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Basilar artery aneurysm: a new finding in classic infantile Pompe disease.

作者信息

Patel Trusha T, Banugaria Suhrad G, Frush Donald P, Enterline David S, Tanpaiboon Pranoot, Kishnani Priya S

出版信息

Muscle Nerve. 2013 Apr;47(4):613-5. doi: 10.1002/mus.23659. Epub 2013 Feb 10.

Abstract
摘要

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本文引用的文献

1
The emerging phenotype of long-term survivors with infantile Pompe disease.
Genet Med. 2012 Sep;14(9):800-10. doi: 10.1038/gim.2012.44. Epub 2012 Apr 26.
3
Abnormalities of cerebral arteries are frequent in patients with late-onset Pompe disease.
J Neurol. 2010 Oct;257(10):1730-3. doi: 10.1007/s00415-010-5618-0. Epub 2010 Jun 18.
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Dilative arteriopathy and basilar artery dolichoectasia complicating late-onset Pompe disease.
Neurology. 2008 May 27;70(22):2063-6. doi: 10.1212/01.wnl.0000313367.09469.13.
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Characterization of pre- and post-treatment pathology after enzyme replacement therapy for Pompe disease.
Lab Invest. 2006 Dec;86(12):1208-20. doi: 10.1038/labinvest.3700484. Epub 2006 Oct 30.
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Alpha-glucosidase deficiency and basilar artery aneurysm: report of a sibship.
Ann Neurol. 1987 Nov;22(5):629-33. doi: 10.1002/ana.410220512.

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