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Heterozygote detection in phenylketonuria. Measurement of discriminatory ability and interpretation of the phenylalanine loading test by determination of the heterozygote likelihood ratio

Journal of medical genetics, 1975-12, Vol.12 (4), p.327-333

1975

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Biopterin derivatives in normal and phenylketonuric patients after oral loads of L-phenylalanine, L-tyrosine, and L-tryptophan

Archives of disease in childhood, 1976-10, Vol.51 (10), p.771-777

1976

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Effect of treatment on tryptophan metabolism in childhood epilepsy

Annals of the New York Academy of Sciences, 1969-09, Vol.166 (1), p.297-305

Raine, D N

1969

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Tay, Sachs et al

The Lancet (British edition), 1969-11, Vol.2 (7627), p.959-960

Raine, D N

1969

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Lead Intoxication in Children in Birmingham

BMJ, 1973-02, Vol.1 (5850), p.402-406

1973

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Estimation of Thiotepa in Urine

Journal of pharmacy and pharmacology, 1962-09, Vol.14 (1), p.614-615

Raine, D. N.

1962

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Macroscopic demonstration of infarction in fresh brain slices

Journal of clinical pathology, 1962-11, Vol.15 (6), p.593-593

Raine, D. N.

1962

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Varicella infection contracted in utero: Sex incidence and incubation period

American journal of obstetrics and gynecology, 1966-04, Vol.94 (8), p.1144-1145

Raine, D.N.

1966

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Faecal composition after surgery for Hirschsprung's disease

Archives of disease in childhood, 1976-10, Vol.51 (10), p.784-789

1976

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A salt-losing syndrome in infancy. Pseudo-hypoadrenocorticalism

Archives of disease in childhood, 1962-10, Vol.37 (195), p.548-556

1962

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In vivo formation of pyridoxal phosphate schiff's base—an inherent defect in the tryptophan load test

Clinica chimica acta, 1966-09, Vol.14 (3), p.399-402

1966

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Immunoelectrophoretic study of proteins in middle ear effusion. A study of secretory otitis media in children

Journal of laryngology and otology, 1976-11, Vol.90 (11), p.1033-1040

1976

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An improved estimation of phosphorus following digestion with hydrogen peroxide

Analytical biochemistry, 1964-12, Vol.9 (4), p.492-495

1964

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The need for a national policy for the management of inherited metabolic disease

Journal of clinical pathology, 1974, Vol.27 (Suppl 8), p.156-163

Raine, D. N.

1974

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Metabolism of tryptophan in childhood epilepsy

Archives of disease in childhood, 1966-12, Vol.41 (220), p.642-651

1966

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Effect of treatment on the metabolism of tryptophan in childhood epilepsy

Archives of disease in childhood, 1967-06, Vol.42 (223), p.281-288

1967

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Early detection of phenylketonuria and other aminoacidopathies in a large city using plasma chromatography

Archives of disease in childhood, 1971-12, Vol.46 (250), p.885-885

Raine, D N

1971

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Screening for several amino acidopathies in neonates in Birmingham by plasma chromatography

Archives of disease in childhood, 1971-12, Vol.46 (250), p.881-881

Raine, D N

1971

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Neonatal screening for sickle haemoglobinopathies in Birmingham

BMJ, 1982-03, Vol.284 (6320), p.933-935

1982

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Leucocyte hydrolytic enzymes in the diagnosis of some neurological disorders

Archives of disease in childhood, 1970-10, Vol.45 (243), p.708-708

Raine, D N

1970

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Screening for Inherited Metabolic Disease by Plasma Chromatography (Scriver) in a Large City

BMJ, 1972-07, Vol.3 (5817), p.7-13

1972

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Inherited metabolic disease

The Lancet (British edition), 1974-10, Vol.2 (7887), p.996-998

Raine, D N

1974

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The need for a national policy for the management of inherited metabolic disease

Journal of clinical pathology. Supplement. Royal College of Pathologists symposia, 1974, Vol.8, p.156

Raine, D N

1974

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Separation of three isoenzymes of N-acetyl-β-D-hexosaminidase from human tissues by cellulose acetate membrane electrophoresis

Journal of clinical pathology, 1974-11, Vol.27 (11), p.913-915

1974

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An ether-soluble precursor of coproporphyrin in urine

Biochemical journal, 1950-08, Vol.47 (2), p.xiv-v

RAINE, D N

1950

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Heterozygote detection in phenylketonuria. Measurement of discriminatory ability and interpretation of the phenylalanine loading test by determination of the heterozygote likelihood ratio

Biopterin derivatives in normal and phenylketonuric patients after oral loads of L-phenylalanine, L-tyrosine, and L-tryptophan

Effect of treatment on tryptophan metabolism in childhood epilepsy

Tay, Sachs et al

Lead Intoxication in Children in Birmingham

Estimation of Thiotepa in Urine

Macroscopic demonstration of infarction in fresh brain slices

Varicella infection contracted in utero: Sex incidence and incubation period

Faecal composition after surgery for Hirschsprung's disease

A salt-losing syndrome in infancy. Pseudo-hypoadrenocorticalism

In vivo formation of pyridoxal phosphate schiff's base—an inherent defect in the tryptophan load test

Immunoelectrophoretic study of proteins in middle ear effusion. A study of secretory otitis media in children

An improved estimation of phosphorus following digestion with hydrogen peroxide

The need for a national policy for the management of inherited metabolic disease

Metabolism of tryptophan in childhood epilepsy

Effect of treatment on the metabolism of tryptophan in childhood epilepsy

Early detection of phenylketonuria and other aminoacidopathies in a large city using plasma chromatography

Screening for several amino acidopathies in neonates in Birmingham by plasma chromatography

Neonatal screening for sickle haemoglobinopathies in Birmingham

Leucocyte hydrolytic enzymes in the diagnosis of some neurological disorders

Screening for Inherited Metabolic Disease by Plasma Chromatography (Scriver) in a Large City

Inherited metabolic disease

The need for a national policy for the management of inherited metabolic disease

Separation of three isoenzymes of N-acetyl-β-D-hexosaminidase from human tissues by cellulose acetate membrane electrophoresis

An ether-soluble precursor of coproporphyrin in urine

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