Published in J Ment Defic Res on December 01, 1968
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Purine nucleoside phosphorylase deficiency associated with selective cellular immunodeficiency. N Engl J Med (1977) 2.12
Catecholamines in attention-deficit hyperactivity disorder: current perspectives. J Am Acad Child Adolesc Psychiatry (1996) 1.89
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Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: identification of a new inborn error of mitochondrial fatty acid beta-oxidation. J Inherit Metab Dis (1990) 1.55
Glutaric aciduria type II: report on a previously undescribed metabolic disorder. Clin Chim Acta (1976) 1.44
Inborn errors of molybdenum metabolism: combined deficiencies of sulfite oxidase and xanthine dehydrogenase in a patient lacking the molybdenum cofactor. Proc Natl Acad Sci U S A (1980) 1.39
Determination of the absolute configuration of some biologically important urinary 2-hydroxydicarboxylic acids by capillary gas--liquid chromatography. J Chromatogr (1981) 1.36
Sudden child death and 'healthy' affected family members with medium-chain acyl-coenzyme A dehydrogenase deficiency. Pediatrics (1986) 1.33
Hereditary mitochondrial myopathy with lactic acidemia, a De Toni-Fanconi-Debré syndrome, and a defective respiratory chain in voluntary striated muscles. Pediatr Res (1977) 1.29
Biogenic amines and depression. Biochemical and pharmacological separation of two types of depression. Arch Gen Psychiatry (1975) 1.17
Treatment of a patient with histidinemia. Acta Paediatr Scand (1967) 1.15
Sudden infant death and long-chain 3-hydroxyacyl-CoA dehydrogenase. Lancet (1989) 1.15
Catecholamine metabolism, depressive illness, and drug response. Arch Gen Psychiatry (1972) 1.14
3-Hydroxydicarboxylic aciduria due to long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency associated with sudden neonatal death: protective effect of medium-chain triglyceride treatment. Eur J Pediatr (1991) 1.11
Distinct regional and subcellular localization of adenylyl cyclases type 1 and 8 in mouse brain. Neuroscience (2007) 1.08
New defects of pyrimidine metabolism. Adv Exp Med Biol (1984) 1.08
Adenylosuccinase deficiency: an inborn error of purine nucleotide synthesis. Eur J Pediatr (1988) 1.08
D-lactic aciduria, an inborn error of metabolism? Clin Chim Acta (1977) 1.08
Dihydropyrimidine dehydrogenase deficiency leading to thymine-uraciluria. An inborn error of pyrimidine metabolism. Clin Chim Acta (1984) 1.07
Prenatal diagnosis of glutaric aciduria type II by direct chemical analysis of dicarboxylic acids in amniotic fluid. Eur J Pediatr (1984) 1.06
Combined deficiency of xanthine oxidase and sulphite oxidase: a defect of molybdenum metabolism or transport? J Inherit Metab Dis (1978) 1.04
Octanoic acidemia and octanoylcarnitine excretion with dicarboxylic aciduria due to defective oxidation of medium-chain fatty acids. J Pediatr (1985) 1.02
Behavioral effects of stimulation of the nucleus locus coeruleus in the stump-tailed monkey Macaca arctoides. Brain Res (1976) 1.00
Inherited 3-methylglutaconic aciduria in two brothers--another defect of leucine metabolism. J Pediatr (1982) 1.00
A patient with alpha-ketoadipic and alpha-aminoadipic aciduria. J Inherit Metab Dis (1984) 0.99
Alpha-ketoadipic aciduria, a new inborn error of lysine metabolism; biochemical studies. Clin Chim Acta (1975) 0.99
Medium-chain acyl-CoA dehydrogenase deficiency in two siblings with a Reye-like syndrome. J Pediatr (1985) 0.98
Adenosine triphosphate--metal--norepinephrine ternary complexes and catecholamine binding. Nature (1965) 0.96
(2-Ethoxyethoxy)acetic acid: an unusual compound found in the gas chromatographic analysis of urinary organic acids. Clin Chim Acta (1977) 0.95
Diverse spore rains and limited local exchange shape fern genetic diversity in a recently created habitat colonized by long-distance dispersal. Ann Bot (2012) 0.93
Deficiency of fumarylacetoacetase in a patient with hereditary tyrosinemia. Clin Chim Acta (1981) 0.93
The timing, specificity and clinical prediction of tricyclic drug effects in depression. Psychol Med (1987) 0.93
Erythrocyte metabolism in purine nucleoside phosphorylase deficiency after enzyme replacement therapy by infusion of erythrocytes. J Clin Invest (1980) 0.93
A variant form of branched-chain keto aciduria. Acta Paediatr Scand (1971) 0.92
Central biogenic amine metabolism in children with the syndrome of chronic multiple tics of Gilles de la Tourette: norepinephrine, serotonin, and dopamine. J Am Acad Child Psychiatry (1979) 0.92
Beta-mannosidosis in two brothers with hearing loss. J Inherit Metab Dis (1988) 0.91
Cis-4-decenoic acid in plasma: a characteristic metabolite in medium-chain acyl-CoA dehydrogenase deficiency. Clin Chem (1988) 0.91
Report on a new patient with combined deficiencies of sulphite oxidase and xanthine dehydrogenase due to molybdenum cofactor deficiency. Eur J Pediatr (1988) 0.91
Absence of hepatic molybdenum cofactor: an inborn error of metabolism leading to a combined deficiency of sulphite oxidase and xanthine dehydrogenase. J Inherit Metab Dis (1983) 0.90
