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Possible genetic defects in regulation of glycosaminoglycans in patients with diabetic nephropathy

Diabetes (New York, N.Y.), 1991-06, Vol.40 (6), p.764-770

1991

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Possible genetic defects in regulation of glycosaminoglycans in patients with diabetic nephropathy

Diabetes (New York, N.Y.), 1991-06, Vol.40 (6), p.764-770

1991

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Increased Vigilance and Dopamine Synthesis by Large Doses of Tyrosine or Phenylalanine Restriction in Phenylketonuria

Acta Paediatrica, 1987-07, Vol.76 (4), p.560-565

1987

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Decreased vigilance and neurotransmitter synthesis after discontinuation of dietary treatment for phenylketonuria in adolescents

European journal of pediatrics, 1985-05, Vol.144 (1), p.17-20

1985

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Increased neurotransmitter biosynthesis in phenylketonuria induced by phenylalanine restriction or by supplementation of unrestricted diet with large amounts of tyrosine

European journal of pediatrics, 1988-12, Vol.148 (3), p.238-245

1988

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Rapid micromethod for flourometric determination of neutral lipids on thin-layer chromatograms

Scandinavian journal of clinical and laboratory investigation, 1979, Vol.39 (5), p.479-483

1979

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Plasma glucagon responses to insulin-induced hypoglycaemia and arginine in normal and alloxan diabetic rats

Scandinavian journal of clinical and laboratory investigation, 1979, Vol.39 (2), p.151-157

1979

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Detection of hyperlipidemia by semiquantitative fluorometric determinations of serum lipids on thin-layer chromatograms

Scandinavian journal of clinical and laboratory investigation, 1980, Vol.40 (4), p.389-391

1980

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Tetrahydrobiopterin and Parkinson's disease

Acta neurologica Scandinavica, 1989-06, Vol.79 (6), p.493-499

1989

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Combined tetrahydrobiopterin-phenylalanine loading test in the detection of partially defective biopterin synthesis

European journal of pediatrics, 1984-06, Vol.142 (2), p.126-129

1984

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Biopterin, neopterin and tyrosine responses to combined oral phenylalanine and tetrahydrobiopterin loading tests in two normal children and in a girl with partial biopterin deficiency

Journal of inherited metabolic disease, 1985-06, Vol.8 (S2), p.95-96

1985

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Reliability of the use of fructose 1-phosphate to detect Hunter cells in fibroblast-cultures of obligate carriers of the Hunter syndrome

Human genetics, 1983-01, Vol.64 (4), p.371-375

1983

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FEASIBILITY OF FIRST TRIMESTER PRENATAL DIAGNOSIS OF HUNTER SYNDROME

The Lancet (British edition), 1983-11, Vol.322 (8359), p.1147-1147

1983

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METACHROMATIC LEUKODYSTROPHY AND PSEUDOARYLSULFATASE A DEFICIENCY IN A DANISH FAMILY

Acta Paediatrica, 1983-03, Vol.72 (2), p.175-178

1983

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Normal excretion of urinary acid mucopolysaccharides in a boy with iduronate sulphatase deficiency, Hunter phenotype and α1-antitrypsin deficiencydeficiency

European journal of pediatrics, 1986-12, Vol.145 (6), p.572-575

1986

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Normal excretion of urinary acid mucopolysaccharides in a boy with iduronate sulphatase deficiency, Hunter phenotype and alpha 1-antitrypsin deficiency

European journal of pediatrics, 1986-12, Vol.145 (6), p.572-575

1986

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Diagnosis of Hunter's syndrome carriers; radioactive sulphate incorporation into fibroblasts in the presence or fructose 1-phosphate

Human genetics, 1982-01, Vol.60 (2), p.167-171

1982

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Mucopolysaccharidoses

Ugeskrift for læger, 1987-05, Vol.149 (22), p.1439

1987

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Feasibility of first trimester prenatal diagnosis of Hunter syndrome

The Lancet (British edition), 1983-11, Vol.2 (8359), p.1147

1983

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Prenatal diagnosis of chromosomal and hereditary metabolic disease during the 1st trimester

Ugeskrift for læger, 1984-06, Vol.146 (25), p.1841

1984

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Feasibility of first trimester prenatal diagnosis of Hunter syndrome

Lancet (London, England), 1983, Vol.2 (8359), p.1147-1147

1983

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Possible genetic defects in regulation of glycosaminoglycans in patients with diabetic nephropathy

Possible genetic defects in regulation of glycosaminoglycans in patients with diabetic nephropathy

Increased Vigilance and Dopamine Synthesis by Large Doses of Tyrosine or Phenylalanine Restriction in Phenylketonuria

Decreased vigilance and neurotransmitter synthesis after discontinuation of dietary treatment for phenylketonuria in adolescents

Increased neurotransmitter biosynthesis in phenylketonuria induced by phenylalanine restriction or by supplementation of unrestricted diet with large amounts of tyrosine

Rapid micromethod for flourometric determination of neutral lipids on thin-layer chromatograms

Plasma glucagon responses to insulin-induced hypoglycaemia and arginine in normal and alloxan diabetic rats

Detection of hyperlipidemia by semiquantitative fluorometric determinations of serum lipids on thin-layer chromatograms

Tetrahydrobiopterin and Parkinson's disease

Combined tetrahydrobiopterin-phenylalanine loading test in the detection of partially defective biopterin synthesis

Biopterin, neopterin and tyrosine responses to combined oral phenylalanine and tetrahydrobiopterin loading tests in two normal children and in a girl with partial biopterin deficiency

Reliability of the use of fructose 1-phosphate to detect Hunter cells in fibroblast-cultures of obligate carriers of the Hunter syndrome

FEASIBILITY OF FIRST TRIMESTER PRENATAL DIAGNOSIS OF HUNTER SYNDROME

METACHROMATIC LEUKODYSTROPHY AND PSEUDOARYLSULFATASE A DEFICIENCY IN A DANISH FAMILY

Normal excretion of urinary acid mucopolysaccharides in a boy with iduronate sulphatase deficiency, Hunter phenotype and α1-antitrypsin deficiencydeficiency

Normal excretion of urinary acid mucopolysaccharides in a boy with iduronate sulphatase deficiency, Hunter phenotype and alpha 1-antitrypsin deficiency

Diagnosis of Hunter's syndrome carriers; radioactive sulphate incorporation into fibroblasts in the presence or fructose 1-phosphate

Mucopolysaccharidoses

Feasibility of first trimester prenatal diagnosis of Hunter syndrome

Prenatal diagnosis of chromosomal and hereditary metabolic disease during the 1st trimester

Feasibility of first trimester prenatal diagnosis of Hunter syndrome

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