Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 139

1.

Distal myopathies.

Mastaglia FL, Lamont PJ, Laing NG.

Curr Opin Neurol. 2005 Oct;18(5):504-10. Review.

PMID:
16155432
2.

Distal myopathies a review: highlights on distal myopathies with rimmed vacuoles.

Malicdan MC, Nonaka I.

Neurol India. 2008 Jul-Sep;56(3):314-24. Review.

3.

Distal myopathies.

Illa I.

J Neurol. 2000 Mar;247(3):169-74. Review.

PMID:
10787109
4.

Late-onset distal myopathy with rimmed vacuoles without mutation in the GNE or dysferlin genes.

Suzuki N, Aoki M, Mizuno H, Onodera Y, Takahashi T, Nagata T, Tateyama M, Itoyama Y.

Muscle Nerve. 2005 Dec;32(6):812-4.

PMID:
16116644
5.

[Distal myopathies].

Pénisson-Besnier I.

Rev Neurol (Paris). 2004 Feb;160(2):211-6. Review. French.

PMID:
15034479
6.

Distal myopathies.

Dimachkie MM, Barohn RJ.

Neurol Clin. 2014 Aug;32(3):817-42, x. doi: 10.1016/j.ncl.2014.04.004. Epub 2014 May 15. Review.

7.

Overview of distal myopathies: from the clinical to the molecular.

Barohn RJ, Amato AA, Griggs RC.

Neuromuscul Disord. 1998 Jun;8(5):309-16. Review.

PMID:
9673984
8.

Phenotypic features and genetic findings in 2 chinese families with Miyoshi distal myopathy.

Ro LS, Lee-Chen GJ, Lin TC, Wu YR, Chen CM, Lin CY, Chen ST.

Arch Neurol. 2004 Oct;61(10):1594-9.

PMID:
15477515
9.

Distal myopathy with rimmed vacuoles: report on clinical characteristics in 23 cases.

Nalini A, Gayathri N, Dawn R.

Neurol India. 2010 Mar-Apr;58(2):235-41. doi: 10.4103/0028-3886.63804.

10.

Dysferlin mutation in a Chinese pedigree with Miyoshi myopathy.

Shunchang S, Fan Q, Huacheng W, Leturcq F, Yongjian S, Bingfeng Z, Wen Y, Deburgrave N.

Clin Neurol Neurosurg. 2006 Jun;108(4):369-73. Epub 2005 Jul 14.

PMID:
16023782
11.

Distal myopathies: from clinical classification to molecular understanding.

Kraya T, Zierz S.

J Neural Transm (Vienna). 2013 Sep;120 Suppl 1:S3-7. doi: 10.1007/s00702-013-1058-1. Epub 2013 Jul 11. Review.

PMID:
23842731
12.

Distal myopathies.

Pénisson-Besnier I.

Rev Neurol (Paris). 2013 Aug-Sep;169(8-9):534-45. doi: 10.1016/j.neurol.2012.09.021. Epub 2013 Sep 3. Review.

PMID:
24008050
13.

Myotilinopathy in a family with late onset myopathy.

Pénisson-Besnier I, Talvinen K, Dumez C, Vihola A, Dubas F, Fardeau M, Hackman P, Carpen O, Udd B.

Neuromuscul Disord. 2006 Jul;16(7):427-31. Epub 2006 Jun 21.

PMID:
16793270
14.

Analysis of NCAM helps identify unusual phenotypes of hereditary inclusion-body myopathy.

Broccolini A, Gidaro T, Tasca G, Morosetti R, Rodolico C, Ricci E, Mirabella M.

Neurology. 2010 Jul 20;75(3):265-72. doi: 10.1212/WNL.0b013e3181e8e8f1.

PMID:
20644153
15.

Recent advances in distal myopathy with rimmed vacuoles (DMRV) or hIBM: treatment perspectives.

Malicdan MC, Noguchi S, Nishino I.

Curr Opin Neurol. 2008 Oct;21(5):596-600. doi: 10.1097/WCO.0b013e32830dd595. Review.

PMID:
18769255
16.

Distal myopathies.

Nonaka I.

Curr Opin Neurol. 1999 Oct;12(5):493-9. Review.

PMID:
10590885
17.

GNE myopathy: new name and new mutation nomenclature.

Huizing M, Carrillo-Carrasco N, Malicdan MC, Noguchi S, Gahl WA, Mitrani-Rosenbaum S, Argov Z, Nishino I.

Neuromuscul Disord. 2014 May;24(5):387-9. doi: 10.1016/j.nmd.2014.03.004. Epub 2014 Mar 13. No abstract available.

18.

A Gne knockout mouse expressing human GNE D176V mutation develops features similar to distal myopathy with rimmed vacuoles or hereditary inclusion body myopathy.

Malicdan MC, Noguchi S, Nonaka I, Hayashi YK, Nishino I.

Hum Mol Genet. 2007 Nov 15;16(22):2669-82. Epub 2007 Aug 18.

PMID:
17704511
19.

Distal myopathies--new genetic entities expand diagnostic challenge.

Udd B.

Neuromuscul Disord. 2012 Jan;22(1):5-12. doi: 10.1016/j.nmd.2011.10.003. Epub 2011 Dec 23. Review.

PMID:
22197426
20.

Pattern of skeletal muscle involvement in primary dysferlinopathies: a whole-body 3.0-T magnetic resonance imaging study.

Kesper K, Kornblum C, Reimann J, Lutterbey G, Schröder R, Wattjes MP.

Acta Neurol Scand. 2009 Aug;120(2):111-8. doi: 10.1111/j.1600-0404.2008.01129.x. Epub 2008 Dec 22.

PMID:
19154541

Supplemental Content

Support Center