You are seeing this message because your Web browser does not support basic Web standards. Find out more about why this message is appearing and what you can do to make your experience on this site better.


ABOUT ARCHIVES
Advanced Search

Welcome   | My Account | E-mail Alerts | Access Rights | Sign In


  Vol. 56 No. 11, November 1999 TABLE OF CONTENTS
  Archives
  •  Online Features
  Images in Neurology
 This Article
 •Full text
 •PDF
 • Reply to article
 •Send to a friend
 • Save in My Folder
 •Save to citation manager
 •Permissions
 Citing Articles
 •Citing articles on HighWire
 •Citing articles on ISI (4)
 •Contact me when this article is cited
 Related Content
 •Similar articles in this journal
 Topic Collections
 •Neurology, Other
 •Alert me on articles by topic

Tubular Aggregates

Their Continuity With Sarcoplasmic Reticulum

Arch Neurol. 1999;56:1410-1411.

Since this article does not have an abstract, we have provided the first 150 words of the full text and any section headings.

A 45-YEAR-OLD man complained of exercise-induced muscle pain, cramps, and stiffness. Muscle biopsy specimens revealed tubular aggregates (TAs) on light microscopy (Figure 1) and electron microscopy (Figure 2, A). Tubular aggregates may be found in various neuromuscular disorders1; they occur as irregular basophilic regions that are usually located at the edges in type II fibers (Figure 1).


 
Figure appears in full text version.
Figure 1. Tubular aggregates on light microscopy (hematoxylin and phloxine, original magnification x500).



 
Figure appears in full text version.
Figure 2. Tubular aggregates on electron microscopy (A, original magnification x25,000; B, original magnification x125,000; C, original magnification x125,000).


In this patient, immunohistochemical staining with calcium–adenosine triphosphatase antibodies pointed to a sarcoplasmic reticulum (SR) origin of the TAs (not shown). However, although TAs are thought to be massive proliferations of SR,2 real continuity of the TAs with the SR has never been shown before. Here we see for the . . . [Full Text of this Article]



THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Hypokalaemic periodic paralysis type 2 caused by mutations at codon 672 in the muscle sodium channel gene SCN4A
Sternberg et al.
Brain 2001;124:1091-1099.
ABSTRACT | FULL TEXT  





HOME | CURRENT ISSUE | PAST ISSUES | TOPIC COLLECTIONS | CME | SUBMIT | SUBSCRIBE | HELP
CONDITIONS OF USE | PRIVACY POLICY | CONTACT US | SITE MAP
 
© 1999 American Medical Association. All Rights Reserved.