Published in Cesk Pediatr on August 01, 1970
Subclinical course of cholesteryl ester storage disease in an adult with hypercholesterolemia, accelerated atherosclerosis, and liver cancer. J Hepatol (2000) 1.00
Adenosine and methotrexate polyglutamate concentrations in patients with juvenile arthritis. Rheumatology (Oxford) (2004) 0.94
Comparative effects of methylphenidate on ADD girls and ADD boys. J Am Acad Child Adolesc Psychiatry (1989) 0.92
Oculocerebrorenal syndrome in a female child. Am J Dis Child (1967) 0.90
Sustained release and standard methylphenidate effects on cognitive and social behavior in children with attention deficit disorder. Pediatrics (1987) 0.88
Changes in phenylalanine tolerance while monitoring the dietetic treatment of pregnant women suffering from hyperphenylalaninaemia. J Inherit Metab Dis (1988) 0.87
Soluble adhesion molecules ICAM-1 and E-selectin in juvenile arthritis: clinical and laboratory correlations. Clin Exp Rheumatol (2002) 0.86
Immunological investigation in children with juvenile chronic arthritis. Med Sci Monit (2001) 0.86
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
Neither expression of VEGF-C/D nor lymph vessel density supports lymphatic invasion as the mechanism responsible for local spread of recurrent salivary pleomorphic adenoma. Virchows Arch (2014) 0.83
Analysis of growth curves of fowl. I. Chickens. Br Poult Sci (1991) 0.83
X-chromosomal recessive microcephaly with epilepsy, spastic tetraplegia and absent abdominal reflexes. New variety of "Paine syndrome"? Humangenetik (1973) 0.81
Subtypes of HLA-DRB1*03, *08, *11, *12, *13 and *14 in early onset pauciarticular juvenile chronic arthritis (EOPA) with and without iridocyclitis. Clin Exp Rheumatol (1994) 0.81
A model for the role of HLA-DQ molecules in the pathogenesis of juvenile chronic arthritis. Rheumatol Int (1991) 0.81
Is the common 844ins68 polymorphism in the cystathionine beta-synthase gene associated with atherosclerosis? J Inherit Metab Dis (1999) 0.80
Cerebrospinal fluid. Adv Clin Chem (2001) 0.80
[Clinical picture of homocystinuria with cystathionine beta-synthase deficiency in 19 Czech and Slovak patients]. Cas Lek Cesk (2000) 0.80
Genetic determinants of folate status in Central Bohemia. Physiol Res (2005) 0.80
Psychostimulant rebound in attention deficit disordered boys. J Am Acad Child Adolesc Psychiatry (1988) 0.79
Mevalonic aciduria. J Inherit Metab Dis (1991) 0.78
[Diagnostic significance of the test with ferric chloride in the urine in phenylketonuria]. Cesk Pediatr (1969) 0.78
Speech and language disorders in histidinaemia and other amino acid disturbances. J Inherit Metab Dis (1985) 0.77
'Homocystinuria' and urinary excretion of beta-amino acids in patients treated with 6-azauridine. Clin Chim Acta (1969) 0.77
[Cultivation of amniotic fluid cells and prenatal diagnosis]. Cesk Gynekol (1971) 0.77
Primary cystathioninuria in an infant born out of incest. Acta Univ Carol Med Monogr (1977) 0.77
[Lysosomal acid lipase deficiency. Overview of Czech patients]. Cas Lek Cesk (1999) 0.77
Calciuria in children with juvenile chronic arthritis. Acta Univ Carol Med (Praha) (1994) 0.77
Multilocular pigmented villonodular synovitis in a child (case report). Acta Univ Carol Med (Praha) (1991) 0.76
Class I associations and frequencies of class II HLA-DRB alleles by RFLP analysis in children with rheumatoid-factor-negative juvenile chronic arthritis. Rheumatol Int (1993) 0.76
