Published in Am J Clin Nutr on June 01, 1988
Dietary sources, current intakes, and nutritional role of omega-3 docosapentaenoic acid. Lipid Technol (2015) 0.79
Fatty acid composition of mature human milk in Nigeria. Z Ernahrungswiss (1991) 0.77
Glycerol Monolaurate (GML) inhibits human T cell signaling and function by disrupting lipid dynamics. Sci Rep (2016) 0.76
A review of the biologic and pharmacological role of docosapentaenoic acid. F1000Res (2013) 0.76
Docosahexaenoic acid in maternal and neonatal plasma phospholipids and milk lipids of Taiwanese women in Kinmen: fatty acid composition of maternal blood, neonatal blood and breast milk. Lipids Health Dis (2013) 0.75
Environmental Lead (Pb) Exposure Versus Fatty Acid Content in Blood and Milk of the Mother and in the Blood of Newborn Children. Biol Trace Elem Res (2015) 0.75
The fatty acid composition of subcutaneous fat in German adults. Z Ernahrungswiss (1992) 0.75
Molecular analysis of katG gene mutations in strains of Mycobacterium tuberculosis complex from Africa. Antimicrob Agents Chemother (1997) 1.99
Vitamin A supplementation in malnourished Sudanese children. Int J Vitam Nutr Res (1991) 1.95
Comparison of DNA fingerprint patterns of isolates of Mycobacterium africanum from east and west Africa. J Clin Microbiol (1997) 1.88
Creatine deficiency syndrome caused by guanidinoacetate methyltransferase deficiency: diagnostic tools for a new inborn error of metabolism. J Pediatr (1997) 1.76
A new agent of mycobacterial lymphadenitis in children: Mycobacterium heidelbergense sp. nov. J Clin Microbiol (1997) 1.52
Betaine in the treatment of homocystinuria due to 5,10-methylenetetrahydrofolate reductase deficiency. Eur J Pediatr (1984) 1.47
Body growth in primary de Toni-Debré-Fanconi syndrome. Pediatr Nephrol (1997) 1.44
Glutaric aciduria type II: report on a previously undescribed metabolic disorder. Clin Chim Acta (1976) 1.44
[On phenylketonuria. Carrying out of phenylalanine-low diet]. Dtsch Med Wochenschr (1967) 1.42
Glutaryl-coenzyme A dehydrogenase deficiency: a distinct encephalopathy. Pediatrics (1991) 1.41
Cervical lymphadenitis in a child caused by a previously unknown mycobacterium. J Infect Dis (1993) 1.35
Large neutral amino acids block phenylalanine transport into brain tissue in patients with phenylketonuria. J Clin Invest (1999) 1.35
Rationale for the German recommendations for phenylalanine level control in phenylketonuria 1997. Eur J Pediatr (1999) 1.17
Neurological outcome in adult patients with early-treated phenylketonuria. Eur J Pediatr (1998) 1.17
Transmission dynamics of tuberculosis in a high-incidence country: prospective analysis by PCR DNA fingerprinting. J Clin Microbiol (1999) 1.12
Nutrient intake and food consumption of adolescents and young adults with phenylketonuria. Acta Paediatr (1995) 1.06
The selenium state of children. II. Selenium content of serum, whole blood, hair and the activity of erythrocyte glutathione peroxidase in dietetically treated patients with phenylketonuria and maple-syrup-urine disease. Eur J Pediatr (1978) 1.04
Letter: Absorption of zinc in acrodermatitis enteropathica. Lancet (1975) 1.04
Alpha-ketoadipic aciduria: degradation studies with fibroblasts,. Clin Chim Acta (1975) 1.02
Alpha-ketoadipic aciduria, a new inborn error of lysine metabolism; biochemical studies. Clin Chim Acta (1975) 0.99
Fat content and fatty acid composition of infant formulas. Acta Paediatr Scand (1989) 0.97
Tolerance of phenylalanine after ntravenous administration in phenylketonurics, heterozygous carriers, and normal adults. Nature (1966) 0.95
Fatty acid and lipid composition of children's food. I. Analytical methods; composition of commercially available supplementary foods for juniors. Z Ernahrungswiss (1984) 0.95
Intellectual development of the patients of the German Collaborative Study of children treated for phenylketonuria. Eur J Pediatr (1996) 0.93
Effects of dietary long-chain polyunsaturated fatty acids on the essential fatty acid status of premature infants. Eur J Pediatr (1989) 0.90
Survival time in cystinosis. A collaborative study. Proc Eur Dial Transplant Assoc (1983) 0.90
Neurological manifestations of organic acid disorders. Eur J Pediatr (1994) 0.89
Beta cell nesidioblastosis. Eur J Pediatr (1978) 0.89
Serum-selenium concentrations in patients with maple-syrup-urine disease and phenylketonuria under dieto-therapy. Clin Chim Acta (1975) 0.88
