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Items: 1 to 20 of 94

1.

The significance of pathological spontaneous activity in various myopathies.

Hanisch F, Kronenberger C, Zierz S, Kornhuber M.

Clin Neurophysiol. 2014 Jul;125(7):1485-90. doi: 10.1016/j.clinph.2013.11.021. Epub 2013 Dec 2.

PMID:
24370491
2.

Diagnostic impact of myotonic discharges in myofibrillar myopathies.

Hanisch F, Kraya T, Kornhuber M, Zierz S.

Muscle Nerve. 2013 Jun;47(6):845-8. doi: 10.1002/mus.23716. Epub 2013 Apr 21.

PMID:
23605961
3.

[EMG-findings in typ-II-glycogenosis (Pompe's disease, acid maltase deficiency) (author's transl)].

Gehlen W, Stefan H.

EEG EMG Z Elektroenzephalogr Elektromyogr Verwandte Geb. 1978 Mar;9(1):24-9. German.

PMID:
416945
4.

Abnormal spontaneous activity in primary myopathic disorders.

Nojszewska M, Gawel M, Szmidt-Salkowska E, Kostera-Pruszczyk A, Potulska-Chromik A, Lusakowska A, Kierdaszuk B, Lipowska M, Macias A, Gawel D, Seroka A, Kaminska AM.

Muscle Nerve. 2016 Dec 21. doi: 10.1002/mus.25521. [Epub ahead of print]

PMID:
28000226
5.

Motor unit reorganization in progressive muscular dystrophies and congenital myopathies.

Szmidt-Sałkowska E, Gaweł M, Lipowska M.

Neurol Neurochir Pol. 2015;49(4):223-8. doi: 10.1016/j.pjnns.2015.05.005. Epub 2015 Jun 6.

PMID:
26188938
6.

Vacuolar myopathies in adults with myalgias: value of paraspinal muscle investigation.

Petrella JT, Giuliani MJ, Lacomis D.

Muscle Nerve. 1997 Oct;20(10):1321-3.

PMID:
9324092
7.

[Glycogen storage disease (Pompe's disease) presenting as myopathy in the adult (author's transl)].

Stefan H, Böker DK, Müller J, Gullotta F.

Dtsch Med Wochenschr. 1977 Oct 21;102(42):1512-4. German.

PMID:
269788
8.

Use of Clinical and Electrical Myotonia to Differentiate Childhood Myopathies.

Ghosh PS, Sorenson EJ.

J Child Neurol. 2015 Sep;30(10):1300-6. doi: 10.1177/0883073814559646. Epub 2015 Jan 30.

PMID:
25637645
9.

Evoked isometric muscle contractions in myopathies: analysis of pathophysiological properties by different stimulus patterns.

Dillmann U, Heide G, Krämer G, Hopf HC, Schimrigk K.

Electroencephalogr Clin Neurophysiol. 1998 Feb;109(1):63-9.

PMID:
11003065
10.

The diagnostic significance of large action potentials in myopathy.

Nakashima K, Tabuchi Y, Takahashi K.

J Neurol Sci. 1983 Oct;61(2):161-70.

PMID:
6644325
11.

Risk factors for osteoporosis, falls and fractures in hereditary myopathies and sporadic inclusion body myositis - A cross sectional survey.

Danckworth F, Karabul N, Posa A, Hanisch F.

Mol Genet Metab Rep. 2014 Feb 11;1:85-97. eCollection 2014.

12.

Electromyography in myopathy.

Liguori R, Fuglsang-Frederiksen A, Nix W, Fawcett PR, Andersen K.

Neurophysiol Clin. 1997 Jun;27(3):200-3. Review.

PMID:
9260160
13.

The spectrum of myotonic and myopathic disorders in a pediatric electromyography laboratory over 12 years.

Shah DU, Darras BT, Markowitz JA, Jones HR Jr, Kang PB.

Pediatr Neurol. 2012 Aug;47(2):97-100. doi: 10.1016/j.pediatrneurol.2012.05.003.

PMID:
22759684
14.

Decomposition-based quantitative electromyography in the evaluation of muscular dystrophy severity.

Derry KL, Venance SL, Doherty TJ.

Muscle Nerve. 2012 Apr;45(4):507-13. doi: 10.1002/mus.22341.

PMID:
22431083
15.

Late onset Pompe disease: clinical and neurophysiological spectrum of 38 patients including long-term follow-up in 18 patients.

Müller-Felber W, Horvath R, Gempel K, Podskarbi T, Shin Y, Pongratz D, Walter MC, Baethmann M, Schlotter-Weigel B, Lochmüller H, Schoser B.

Neuromuscul Disord. 2007 Oct;17(9-10):698-706. Epub 2007 Jul 23.

PMID:
17643989
16.

Differential diagnosis of limb girdle syndromes.

Ishpekova B, Milanov I.

Electromyogr Clin Neurophysiol. 1996 Dec;36(8):469-75.

PMID:
8985674
17.

[Pseudodystrophic muscle glycogenosis in adults. (Acid maltase deficiency syndrome) (author's transl)].

Gullotta F, Stefan H, Mattern H.

J Neurol. 1976;213(3):199-216. German.

PMID:
61260
18.

Muscular dystrophies and other genetic myopathies.

Shieh PB.

Neurol Clin. 2013 Nov;31(4):1009-29. doi: 10.1016/j.ncl.2013.04.004. Review.

PMID:
24176421
19.

[A retrospective study of six patients with late-onset Pompe disease].

Saux A, Laforet P, Pagès AM, Figarella-Branger D, Pellissier JF, Pagès M, Labauge P.

Rev Neurol (Paris). 2008 Apr;164(4):336-42. doi: 10.1016/j.neurol.2007.09.008. French.

PMID:
18439925
20.

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