[Secondary reactions of some new antibiotics. Fumagillin]. Lek Veda Zahr (1966) 0.76
Results of screening for phenylalanine and other amino acid disturbances among pregnant women. J Inherit Metab Dis (1980) 0.75
The Czech version of the Childhood Health Assessment Questionnaire (CHAQ) and the Child Health Questionnaire (CHQ). Clin Exp Rheumatol (2001) 0.75
Eosinophilic fasciitis in an adolescent girl with lymphadenopathy and vitiligo-like and linear scleroderma-like changes. A case report. Clin Exp Rheumatol (1996) 0.75
[Maternal hyperphenylalaninemia and intrauterine damage to the CNS]. Cesk Neurol Neurochir (1974) 0.75
[Child of a mother with hyperphenylalaninemia]. Cesk Pediatr (1972) 0.75
[Pregnancy hyperphenylalanemia and its diagnostic importance (author's transl)]. Cas Lek Cesk (1975) 0.75
[Hyperphenylalaninemia]. Cas Lek Cesk (1971) 0.75
[Menkes syndrome]. Cesk Pediatr (1987) 0.75
[Digestive hypertyrosinemia in newborn infants and premature infants fed Tatra condensed milk]. Cesk Pediatr (1983) 0.75
[Cystathioninuria]. Cesk Pediatr (1985) 0.75
[Simple screening tests for the detection of congenital metabolic disorders of amino acids, sugars, and mycopolysaccharides]. Cas Lek Cesk (1968) 0.75
[Leucinosis--a case of congenital metabolic disease in a child]. Cesk Pediatr (1976) 0.75
Screening of amino acid enzymopathies in pregnancy and possibilities of their prenatal diagnosis. Acta Univ Carol Med Monogr (1977) 0.75
[Offspring of mothers with hyperphenylalaninemia treated with a low phenylalanine diet before conception and during pregnancy]. Cas Lek Cesk (1988) 0.75
[Hyperphenylalaninemia during pregnancy]. Cesk Pediatr (1977) 0.75
[Clinical diagnosis of hyperphenylalaninemia in the newborn infant and infant stages]. Cesk Pediatr (1976) 0.75
[Crossed chromatography of sugars in urine on thin cellulose layers]. Vnitr Lek (1976) 0.75
[Hyperaminoaciduria]. Lek Veda Zahr (1967) 0.75
[Free amino acids in the human ejaculate]. Cas Lek Cesk (1977) 0.75
[Homocystinuria]. Cesk Pediatr (1985) 0.75
Growth curves of highly inbred lines of fowl and their F(1 )hybrids. Genet Sel Evol (1983) 0.75
[Changes in the voice in type II mucopolysaccharidosis]. Cesk Pediatr (1986) 0.75
Results of phenylalanine tolerance tests and EEG examination in patients under treatment for phenylketonuria. Acta Univ Carol Med Monogr (1977) 0.75
A screening test for the recognition of increased alpha-amino nitrogen excretion in urine. Clin Chim Acta (1965) 0.75
[Chromatography of amino acids on a thin layer of cellulose in urine exminations in inborn errors of metabolism]. Cas Lek Cesk (1969) 0.75
The effect of insulin load on plasma tryptophan levels in schizophrenic patients. Act Nerv Super (Praha) (1974) 0.75
[Pyridoxine-sensitive homocystinuria in 2 siblings]. Cesk Pediatr (1983) 0.75
[Protein tolerance test in the differential diagnosis of inborn errors amino acid metabolism]. Cas Lek Cesk (1976) 0.75
[Non-ketotic hyperglycinemia]. Cesk Pediatr (1990) 0.75
[Gonosomal recessive heredity of microcephaly with epilepsy and spastic quadruparesis. New variant of the so called Paine's dyndrome?]. Cesk Pediatr (1973) 0.75
[Hyperprolinuria]. Cesk Pediatr (1974) 0.75
[Longitudinal studies of liver function in persons following choledochoduodenoanastomosis based on relative indication]. Cesk Gastroenterol Vyz (1968) 0.75
[Diagnostic significance of the urine smell in inborn errors of the metabolism]. Cesk Pediatr (1973) 0.75