Enhanced urinary excretion of leukotriene E4 in patients with mevalonate kinase deficiency. J Pediatr (1993) 0.87
Influence of n-6 and n-3 polyunsaturated fatty acids on the resistance to experimental tuberculosis. Metabolism (1997) 0.87
Fatty acid composition of plasma lipids in Nigerian children with protein-energy malnutrition. Eur J Pediatr (1986) 0.87
Two cases of phosphoenolpyruvate carboxykinase deficiency. Acta Paediatr Scand (1976) 0.87
The excretion of diamines in human urine. II. Cadaverine, putrescine, 1,3-diaminopropane, 2,2'-dithiobis(ethylamine) and spermidine in urine of patients with cystinuria and cystinlysinuria. Clin Chim Acta (1971) 0.87
Propionyl-CoA carboxylase deficiency with overflow of metabolites of isoleucine catabolism at all levels. Eur J Pediatr (1979) 0.86
Long-chain polyunsaturated fatty acids in plasma and erythrocyte membrane lipids of children with phenylketonuria after controlled linoleic acid intake. J Inherit Metab Dis (1998) 0.85
[Prenatal diagnosis of glycogenosis type II (Pompe) and subsequent therapeutic abortion (author's transl)]. Dtsch Med Wochenschr (1974) 0.85
Increased manganese content and reduced arginase activity in erythrocytes of a patient with prolidase deficiency (iminodipeptiduria). Eur J Pediatr (1986) 0.85
Comparison of the protein quality of dietetically treated phenylketonuria patients with the recommendations of the WHO Expert Consultation. Eur J Pediatr (1996) 0.85
Vacuolated lymphocytes in type II glycogenosis--a diagnostic approach? Eur J Pediatr (1977) 0.85
Nutrition, physical growth, and bone density in treated phenylketonuria. Eur J Pediatr (2000) 0.85
5-Oxoprolinase deficiency associated with severe psychomotor developmental delay, failure to thrive, microcephaly and microcytic anaemia. J Inherit Metab Dis (1995) 0.84
Growth and skeletal maturation in children with phenylketonuria. Acta Paediatr (1994) 0.84
Influence of dietary (n-3)-polyunsaturated fatty acids on leukotriene B4 and prostaglandin E2 synthesis and course of experimental tuberculosis in guinea pigs. Infection (1994) 0.84
The selenium state of healthy children. I. Serum selenium concentration at different ages; activity of glutathione peroxidase of erythrocytes at different ages; selenium content of food of infants. Eur J Pediatr (1977) 0.84
Facts and artefacts in mevalonic aciduria: development of a stable isotope dilution GCMS assay for mevalonic acid and its application to physiological fluids, tissue samples, prenatal diagnosis and carrier detection. Clin Chim Acta (1991) 0.84
[Analysis of di- and polyamines in urine. A chromatographic method for concentration, separation and identification]. J Chromatogr (1966) 0.83
3-Methylglutaconic aciduria in a patient with Pearson syndrome. Eur J Pediatr (1993) 0.82
A metabolic disorder similar to Zellweger syndrome with hepatic acatalasia and absence of peroxisomes, altered content and redox state of cytochromes, and infantile cirrhosis with hemosiderosis. Eur J Pediatr (1977) 0.81
Fatty acid composition of plasma lipids in acrodermatitis enteropathica before and after zinc supplementation. Eur J Pediatr (1985) 0.81
Selenium content of human milk, cow's mild and cow's milk infant formulas. Eur J Pediatr (1978) 0.81
Macrocephaly: an important indication for organic acid analysis. J Inherit Metab Dis (1991) 0.80
Plasma retinol and tocopherols of breast-feeding Sudanese women. Trop Med Parasitol (1989) 0.80
Glycogenosis type Ib complicated by severe granulocytopenia resembling inherited neutropenia. Eur J Pediatr (1981) 0.80
Ornithine transcarbamylase deficiency in a male: strict correlation between metabolic control and plasma arginine concentration. Eur J Pediatr (1989) 0.80
Vitamin E status of Congolese children in a rural area. Int J Vitam Nutr Res (1990) 0.80
[Research on the tyrosine metabolism of premature infants. I. Changes in blood tyrosine and phenylalanine levels in premature infants during the 1st weeks of life]. Ann Paediatr (1966) 0.80
Maple-syrup-urine disease. N Engl J Med (1983) 0.80
Vitamin E status in Sudanese children with protein-energy malnutrition. Z Ernahrungswiss (1990) 0.80
The selenium content of infant food. Z Ernahrungswiss (1984) 0.80
Glutathione and association antioxidant systems in protein energy malnutrition: results of a study in Nigeria. Free Radic Biol Med (1995) 0.80
Mitochondropathy presenting with non-ketotic hypoglycaemia as 3-hydroxydicarboxylic aciduria. J Inherit Metab Dis (1995) 0.80
