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Managed care. Origins, principles, and evolution

BMJ (Online), 1997-06, Vol.314 (7097), p.1823

1997

Volltextzugriff (PDF)

Implications of managed care for health systems, clinicians, and patients

BMJ (Online), 1997-06, Vol.314 (7098), p.1895

1997

Volltextzugriff (PDF)

Normal glycine transport in cultured diploid fibroblasts from hyperglycinaemic subjects

Journal of inherited metabolic disease, 1983-09, Vol.6 (2), p.82-84

1983

Volltextzugriff (PDF)

Antithrombin III deficiency in the nephrotic syndrome. Threatened thrombosis treated with fresh plasma

Ugeskrift for læger, 1984-07, Vol.146 (28), p.2092

1984

Volltextzugriff (PDF)

The trisomy 8 syndrome: report of two further cases

Annales de génétique, 1974-06, Vol.17 (2), p.87

1974

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Managed care: implications of managed care for health systems, clinicians, and patients

British Medical Journal, 1997-06, Vol.314 (7098), p.1895-1898

1997

Volltextzugriff (PDF)

Managed care: origins, principles, and evolution

British Medical Journal, 1997-06, Vol.314 (7097), p.1823-1826

1997

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Brave new world in clinical microbiology?

Ugeskrift for læger, 1991-05, Vol.153 (21), p.1506

Søgaard, P

1991

Volltextzugriff (PDF)

URINARY PHENYLALANINE EXCRETION IN HYPERPHENYL-ALANINEMIC CHILDREN

Acta Paediatrica, 1973-07, Vol.62 (4), p.333-336

1973

Volltextzugriff (PDF)

The genome of the recently domesticated crop plant sugar beet (Beta vulgaris)

Nature (London), 2014-01, Vol.505 (7484), p.546-549

2014

Volltextzugriff (PDF)

Normal glycine transport in cultured diploid fibroblasts from hyperglycinaemic subjects

Journal of inherited metabolic disease, 1982-01, Vol.6 (2), p.82-87

1982

Volltextzugriff (PDF)

Non-ketotic C6-C10-dicarboxylic aciduria: biochemical investigations of two cases

Clinica chimica acta, 1980-03, Vol.102 (2-3), p.179-189

1980

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

4.2. Studies on the required analytical quality of TSH measurements in screening for congenital hypothyroidism

Scandinavian journal of clinical and laboratory investigation, 1980, Vol.40 (S154), p.85-93

1980

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A ring chromosome, diagnosed by quinacrine fluorescence as No. 9, in a mentally retarded girl

Clinical genetics, 1973-01, Vol.4 (5), p.434-441

1973

Volltextzugriff (PDF)

Studies on the required analytical quality of TSH measurements in screening for congenital hypothyroidism

Scandinavian journal of clinical & laboratory investigation. Supplement, 1980, Vol.155, p.85

1980

Volltextzugriff (PDF)

Crop wild relative populations of Beta vulgaris allow direct mapping of agronomically important genes

Nature communications, 2017-06, Vol.8 (1), p.15708-15708, Article 15708

2017

Volltextzugriff (PDF)

Urinary phenylalanine excretion in hyperphenylalaninemic children

Acta pædiatrica Scandinavica, 1973-07, Vol.62 (4), p.333

1973

Volltextzugriff (PDF)

Hyperprolinemia type II

Ugeskrift for læger, 1974-11, Vol.136 (45), p.2530

1974

Volltextzugriff (PDF)

Hyperprolinemia type I

Ugeskrift for læger, 1974-10, Vol.136 (44), p.2460

1974

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Managed care. Origins, principles, and evolution

Implications of managed care for health systems, clinicians, and patients

Normal glycine transport in cultured diploid fibroblasts from hyperglycinaemic subjects

Antithrombin III deficiency in the nephrotic syndrome. Threatened thrombosis treated with fresh plasma

The trisomy 8 syndrome: report of two further cases

Managed care: implications of managed care for health systems, clinicians, and patients

Managed care: origins, principles, and evolution

Brave new world in clinical microbiology?

URINARY PHENYLALANINE EXCRETION IN HYPERPHENYL-ALANINEMIC CHILDREN

The genome of the recently domesticated crop plant sugar beet (Beta vulgaris)

Normal glycine transport in cultured diploid fibroblasts from hyperglycinaemic subjects

Non-ketotic C6-C10-dicarboxylic aciduria: biochemical investigations of two cases

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

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

4.2. Studies on the required analytical quality of TSH measurements in screening for congenital hypothyroidism

A ring chromosome, diagnosed by quinacrine fluorescence as No. 9, in a mentally retarded girl

Studies on the required analytical quality of TSH measurements in screening for congenital hypothyroidism

Crop wild relative populations of Beta vulgaris allow direct mapping of agronomically important genes

Urinary phenylalanine excretion in hyperphenylalaninemic children

Hyperprolinemia type II

Hyperprolinemia type I

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