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The Journal of Clinical Investigation
|
September 1, 1976
Type II hyperprolinemia. Delta1-pyrroline-5-carboxylic acid dehydrogenase deficiency in cultured skin fibroblasts and circulating lymphocytes
D Valle, S I Goodman, D A Applegarth, et al.
The Journal of Pediatrics
|
September 1, 1983
Multiple acyl-CoA dehydrogenase deficiency occurring in pregnancy and caused by a defect in riboflavin metabolism in the mother. Study of a kindred with seven deaths in infancy: Value of riboflavin therapy in preventing this syndrome
J P Harpey, C Charpentier, S I Goodman, et al.
The Journal of Pediatrics
|
January 1, 1978
Propionic acidemia with severe hyperammonemia and defective glycine metabolism
T Shafai, L Sweetman, W Weyler, et al.
Biochemical Medicine
|
January 1, 1975
Glutaric aciduria; a "new" disorder of amino acid metabolism
S I Goodman, S P Markey, P G Moe, et al.
Biochemical Medicine
|
December 1, 1970
Homocystinuria with methylmalonic aciduria: two cases in a sibship
S I Goodman, P G Moe, K B Hammond, et al.
Pediatric Pathology
|
July 1, 1992
X-linked myotubular myopathy: a case report of prenatal and perinatal aspects
R W Tyson, S P Ringel, D K Manchester, et al.
The Journal of Pediatrics
|
May 1, 1977
Glutaric aciduria: biochemical and morphologic considerations
S I Goodman, M D Norenberg, R H Shikes, et al.
Biochemical Medicine
|
August 1, 1974
Defective hydroxyproline metabolism in type II hyperprolinemia
S I Goodman, J W Mace, B S Miles, et al.
Annals of Internal Medicine
|
January 1, 1980
Fanconi's syndrome and distal renal tubular acidosis after glue sniffing
A H Moss, P A Gabow, W D Kaehny, et al.
The Journal of Biological Chemistry
|
December 23, 1994
Expression and characterization of human and chimeric human-Paracoccus denitrificans electron transfer flavoproteins
K R Herrick, D Salazar, S I Goodman, et al.
Page
of 13
Search research articles
Search
Showing results (71-80 of 130) with videos related to
Sort By:
Page
of 13
The Journal of Clinical Investigation
|
September 1, 1976
Type II hyperprolinemia. Delta1-pyrroline-5-carboxylic acid dehydrogenase deficiency in cultured skin fibroblasts and circulating lymphocytes
D Valle, S I Goodman, D A Applegarth, et al.
The Journal of Pediatrics
|
September 1, 1983
Multiple acyl-CoA dehydrogenase deficiency occurring in pregnancy and caused by a defect in riboflavin metabolism in the mother. Study of a kindred with seven deaths in infancy: Value of riboflavin therapy in preventing this syndrome
J P Harpey, C Charpentier, S I Goodman, et al.
The Journal of Pediatrics
|
January 1, 1978
Propionic acidemia with severe hyperammonemia and defective glycine metabolism
T Shafai, L Sweetman, W Weyler, et al.
Biochemical Medicine
|
January 1, 1975
Glutaric aciduria; a "new" disorder of amino acid metabolism
S I Goodman, S P Markey, P G Moe, et al.
Biochemical Medicine
|
December 1, 1970
Homocystinuria with methylmalonic aciduria: two cases in a sibship
S I Goodman, P G Moe, K B Hammond, et al.
Pediatric Pathology
|
July 1, 1992
X-linked myotubular myopathy: a case report of prenatal and perinatal aspects
R W Tyson, S P Ringel, D K Manchester, et al.
The Journal of Pediatrics
|
May 1, 1977
Glutaric aciduria: biochemical and morphologic considerations
S I Goodman, M D Norenberg, R H Shikes, et al.
Biochemical Medicine
|
August 1, 1974
Defective hydroxyproline metabolism in type II hyperprolinemia
S I Goodman, J W Mace, B S Miles, et al.
Annals of Internal Medicine
|
January 1, 1980
Fanconi's syndrome and distal renal tubular acidosis after glue sniffing
A H Moss, P A Gabow, W D Kaehny, et al.
The Journal of Biological Chemistry
|
December 23, 1994
Expression and characterization of human and chimeric human-Paracoccus denitrificans electron transfer flavoproteins
K R Herrick, D Salazar, S I Goodman, et al.
Page
of 13