Published in Arch Dis Child on January 01, 1975
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The chemical composition of idiopathic nonarteriosclerotic cerebral calcifications. Neurology (1975) 1.59
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Urine analysis performed by flow cytometry: reference range determination and comparison to morphological findings, dipstick chemistry and bacterial culture results--a multicenter study. Clin Nephrol (2001) 1.19
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The effect of enzyme induction on diazepam metabolism in man. Br J Clin Pharmacol (1979) 1.05
Purification and properties of arginase from human liver and erythrocytes. Biochem J (1978) 1.05
A new neonatal case of N-acetylglutamate synthase deficiency treated by carbamylglutamate. J Inherit Metab Dis (1995) 1.05
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Defective measles virus in human subacute sclerosing panencephalitis brain. Virology (1994) 1.04
Long-term follow-up of 12 patients with the late-onset variant of argininosuccinic acid lyase deficiency: no impairment of intellectual and psychomotor development during therapy. Pediatrics (1992) 1.03
Morphological, structural and chemical study of small calcifications. Acta Neurol Belg (1974) 1.01
Early diagnosis and treatment of neonatal medium-chain acyl-CoA dehydrogenase deficiency: report of two siblings. Eur J Pediatr (1990) 1.01
N-Acetylglutamate synthetase deficiency responding to carbamylglutamate. J Inherit Metab Dis (1997) 1.01
Diagnosis and treatment of herpes encephalitis. A multidisciplinary approach. J Neurol Sci (1971) 0.99
Prenatal diagnosis of carbamoyl phosphate synthetase I deficiency by identification of a missense mutation in CPS1. Hum Mutat (1998) 0.99
Serological identification of viral antigens after electrophoretic transfer. J Immunol Methods (1981) 0.98
L-Lysine dehydrogenase deficiency in a patient with congenital lysine intolerance. Nature (1966) 0.98
Increased tryptophan uptake into the brain in hyperammonemia. Life Sci (1983) 0.97
Periodic attacks of lethargy in a baby with ammonia intoxication due to a congenital defect in ureogenesis. Arch Dis Child (1969) 0.97
Brain development: 1H magnetic resonance spectroscopy of rat brain extracts compared with chromatographic methods. Neurochem Res (1990) 0.97
[Hyperargininemia wityh arginase deficiency. A new familial metabolic disease. I. Clinical studies]. Z Kinderheilkd (1970) 0.97
Incidence of disorders tested by systematic screening: confidence limits and comparison of programmes. J Inherit Metab Dis (1982) 0.96
Familial cerebellar ataxia with hypogonadism. J Neurol (1979) 0.95
Induction of arginase activity with the Shope papilloma virus in tissue culture cells from an argininemic patient. J Exp Med (1973) 0.94
Enzyme induction and renal function in man. Br J Clin Pharmacol (1977) 0.94
Phenylketonuria, a family study. Borderline intelligence in two siblings with mentally retarded children. Helv Paediatr Acta (1967) 0.92
Bound and free light chains in subacute sclerosing panencephalitis and multiple sclerosis serum and cerebrospinal fluid. Z Klin Chem Klin Biochem (1975) 0.91
Diagnostic value of orotic acid excretion in heritable disorders of the urea cycle and in hyperammonemia due to organic acidurias. Eur J Pediatr (1980) 0.91
Ornithine transcarbamylase deficiency: new sites with increased probability of mutation. Hum Genet (1995) 0.91
Ornithine transcarbamylase deficiency: characterization of gene mutations and polymorphisms. Hum Mutat (1996) 0.90
Cerebrospinal fluid proteins in neurology. Int Rev Neurobiol (1984) 0.90
Guanidino compound analysis as a complementary diagnostic parameter for hyperargininemia: follow-up of guanidino compound levels during therapy. Pediatr Res (1990) 0.90
Cellular composition of primary cultures from cerebral cortex, striatum, hippocampus, brainstem and cerebellum. Brain Res (1984) 0.89
Blood-brain barrier in chronic relapsing experimental allergic encephalomyelitis: a correlative study between cerebrospinal fluid protein concentrations and tracer leakage in the central nervous system. Acta Neuropathol (1984) 0.88
A morphological and chemical study of calcification of the pineal gland. J Neurol (1977) 0.88
Isolation and characterization of IgG globulins in subacute sclerosing panencephalitis. Immunology (1972) 0.88
Isolation and identification of the urinary pigment uroerythrin. Eur J Biochem (1975) 0.88
[The XXXXY syndrome. Report of 7 new cases and review of the literature (author's transl)]. Z Kinderheilkd (1973) 0.88
Quantitative overestimation of free taurocyamine using short liquid cation-exchange chromatography columns? J Chromatogr (1985) 0.87
