(Q39107247)
Statements
1 reference
Organic Acidemias (English)
1 March 1976
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1 reference
61-78
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293
314
Prenatal therapy of a patient with vitamin B^-responsive methylmalonic acidemia (English)
Ampola
1975
78
827
Propionic acidemia in patients with ketotic hyperglycinemia (English)
Ando
1971
2
244
Biotin-responsive propionic acidemia (English)
Barnes
1970
49
423
A defect in pyruvate decarboxylase in a child with an intermittent movement disorder (English)
Blass
1970
51
1845
An inherited defect affecting the tricar boxylic acid cycle in a patient with congenital lactic acidosis (English)
Blass
0 references
7
149
An inherited disorder of isoleucine ca tabolism causing accumulation of a-methyl-/3-hydroxybutyrate, and intermittent metabolic acidosis (English)
Daum
1973
187
1082
Absence of pyruvate decarboxylase activity in man: A cause of congenital lactic acidosis (English)
Farrell
1975
1
1140
Localization of enzymic defect in propionic acidemia (English)
Gompertz
1970
2
22
Biotin-responsiveβ-methylcrotonylglycin- uria (English)
Gompertz
1971
48
975
Child with a defect in leucine metabolism as sociated with /3-hydroxyisovaleric aciduria and /3-methylcrotonylglycinuria (English)
Gompertz
1973
57
269
A defect in Z-isoleucine metabo lism associated with ?-methyl-β-hydroxybutyric and a-methylacetoacetic aciduria: Quantitative in vivo and in vitro studies (English)
Gompertz
1974
8
244
Prenatal diagnosis and family studies in a case of propionic acidemia (English)
Gompertz
1975
4
500
Homocystinuria with methylmalonic- aciduria: Two cases in a sibship (English)
Goodman
1970
12
12
Glutaric aciduria: A "new" disorder of amino acid metabolism (English)
Goodman
1975
43
423
Leigh's encephalopathy: An inborn error of gluconeogenesis (English)
Hommes
1968
2
519
Propionic acidemia, a new inborn error of metabolism (English)
Hommes
1968
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Identifiers
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