[Transitory hyperphenylalaninemia with a tetrahydrobiopterin synthesis deficiency]. Cesk Pediatr (1987) 0.75
[Hyperlysinuria]. Cas Lek Cesk (1967) 0.75
[Cystinuria and lysinuria in Down's syndrome]. Cas Lek Cesk (1970) 0.75
[Metabolic studies in 28 families of patients with cystinuria]. Cesk Pediatr (1988) 0.75
[Results of screening for aminoacidopathies in pregnant women]. Cesk Pediatr (1977) 0.75
Incidence of phenylketonuria and other inborn errors of the amino acid metabolism in the normal and mentally retarded population. Rev Czech Med (1974) 0.75
[Malignant hyperphenylalaninemia with dihydropteridine reductase deficiency]. Cesk Pediatr (1986) 0.75
[Use of 1-amine oxidase from snake venom in enzymatic determination of 1-phenylalanine in serum]. Cas Lek Cesk (1968) 0.75
[Hyperphenylalaninemia and other hyperaminoacidurias with mental retardation, detected by multiple screening]. Cas Lek Cesk (1972) 0.75
[Isovaleric aciduria]. Cas Lek Cesk (1983) 0.75
[Changes in phenylalanine tolerance during the monitoring of diet therapy of pregnant women with phenylketonuria]. Cesk Gynekol (1988) 0.75
[On methods for the determination of amino acids in the urine]. Z Med Labortech (1967) 0.75
[A program for evaluating ligand-receptor binding based on strong linear regression]. Cesk Fysiol (1988) 0.75
[Results of screening for inborn errors of aminoacid metabolism in adult and infant patients from psychiatric institutions (author's transl)]. Cas Lek Cesk (1975) 0.75
[Typical hyperaminoaciduria in patients with mycosis fungoides and primary progressive polyarthritis following 6-azauridine triacetate administration]. Cas Lek Cesk (1970) 0.75
[Phenylketonuria undiagnosed, unrecognizable and neglected. Review of failures in diagnosis, therapy, and prevention of hereditary disorders of phenylalanine]. Cesk Pediatr (1987) 0.75
[Disorders of tyrosine metabolism and their diagnostic value]. Cesk Pediatr (1977) 0.75
[Prolonged hypertyrosinemia resistant to vitamins]. Cesk Pediatr (1977) 0.75
[Results of screening test for cystinuria in schoolchildren]. Cas Lek Cesk (1970) 0.75
[Typical hyperaminoaciduria and disulfiduria associated with mental retardation in an incest-born child]. Cesk Pediatr (1970) 0.75
The results of chromatographic screening for the detection of inborn metabolic errors in normal and mentally retarded population. Acta Univ Carol Med Monogr (1973) 0.75
Quantification of some glycols in urinary organic acid profiles of acutely ill newborns. J Chromatogr (1987) 0.75
[Hyperaminoacidemia and hyperaminoaciduria of benign nature and their diagnostic values]. Cesk Pediatr (1977) 0.75
[Urinary excretion of free amino acids, sugars and mucopolysaccharides in mentally retarded children from social welfare homes in Czechoslovakia]. Cesk Pediatr (1970) 0.75
[Excretion of free histidine in urine in the course of normal and endangered pregnancy]. Cesk Gynekol (1971) 0.75
Morphological differences in the skeletal system in highly inbred lines of chickens. Folia Biol (Praha) (1977) 0.75
[Structure and function of the liver in persons with choledochoduodenal anastomosis]. Cesk Gastroenterol Vyz (1972) 0.75
Speech disorders associated with histidinemia and other hereditary disorders of amino acid metabolism. Folia Phoniatr (Basel) (1986) 0.75
[Metabolic study of the classic form of leucinosis during exchange transfusion therapy]. Cesk Pediatr (1987) 0.75
[Hyperglycinemia]. Cesk Pediatr (1975) 0.75