Extracerebrospinal metastases in glioblastoma. Case report and review of the literature. Eur J Pediatr (1977) 0.87
Multiple sclerosis in a black Cameroonian woman. Acta Neurol Belg (1990) 0.86
Prenatal diagnosis of the urea cycle diseases: a survey of the European cases. Am J Med Genet (1995) 0.86
Arachnoiditis ossificans with arachnoid cyst after cranial tuberculous meningitis. Neurology (1990) 0.86
Human gamma gamma-enolase: two-site immunoradiometric assay with a single monoclonal antibody. J Neurochem (1987) 0.86
Increase of tryptophan and 5-hydroxyindole acetic acid in the brain of ornithine carbamoyltransferase deficient sparse-fur mice. Pediatr Res (1984) 0.86
Enzymatic determination of red cell creatine as an index of hemolysis. Clin Biochem (1987) 0.86
Unsuccessful trial of gene replacement in arginase deficiency. Z Kinderheilkd (1975) 0.85
Determination of orotic acid in children's urine. J Clin Chem Clin Biochem (1980) 0.85
[Hypoplastic anemia accompanied by triphalangeal thumbs (author's transl)]. Z Kinderheilkd (1974) 0.85
Glutaric aciduria type I: ultrasonographic demonstration of early signs. Pediatr Radiol (1999) 0.85
Serum gamma globulins in 84 typical cases of subacute sclerosing panencephalitis. Neurology (1971) 0.84
The renal handling of carnitine in patients with selective tubulopathy and with Fanconi syndrome. Pediatr Res (1987) 0.83
Guanidino compounds in uraemic dialysed patients. Clin Chim Acta (1986) 0.83
[The determination of bilirubin as azobilirubin in plasma and serum with the Greiner electronic selective analyzer GSA II (author's transl)]. Z Klin Chem Klin Biochem (1974) 0.83
A morphological and chemical study of calcification of the choroid plexus. J Neurol (1977) 0.83
Late-onset form of partial N-acetylglutamate synthetase deficiency. Eur J Pediatr (1990) 0.82
[Hyperargininemia with arginase deficiency. A new familial metabolic disease. II. Biochemical studies]. Z Kinderheilkd (1970) 0.82
N-acetylglutamate synthetase deficiency, a second patient. J Inherit Metab Dis (1988) 0.82
[Wilson's disease in Switzerland. Clinical, genetic and biochemical studies]. Schweiz Med Wochenschr (1973) 0.82
Juvenile dystonic lipidosis (variant of Niemann-Pick disease type C). J Neurol Sci (1984) 0.81
The European Stroke Prevention Study: results according to sex. Neurology (1991) 0.81
Carbamyl phosphate synthetase-1 deficiency discovered after valproic acid-induced coma. Acta Neurol Scand (1992) 0.81
[Hyperammonemia due to ornithine transcarbamylase deficiency--a cause of lethal metabolic crisis during the newborn period and infancy (author's transl)]. Klin Padiatr (1980) 0.81
Increased GFAp levels in CSF as a marker of organicity in patients with Alzheimer's disease and other types of irreversible chronic organic brain syndrome. J Neurol (1986) 0.81
Partial N-acetylglutamate synthetase deficiency: a new case with uncontrollable movement disorders. J Inherit Metab Dis (1992) 0.81
[Periodic stupor and ammonia intoxication in a child with anicteric subacute hepatitis]. Helv Paediatr Acta (1967) 0.81
Methylmalonic acidaemia and nonketotic hyperglycinaemia. Clinical and biochemical aspects. Arch Dis Child (1975) 0.81
Determination in human cerebrospinal fluid of glial fibrillary acidic protein, S-100 and myelin basic protein as indices of non-specific or specific central nervous tissue pathology. Clin Chim Acta (1986) 0.80
Second European Stroke Prevention Study: antiplatelet therapy is effective regardless of age. ESPS2 Working Group. Acta Neurol Scand (1999) 0.80
Detection of neuron specific enolase concentrations in cerebrospinal fluid from patients with neurological disorders by means of a sensitive enzyme immunoassay. Clin Chim Acta (1990) 0.80
Antiplatelet treatment does not reduce the severity of subsequent stroke. European Stroke Prevention Study 2 Working Group. Neurology (1999) 0.80
Effect of L-dopa on visual evoked potentials and neuropsychological tests in adult phenylketonuria patients. Eur J Pediatr (1996) 0.80
Measles antibodies in patients with various types of measles infection. Arch Gesamte Virusforsch (1969) 0.79
Cytosolic phospholipase A2 is required for the activation of the NADPH oxidase associated H+ channel in phagocyte-like cells. Adv Exp Med Biol (2000) 0.79
Excretion of guanidino-derivates in urine of hyperargininemic patients. J Genet Hum (1976) 0.79
The defect of uric acid metabolism in Eck-fistula rats. J Lab Clin Med (1977) 0.79
Clinical biochemistry of epilepsy. Epilepsia (1965) 0.79
Guanidino compounds in plasma, urine and cerebrospinal fluid of hyperargininemic patients during therapy. Clin Chim Acta (1985) 0.79
Pergolide therapy in Parkinson's disease. J Neurol (1984) 0.79