Glutaric aciduria type 1 in South Africa—high incidence of glutaryl-CoA dehydrogenase deficiency in black South Africans G van der Watt, EP Owen, P Berman, S Meldau, N Watermeyer, SE Olpin, ... Molecular genetics and metabolism 101 (2-3), 178-182, 2010 | 64 | 2010 |
Reference change values: how useful are they? F Omar, GF van der Watt, TS Pillay Journal of Clinical Pathology 61 (4), 426-427, 2008 | 39 | 2008 |
The first case of riboflavin transporter deficiency in sub-Saharan Africa S Chaya, M Zampoli, D Gray, J Booth, G Riordan, A Ndondo, K Fieggen, ... Seminars in Pediatric Neurology 26, 10-14, 2018 | 30 | 2018 |
Plasma sarcosine does not distinguish early and advanced stages of prostate cancer L Bohm, AM Serafin, P Fernandez, G Van der Watt, PJD Bouic, J Harvey SAMJ: South African Medical Journal 102 (8), 677-679, 2012 | 26 | 2012 |
Euthyroid patient with elevated serum free thyroxine G van der Watt, D Haarburger, P Berman Clinical chemistry 54 (7), 1239-1241, 2008 | 24 | 2008 |
Laboratory investigation of the child with suspected renal disease G Van der Watt, F Omar, A Brink, M McCulloch Pediatric Nephrology, 7th Edn. Heidelberg: Springer-Verlag, 613-636, 2016 | 19 | 2016 |
Common mutation causes cystinosis in the majority of black South African patients EP Owen, J Nandhlal, F Leisegang, G Van der Watt, P Nourse, P Gajjar Pediatric Nephrology 30, 595-601, 2015 | 18 | 2015 |
Vitamin D abnormalities and bone turn over analysis in children with epilepsy in the Western Cape of South Africa. E Kija, BE Gidal, A Shapson-Coe, S Cader, G van der Watt, S Delport, ... Seizure 69, 186-192, 2019 | 16 | 2019 |
Identification of a single MPV17 nonsense‐associated altered splice variant in 24 South African infants with mitochondrial neurohepatopathy S Meldau, RJ De Lacy, GTM Riordan, EA Goddard, K Pillay, KJ Fieggen, ... Clinical genetics 93 (5), 1093-1096, 2018 | 16 | 2018 |
Pseudoparaproteinemia after iopamidol infusion for coronary angiography G van der Watt, P Berman Clinical chemistry 51 (1), 273-274, 2005 | 16 | 2005 |
Residual allergenicity of amino acid-based and extensively hydrolysed cow’s milk formulas ME Levin, DM Blackhurst, F Kirstein, D Kok, GF Van der Watt, AD Marais South African Medical Journal 107 (9), 763-767, 2017 | 13 | 2017 |
Cystine urolithiasis in a caracal (Caracal caracal) ASW Tordiffe, GF Van Der Watt, F Reyers Journal of Zoo and Wildlife Medicine 43 (3), 649-651, 2012 | 10 | 2012 |
Mitochondrial dysfunction and human immunodeficiency virus infection G Van der Watt Journal of Endocrinology, Metabolism and Diabetes of South Africa 16 (2), 94-100, 2011 | 6 | 2011 |
Hemiatrophy of the spinal cord in a patient with mucopolysaccharidosis type IIIB P Samia, N Wieselthaler, GF Van Der Watt, JM Wilmshurst Journal of child neurology 25 (10), 1288-1291, 2010 | 5 | 2010 |
Plasma free fatty acid reference interval in South African neonates in the first week of life F Omar, G van der Watt, V November, TS Pillay Annals of clinical biochemistry 47 (4), 381-382, 2010 | 5 | 2010 |
Teenaged siblings with progressive neurocognitive disease D Haarburger, R Renison, S Meldau, R Eastman, G van der Watt Clinical Chemistry 59 (8), 1160-1164, 2013 | 4 | 2013 |
Whole blood mitochondrial DNA depletion in South African HIV-infected children GF van der Watt, B Eley, H Henderson Journal of Pediatric Biochemistry 1 (3), 225-232, 2010 | 2 | 2010 |
Clinical, biochemical, and genetic spectrum of MADD in a South African cohort: an ICGNMD study M Bisschoff, I Smuts, M Dercksen, M Schoonen, BC Vorster, ... Orphanet Journal of Rare Diseases 19 (1), 15, 2024 | 1 | 2024 |
Extensively hydrolysed infant formulas: Need for aligned definition of peptide size characteristics and standardisation of analytical methods S Nutten, M Kuslys, F Maynard, M Affolter, RG Heine South African Medical Journal 108 (11), 887-888, 2018 | 1 | 2018 |
A novel mitochondrial DNA variant in MT-ND6: m. 14430A> C p.(Trp82Gly) identified in a patient with Leigh syndrome and complex I deficiency S Meldau, S Ackermann, G Riordan, GF van der Watt, C Spencer, S Raga, ... Molecular Genetics and Metabolism Reports 39, 101078, 2024 | | 2024 |