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M Korson

Showing results (1-10 of 7) with videos related to

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Journal of Pediatric Gastroenterology and Nutrition|January 1, 1995
Metabolic etiologies of cyclic or recurrent vomitingM Korson
Journal of Child Neurology|January 1, 1996
Infantile onset of hereditary ascending spastic paralysis with bulbar involvementT Lerman-Sagie, J Filiano, D W Smith, et al.
Pediatric Cardiology|November 1, 1996
Cardiac mitochondrial dysfunction in Leigh syndromeJ Marin-Garcia, R Ananthakrishnan, M Korson, et al.
European Journal of Human Genetics : EJHG|January 1, 1994
The 8993 mtDNA mutation: heteroplasmy and clinical presentation in three familiesY Tatuch, R A Pagon, B Vlcek, et al.
The Journal of Pediatrics|January 15, 1998
Infantile phosphofructokinase deficiency with arthrogryposis: clinical benefit of a ketogenic dietK J Swoboda, L Specht, H R Jones, et al.
Journal of the American College of Nutrition|April 16, 1999
Protein status of infants with phenylketonuria undergoing nutrition managementP B Acosta, S Yannicelli, B Marriage, et al.
Journal of Inherited Metabolic Disease|March 18, 2003
Newborn screening compared to clinical identification of biochemical genetic disordersS E Waisbren, C Y Read, M Ampola, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Journal of Pediatric Gastroenterology and Nutrition|January 1, 1995
Metabolic etiologies of cyclic or recurrent vomitingM Korson
Journal of Child Neurology|January 1, 1996
Infantile onset of hereditary ascending spastic paralysis with bulbar involvementT Lerman-Sagie, J Filiano, D W Smith, et al.
Pediatric Cardiology|November 1, 1996
Cardiac mitochondrial dysfunction in Leigh syndromeJ Marin-Garcia, R Ananthakrishnan, M Korson, et al.
European Journal of Human Genetics : EJHG|January 1, 1994
The 8993 mtDNA mutation: heteroplasmy and clinical presentation in three familiesY Tatuch, R A Pagon, B Vlcek, et al.
The Journal of Pediatrics|January 15, 1998
Infantile phosphofructokinase deficiency with arthrogryposis: clinical benefit of a ketogenic dietK J Swoboda, L Specht, H R Jones, et al.
Journal of the American College of Nutrition|April 16, 1999
Protein status of infants with phenylketonuria undergoing nutrition managementP B Acosta, S Yannicelli, B Marriage, et al.
Journal of Inherited Metabolic Disease|March 18, 2003
Newborn screening compared to clinical identification of biochemical genetic disordersS E Waisbren, C Y Read, M Ampola, et al.
Pageof 1