Details
Role
Clinical Geneticist
Group
Clinical Services
Top Publications
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Amor, DJ, Marsh, APL, Storey, E, Tankard, R, Gillies, G, Delatycki, MB, Pope, K, Bromhead, C, Leventer, RJ, Bahlo, M, et al.
Heterozygous mutations in HSD17B4 cause juvenile peroxisomal D-bifunctional protein deficiency.
Neurology Genetics
2(6)
:
&na
2016
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Harding, IH, Raniga, P, Delatycki, MB, Stagnitti, MR, Corben, LA, Storey, E, Georgiou-Karistianis, N, Egan, GF.
Tissue atrophy and elevated iron concentration in the extrapyramidal motor system in Friedreich ataxia: the IMAGE-FRDA study.
Journal of Neurology Neurosurgery & Psychiatry
87(11)
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1261
2016
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Selvadurai, LP, Harding, IH, Corben, LA, Stagnitti, MR, Storey, E, Egan, GF, Delatycki, MB, Georgiou-Karistianis, N.
Cerebral and cerebellar grey matter atrophy in Friedreich ataxia: the IMAGE-FRDA study.
Journal of Neurology
263(11)
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2215 -2223
2016
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Stark, Z, Wallace, J, Gillam, L, Burgess, M, Delatycki, MB.
Predictive genetic testing for neurodegenerative conditions: how should conflicting interests within families be managed?.
Journal of Medical Ethics
42(10)
:
640
2016
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Delatycki, M, Churchyard, A, Yiu, E, Davis, M, Beecroft, S, Ravenscroft, G, McLean, C, Laing, N.
P.90 Autosomal dominant lower limb restricted congenital myopathy.
Neuromuscular Disorders
26:
s116
2016
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