DOI: 10.1097/nen.0b013e31821d3194. Rare Intranuclear Inclusions in the Brains of 3 Older Adult Males With Fragile X Syndrome: Implications for the Spectrum of Fragile X-Associated Disorders

Rare Intranuclear Inclusions in the Brains of 3 Older Adult Males With Fragile X Syndrome: Implications for the Spectrum of Fragile X-Associated Disorders

10.1097/nen.0b013e31821d3194

Crossref journal-article

Oxford University Press (OUP)

Journal of Neuropathology & Experimental Neurology (286)

Bibliography

Hunsaker, M. R., Greco, C. M., Tassone, F., Berman, R. F., Willemsen, R., Hagerman, R. J., & Hagerman, P. J. (2011). Rare Intranuclear Inclusions in the Brains of 3 Older Adult Males With Fragile X Syndrome: Implications for the Spectrum of Fragile X-Associated Disorders. Journal of Neuropathology & Experimental Neurology, 70(6), 462â469.

Authors 7

Michael R. Hunsaker (first)
Claudia M. Greco (additional)
Flora Tassone (additional)
Robert F. Berman (additional)
Rob Willemsen (additional)
Randi J. Hagerman (additional)
Paul J. Hagerman (additional)

References 44 Referenced 30

10.1016/0092-8674(91)90283-5
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10.1016/0092-8674(91)90397-H
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10.1016/j.yapd.2009.08.008
10.1016/j.fertnstert.2006.09.004
10.1097/DBP.0b013e3181c35f25
10.1002/ajmg.a.32060 / Am J Med Genet A / Expanded clinical phenotype of women with the FMR1 premutation by Coffey (2008)
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10.4088/JCP.09m05407blu
10.1111/j.1399-0004.2010.01448.x / Clin Genet / Clinical involvement in daughters of men with fragile X-associated tremor/ataxia syndrome by Chonchaiya (2010)
10.1097/00004703-200604002-00012 / J Dev Behav Pediatr / Autism spectrum disorders and attention-deficit/hyperactivity disorder in boys with the fragile X premutation by Farzin (2006)
10.1007/s00439-010-0882-8 / Hum Genet / Autoimmune disease in mothers with the FMR1 premutation is associated with seizures in their children with fragile X syndrome by Chonchaiya (2010)
10.1136/jnnp.2008.160960
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10.1136/jmg.2003.012518 / J Med Genet / Intranuclear inclusions in neural cells with premutation alleles in fragile X-associated tremor/ataxia syndrome by Tassone (2004)
10.4161/rna.1.2.1035
10.1002/1096-8628(20000918)94:3<232::AID-AJMG9>3.0.CO;2-H
10.1136/jmg.38.7.453 / J Med Genet / A majority of fragile X males with methylated, full mutation alleles have significant levels of FMR1 messenger RNA by Tassone (2001)
10.1002/1096-8628(200023)97:3<195::AID-AJMG1037>3.0.CO;2-R
10.1002/ajmg.1320510444
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10.2353/jmoldx.2008.070073
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10.1016/j.nbd.2005.08.019
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10.1016/j.gene.2007.02.026 / Gene / Regional FMRP deficits and large repeat expansions into the full mutation range in a new Fragile X premutation mouse model by Entezam (2007)
10.1007/s11689-010-9047-2

Dates

Type	When
Created	14 years, 3 months ago (May 13, 2011, 1:20 a.m.)
Deposited	8 years, 2 months ago (June 19, 2017, 4:09 p.m.)
Indexed	1 month ago (July 30, 2025, 8:29 p.m.)
Issued	14 years, 3 months ago (June 1, 2011)
Published	14 years, 3 months ago (June 1, 2011)
Published Online	14 years, 3 months ago (June 1, 2011)
Published Print	14 years, 3 months ago (June 1, 2011)

Funders 0

None

BibTeX

@article{Hunsaker_2011, title={Rare Intranuclear Inclusions in the Brains of 3 Older Adult Males With Fragile X Syndrome: Implications for the Spectrum of Fragile X-Associated Disorders}, volume={70}, ISSN={1554-6578}, url={http://dx.doi.org/10.1097/nen.0b013e31821d3194}, DOI={10.1097/nen.0b013e31821d3194}, number={6}, journal={Journal of Neuropathology & Experimental Neurology}, publisher={Oxford University Press (OUP)}, author={Hunsaker, Michael R. and Greco, Claudia M. and Tassone, Flora and Berman, Robert F. and Willemsen, Rob and Hagerman, Randi J. and Hagerman, Paul J.}, year={2011}, month=jun, pages={462–469} }

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