Van der Watt G - Search Results

1

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

Owen EP, Nandhlal J, Leisegang F, Van der Watt G, Nourse P, Gajjar P. Owen EP, et al. Among authors: van der watt g. Pediatr Nephrol. 2015 Apr;30(4):595-601. doi: 10.1007/s00467-014-2980-7. Epub 2014 Oct 18. Pediatr Nephrol. 2015. PMID: 25326109

2

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

van der Watt G, Owen EP, Berman P, Meldau S, Watermeyer N, Olpin SE, Manning NJ, Baumgarten I, Leisegang F, Henderson H. van der Watt G, et al. Mol Genet Metab. 2010 Oct-Nov;101(2-3):178-82. doi: 10.1016/j.ymgme.2010.07.018. Epub 2010 Aug 3. Mol Genet Metab. 2010. PMID: 20732827

3

Plasma free fatty acid reference interval in South African neonates in the first week of life.

Omar F, van der Watt G, November V, Pillay TS. Omar F, et al. Among authors: van der watt g. Ann Clin Biochem. 2010 Jul;47(Pt 4):381-2. doi: 10.1258/acb.2010.009281. Ann Clin Biochem. 2010. PMID: 20592337

4

Identification of a single MPV17 nonsense-associated altered splice variant in 24 South African infants with mitochondrial neurohepatopathy.

Meldau S, De Lacy RJ, Riordan GTM, Goddard EA, Pillay K, Fieggen KJ, Marais AD, Van der Watt GF. Meldau S, et al. Among authors: van der watt gf. Clin Genet. 2018 May;93(5):1093-1096. doi: 10.1111/cge.13208. Epub 2018 Mar 25. Clin Genet. 2018. PMID: 29318572

5

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

Kija E, Gidal BE, Shapson-Coe A, Cader S, van der Watt G, Delport S, Wilmshurst JM. Kija E, et al. Among authors: van der watt g. Seizure. 2019 Dec;73:84. doi: 10.1016/j.seizure.2019.07.018. Epub 2019 Aug 13. Seizure. 2019. PMID: 31420230 Free article. No abstract available.

6

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

Kija E, Gidal BE, Shapson-Coe A, Cader S, van der Watt G, Delport S, Wilmshurst JM. Kija E, et al. Among authors: van der watt g. Seizure. 2019 Jul;69:186-192. doi: 10.1016/j.seizure.2019.04.020. Epub 2019 Apr 29. Seizure. 2019. PMID: 31075750 Free article.

7

Clinical, biochemical, and genetic spectrum of MADD in a South African cohort: an ICGNMD study.

Bisschoff M, Smuts I, Dercksen M, Schoonen M, Vorster BC, van der Watt G, Spencer C, Naidu K, Henning F, Meldau S, McFarland R, Taylor RW, Patel K, Fassad MR, Vandrovcova J; ICGNMD Consortium; Wanders RJA, van der Westhuizen FH. Bisschoff M, et al. Among authors: van der watt g. Orphanet J Rare Dis. 2024 Jan 14;19(1):15. doi: 10.1186/s13023-023-03014-8. Orphanet J Rare Dis. 2024. PMID: 38221620 Free PMC article.

8

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

Chaya S, Zampoli M, Gray D, Booth J, Riordan G, Ndondo A, Fieggen K, Rusch J, van der Watt G, Pillay K, van der Westhuizen F, Menezes M, Wilmshurst J. Chaya S, et al. Among authors: van der watt g. Semin Pediatr Neurol. 2018 Jul;26:10-14. doi: 10.1016/j.spen.2017.03.002. Epub 2017 Apr 4. Semin Pediatr Neurol. 2018. PMID: 29961494

9

Pseudoparaproteinemia after iopamidol infusion for coronary angiography.

van der Watt G, Berman P. van der Watt G, et al. Clin Chem. 2005 Jan;51(1):273-4. doi: 10.1373/clinchem.2004.043505. Clin Chem. 2005. PMID: 15613732 No abstract available.

10

Euthyroid patient with elevated serum free thyroxine.

van der Watt G, Haarburger D, Berman P. van der Watt G, et al. Clin Chem. 2008 Jul;54(7):1239-41. doi: 10.1373/clinchem.2007.101428. Clin Chem. 2008. PMID: 18593963 No abstract available.

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