Published in J Clin Pathol on February 01, 1976
Diagnosing mucopolysaccharidosis IVA. J Inherit Metab Dis (2013) 1.14
Analysis of glycosaminoglycans in urine by using acridine orange fluorescence. Biochem J (1978) 1.07
Mucopolysaccharides in suspensions of Treponema pallidum extracted from infected rabbit testes. Genitourin Med (1985) 1.00
Mucopolysacccharidoses: From understanding to treatment, a century of discoveries. Genet Mol Biol (2012) 0.94
Biochemical and histopathological studies on patients with mucopolysaccharidoses, two of whom had been treated by fibroblast transplantation. J Clin Pathol (1983) 0.82
Serum hyaluronidase aberrations in metabolic and morphogenetic disorders. Glycoconj J (2005) 0.81
GM1 gangliosidosis (type 1) in a cat. Biochem J (1986) 0.79
Urinary glycosaminoglycan excretion in urolithiasis. Arch Dis Child (1999) 0.79
Urinary excretion of glycosaminoglycans in psoriasis. Arch Dermatol Res (1988) 0.76
Genotypic and bioinformatic evaluation of the alpha-l-iduronidase gene and protein in patients with mucopolysaccharidosis type I from Colombia, Ecuador and Peru. Mol Genet Metab Rep (2014) 0.75
Diagnosis of Sanfilippo disease correlating clinical, radiological and biochemical findings-a case report. Indian J Clin Biochem (2012) 0.75
A Case of Sanfillippo's Disease Correlating Clinical and Biochemical Findings. Indian J Clin Biochem (2014) 0.75
Urinary Glycosaminoglycan Estimation as a Routine Clinical Service. Indian J Clin Biochem (2014) 0.75
Screening for Attenuated Forms of Mucopolysaccharidoses in Patients with Osteoarticular Problems of Unknown Etiology. JIMD Rep (2015) 0.75
Screening method for mucopolysaccharidoses. J Clin Pathol (1983) 0.75
Validation of Urinary Glycosaminoglycans in Iranian patients with Mucopolysaccharidase type I: The effect of urine sedimentation characteristics. Iran J Child Neurol (2014) 0.75
Investigation of newborns with abnormal results in a newborn screening program for four lysosomal storage diseases in Brazil. Mol Genet Metab Rep (2017) 0.75
A modified uronic acid carbazole reaction. Anal Biochem (1962) 34.83
Aliphatic ammonium salts in the assay of acidic polysaccharides from tissues. Methods Biochem Anal (1960) 6.00
Metabolic abnormalities detected in a survey of mentally backward individuals in Northern Ireland. Arch Dis Child (1962) 4.02
Beta glucuronidase deficiency: report of clinical, radiologic, and biochemical features of a new mucopolysaccharidosis. J Pediatr (1973) 3.44
The defect in Hurler's and Hunter's syndromes: faulty degradation of mucopolysaccharide. Proc Natl Acad Sci U S A (1968) 2.89
Analytical and preparative separation of acidic glycosaminoglycans by electrophoresis in barium acetate. Anal Biochem (1968) 2.59
OCCURRENCE OF URINARY ACID MUCOPOLYSACCHARIDES IN THE HURLER SYNDROME. Proc Natl Acad Sci U S A (1957) 2.42
Hurler and Hunter syndromes: mutual correction of the defect in cultured fibroblasts. Science (1968) 2.40
The defect in the Hurler and Scheie syndromes: deficiency of -L-iduronidase. Proc Natl Acad Sci U S A (1972) 2.32
Thrombosis and oestrogens. Lancet (1967) 2.06
The genetic mucopolysaccharidoses. Medicine (Baltimore) (1965) 2.04
Excretion of sulfated mucopolysaccharides in gargoylism (Hurler's syndrome). Proc Soc Exp Biol Med (1958) 1.89
The quantitative measurement of Alcian Blue-glycosaminoglycan complexes. Biochem J (1973) 1.89
The defect in the Hunter syndrome: deficiency of sulfoiduronate sulfatase. Proc Natl Acad Sci U S A (1973) 1.86
A rapid and micro method for separation of acidic glycosaminoglycans by two-dimensional electrophoresis. Anal Biochem (1972) 1.76
A paper spot test useful in study of Hurler's syndrome. J Lab Clin Med (1960) 1.63
The nomenclature of mucopolysaccharides. Arthritis Rheum (1960) 1.57
The mucopolysaccharide of normal human urine. Clin Chim Acta (1957) 1.54
Excretion patterns of glycosaminoglycans and glycoproteins in normal human urine. J Clin Pathol (1968) 1.50
Hurler's syndrome, an -L-iduronidase deficiency. Biochem Biophys Res Commun (1972) 1.45
Urinary excretion of acid mucopolysaccharides in normal children and patients with gargoylism. J Lab Clin Med (1962) 1.44
Sanfilippo syndrome: profound deficiency of alpha-acetylglucosaminidase activity in organs and skin fibroblasts from type-B patients. Proc Natl Acad Sci U S A (1972) 1.38
