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Items: 1 to 20 of 412

1.

Leukocyte CTG repeat length correlates with severity of myotonia in myotonic dystrophy type 1.

Logigian EL, Moxley RT 4th, Blood CL, Barbieri CA, Martens WB, Wiegner AW, Thornton CA, Moxley RT 3rd.

Neurology. 2004 Apr 13;62(7):1081-9.

PMID:
15079005
2.

Computerized hand grip myometry reliably measures myotonia and muscle strength in myotonic dystrophy (DM1).

Moxley RT 3rd, Logigian EL, Martens WB, Annis CL, Pandya S, Moxley RT 4th, Barbieri CA, Dilek N, Wiegner AW, Thornton CA.

Muscle Nerve. 2007 Sep;36(3):320-8.

PMID:
17587223
3.

Evoked myotonia can be "dialed-up" by increasing stimulus train length in myotonic dystrophy type 1.

Logigian EL, Twydell P, Dilek N, Martens WB, Quinn C, Wiegner AW, Heatwole CR, Thornton CA, Moxley RT 3rd.

Muscle Nerve. 2010 Feb;41(2):191-6. doi: 10.1002/mus.21481.

4.

Quantitative analysis of the "warm-up" phenomenon in myotonic dystrophy type 1.

Logigian EL, Blood CL, Dilek N, Martens WB, Moxley RT 4th, Wiegner AW, Thornton CA, Moxley RT 3rd.

Muscle Nerve. 2005 Jul;32(1):35-42.

PMID:
15880468
5.

Severity, type, and distribution of myotonic discharges are different in type 1 and type 2 myotonic dystrophy.

Logigian EL, Ciafaloni E, Quinn LC, Dilek N, Pandya S, Moxley RT 3rd, Thornton CA.

Muscle Nerve. 2007 Apr;35(4):479-85.

PMID:
17230537
6.

Stapedial reflex in myotonic dystrophy type 1 and CTG repeat expansion.

Osanai R, Kinoshita M, Hirose K.

J Neurol. 2001 Dec;248(12):1056-61.

PMID:
12013582
7.

Neuromuscular excitability properties in myotonic dystrophy type 1.

Boërio D, Hogrel JY, Bassez G, Lefaucheur JP.

Clin Neurophysiol. 2007 Nov;118(11):2375-82. Epub 2007 Sep 24.

PMID:
17890147
8.

The correlation of CTG repeat length with material and social deprivation in myotonic dystrophy.

Laberge L, Veillette S, Mathieu J, Auclair J, Perron M.

Clin Genet. 2007 Jan;71(1):59-66.

PMID:
17204048
9.

The CTG repeat expansion size correlates with the splicing defects observed in muscles from myotonic dystrophy type 1 patients.

Botta A, Rinaldi F, Catalli C, Vergani L, Bonifazi E, Romeo V, Loro E, Viola A, Angelini C, Novelli G.

J Med Genet. 2008 Oct;45(10):639-46. doi: 10.1136/jmg.2008.058909. Epub 2008 Jul 8.

PMID:
18611984
10.

Electrophysiological evaluation in myotonic dystrophy: correlation with CTG length expansion.

Pfeilsticker BH, Bertuzzo CS, Nucci A.

Arq Neuropsiquiatr. 2001 Jun;59(2-A):186-91.

11.

Heart rate variability declines with increasing age and CTG repeat length in patients with myotonic dystrophy type 1.

Hardin BA, Lowe MR, Bhakta D, Groh WJ.

Ann Noninvasive Electrocardiol. 2003 Jul;8(3):227-32.

PMID:
14510658
12.

Cognitive/personality pattern and triplet expansion size in adult myotonic dystrophy type 1 (DM1): CTG repeats, cognition and personality in DM1.

Sistiaga A, Urreta I, Jodar M, Cobo AM, Emparanza J, Otaegui D, Poza JJ, Merino JJ, Imaz H, Martí-Massó JF, López de Munain A.

Psychol Med. 2010 Mar;40(3):487-95. doi: 10.1017/S0033291709990602. Epub 2009 Jul 23.

PMID:
19627641
13.

Satellite cell dysfunction contributes to the progressive muscle atrophy in myotonic dystrophy type 1.

Thornell LE, Lindstöm M, Renault V, Klein A, Mouly V, Ansved T, Butler-Browne G, Furling D.

Neuropathol Appl Neurobiol. 2009 Dec;35(6):603-13. doi: 10.1111/j.1365-2990.2009.01014.x. Epub 2009 Jan 21.

PMID:
19207265
14.

[Disease picture of myotonic muscular dystrophy in patients with large CTG triplet expansion].

Spranger M, Janssen B, Rating D, Spranger S.

Nervenarzt. 1999 Feb;70(2):131-5. German.

PMID:
10098148
15.

Mice transgenic for the human myotonic dystrophy region with expanded CTG repeats display muscular and brain abnormalities.

Seznec H, Agbulut O, Sergeant N, Savouret C, Ghestem A, Tabti N, Willer JC, Ourth L, Duros C, Brisson E, Fouquet C, Butler-Browne G, Delacourte A, Junien C, Gourdon G.

Hum Mol Genet. 2001 Nov 1;10(23):2717-26.

16.

Myotonic dystrophies.

Huang CC, Kuo HC.

Chang Gung Med J. 2005 Aug;28(8):517-26. Review.

17.

Correlation among subcortical white matter lesions, intelligence and CTG repeat expansion in classic myotonic dystrophy type 1.

Kuo HC, Hsieh YC, Wang HM, Chuang WL, Huang CC.

Acta Neurol Scand. 2008 Feb;117(2):101-7. doi: 10.1111/j.1600-0404.2007.00911.x.

PMID:
18184345
18.

Clinical characteristics of myotonic dystrophy type 1 patients with small CTG expansions.

Arsenault ME, Prévost C, Lescault A, Laberge C, Puymirat J, Mathieu J.

Neurology. 2006 Apr 25;66(8):1248-50.

PMID:
16636244
19.

Differential susceptibility of muscles to myotonia and force impairment in a mouse model of myotonic dystrophy.

Moyer M, Berger DS, Ladd AN, Van Lunteren E.

Muscle Nerve. 2011 Jun;43(6):818-27. doi: 10.1002/mus.21988. Epub 2011 Mar 14.

PMID:
21404300
20.

[Effects of CTG repeat expansion on quantitative muscle histopathology in myotonic dystrophy].

Utsugisawa K, Yamagata M, Nagane Y, Tohgi H.

Nihon Rinsho. 1997 Dec;55(12):3214-8. Review. Japanese.

PMID:
9436439
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