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. 19 No. 4, October 1968 TABLE OF CONTENTS
  Archives
  •  Online Features
  ORIGINAL ARTICLES
 This Article
 •References
 •Full text PDF
 • Reply to article
 •Send to a friend
 • Save in My Folder
 •Save to citation manager
 •Permissions
 Citing Articles
 •Citation map
 •Citing articles on HighWire
 •Contact me when this article is cited
 Related Content
 •Similar articles in this journal
 Social Bookmarking
  Add to CiteULike Add to Connotea Add to Del.icio.us Add to Digg Add to Reddit Add to Technorati Add to Twitter What's this?

Cryoglobulinemic Neuropathy

Incidence and Clinical Characteristics

John Logothetis, MD; William R. Kennedy, MD; Anna Ellington, MD; Ralph C. Williams, MD

Arch Neurol. 1968;19(4):389-397.

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

CRYOGLOBULINEMIA has been the focus of considerable attention in recent years because it has become apparent that cryoproteins may provoke symptoms more frequently than previously recognized. A number of good reviews on the subject have appeared in the literature during the last 15 years.1-7

Cryoglobulins are serum proteins which reversibly precipitate from blood during cooling. Although most commonly found in association with multiple myeloma and macroglobulinemia, they are encountered in lymphomatous and various connective tissue disorders. The protein abnormality has been referred to as secondary cryoglobulinemia when it occurs in combination with such disorders. In the absence of associated disease the term essential cryoglobulinemia is often used. Meltzer et al7 have described a group of essential cryoglobulinemic patients having purpura, weakness, arthralgias, and in some instances, acute renal failure secondary to diffuse glomerulonephitis.

In both the secondary and essential groups, the cold precipitating protein is usually characterized . . . [Full Text PDF of this Article]


Author Affiliations

Minneapolis

From the departments of neurology (Drs. Logothetis, Kennedy, and Ellington), and internal medicine (Dr. Williams), University of Minnesota Medical School, Minneapolis.


Footnotes

Submitted for publication Jan 11, 1968; accepted March 25.

Reprint requests to Division of Neurology, University of Minnesota Medical School, Minneapolis 55455.



Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter     What's this?





HOME | CURRENT ISSUE | PAST ISSUES | TOPIC COLLECTIONS | CME | SUBMIT | SUBSCRIBE | HELP
CONDITIONS OF USE | PRIVACY POLICY | CONTACT US | SITE MAP
 
© 1968 American Medical Association. All Rights Reserved.