The quantitative determination of glycosaminoglycans in urine with Alcian Blue 8GX. Biochem J (1973) 1.33
Sequential thin layer chromatography of urinary acidic glycosaminglycans. Clin Chim Acta (1972) 1.33
Scheie and Hurler syndromes: apparent identity of the biochemical defect. Science (1970) 1.30
The measurement of urinary mucopolysaccharides. Anal Biochem (1967) 1.30
Studies on the biochemistry of connective tissue. Pediatrics (1958) 1.25
Hunter's syndrome: a deficiency of L-idurono-sulfate sulfatase. Biochem Biophys Res Commun (1973) 1.21
Morquio's syndrome: deficiency of a chondroitin sulfate N-acetylhexosamine sulfate sulfatase. Biochem Biophys Res Commun (1974) 1.19
Mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome). I. Sulfatase B deficiency in tissues. Am J Dis Child (1973) 1.16
Classification of the mucopolysaccharidoses based on the pattern of mucopolysacchariduria. Am J Med (1969) 1.14
Colorimetric measurement of dermatan sulphate. Biochem J (1971) 1.12
Mucopolysaccharidosis 3 A (Sanfilippo A disease): deficiency of a heparin sulfamidase in skin fibroblasts and leucocytes. Biochem Biophys Res Commun (1973) 1.12
The structure and metabolism of mucopolysaccharides (glycosaminoglycans) and the problem of the mucopolysaccharidoses. Am J Med (1969) 1.12
The Hunter corrective factor. Purification and preliminary characterization. J Biol Chem (1972) 1.11
Morquio's disease: An abnormality of mucopolysaccharide metabolism. J Pediatr (1963) 1.09
Isolation and identification of keratosulphate in urine of patients affected by Morquio-Ullrich disease. Proc Soc Exp Biol Med (1962) 1.07
Hurler's, Hunter's and Morquio's syndromes. A biochemical study in the light of current views of the underlying defects. Biochem J (1971) 1.03
Urinary excretion of acid mucopolysaccharides by patients with lupus erythematosus. J Lab Clin Med (1957) 1.00
Diagnosis of Hurler's syndrome in the hospital laboratory and the determination of its genetic type. Arch Dis Child (1966) 0.98
Hunter-Hurler syndrome: gel filtration and dialysis of urinary acid mucopolysaccharides. Nature (1968) 0.98
DIAGNOSTIC TEST FOR GARGOYLISM. Lancet (1964) 0.98
Screening for inborn errors of metabolism associated with mental deficiency or neurologic disorders or both. N Engl J Med (1966) 0.97
The nosology of the mucopolysaccharidoses. Am J Med (1969) 0.97
The glycosaminoglycans of neonatal rat skin. Biochem J (1970) 0.96
[ULTRASTRUCTURE OF THE HEPATIC CELLS IN HURLER'S DISEASE (GARGOYLISM)]. C R Hebd Seances Acad Sci (1964) 0.96
Morquio's disease and mucopolysaccharide excretion. J Pediatr (1970) 0.93
Keratosulfate-chondroitin sulfate peptide from normal urine and from urine of patients with Morquio syndrome (mucopolysaccharidosis IV). J Lab Clin Med (1968) 0.92
Urinary excretion of mucopolysaccharides in normal individuals and in the Marfan syndrome. Biochim Biophys Acta (1965) 0.92
A modified screening test for glycosaminoglycan excretion. J Clin Pathol (1969) 0.88
Sanfilippo B disease: serum assays for detection of homozygous and heterozygous individuals in three families. J Pediatr (1973) 0.87
Gas-liquid chromatographic measurement of glucosamine and galactosamine content of urinary glycosaminoglycans. Clin Chim Acta (1974) 0.87
CPC precipitable uronic acid: creatinine ratio in random urine samples collected from normal children. Acta Paediatr Scand (1972) 0.85
Characterization of the factor deficient in the Hunter syndrome by polyacrylamide gel electrophoresis. Biochem Biophys Res Commun (1970) 0.84
Commonly used tests in the detection of Hurler's syndrome. J Pediatr (1968) 0.84
Determination of acidic glycosaminoglycans (mucopolysaccharides) in urine by an ion exchange method. Application to "collagenoses", gargoylism, the nail-patella syndrome and Farber's disease. Clin Chim Acta (1967) 0.84
Thin-layer chromatographic separation of the isomeric chondroitin sulfates, dermatan sulfate, and keratan sulfate. Anal Biochem (1971) 0.84
MUCOPOLYSACCHARIDES IN DISEASE. Adv Clin Chem (1964) 0.83
Urinary glycosaminoglycan excretion in the neonatal period. Acta Paediatr Scand (1971) 0.83
