M B Delatycki
Overview
Explore the profile of M B Delatycki including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
58
Citations
753
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
11.
Georgiou-Karistianis N, Akhlaghi H, Corben L, Delatycki M, Storey E, Bradshaw J, et al.
Brain Cogn
. 2012 May;
79(3):200-8.
PMID: 22542844
The present study applied the Simon effect task to examine the pattern of functional brain reorganization in individuals with Friedreich ataxia (FRDA), using functional magnetic resonance imaging (fMRI). Thirteen individuals...
12.
Corben L, Georgiou-Karistianis N, Bradshaw J, Hocking D, Churchyard A, Delatycki M
Neuroscience
. 2011 Jul;
192:382-90.
PMID: 21749914
Friedreich ataxia (FRDA) is the most common of the inherited ataxias. We have suggested that people with FRDA may have impairment in cognitive and/or psychomotor capacity either due to disturbance...
13.
Corben L, Akhlaghi H, Georgiou-Karistianis N, Bradshaw J, Egan G, Storey E, et al.
Brain Cogn
. 2011 Mar;
76(1):140-5.
PMID: 21354685
Friedreich ataxia (FRDA) is the most common of the genetically inherited ataxias. We recently demonstrated that people with FRDA have impairment in motor planning - most likely because of pathology...
14.
Rance G, Corben L, Du Bourg E, King A, Delatycki M
Neuroscience
. 2010 Sep;
171(2):552-5.
PMID: 20849937
Friedreich ataxia (FRDA) is a neurodegenerative disease affecting motor and sensory systems. This study aimed to investigate the presence and perceptual consequences of auditory neuropathy (AN) in affected individuals and...
15.
Ioannou L, Massie J, Lewis S, Petrou V, Gason A, Metcalfe S, et al.
Clin Genet
. 2010 Jul;
78(1):21-31.
PMID: 20597919
A screening programme for Tay Sachs disease (TSD) carrier status was introduced in high schools in Victoria, Australia in 1997, and was expanded to screen for six other genetic conditions...
16.
Ioannou L, Massie J, Collins V, McClaren B, Delatycki M
Public Health Genomics
. 2010 Jan;
13(7-8):449-56.
PMID: 20090299
A population-based cystic fibrosis (CF) carrier screening program was introduced in Victoria, Australia in 2006, and was offered to couples planning a pregnancy or in early pregnancy for a fee....
17.
Mand C, Duncan R, Gillam L, Collins V, Delatycki M
J Med Ethics
. 2009 Dec;
35(12):722-8.
PMID: 19948926
The concept of selecting for a disability, and deafness in particular, has triggered a controversial and sometimes acrimonious debate between key stakeholders. Previous studies have concentrated on the views of...
18.
Delatycki M, Wolthuizen M, Collins V, Varley E, Craven J, Allen K, et al.
Clin Genet
. 2009 Nov;
77(3):241-8.
PMID: 19930418
Hereditary hemochromatosis (HH), most often due to HFE C282Y homozygosity, is an iron overload disorder that can result in severe morbidity including hepatic cirrhosis. Predisposition to HH is easily diagnosed...
19.
Hulsebos T, Kenter S, Jakobs M, Baas F, Chong B, Delatycki M
Clin Genet
. 2009 Nov;
77(1):86-91.
PMID: 19912265
Schwannomatosis is characterized by the development of multiple schwannomas of the nervous system, but without the occurrence of vestibular schwannomas. Most cases of schwannomatosis are thought to be sporadic, representing...
20.
Corben L, Tai G, Wilson C, Collins V, Churchyard A, Delatycki M
J Neurol
. 2009 Oct;
257(4):518-23.
PMID: 19823893
Friedreich Ataxia (FRDA) is the commonest inherited ataxia. Clinical trials of pharmaceuticals are increasingly being conducted in this condition. This requires the most accurate outcome measures to enable trials to...