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S H MUDD

Showing results (51-60 of 67) with videos related to

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The Journal of Clinical Investigation|October 1, 1995
Molecular mechanisms of an inborn error of methionine pathway. Methionine adenosyltransferase deficiencyT Ubagai, K J Lei, S Huang, et al.
The Journal of Clinical Investigation|August 15, 1996
Demyelination of the brain is associated with methionine adenosyltransferase I/III deficiencyM E Chamberlin, T Ubagai, S H Mudd, et al.
The New England Journal of Medicine|December 2, 1976
Platelet survival and morphology in homocystinuria due to cystathionine synthase deficiencyE R Uhlemann, J H TenPas, A W Lucky, et al.
Journal of Inherited Metabolic Disease|October 2, 2003
Maternal methionine adenosyltransferase I/III deficiency: reproductive outcomes in a woman with four pregnanciesS H Mudd, A Tangerman, S P Stabler, et al.
Journal of Inherited Metabolic Disease|April 23, 2003
Methionine adenosyltransferase I/III deficiency: two Korean compound heterozygous siblings with a novel mutationS Z Kim, E Santamaria, T E Jeong, et al.
Journal of Inherited Metabolic Disease|January 24, 2004
Glycine N -methyltransferase deficiency: a new patient with a novel mutationP Augoustides-Savvopoulou, Z Luka, S Karyda, et al.
The Journal of Biological Chemistry|March 30, 2001
Biochemical basis for the dominant inheritance of hypermethioninemia associated with the R264H mutation of the MAT1A gene. A monomeric methionine adenosyltransferase with tripolyphosphatase activityI Pérez Mato, M M Sanchez del Pino, M E Chamberlin, et al.
Journal of Inherited Metabolic Disease|May 27, 2008
Hypermethioninaemia due to methionine adenosyltransferase I/III (MAT I/III) deficiency: diagnosis in an expanded neonatal screening programmeM L Couce, M D Bóveda, D E Castiñeiras, et al.
The Journal of Clinical Investigation|February 1, 1988
Transsulfuration in an adult with hepatic methionine adenosyltransferase deficiencyW A Gahl, I Bernardini, J D Finkelstein, et al.
American Journal of Human Genetics|October 1, 1995
Isolated persistent hypermethioninemiaS H Mudd, H L Levy, A Tangerman, et al.
Pageof 7

Showing results (51-60 of 67) with videos related to

Sort By:
Pageof 7
The Journal of Clinical Investigation|October 1, 1995
Molecular mechanisms of an inborn error of methionine pathway. Methionine adenosyltransferase deficiencyT Ubagai, K J Lei, S Huang, et al.
The Journal of Clinical Investigation|August 15, 1996
Demyelination of the brain is associated with methionine adenosyltransferase I/III deficiencyM E Chamberlin, T Ubagai, S H Mudd, et al.
The New England Journal of Medicine|December 2, 1976
Platelet survival and morphology in homocystinuria due to cystathionine synthase deficiencyE R Uhlemann, J H TenPas, A W Lucky, et al.
Journal of Inherited Metabolic Disease|October 2, 2003
Maternal methionine adenosyltransferase I/III deficiency: reproductive outcomes in a woman with four pregnanciesS H Mudd, A Tangerman, S P Stabler, et al.
Journal of Inherited Metabolic Disease|April 23, 2003
Methionine adenosyltransferase I/III deficiency: two Korean compound heterozygous siblings with a novel mutationS Z Kim, E Santamaria, T E Jeong, et al.
Journal of Inherited Metabolic Disease|January 24, 2004
Glycine N -methyltransferase deficiency: a new patient with a novel mutationP Augoustides-Savvopoulou, Z Luka, S Karyda, et al.
The Journal of Biological Chemistry|March 30, 2001
Biochemical basis for the dominant inheritance of hypermethioninemia associated with the R264H mutation of the MAT1A gene. A monomeric methionine adenosyltransferase with tripolyphosphatase activityI Pérez Mato, M M Sanchez del Pino, M E Chamberlin, et al.
Journal of Inherited Metabolic Disease|May 27, 2008
Hypermethioninaemia due to methionine adenosyltransferase I/III (MAT I/III) deficiency: diagnosis in an expanded neonatal screening programmeM L Couce, M D Bóveda, D E Castiñeiras, et al.
The Journal of Clinical Investigation|February 1, 1988
Transsulfuration in an adult with hepatic methionine adenosyltransferase deficiencyW A Gahl, I Bernardini, J D Finkelstein, et al.
American Journal of Human Genetics|October 1, 1995
Isolated persistent hypermethioninemiaS H Mudd, H L Levy, A Tangerman, et al.
Pageof 7