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K Michals

Showing results (11-20 of 30) with videos related to

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American Journal of Public Health|January 1, 1985
Reinstitution of diet therapy in PKU patients from twenty-two US clinicsV E Schuett, E S Brown, K Michals
Journal of Inherited Metabolic Disease|January 1, 1988
Carrier detection for Sanfilippo A syndromeR Matalon, M Deanching, R Marback, et al.
Journal of the American College of Nutrition|April 1, 1997
Phenylketonuria: current dietary treatment practices in the United States and CanadaR O Fisch, R Matalon, S Weisberg, et al.
Journal of Inherited Metabolic Disease|January 1, 1982
The use of deuterated phenylalanine for the in vivo assay of phenylalanine hydroxylase activity in childrenR Matalon, D E Matthews, K Michals, et al.
Pediatrics|April 1, 1983
Nonketotic hyperglycinemia: treatment with diazepam--a competitor for glycine receptorsR Matalon, S Naidu, J R Hughes, et al.
Biochemical Medicine|August 1, 1983
Glucose-6-phosphatase as a marker for tumors of liver and kidney originK Michals, K Pringle, E J Pang, et al.
Journal of the American Dietetic Association|October 1, 1988
Blood phenylalanine levels and intelligence of 10-year-old children with PKU in the National Collaborative StudyK Michals, C Azen, P Acosta, et al.
Clinical Pediatrics|June 1, 1992
A treatment program for adolescents with phenylketonuriaL A Gleason, K Michals, R Matalon, et al.
American Journal of Medical Genetics|February 1, 1988
Aspartoacylase deficiency and N-acetylaspartic aciduria in patients with Canavan diseaseR Matalon, K Michals, D Sebesta, et al.
American Journal of Human Genetics|July 1, 1994
Canavan disease: mutations among Jewish and non-Jewish patientsR Kaul, G P Gao, M Aloya, et al.
Pageof 3

Showing results (11-20 of 30) with videos related to

Sort By:
Pageof 3
American Journal of Public Health|January 1, 1985
Reinstitution of diet therapy in PKU patients from twenty-two US clinicsV E Schuett, E S Brown, K Michals
Journal of Inherited Metabolic Disease|January 1, 1988
Carrier detection for Sanfilippo A syndromeR Matalon, M Deanching, R Marback, et al.
Journal of the American College of Nutrition|April 1, 1997
Phenylketonuria: current dietary treatment practices in the United States and CanadaR O Fisch, R Matalon, S Weisberg, et al.
Journal of Inherited Metabolic Disease|January 1, 1982
The use of deuterated phenylalanine for the in vivo assay of phenylalanine hydroxylase activity in childrenR Matalon, D E Matthews, K Michals, et al.
Pediatrics|April 1, 1983
Nonketotic hyperglycinemia: treatment with diazepam--a competitor for glycine receptorsR Matalon, S Naidu, J R Hughes, et al.
Biochemical Medicine|August 1, 1983
Glucose-6-phosphatase as a marker for tumors of liver and kidney originK Michals, K Pringle, E J Pang, et al.
Journal of the American Dietetic Association|October 1, 1988
Blood phenylalanine levels and intelligence of 10-year-old children with PKU in the National Collaborative StudyK Michals, C Azen, P Acosta, et al.
Clinical Pediatrics|June 1, 1992
A treatment program for adolescents with phenylketonuriaL A Gleason, K Michals, R Matalon, et al.
American Journal of Medical Genetics|February 1, 1988
Aspartoacylase deficiency and N-acetylaspartic aciduria in patients with Canavan diseaseR Matalon, K Michals, D Sebesta, et al.
American Journal of Human Genetics|July 1, 1994
Canavan disease: mutations among Jewish and non-Jewish patientsR Kaul, G P Gao, M Aloya, et al.
Pageof 3