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S H Mudd

Showing results (81-90 of 93) with videos related to

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Trends in Genetics : TIG|February 1, 1997
Consensus nomenclature for the mammalian methionine adenosyltransferase genes and gene productsM Kotb, S H Mudd, J M Mato, 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.
American Journal of Human Genetics|January 1, 1987
Hepatic methionine adenosyltransferase deficiency in a 31-year-old manW A Gahl, J D Finkelstein, K D Mullen, et al.
American Journal of Human Genetics|March 21, 2000
Methionine adenosyltransferase I/III deficiency: novel mutations and clinical variationsM E Chamberlin, T Ubagai, S H Mudd, et al.
American Journal of Human Genetics|January 1, 1985
The natural history of homocystinuria due to cystathionine beta-synthase deficiencyS H Mudd, F Skovby, H L Levy, et al.
Journal of Inherited Metabolic Disease|June 1, 2006
S-adenosylhomocysteine hydrolase deficiency in a 26-year-old manN R M Buist, B Glenn, O Vugrek, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Persistent hypermethioninaemia with dominant inheritanceH J Blom, A J Davidson, J D Finkelstein, et al.
Journal of Inherited Metabolic Disease|January 26, 2006
S-Adenosylhomocysteine hydrolase deficiency: a second patient, the younger brother of the index patient, and outcomes during therapyI Barić, M Cuk, K Fumić, et al.
Pageof 10

Showing results (81-90 of 93) with videos related to

Sort By:
Pageof 10
Trends in Genetics : TIG|February 1, 1997
Consensus nomenclature for the mammalian methionine adenosyltransferase genes and gene productsM Kotb, S H Mudd, J M Mato, 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.
American Journal of Human Genetics|January 1, 1987
Hepatic methionine adenosyltransferase deficiency in a 31-year-old manW A Gahl, J D Finkelstein, K D Mullen, et al.
American Journal of Human Genetics|March 21, 2000
Methionine adenosyltransferase I/III deficiency: novel mutations and clinical variationsM E Chamberlin, T Ubagai, S H Mudd, et al.
American Journal of Human Genetics|January 1, 1985
The natural history of homocystinuria due to cystathionine beta-synthase deficiencyS H Mudd, F Skovby, H L Levy, et al.
Journal of Inherited Metabolic Disease|June 1, 2006
S-adenosylhomocysteine hydrolase deficiency in a 26-year-old manN R M Buist, B Glenn, O Vugrek, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Persistent hypermethioninaemia with dominant inheritanceH J Blom, A J Davidson, J D Finkelstein, et al.
Journal of Inherited Metabolic Disease|January 26, 2006
S-Adenosylhomocysteine hydrolase deficiency: a second patient, the younger brother of the index patient, and outcomes during therapyI Barić, M Cuk, K Fumić, et al.
Pageof 10