Delatycki MB - Search Results

1

Implementation of HaemScreen, a workplace-based genetic screening program for hemochromatosis.

Nisselle AE, Delatycki MB, Collins V, Metcalfe S, Aitken MA, du Sart D, Halliday J, Macciocca I, Wakefield A, Hill V, Gason A, Warner B, Calabro V, Williamson R, Allen KJ. Nisselle AE, et al. Among authors: delatycki mb. Clin Genet. 2004 May;65(5):358-67. doi: 10.1111/j.1399-0004.2004.0239.x. Clin Genet. 2004. PMID: 15099342

2

Sperm DNA analysis in a Friedreich ataxia premutation carrier suggests both meiotic and mitotic expansion in the FRDA gene.

Delatycki MB, Paris D, Gardner RJ, Forshaw K, Nicholson GA, Nassif N, Williamson R, Forrest SM. Delatycki MB, et al. J Med Genet. 1998 Sep;35(9):713-6. doi: 10.1136/jmg.35.9.713. J Med Genet. 1998. PMID: 9733027 Free PMC article.

3

Direct evidence that mitochondrial iron accumulation occurs in Friedreich ataxia.

Delatycki MB, Camakaris J, Brooks H, Evans-Whipp T, Thorburn DR, Williamson R, Forrest SM. Delatycki MB, et al. Ann Neurol. 1999 May;45(5):673-5. Ann Neurol. 1999. PMID: 10319894

4

Clinical and genetic study of Friedreich ataxia in an Australian population.

Delatycki MB, Paris DB, Gardner RJ, Nicholson GA, Nassif N, Storey E, MacMillan JC, Collins V, Williamson R, Forrest SM. Delatycki MB, et al. Am J Med Genet. 1999 Nov 19;87(2):168-74. doi: 10.1002/(sici)1096-8628(19991119)87:2<168::aid-ajmg8>3.0.co;2-2. Am J Med Genet. 1999. PMID: 10533031

5

G130V, a common FRDA point mutation, appears to have arisen from a common founder.

Delatycki MB, Knight M, Koenig M, Cossée M, Williamson R, Forrest SM. Delatycki MB, et al. Hum Genet. 1999 Oct;105(4):343-6. doi: 10.1007/s004399900142. Hum Genet. 1999. PMID: 10543403

6

Friedreich ataxia: an overview.

Delatycki MB, Williamson R, Forrest SM. Delatycki MB, et al. J Med Genet. 2000 Jan;37(1):1-8. doi: 10.1136/jmg.37.1.1. J Med Genet. 2000. PMID: 10633128 Free PMC article. Review.

7

The correlation of clinical phenotype in Friedreich ataxia with the site of point mutations in the FRDA gene.

Forrest SM, Knight M, Delatycki MB, Paris D, Williamson R, King J, Yeung L, Nassif N, Nicholson GA. Forrest SM, et al. Among authors: delatycki mb. Neurogenetics. 1998 Aug;1(4):253-7. doi: 10.1007/s100480050037. Neurogenetics. 1998. PMID: 10732799

8

Insurance agreement to facilitate genetic testing.

Delatycki M, Allen K, Williamson R. Delatycki M, et al. Lancet. 2002 Apr 20;359(9315):1433. doi: 10.1016/S0140-6736(02)08369-1. Lancet. 2002. PMID: 11978360 No abstract available.

9

Haemochromatosis and family testing. What should a GP do?

Newstead J, Delatycki M, Aitken MA. Newstead J, et al. Aust Fam Physician. 2002 Jun;31(6):533-7. Aust Fam Physician. 2002. PMID: 12154600 Review.

10

Clinical haemochromatosis in HFE mutation carriers.

Allen KJ, Warner B, Delatycki MB. Allen KJ, et al. Among authors: delatycki mb. Lancet. 2002 Aug 3;360(9330):412-3; author reply 413-4. doi: 10.1016/s0140-6736(02)09583-1. Lancet. 2002. PMID: 12241805 No abstract available.

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