Correlations between branched-chain amino acids and branched-chain alpha-keto acids in blood in maple syrup urine disease. Clin Chim Acta (1978) 0.79
Trans fatty acid content of selected brands of West German nut-nougat cream. Z Ernahrungswiss (1988) 0.79
Long-term outcome of paediatric patients with hereditary tubular disorders. Nephron (1999) 0.79
Serum zinc concentration during childhood. Eur J Pediatr (1977) 0.79
Thin layer chromatographic screening test for amino acid anomalies in urine without desalting using internal standards. Clin Chim Acta (1971) 0.79
Inflammatory bowel disease in glycogen storage disease type Ib. J Pediatr (1987) 0.79
Reversibility of urinary tract abnormalities due to Schistosoma haematobium infection. Kidney Int (1986) 0.79
Selenium requirements in patients with inborn errors of amino acid metabolism and selenium deficiency. Eur J Pediatr (1980) 0.78
Fatty acid composition of phospholipids of plasma and of mononuclear blood cells in children with allergic asthma and the influence of glucocorticoids. Eur J Pediatr (1990) 0.78
[Lysosomal glycogen storage in lymphocytes in patients with glycogenosis type II]. Monatsschr Kinderheilkd (1976) 0.78
[Surgical therapy of nesidioblastosis]. Z Kinderchir (1984) 0.78
Primary hypomagnesemia. I. Absorption Studies. Z Kinderheilkd (1975) 0.78
'Homocystinuria' and urinary excretion of beta-amino acids in patients treated with 6-azauridine. Clin Chim Acta (1969) 0.77
Clinical, morphological, and biochemical investigations on a patient with an unusual form of neuronal ceroid-lipofuscinosis. Eur J Pediatr (1979) 0.77
Maple syrup urine disease--therapeutic use of insulin in catabolic states. Eur J Pediatr (1982) 0.77
D-Glyceric acidemia in a patient with chronic metabolic acidosis. Clin Chim Acta (1976) 0.77
Comparison of fatty acid composition of plasma lipid fractions in well-nourished Nigerian and German infants and toddlers. J Pediatr Gastroenterol Nutr (1986) 0.77
[Primary hypomagnesemia. Clinical, diagnostic and therapeutic studies in three children (author's transl)]. Monatsschr Kinderheilkd (1979) 0.77
Milk protein intake in the term infant. II. Effects on plasma amino acid concentrations. Acta Paediatr Scand (1986) 0.77
Preoperative diagnosis of Mycobacterium avium lymphadenitis in two immunocompetent children by polymerase chain reaction of gastric aspirates. Pediatr Infect Dis J (1998) 0.77
[Macrocephaly as the initial manifestation of glutaryl-CoA-dehydrogenase deficiency (glutaric aciduria type I)]. Monatsschr Kinderheilkd (1991) 0.77
Status of plasma and erythrocyte fatty acids and vitamin A and E in young children with cystic fibrosis. Scand J Gastroenterol Suppl (1988) 0.76
Rubidium-A possible essential trace element : 1. The rubidium content of whole blood of healthy and dietetically treated children. Biol Trace Elem Res (1980) 0.76
Trace element disturbances in dietetically treated patients with phenylketonuria and maple syrup urine disease. Monogr Hum Genet (1978) 0.76
Exchange transfusion in acute episodes of maple syrup urine disease. Studies on branched-chain amino and keto acids. Eur J Pediatr (1982) 0.75
Zinc status of Libyan children -- a pilot study. Z Ernahrungswiss (1983) 0.75
[p-Tyramine excretion in urine. p-Tyramine excretion in healthy children of various age groups, in children with protein utilization disorders of the gut, and in children with severe enteritis]. Z Kinderheilkd (1966) 0.75
[Early diagnosis of inborn errors of metabolism]. Schwest Rev (1969) 0.75
Fatty acid composition of the milk of well-nourished Sudanese women. Int J Food Sci Nutr (1995) 0.75
[Gluten induced enteropathy (celiac disease) in children. II. Diet therapy]. Med Klin (1969) 0.75
[On disorders of tyrosine metabolism in newborn infants: vitamin C dependency of tyrosine blood levels in premature infants]. Helv Paediatr Acta (1966) 0.75
[Gluten induced enteropathy (celiac disease) in children. I. Pathogenesis and clinical aspects]. Med Klin (1969) 0.75
[Amines in human stools. II. Determination of the p-tyramine content in feces from children of various age groups]. Z Kinderheilkd (1966) 0.75
[Studies on the nutritive dependency of tyrosine metabolism disorders in premature infants]. Monatsschr Kinderheilkd (1966) 0.75
[Transitory hypertyrosinemia of young infants and its relation to vitamin C]. Monatsschr Kinderheilkd (1969) 0.75
[Glucose tolerance of eutrophic and dystrophic infants following intravenous injection of glucose]. Z Kinderheilkd (1966) 0.75