Loesch DZ - Search Results

1

White matter changes in patients with Parkinson's disease carrying small CGG expansion FMR1 alleles: a pilot study.

Trost N, Cook M, Hammersley E, Bui MQ, Brotchie P, Burgess T, Slater H, Storey E, Loesch DZ. Trost N, et al. Among authors: loesch dz. Neurodegener Dis. 2014;14(2):67-76. doi: 10.1159/000356190. Epub 2013 Dec 24. Neurodegener Dis. 2014. PMID: 24401315

2

Expansion of the CGG repeat in fragile X in the FMR1 gene depends on the sex of the offspring.

Loesch DZ, Huggins R, Petrovic V, Slater H. Loesch DZ, et al. Am J Hum Genet. 1995 Dec;57(6):1408-13. Am J Hum Genet. 1995. PMID: 8533771 Free PMC article.

3

"Reduction" of CGG trinucleotide expansion from mother to offspring in seven fragile-X families.

Loesch DZ, Petrovic V, Francis DI, Oertel R, Slater H. Loesch DZ, et al. Clin Genet. 1997 Jan;51(1):1-6. doi: 10.1111/j.1399-0004.1997.tb02405.x. Clin Genet. 1997. PMID: 9084926

4

FMR1 alleles in Tasmania: a screening study of the special educational needs population.

Mitchell RJ, Holden JJ, Zhang C, Curlis Y, Slater HR, Burgess T, Kirkby KC, Carmichael A, Heading KD, Loesch DZ. Mitchell RJ, et al. Among authors: loesch dz. Clin Genet. 2005 Jan;67(1):38-46. doi: 10.1111/j.1399-0004.2004.00344.x. Clin Genet. 2005. PMID: 15617547

5

Evidence for, and a spectrum of, neurological involvement in carriers of the fragile X pre-mutation: FXTAS and beyond.

Loesch DZ, Churchyard A, Brotchie P, Marot M, Tassone F. Loesch DZ, et al. Clin Genet. 2005 May;67(5):412-7. doi: 10.1111/j.1399-0004.2005.00425.x. Clin Genet. 2005. PMID: 15811008

6

Magnetic resonance imaging study in older fragile X premutation male carriers.

Loesch DZ, Litewka L, Brotchie P, Huggins RM, Tassone F, Cook M. Loesch DZ, et al. Ann Neurol. 2005 Aug;58(2):326-30. doi: 10.1002/ana.20542. Ann Neurol. 2005. PMID: 16049924

7

Effect of Turner's syndrome and X-linked imprinting on cognitive status: analysis based on pedigree data.

Loesch DZ, Bui QM, Kelso W, Huggins RM, Slater H, Warne G, Bergman PB, Rodda C, Mitchell RJ, Prior M. Loesch DZ, et al. Brain Dev. 2005 Oct;27(7):494-503. doi: 10.1016/j.braindev.2004.12.009. Brain Dev. 2005. PMID: 16198207

8

Transcript levels of the intermediate size or grey zone fragile X mental retardation 1 alleles are raised, and correlate with the number of CGG repeats.

Loesch DZ, Bui QM, Huggins RM, Mitchell RJ, Hagerman RJ, Tassone F. Loesch DZ, et al. J Med Genet. 2007 Mar;44(3):200-4. doi: 10.1136/jmg.2006.043950. Epub 2006 Aug 11. J Med Genet. 2007. PMID: 16905681 Free PMC article.

9

Tremor/ataxia syndrome and fragile X premutation: diagnostic caveats.

Loesch DZ, Litewka L, Churchyard A, Gould E, Tassone F, Cook M. Loesch DZ, et al. J Clin Neurosci. 2007 Mar;14(3):245-8. doi: 10.1016/j.jocn.2006.01.015. Epub 2006 Dec 27. J Clin Neurosci. 2007. PMID: 17194594

10

A low symptomatic form of neurodegeneration in younger carriers of the FMR1 premutation, manifesting typical radiological changes.

Loesch DZ, Cook M, Litewka L, Gould E, Churchyard A, Tassone F, Slater HR, Storey E. Loesch DZ, et al. J Med Genet. 2008 Mar;45(3):179-81. doi: 10.1136/jmg.2007.054171. Epub 2007 Dec 5. J Med Genet. 2008. PMID: 18057083

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