关注
George Frederick Van Der Watt
George Frederick Van Der Watt
未知所在单位机构
在 uct.ac.za 的电子邮件经过验证
标题
引用次数
引用次数
年份
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
642010
Reference change values: how useful are they?
F Omar, GF van der Watt, TS Pillay
Journal of Clinical Pathology 61 (4), 426-427, 2008
392008
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
302018
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
262012
Euthyroid patient with elevated serum free thyroxine
G van der Watt, D Haarburger, P Berman
Clinical chemistry 54 (7), 1239-1241, 2008
242008
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
192016
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
182015
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
162019
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
162018
Pseudoparaproteinemia after iopamidol infusion for coronary angiography
G van der Watt, P Berman
Clinical chemistry 51 (1), 273-274, 2005
162005
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
132017
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
102012
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
62011
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
52010
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
52010
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
42013
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
22010
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
12024
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
12018
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
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