G. Berger

发表

HMG-CoA reductase is not the site of the primary defect in phytosterolemia.

A. Marais, R. Naoumova, P. Naidu, 1998, Journal of lipid research.

Dietary cholesterol--the role of eggs in the prudent diet.

A. Beynen, H. Vorster, G. Berger, 1995, South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde.

A diversity of genetic hyperlipoproteinaemias in black patients. Experience at the Lipid Clinics at Groote Schuur Hospital and Red Cross War Memorial Children's Hospital, Cape Town.

A. Marais, G. Berger, 1986, South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde.

Action limits for serum total cholesterol. A statement for the medical profession by an ad hoc committee of the Heart Foundation of Southern Africa.

J. Rossouw, K. Steyn, G. Berger, 1988, South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde.

Molecular diagnosis of multiple endocrine neoplasia type 2A.

R. Pegoraro, G. Berger, L. Rom, 1998, South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde.

Absence of Serum-Stimulated Lipase Activity and Altered Lipid Content in Milk from a Patient with Type I Hyperlipoproteinaemia

J. Huskisson, G. Berger, A. Spark, 1983, Pediatric Research.

Continuous flow plasma exchange in the treatment of homozygous familial hypercholesterolemia.

G. Berger, H. S. Joffe, F. Bonnici, 1978, The American journal of medicine.

Treatment of hypercholesterolemia with the HMG CoA reductase inhibitor, simvastatin

A. Marais, G. Berger, B. Joffe, 1989, Cardiovascular Drugs and Therapy.

A new LDL receptor gene deletion mutation in the South African population

A. Marais, G. Berger, H. Henderson, 1988, Human Genetics.

Multiple mutations underlying familial hypercholesterolemia in the South African population

M. Kotze, G. Berger, H. Henderson, 1989, Human Genetics.

The lipoprotein lipase Gly188----Glu mutation in South Africans of Indian descent: evidence suggesting common origins and an increased frequency.

M. Hayden, G. Berger, H. Henderson, 1992, Journal of medical genetics.

Three different schedules of low-density lipoprotein apheresis compared with plasmapheresis in patients with homozygous familial hypercholesterolemia.

A. Marais, J. Firth, G. Berger, 1990, The American journal of medicine.

Alpha fetoprotein in the antenatal diagnosis of the congenital nephrotic syndrome.

G. Berger, R. Kaschula, J. Wiggelinkhuizen, 1976, The Journal of pediatrics.

Apolipoprotein E allele frequencies in a South African Indian female population

R. Pegoraro, G. Berger, N. Gounden, 1995, Clinical genetics.

Phytosterolaemia in three unrelated South African families.

A. Marais, G. Berger, W. Deppe, 1994, Postgraduate medical journal.

Automation of serum cholinesterase assay--paediatric and adult reference ranges.

B. Fuller, G. Berger, 1990, South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde.

Amylase: creatinine clearance ratio and urinary excretion of lysozyme in acute pancreatitis and acute duodenal perforation.

G. Berger, J. Cowlin, T. J. Turner, 1976, South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde.

The raised anion gap in Bartter's syndrome.

G. Berger, K. Sprenger, 1983, South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde.

Acute dehydrating gastro-enteritis in undernourished infants. The diagnosis and correction of electrolyte and metabolic abnormalities.

G. Berger, H. D. Heese, M. Mann, 1974, South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde.

Analbuminaemia. Clinical and laboratory features in a South African patient.

C. R. Stephen, G. Berger, A. Finestone, 1985, South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde.

Low serum cholinesterase levels in rural workers exposed to organophosphate pesticide sprays.

B. Fuller, G. Berger, D. Innes, 1990, South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde.

Association of a DNA polymorphism in the apolipoprotein C-III gene with diverse hyperlipidaemic phenotypes

G. Berger, H. Henderson, S. V. Landon, 1987, Human Genetics.

Apolipoprotein B detected in the plasma of a patient with homozygous hypobetalipoproteinaemia: implications for aetiology.

G. Berger, H. Henderson, F. Bonnici, 1983, Journal of medical genetics.

Marked Hyperinsulinaemia in Postmenopausal, Healthy Indian (Asian) Women

E. Gouws, G. Berger, N. Gounden, 1995, Diabetic medicine : a journal of the British Diabetic Association.

Portacaval shunt in two patients with homozygous type II hyperlipoproteinaemia.

J. Louw, M. Davies, G. Berger, 1976, South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde.

Nutritional status, dietary intake and disease patterns in rural Hereros, Kavangos and Bushmen in South West Africa/Namibia.

S. O'keefe, N. Marot, K. Symmonds, 1988, South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde.