Sporadic late-onset nemaline myopathy: clinico-pathological characteristics and review of 76 cases

Author:

Schnitzler Lukas J.,Schreckenbach Tobias,Nadaj-Pakleza Aleksandra,Stenzel Werner,Rushing Elisabeth J.,Van Damme Philip,Ferbert Andreas,Petri Susanne,Hartmann Christian,Bornemann Antje,Meisel Andreas,Petersen Jens A.,Tousseyn Thomas,Thal Dietmar R.,Reimann Jens,De Jonghe Peter,Martin Jean-Jacques,Van den Bergh Peter Y.,Schulz Jörg B.,Weis Joachim,Claeys Kristl G.

Funder

Deutsche Gesellschaft für Muskelkranke (DGM) e.V.

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Genetics (clinical),General Medicine

Reference63 articles.

1. Engel AG. Late-onset rod myopathy (a new syndrome?): light and electron microscopic observations in two cases. Mayo Clin Proc. 1966;41(11):713–41.

2. Engel WK, Resnick JS. Late-onset rod myopathy: a newly recognized, acquired, and progressive disease. Neurology. 1966;16:308–9.

3. Palmucci L, Doriguzzi C, Mongini T, Chiado-Piat L. Adult onset nemaline myopathy: a distinct nosologic entity? Clin Neuropathol. 1993;12(3):153–5.

4. Engel WK, Oberc MA. Abundant nuclear rods in adult-onset rod disease. J Neuropathol Exp Neurol. 1975;34(2):119–32.

5. Lomen-Hoerth C, Simmons ML, Dearmond SJ, Layzer RB. Adult-onset nemaline myopathy: another cause of dropped head. Muscle Nerve. 1999;22(8):1146–50.

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