» Articles » PMID: 4169453

Nemaline Myopathy: Report of a Fatal Case, with Histochemical and Electron Microscopic Studies

Overview
Journal Brain
Specialty Neurology
Date 1967 Dec 1
PMID 4169453
Citations 22
Authors
Affiliations
Soon will be listed here.
Citing Articles

Nebulin nemaline myopathy recapitulated in a compound heterozygous mouse model with both a missense and a nonsense mutation in Neb.

Laitila J, McNamara E, Wingate C, Goullee H, Ross J, Taylor R Acta Neuropathol Commun. 2020; 8(1):18.

PMID: 32066503 PMC: 7027239. DOI: 10.1186/s40478-020-0893-1.


Loss of LMOD1 impairs smooth muscle cytocontractility and causes megacystis microcolon intestinal hypoperistalsis syndrome in humans and mice.

Halim D, Wilson M, Oliver D, Brosens E, Verheij J, Han Y Proc Natl Acad Sci U S A. 2017; 114(13):E2739-E2747.

PMID: 28292896 PMC: 5380076. DOI: 10.1073/pnas.1620507114.


Phenotypes of myopathy-related beta-tropomyosin mutants in human and mouse tissue cultures.

Abdul-Hussein S, Rahl K, Moslemi A, Tajsharghi H PLoS One. 2013; 8(9):e72396.

PMID: 24039757 PMC: 3769345. DOI: 10.1371/journal.pone.0072396.


Nemaline myopathy: two autopsy reports.

Bergmann M, Kamarampaka M, Kuchelmeister K, Klein H, Koch H Childs Nerv Syst. 1995; 11(10):610-5.

PMID: 8556730 DOI: 10.1007/BF00301002.


Nemaline myopathy associated with consanguinity.

Glynn M, Dervan P, Mulvihill N Ir J Med Sci. 1980; 149(11):436-8.

PMID: 7228590 DOI: 10.1007/BF02939186.