0
We're unable to sign you in at this time. Please try again in a few minutes.
Retry
We were able to sign you in, but your subscription(s) could not be found. Please try again in a few minutes.
Retry
There may be a problem with your account. Please contact the AMA Service Center to resolve this issue.
Contact the AMA Service Center:
Telephone: 1 (800) 262-2350 or 1 (312) 670-7827  *   Email: subscriptions@jamanetwork.com
Error Message ......
RSS Email Alerts
Please Wait... Processing your request... Please Wait.

Lab Reports | 
Tracy Hampton, PhD
JAMA. 2013;310(1):22. doi:10.1001/jama.2013.7876.

JAMA Clinical Challenge | 
Brian J. Dlouhy, MD; Jeremy D. W. Greenlee, MD
JAMA. 2012;307(20):2195-2196. doi:10.1001/jama.2012.3447.

Original Contribution |  FREE
Sébastien Jacquemont, MD; Randi J. Hagerman, MD; Maureen A. Leehey, MD; et al.
JAMA. 2004;291(4):460-469. doi:10.1001/jama.291.4.460.

Sign in

Create a free personal account to sign up for alerts, share articles, and more.

Purchase Options

• Subscribe to the journal
From The JAMA Network
JAMA Neurology
Original Investigation  | 
Exome Sequencing in the Clinical Diagnosis of Sporadic or Familial Cerebellar Ataxia
Brent L. Fogel, MD, PhD; Hane Lee, PhD; Joshua L. Deignan, PhD; et al.
JAMA Neurology
Case Report/Case Series  | 
Autosomal Recessive Cerebellar Ataxia Type 3 Due to ANO10 Mutations:  Delineation and Genotype-Phenotype Correlation Study
Mathilde Renaud, MD; Mathieu Anheim, MD, PhD; Erik-Jan Kamsteeg, PhD; et al.
JAMA Neurology
Original Investigation  | 
Cerebellar Ataxia and Glutamic Acid Decarboxylase Antibodies:  Immunologic Profile and Long-term Effect of Immunotherapy
Helena Ariño, MD; Nuria Gresa-Arribas, PhD; Yolanda Blanco, MD, PhD; et al.
JAMA Neurology
Editorial  | 
Coexpression Networks Predict Ataxia Genes
Stefan M. Pulst, MD; Lance T. Pflieger, BS