Morquio-Brailsford disease. A report of four affected sisters with absence of excessive keratan sulphate in the urine. Br J Radiol (1973) 0.83
Specific isolation and analysis of mucopolysaccharides (glycosaminoglycans) from human urine. Clin Chim Acta (1972) 0.83
Excess glycosaminoglycan excretion in infancy and childhood. Acta Paediatr Scand (1973) 0.82
The determination of galactose in urinary acidic glycosaminoglycans as a measure of keratan sulfate-like substances in urine. Biochem Med (1972) 0.80
A reliable spot test for mucopolysaccharidoses. Clin Chem (1971) 0.80
Screening for mucopolysaccharidoses. Clin Chim Acta (1970) 0.80
Thin-layer chromatography and the rapid identification of common acidic glycosaminoglycans. J Chromatogr (1966) 0.80
Glycosaminoglycan fractions in normal human urine. Ann Clin Biochem (1975) 0.78
Excretion in the urine of aminoacridine precipitable polyuronides (acid mucopolysaccharides) in patients with rheumatoid arthritis. Ann Rheum Dis (1970) 0.78
Acid mucopolysaccharides of normal human urine. J Lab Clin Med (1963) 0.78
[Biochemical differentiation of Hurler's and Hunter's diseases by fracionation of heparitin sulfate]. Rev Eur Etud Clin Biol (1970) 0.78
Biochemical definition of the mucopolysaccharidoses. Z Kinderheilkd (1970) 0.78
Thin layer chromatography of urinary acid glycosaminoglycans as screening procedure for mucopolysaccharidoses. Horm Metab Res (1969) 0.78
Early diagnosis of hypermucopolysacchariduria. Clin Chim Acta (1973) 0.78
Screening tests for mucopolysaccharidosis. J Ment Defic Res (1968) 0.77
Quantitative levels of the constituents of acid mucopolysaccharides and other carbohydrate polymers in dialyzed normal human urine. Clin Chim Acta (1971) 0.77
Urinary glycosaminoglycans versus creatinine excretion: a used and abused parameter. Clin Chim Acta (1970) 0.77
Phosphatase reaction of coagulase-negative staphylococci and micrococci. J Pathol Bacteriol (1967) 2.49
Impact of home blood glucose monitoring on childhood diabetes. Arch Dis Child (1982) 1.65
A comparison of autoanalyser methods for the estimation of glucose in blood. Clin Chim Acta (1973) 1.63
A collaborative study of the measurement of glycosylated haemoglobin by several methods in seven laboratories in the United Kingdom. Diabetologia (1983) 1.17
Mannosidosis in two brothers: prolonged survival in the severe phenotype. Clin Genet (1982) 1.16
Histochemical investigation of acid mucosubstances in secondary amyloidosis. J Clin Pathol (1968) 1.15
The specificity of the staining of amyloid deposits with thioflavine T. J Pathol Bacteriol (1967) 1.14
Estimation of hydroxyproline in urine. J Med Lab Technol (1970) 1.10
Urinary total hydroxyproline: creatinine ratio. Range of normal, and clinical application in British children. Arch Dis Child (1972) 1.07
Practical considerations in kinetics of continuous flow analysis. Clin Chim Acta (1970) 1.03
Sialic acid and cardiovascular mortality. BMJ (1991) 1.01
The generalized aminoaciduria seen in patients with hepatocyte nuclear factor-1alpha mutations is a feature of all patients with diabetes and is associated with glucosuria. Diabetes (2001) 1.01
Estimation of cerebrospinal fluid protein. J Clin Pathol (1968) 0.94
An improved rapid automated method for the estimation of blood glucose. Clin Chim Acta (1972) 0.91
The relationship of height and weight velocities of adolescent boys to the total hydroxyproline: creatinine ratio in their random urines. Clin Sci (1973) 0.90
Hurler syndrome with cardiomyopathy in infancy. J Pediatr (1989) 0.90
A comparison of three methods for the estimation of capillary blood glucose in filter paper spots. Ann Clin Biochem (1982) 0.90
Measurement of sialic acid in serum and urine: clinical applications and limitations. Ann Clin Biochem (1992) 0.90
A modified screening test for glycosaminoglycan excretion. J Clin Pathol (1969) 0.88
Screening for diabetic microalbuminuria in routine clinical care: which method? Arch Dis Child (1995) 0.88
Gas-liquid chromatographic measurement of glucosamine and galactosamine content of urinary glycosaminoglycans. Clin Chim Acta (1974) 0.87
Effect of hyperbaric oxygen on the growth of aerobic organisms in deep culture. Lancet (1966) 0.86
CPC precipitable uronic acid: creatinine ratio in random urine samples collected from normal children. Acta Paediatr Scand (1972) 0.85
