Loading…
Addressing the gap for racially diverse research involvement: The King's Model for minority ethnic research participant recruitment
Ray Chaudhuri, K., Podlewska, A., Hui Lau, Yue, Gonde, C., McIntosh, A., Qamar, M.A., O'Donoghue, S., Larcombe, K., Adeeko, M., Gupta, A., Bajwah, S., Lafond, S., Awogbemila, O., van Coller, R., Murtagh, A.M., Ocloo, J.E.
Published in Public health in practice (Oxford, England) (01.12.2023)
Published in Public health in practice (Oxford, England) (01.12.2023)
Get full text
Journal Article
Loading…
Genetic screening of South African families with Parkinson’s disease
Bardien, S, Braun, A, Van Coller, R, Hassan Amod, F, Carr, J, Moosa, S
Published in South African medical journal (13.02.2024)
Published in South African medical journal (13.02.2024)
Get full text
Journal Article
Loading…
TOR1A mutation-related isolated childhood-onset generalised dystonia in South Africa
van Coller, R, Schutte, C-M, Lubbe, E, Ngele, B
Published in South African medical journal (01.10.2021)
Published in South African medical journal (01.10.2021)
Get full text
Journal Article
Loading…
Loading…
Severe porphyric neuropathy--importance of screening for porphyria in Guillain-Barré syndrome
Schutte, Clara-Maria, van der Meyden, Cornelius H, van Niekerk, Linette, Kakaza, Mandisa, van Coller, Riaan, Ueckermann, Veronica, Oosthuizen, Nicky M
Published in South African medical journal (01.01.2016)
Published in South African medical journal (01.01.2016)
Get full text
Journal Article
Loading…
Loading…
Loading…
Loading…
A South African family with oculopharyngeal muscular dystrophy : clinical and molecular genetic characteristics : forum - genetics
van Rensburg, E.J., van Rensburg, E.J., van Coller, R., Schutte, C.M., Dorfling, C.M.
Published in South African medical journal (01.07.2015)
Published in South African medical journal (01.07.2015)
Get full text
Journal Article
Loading…
Severe porphyric neuropathy - importance of screening for porphyria in Guillain-Barre syndrome : clinical alert
Oosthuizen, N.M., Van der Meyden, C.H., Van Coller, R., Ueckermann, V., Van Niekerk, L., Kakaza, M., Schutte, C.M.
Published in South African medical journal (01.01.2016)
Published in South African medical journal (01.01.2016)
Get full text
Journal Article
Loading…
Loading…
A South African family with oculopharyngeal muscular dystrophy: Clinical and molecular genetic characteristics
Schutte, Clara Maria, Dorfling, Cecelia M, van Coller, Riaan, Honey, Engela M, van Rensburg, Elizabeth Jansen
Published in South African medical journal (01.07.2015)
Published in South African medical journal (01.07.2015)
Get full text
Journal Article