Co-ordination chemistry and membrane function with particular reference to the synapse and catecholamine transport. Nature (1965) 0.90
Secondary carnitine deficiency. J Clin Chem Clin Biochem (1990) 0.90
Biochemical basis of prolidase deficiency. Polypeptide and RNA phenotypes and the relation to clinical phenotypes. J Clin Invest (1990) 0.90
Pretreatment DST and hypothalamic-pituitary-adrenocortical function in depressed patients and comparison groups. A multicenter study. Arch Gen Psychiatry (1984) 0.89
The urinary excretion of ethylmalonic acid: what level requires further attention? Biochem Med (1983) 0.89
The effect of deoxyguanosine on human lymphocyte function. I. Analysis of the interference with lymphocyte proliferation in vitro. J Immunol (1984) 0.89
5-oxoprolinuria due to hereditary 5-oxoprolinase deficiency in two brothers--a new inborn error of the gamma-glutamyl cycle. Acta Paediatr Scand (1981) 0.88
Stable isotope dilution analysis of succinylacetone using electron capture negative ion mass fragmentography: an accurate approach to the pre- and neonatal diagnosis of hereditary tyrosinemia type I. Clin Chim Acta (1988) 0.88
Familial hyperlysinaemia due to L-lysine alpha-ketoglutarate reductase deficiency: results of attempted treatment. J Inherit Metab Dis (1978) 0.88
Effects of fire ant venom alkaloids on platelet and neutrophil function. Life Sci (1993) 0.88
An improved procedure of 3-methoxy-4-hydroxyphenyl-ethylene glycol determination by gas-liquid chromatography. Anal Biochem (1970) 0.88
In vivo studies of the metabolism of norepinephrine in the central nervous system. J Pharmacol Exp Ther (1968) 0.87
The time course of noradrenergic pre- and postsynaptic activity during chronic desipramine treatment. Eur J Pharmacol (1980) 0.87
Isolated biotin-resistant 3-methylcrotonyl-CoA carboxylase deficiency in two sibs. Eur J Pediatr (1982) 0.87
Effects of thiamine in a patient with a variant form of branched-chian ketoaciduria. Acta Paediatr Scand (1978) 0.87
O-phosphohydroxylysinuria: a new inborn error of metabolism? Clin Chim Acta (1990) 0.87
Can the spread of agriculture in Europe be followed by tracing the spread of the weed Silene latifolia. A RAPD study. Theor Appl Genet (1996) 0.86
Adrenocortical steroid hormones, electrolytes, and the disposition of the catecholamines with particular reference to depressive states. J Psychiatr Res (1972) 0.86
CSF and urinary biogenic amines and metabolites in depression and mania. A controlled, univariate analysis. Arch Gen Psychiatry (1983) 0.86
Human molybdenum cofactor deficiency. Adv Exp Med Biol (1993) 0.86
Propionyl-CoA carboxylase deficiency with overflow of metabolites of isoleucine catabolism at all levels. Eur J Pediatr (1979) 0.86
Diagnosis of medium-chain acyl-CoA dehydrogenase deficiency in lymphocytes and liver by a gas chromatographic method: the effect of oral riboflavin supplementation. Pediatr Res (1992) 0.85
Primary affective disorder, clinical state change, and MHPG excretion: a longitudinal study. Arch Gen Psychiatry (1978) 0.85
The cerebro-costo-mandibular syndrome: third report of familial occurrence. Clin Genet (1985) 0.85
Dihydropyrimidine dehydrogenase deficiency leading to thymine-uraciluria. An inborn error of pyrimidine metabolism. J Inherit Metab Dis (1985) 0.85
Linear relationship between the R- and S-enantiomers of a beta-aminoisobutyric acid in human urine. Clin Chim Acta (1981) 0.85
Group tests for selective screening of inborn errors of metabolism. Eur J Pediatr (1994) 0.84
Urinary excretion of deuterated metabolites in patients with tyrosinemia type I after oral loading with deuterated L-tyrosine. Clin Chim Acta (1983) 0.84
Computer analysis of the EEG as an aid in the evaluation of dietetic treatment in phenylketonuria. Electroencephalogr Clin Neurophysiol (1979) 0.84
Mechanisms of deoxyguanosine toxicity for human T and B lymphocytes. Adv Exp Med Biol (1986) 0.84
Urinary purines and pyrimidines in patients with hyperammonemia of various origins. Clin Chim Acta (1980) 0.83
N-EPSILON-(CARBOXYMETHYL)LYSINE, A CONSTITUENT OF HUMAN URINE. Clin Chim Acta (1975) 0.83
Social behavior of monkeys selectively depleted of monoamines. Science (1971) 0.83
Two sisters with isovaleric acidaemia, multiple attacks of ketoacidosis and normal development. Eur J Pediatr (1979) 0.83
MHPG excretion by patients with affective disorders. Int Pharmacopsychiatry (1974) 0.83
Mania. Diagnosis, state measurement and prediction of treatment response. J Affect Disord (1985) 0.83
Intracellular purine and pyrimidine nucleotide pools of human T and B lymphocytes. Adv Exp Med Biol (1986) 0.83
Lanthionine detected in human urine. Clin Chim Acta (1978) 0.83
Deficiency of 3-methylglutaconyl-coenzyme A hydratase in two siblings with 3-methylglutaconic aciduria. J Clin Invest (1986) 0.83
Drug-induced actions on brain neurotransmitter systems and changes in the behaviors and emotions of depressed patients. Neuropsychopharmacology (1994) 0.83
Increased ouabain binding after repeated noradrenergic stimulation. Brain Res (1981) 0.83