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. 10 No. 6, June 1964 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?

Myoglobinuria

LEWIS P. ROWLAND, MD; STANLEY FAHN, MD; ERICH HIRSCHBERG, PhD; DONALD H. HARTER, MD

Arch Neurol. 1964;10(6):537-562.

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

Introduction

Human myoglobinuria has been regarded as a rare syndrome, but, as in other rare syndromes, increasing awareness has led to an increasing number of reports. The first description is usually attributed to Meyer-Betz in 1910,96 and there have been about 118 cases in the world literature until the present, 103 since 1951 (Table 1).

The total of 118 is only an approximation because selection of cases has been somewhat arbitrary. On the one hand, the urinary pigment has not been strictly identified in all cases (although the clinical and pathological descriptions were felt to be compatible with the diagnosis). On the other hand, the compilation includes only those cases considered to be primarily "idiopathic," not those due to exogenous causes, but this distinction is not precise. Furthermore, some cases of probable myoglobinuria have been reported with other diagnoses and have not been included.43,48,49 It is a major . . . [Full Text PDF of this Article]


Author Affiliations

NEW YORK

Departments of Neurology and Biochemistry, College of Physicians and Surgeons, Columbia University; Neurological Clinical Research Center, Neurological Institute, Columbia-Presbyterian Medical Center, New York City, and Neurology Service, Department of Medicine, Wilford Hall USAF Hospital, Aerospace Medical Division (AFSC), Lackland Air Force Base, Texas.


Footnotes

Received for publication March 3, 1964; accepted March 17.

Associate Professor of Neurology, College of Physicians and Surgeons, Columbia University; Co-Director, Neurological Clinical Research Center, Neurological Institute (Dr. Rowland); formerly Assistant Resident in Neurology, Presbyterian Hospital, New York City; present address: National Institute of Neurological Diseases and Blindness, National Institutes of Health, Bethesda, Md (Dr. Fahn); Assistant Professor of Biochemistry, College of Physicians and Surgeons, Columbia University (Dr. Hirschberg); formerly Captain, USAF, MC, Wilford Hall USAF Hospital; present address: The Rockefeller Institute, New York City (Dr. Harter).

Supported by USPHS grants B-3359, B-3102, and CA-02332.



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
 
© 1964 American Medical Association. All Rights Reserved.