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M R Seashore

Showing results (21-30 of 42) with videos related to

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Pediatrics|February 1, 1985
Loss of intellectual function in children with phenylketonuria after relaxation of dietary phenylalanine restrictionM R Seashore, E Friedman, R A Novelly, et al.
Journal of Medical Genetics|October 1, 1981
Complete trisomy 9 in two liveborn infantsS Mantagos, J W McReynolds, M R Seashore, et al.
Pediatrics|December 10, 1999
Development of guidelines for treatment of children with phenylketonuria: report of a meeting at the National Institute of Child Health and Human Development held August 15, 1995, National Institutes of Health, Bethesda, MarylandM R Seashore, R Wappner, S Cho, et al.
Pediatrics|December 10, 1999
Management of phenylketonuria for optimal outcome: a review of guidelines for phenylketonuria management and a report of surveys of parents, patients, and clinic directorsR Wappner, S Cho, R A Kronmal, et al.
The Yale Journal of Biology and Medicine|January 1, 1990
Idiopathic Fanconi syndrome with progressive renal failure: a case report and discussionW S Long, M R Seashore, N J Siegel, et al.
Pediatrics|October 1, 1987
Familial apple peel jejunal atresia: surgical, genetic, and radiographic aspectsJ H Seashore, F S Collins, R I Markowitz, et al.
Obstetrics and Gynecology|June 1, 1988
Prenatal findings in a case of spondylocostal dysplasia type I (Jarcho-Levin syndrome)R Romero, A Ghidini, M S Eswara, et al.
The American Journal of Clinical Nutrition|August 1, 1973
Defective propionate oxidation in leukocytes of vitamin B12-deficient pigs: in vitro correctionM R Seashore, Y E Hsia, K Scully, et al.
JAMA|January 11, 1980
Detection of phenylketonuria in autistic and psychotic childrenT L Lowe, K Tanaka, M R Seashore, et al.
Lancet (London, England)|November 5, 1977
New defect in fatty-acid metabolism with hypoglycemia and organic aciduriaK Tanaka, S Mantagos, M Genel, et al.
Pageof 5

Showing results (21-30 of 42) with videos related to

Sort By:
Pageof 5
Pediatrics|February 1, 1985
Loss of intellectual function in children with phenylketonuria after relaxation of dietary phenylalanine restrictionM R Seashore, E Friedman, R A Novelly, et al.
Journal of Medical Genetics|October 1, 1981
Complete trisomy 9 in two liveborn infantsS Mantagos, J W McReynolds, M R Seashore, et al.
Pediatrics|December 10, 1999
Development of guidelines for treatment of children with phenylketonuria: report of a meeting at the National Institute of Child Health and Human Development held August 15, 1995, National Institutes of Health, Bethesda, MarylandM R Seashore, R Wappner, S Cho, et al.
Pediatrics|December 10, 1999
Management of phenylketonuria for optimal outcome: a review of guidelines for phenylketonuria management and a report of surveys of parents, patients, and clinic directorsR Wappner, S Cho, R A Kronmal, et al.
The Yale Journal of Biology and Medicine|January 1, 1990
Idiopathic Fanconi syndrome with progressive renal failure: a case report and discussionW S Long, M R Seashore, N J Siegel, et al.
Pediatrics|October 1, 1987
Familial apple peel jejunal atresia: surgical, genetic, and radiographic aspectsJ H Seashore, F S Collins, R I Markowitz, et al.
Obstetrics and Gynecology|June 1, 1988
Prenatal findings in a case of spondylocostal dysplasia type I (Jarcho-Levin syndrome)R Romero, A Ghidini, M S Eswara, et al.
The American Journal of Clinical Nutrition|August 1, 1973
Defective propionate oxidation in leukocytes of vitamin B12-deficient pigs: in vitro correctionM R Seashore, Y E Hsia, K Scully, et al.
JAMA|January 11, 1980
Detection of phenylketonuria in autistic and psychotic childrenT L Lowe, K Tanaka, M R Seashore, et al.
Lancet (London, England)|November 5, 1977
New defect in fatty-acid metabolism with hypoglycemia and organic aciduriaK Tanaka, S Mantagos, M Genel, et al.
Pageof 5