George van der Watt

Glutaric aciduria type 1 in South Africa—high incidence of glutaryl-CoA dehydrogenase deficiency in black South Africans

George van der Watt, E. Owen, Peter Berman et al. · Molecular Genetics and Metabolism · 2010 · 52 citations

Life Sciences, Biochemistry, Genetics +4

The First Case of Riboflavin Transporter Deficiency in sub-Saharan Africa

Shaakira Chaya, Marco Zampoli, Diane Gray et al. · Seminars in Pediatric Neurology · 2017 · 25 citations

Public Health, Biochemistry, Nutrition +14

Euthyroid Patient with Elevated Serum Free Thyroxine

George van der Watt, David Haarburger, Peter Berman · Clinical Chemistry · 2008 · 22 citations · Full text

Medicine, Dermatology, Endocrinology +17

Vitamin D abnormalities and bone turn over analysis in children with epilepsy in the Western Cape of South Africa.

Edward Kija, Barry E. Gidal, Alexander Shapson-Coe et al. · Seizure · 2019 · 17 citations · Full text

Medicine, Nutritional Sciences, Pediatrics +17

Common mutation causes cystinosis in the majority of black South African patients

E. Owen, Jenisha Nandhlal, Felicity Leisegang et al. · Pediatric Nephrology · 2014 · 16 citations

Life Sciences, Genetics, Molecular Genetics +9