0
RSS Email Alerts
Please Wait... Processing your request... Please Wait.

JAMA Ophthalmology | 
Ophthalmic Molecular Genetics |  June 13, 2013 ONLINE FIRST
Distinct Ocular Expression in Infants and Children With Down Syndrome in Cairo, Egypt:  Myopia and Heart Disease
Hanan H. Afifi, MD, PhD; Amira A. Abdel Azeem, MD; Hala T. El-Bassyouni, MD, PhD; et al.
JAMA Ophthalmol. 2013;():1-9. doi:10.1001/jamaophthalmol.2013.644.
JAMA Neurology | 
Original Contribution |  June 10, 2013 ONLINE FIRST
Fragile X–Associated Tremor/Ataxia Syndrome:  Influence of the FMR1 Gene on Motor Fiber Tracts in Males With Normal and Premutation Alleles
Jun Yi Wang, PhD; David Hessl, PhD; Andrea Schneider, PhD; et al.
JAMA Neurol. 2013;():1-8. doi:10.1001/jamaneurol.2013.2934.
INCLUDES: , Supplemental Content
JAMA Dermatology | 
Off-Center Fold |  June 05, 2013 ONLINE FIRST
Scleroderma-Like Hands in a 16-Year-Old Boy—Diagnosis
JAMA Dermatol. 2013;():2. doi:10.1001/jamadermatol.2013.3370b.
JAMA Neurology | 
Original Contribution |  June 01, 2013
Systemic Metabolic Abnormalities in Adult-onset Acid Maltase Deficiency:  Beyond Muscle Glycogen Accumulation
Juan M. Pascual, MD, PhD; Charles R. Roe, MD
JAMA Neurol. 2013;70(6):756-763. doi:10.1001/jamaneurol.2013.1507.
JAMA Neurology | 
Original Contribution |  June 01, 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 Neurol. 2013;70(6):746-755. doi:10.1001/jamaneurol.2013.1707.
INCLUDES: , Supplemental Content
JAMA Neurology | 
Observation |  June 01, 2013
Improvement of White Matter Changes on Neuroimaging Modalities After Stem Cell Transplant in Metachromatic Leukodystrophy
Martje E. van Egmond, MD; Petra J. W. Pouwels, PhD; Jaap-Jan Boelens, MD, PhD; et al.
JAMA Neurol. 2013;70(6):779-782. doi:10.1001/jamaneurol.2013.629.
JAMA Neurology | 
Original Contribution |  June 01, 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 Neurol. 2013;70(6):764-771. doi:10.1001/jamaneurol.2013.2311.
INCLUDES: , Supplemental Content
JAMA Ophthalmology | 
Clinical Sciences |  May 16, 2013 ONLINE FIRST
Phenotypic Conservation in Patients With X-Linked Retinitis Pigmentosa Caused by RPGR Mutations
Sarwar Zahid, MD, MS; Naheed Khan, PhD; Kari Branham, MS; et al.
JAMA Ophthalmol. 2013;():1-10. doi:10.1001/jamaophthalmol.2013.120.
INCLUDES: , Supplemental Content
JAMA Neurology | 
Clinical Implications of Basic Neuroscience Research |  May 13, 2013 ONLINE FIRST
TRIM Proteins in Therapeutic Membrane Repair of Muscular Dystrophy
Jenna Alloush; Noah Weisleder, PhD
JAMA Neurol. 2013;():1-5. doi:10.1001/jamaneurol.2013.469.
JAMA Ophthalmology | 
Clinical Trials |  May 09, 2013 ONLINE FIRST
Treatment With 9- cis β-Carotene–Rich Powder in Patients With Retinitis Pigmentosa:  A Randomized Crossover Trial
Ygal Rotenstreich, MD; Michael Belkin, MD; Siegal Sadetzki, MD; et al.
JAMA Ophthalmol. 2013;():1-8. doi:10.1001/jamaophthalmol.2013.147.
INCLUDES: , Supplemental Content

Sign In

Register for a FREE personal account

and access these and other features:

Register Now

Want to Subscribe?

Learn More about subscription options.

Don't have Access?

Register and get free email Table of Contents alerts, saved searches, PowerPoint downloads, CME quizzes, and more

Subscribe for full-text access to content from 1998 forward and a host of useful features

Activate your current subscription (AMA members and current subscribers)

From The JAMA Network
JAMA Ophthalmology
Ophthalmic Molecular Genetics  |  June 13, 2013
Distinct Ocular Expression in Infants and Children With Down Syndrome in Cairo, Egypt:  Myopia and Heart Disease
Hanan H. Afifi, MD, PhD; Amira A. Abdel Azeem, MD; Hala T. El-Bassyouni, MD, PhD; et al.
JAMA Neurology
Original Contribution  |  June 10, 2013
Fragile X–Associated Tremor/Ataxia Syndrome:  Influence of the FMR1 Gene on Motor Fiber Tracts in Males With Normal and Premutation Alleles
Jun Yi Wang, PhD; David Hessl, PhD; Andrea Schneider, PhD; et al.
JAMA Dermatology
Off-Center Fold  |  June 5, 2013
Scleroderma-Like Hands in a 16-Year-Old Boy—Diagnosis
JAMA Neurology
Original Contribution  |  April 22, 2013
Systemic Metabolic Abnormalities in Adult-onset Acid Maltase Deficiency:  Beyond Muscle Glycogen Accumulation
Juan M. Pascual, MD, PhD; Charles R. Roe, MD
© 2013 American Medical Association. All Rights Reserved.
Powered bySilverchair Information Systems