Adelaide Research & Scholarship
Browsing "Genetics publications" by Author Ketteridge, D.
Showing results 1 to 2 of 2
Preview | Issue Date | Title | Author(s) |
| 2014 | Natural history and galsulfase treatment in mucopolysaccharidosis VI (MPS VI, Maroteaux-Lamy syndrome)-10-year follow-up of patients who previously participated in an MPS VI survey study | Giugliani, R.; Lampe, C.; Guffon, N.; Ketteridge, D.; Leão-Teles, E.; Wraith, J.E.; Jones, S.A.; Piscia-Nichols, C.; Lin, P.; Quartel, A.; Harmatz, P. |
| 2017 | Unique presentation of cutis laxa with Leigh-like syndrome due to ECHS1 deficiency | Balasubramaniam, S.; Riley, L.; Bratkovic, D.; Ketteridge, D.; Manton, N.; Cowley, M.; Gayevskiy, V.; Roscioli, T.; Mohamed, M.; Gardeitchik, T.; Morava, E.; Christodoulou, J. |