Published in Acta Paediatr Scand on September 01, 1982
Review of neonatal screening programme for phenylketonuria. BMJ (1991) 3.43
Cows' milk allergy in the syndrome of thrombocytopenia with absent radius. Arch Dis Child (1976) 1.84
Ciprofloxacin for treating urethral gonorrhoea in men. Genitourin Med (1986) 1.78
Partial trisomy for long arm of chromosome 16. J Med Genet (1981) 1.28
Oral calcium-loading test in infancy, with particular reference to idiopathic hypercalcaemia. Br Med J (1969) 1.24
GNAS1 mutational analysis in pseudohypoparathyroidism. Clin Endocrinol (Oxf) (1998) 1.17
Transient neonatal hyperparathyroidism secondary to maternal pseudohypoparathyroidism. Arch Dis Child (1981) 1.12
Persisting vitamin D deficiency in the Asian adolescent. Arch Dis Child (1984) 1.01
Catch-up growth in malnutrition, studied in celiac disease after institution of gluten-free diet. Pediatr Res (1972) 1.01
Vital signs for children at triage: a multicentre validation of the revised South African Triage Scale (SATS) for children. S Afr Med J (2013) 1.00
Salmonella gona infection in sheep. Vet Rec (1978) 0.99
Measurement of osmolality and sodium concentration in heated-cup sweat collections for the investigation of cystic fibrosis. Ann Clin Biochem (1983) 0.93
Immunisation against plague by transcutaneous and intradermal application of subunit antigens. Vaccine (2004) 0.91
Chronic hypoparathyroidism in two generations. Helv Paediatr Acta (1971) 0.88
Acute iron poisoning in children: role of chelating agents. Br Med J (1968) 0.87
Plasma cyclic AMP response to intravenous parathyroid hormone in pseudohypoparathyroidism. Acta Paediatr Scand (1991) 0.86
Childhood in-hospital mortality from acute gastro-enteritis in Cape Town. S Afr Med J (2010) 0.86
Arterial plasma histamine after exercise in normal individuals an in patients with exercise-induced asthma. Clin Sci (Lond) (1981) 0.85
Direct current cardioversion in a case of congenital atrial flutter. Arch Dis Child (1972) 0.84
Preliminary report on inverse diurnal variation of phenylalanine: implications in maternal phenylketonuria. Hum Nutr Appl Nutr (1985) 0.83
Neurogenic chronic idiopathic intestinal pseudo-obstruction, patent ductus arteriosus, and thrombocytopenia segregating as an X linked recessive disorder. J Med Genet (1997) 0.82
Nager acrofacial dysostosis: minor familial manifestations supporting dominant inheritance. Clin Genet (1993) 0.82
Organisation of the human PAX4 gene and its exclusion as a candidate for the Wolcott-Rallison syndrome. J Med Genet (1998) 0.81
An improved radioenzymatic assay for histamine in human plasma, whole blood, urine, and gastric juice. Ann Clin Biochem (1979) 0.81
Short report: Hyperammonaemia in critically ill septic infants. Arch Dis Child (2001) 0.81
Rickets of prematurity: calcium and phosphorus supplementation. J Pediatr (1985) 0.81
Heterozygote detection in phenylketonuria. Measurement of discriminatory ability and interpretation of the phenylalanine loading test by determination of the heterozygote likelihood ratio. J Med Genet (1975) 0.81
An adapted triage tool (ETAT) at Red Cross War Memorial Children's Hospital Medical Emergency Unit, Cape Town: an evaluation. S Afr Med J (2012) 0.81
Catch-up growth in cortisone-treated rats: effects of calcium and vitamin D. Pediatr Res (1978) 0.80
Prostaglandin synthetase inhibitor in an infant with congenital chloride diarrhoea. Arch Dis Child (1980) 0.80
Oral calcium-loading test in rickets and in neonatal tetany: effect of vitamin D. Br Med J (1969) 0.80
Familial growth hormone releasing factor deficiency in pseudopseudohypoparathyroidism. Arch Dis Child (1991) 0.79
Separation of three isoenzymes of N-acetyl-beta-D-hexosaminidase from human tissues by cellulose acetate membrane electrophoresis. J Clin Pathol (1974) 0.78
Safety and efficacy of three oral rehydration solutions for children with diarrhoea (Edinburgh 1984-85). Acta Paediatr Scand (1989) 0.78
Interpretation of sweat sodium results--the effect of patient age. Ann Clin Biochem (1989) 0.78
Transition from child- to adult-orientated care for children with long-term health conditions: a process, not an event. S Afr Med J (2014) 0.76
Identification of the correct lumbar level using passive intersegmental motion testing. Anaesthesia (2007) 0.76
C-trisomy in a case of neonatal leukaemia. Arch Dis Child (1980) 0.75
Parental consanguinity in the blepharophimosis, heart defect, hypothyroidism, mental retardation syndrome (Young-Simpson syndrome). J Med Genet (1993) 0.75
Hypercarotenaemia and vitamin A overdosage from proprietary baby food. Lancet (1986) 0.75
Biochemical observations on a non-elite marathon runner. J Clin Chem Clin Biochem (1984) 0.75
Colorimetric method for determination of urinary methylmalonic acid. Ann Clin Biochem (1979) 0.75
Proceedings: Bone deficiency in Turner's syndrome measured by metacarpal dimensions. Arch Dis Child (1974) 0.75
Serum ALT levels in patients with primary hypogammaglobulinaemia receiving replacement therapy with intravenous immunoglobulin or fresh frozen plasma. Vox Sang (1986) 0.75
Erysipelas in the guinea-fowl. Vet Rec (1971) 0.75
Determination of total and direct bilirubin in plasma by means of a bichromatic method on a centrifugal analyser. Ann Clin Biochem (1982) 0.75
An examination of the hexokinase method for serum glucose assay using external quality assessment data. Ann Clin Biochem (1986) 0.75
Climate change is catchy - but when will it really hurt? S Afr Med J (2015) 0.75
Galactose-I-phosphate uridyl transferase: a new manometric assay specially suited to erythrocyte studies in galactosaemia. Clin Chim Acta (1973) 0.75