Association of acid mucopolysaccharides with isolated amyloid fibrils. Nature (1968) 0.85
Maternal leucocyte zinc deficiency at start of third trimester as a predictor of fetal growth retardation. Br Med J (Clin Res Ed) (1987) 0.84
Hepatic beta galactosidase and feline GMI gangliosidosis. Neuropathol Appl Neurobiol (1982) 0.83
Urinary glycosaminoglycan excretion in the neonatal period. Acta Paediatr Scand (1971) 0.83
Fructosamine and glycated haemoglobin in the assessment of long term glycaemic control in diabetes. Arch Dis Child (1994) 0.82
Are frozen urine samples acceptable for estimating albumin excretion in research? Diabet Med (1995) 0.82
Excess glycosaminoglycan excretion in infancy and childhood. Acta Paediatr Scand (1973) 0.82
Increases in plasma lysosomal enzymes in type 1 (insulin-dependent) diabetes mellitus: relationship to diabetic complications and glycaemic control. Diabetologia (1992) 0.81
Interaction of 1,9-dimethylmethylene blue with glycosaminoglycans. Ann Clin Biochem (1994) 0.81
Urinary hydroxyproline in children with growth hormone deficiency. Clinical value in diagnosis and prognosis. Arch Dis Child (1974) 0.80
Screening for mucopolysaccharidoses. Clin Chim Acta (1970) 0.80
Abnormal keratan sulphate excretion. Ann Clin Biochem (1979) 0.80
Proceedings: Enzyme defects in mucopolysaccharidoses. J Clin Pathol (1976) 0.79
Faecal excretion of oligosaccharides and other carbohydrates in normal neonates. Arch Dis Child (1978) 0.78
Epiphyseal cartilage chemistry in thanatophoric dwarfism. Lancet (1977) 0.78
Interaction of water-soluble amyloid fibrils with Congo Red and thioflavine T. Clin Chim Acta (1969) 0.78
Gas chromatographic measurement of blood and urine glucose and other monosaccharides. Clin Chim Acta (1972) 0.78
Decreased sialidase activity in mononuclear leucocytes of type 1 diabetic subjects: relationship to diabetic complications and glycaemic control. Diabet Med (1995) 0.76
The mucopolysaccharidoses. J Med Genet (1976) 0.76
Urinary heparan sulphate proteoglycan excretion is abnormal in insulin dependent diabetes. Ann Clin Biochem (1995) 0.76
Effect of ethylene-diamine-tetra-acetic acid (dipotassium salt) and heparin on the estimation of packed cell volume. J Clin Pathol (1966) 0.75
Relation of urinary total hydroxyproline: Creatinine ratio to height velocity in children with retarded growth. Arch Dis Child (1976) 0.75
Freeze-stable sialidase activity in human leucocytes: substrate specificity, inhibitor susceptibility, detergent requirements and subcellular localization. Biochem J (1994) 0.75
Urinary hydroxyproline and thyroid disease. Br Med J (1971) 0.75
Management of acute salicylate poisoning. Br Med J (1969) 0.75
Identity of an oligosaccharide present in faeces in breast-fed neonates. Ann Clin Biochem (1979) 0.75
Carrier detection for Sanfilippo A syndrome. J Inherit Metab Dis (1990) 0.75
Abnormal ganglioside in neuroblastoma. Lancet (1986) 0.75
The ammonia checker. Ann Clin Biochem (1984) 0.75
The attainment of increased sampling rates in continuous flow analysis. Med Lab Technol (1973) 0.75
Factors affecting the assay of urinary free and bound sialic acid. Biochem Soc Trans (1992) 0.75
Amniotic fluid total hydroxyproline and intrauterine growth. J Obstet Gynaecol Br Commonw (1971) 0.75
Amniotic fluid creatinine: an unreliable index of fetal maturity. J Obstet Gynaecol Br Commonw (1972) 0.75
Association between serum cholesterol and leucocyte lysosomal function. Ann Clin Biochem (1994) 0.75
The chemistry of human neonatal femoral epiphyseal cartilage. Clin Chim Acta (1976) 0.75
The systemic effect of bromhexine ('Bisolvon') in normal subjects. Curr Med Res Opin (1972) 0.75
Brain gangliosides: an improved simple method for their extraction and identification. J Chromatogr (1980) 0.75
Keratan sulphate excretion in a patient with Kniest dysplasia. J Inherit Metab Dis (1980) 0.75
Simple gas chromatographic screening procedure for lactic and pyruvic acids in human plasma. J Chromatogr (1979) 0.75
Diabetes-related changes in sialic acid content of leucocytes: an assay-dependent artefact? Biochem Soc Trans (1993) 0.75
Cord blood C-peptide:glucose ratio - a good indicator of B cell function in infants of diabetic mothers. Diabetologia (1981) 0.75