/genomics testing: A points to consider statement of the American College of Medical Genetics and Genomics (ACMG)Dena R Matalon, Cinthya J Zepeda-Mendoza, Mahmoud Aarabi, et al.
European Journal of Clinical Nutrition|August 3, 2017
Long-term treatment of phenylketonuria with a new medical food containing large neutral amino acidsD Concolino, I Mascaro, M T Moricca, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Maternal PKU collaborative study: the effect of nutrient intake on pregnancy outcomeR Matalon, K Michals, C Azen, et al.
European Journal of Pediatrics|July 1, 1996
The International Collaborative Study on maternal phenylketonuria: organization, study design and description of the sampleE G Friedman, R Koch, C Azen, et al.
European Journal of Clinical Nutrition|September 15, 2016
Long-term treatment of phenylketonuria with a new medical food containing large neutral amino acidsD Concolino, I Mascaro, M T Moricca, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Prenatal diagnosis for Canavan disease: the use of DNA markersR Matalon, R Kaul, G P Gao, 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.
American Journal of Human Genetics|July 1, 1996
Identification and expression of eight novel mutations among non-Jewish patients with Canavan diseaseR Kaul, G P Gao, R Matalon, et al.
Pageof 19