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JAMA Neurology | 
Original Contribution |  April 29, 2013 ONLINE FIRST
New Subtype of Spinocerebellar Ataxia With Altered Vertical Eye Movements Mapping to Chromosome 1p32
Carmen Serrano-Munuera, MD; Marc Corral-Juan, BSc; Giovanni Stevanin, PhD; et al.
JAMA Neurol. 2013;():1-8. doi:10.1001/jamaneurol.2013.2311.
INCLUDES: , Supplemental Content
JAMA Neurology | 
Observation |  April 29, 2013 ONLINE FIRST
Clinical Application of Whole-Exome Sequencing:  A Novel Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay Sequence Variation in a Child With Ataxia
Wendy K. M. Liew, MBChB, MRCPCH; Tawfeg Ben-Omran, MD, FRCPC, FCCMG; Basil T. Darras, MD; et al.
JAMA Neurol. 2013;():1-4. doi:10.1001/jamaneurol.2013.247.
JAMA Neurology | 
Original Contribution |  April 22, 2013 ONLINE FIRST
Hereditary Ataxia and Spastic Paraplegia in Portugal:  A Population-Based Prevalence Study
Paula Coutinho, MD, PhD; Luis Ruano, MD, MPH; José L. Loureiro, MD, PhD; et al.
JAMA Neurol. 2013;():1-10. doi:10.1001/jamaneurol.2013.1707.
INCLUDES: , Supplemental Content
JAMA Neurology | 
Observation |  April 01, 2013
Patient With Homer-3 Antibodies and Cerebellitis
Romana Höftberger, MD; Lidia Sabater, PhD; Angel Ortega, MD; et al.
JAMA Neurol. 2013;70(4):506-509. doi:10.1001/jamaneurol.2013.1955.
JAMA Ophthalmology | 
Research Letters |  April 01, 2013
Novel Maculopathy in Patients With Spinocerebellar Ataxia Type 1 Autofluorescence Findings and Functional Characteristics
Veronika Vaclavik, MD; François-Xavier Borruat, MD; Aude Ambresin, MD; et al.
JAMA Ophthalmol. 2013;131(4):536-538. doi:10.1001/jamaophthalmol.2013.1127.
JAMA Neurology | 
Original Contribution |  February 01, 2013
Cerebellar Ataxia, Hemiplegic Migraine, and Related Phenotypes Due to a CACNA1A Missense Mutation:  12-Year Follow-up of a Large Portuguese Family
José Barros, MD; Joana Damásio, MD; Assunção Tuna, MD, Msc; et al.
JAMA Neurol. 2013;70(2):235-240. doi:10.1001/jamaneurol.2013.591.
INCLUDES: , Supplemental Content
JAMA Neurology | 
Correspondence |  December 01, 2012
Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay in the Time of Next-Generation Sequencing
Gabriella Silvestri, MD, PhD; Marcella Masciullo, MD; Filippo M. Santorelli, MD
Arch Neurol. 2012;69(12):1661-1662. doi:10.1001/2013.jamaneurol.70.
JAMA Neurology | 
Correspondence |  December 01, 2012
Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay in the Time of Next-Generation Sequencing—Reply
Angela Pyle, PhD; Rita Horvath, MD; Patrick F. Chinnery, PhD, FRCP, FMedSci
Arch Neurol. 2012;69(12):1661-1662. doi:10.1001/2013.jamaneurol.389.
JAMA Neurology | 
Correspondence |  November 01, 2012
Spinocerebellar Ataxia Types 2 and 10: More Than a Coincidental Association?—Reply
Sachin S. Kapur, MD, MS; Jennifer G. Goldman, MD, MS
Arch Neurol. 2012;69(11):1524-1525. doi:10.1001/archneurol.2012.2771.
JAMA Neurology | 
Clinical Pathologic Conference |  October 01, 2012
Slowly Progressive Ataxia, Neuropathy, and Oculomotor Dysfunction
Justin T. Jordan, MD; Gincy Samuel, MD; Steven Vernino, MD, PhD; et al.
Arch Neurol. 2012;69(10):1366-1371. doi:10.1001/archneurol.2012.2356.

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From The JAMA Network
JAMA Neurology
Observation  |  April 29, 2013
Clinical Application of Whole-Exome Sequencing:  A Novel Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay Sequence Variation in a Child With Ataxia
Wendy K. M. Liew, MBChB, MRCPCH; Tawfeg Ben-Omran, MD, FRCPC, FCCMG; Basil T. Darras, MD; et al.
JAMA Neurology
Original Contribution  |  April 29, 2013
New Subtype of Spinocerebellar Ataxia With Altered Vertical Eye Movements Mapping to Chromosome 1p32
Carmen Serrano-Munuera, MD; Marc Corral-Juan, BSc; Giovanni Stevanin, PhD; et al.
JAMA Neurology
Original Contribution  |  April 22, 2013
Hereditary Ataxia and Spastic Paraplegia in Portugal:  A Population-Based Prevalence Study
Paula Coutinho, MD, PhD; Luis Ruano, MD, MPH; José L. Loureiro, MD, PhD; et al.
JAMA Neurology
Observation  |  February 11, 2013
Patient With Homer-3 Antibodies and Cerebellitis
Romana Höftberger, MD; Lidia Sabater, PhD; Angel Ortega, MD; et al.
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