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In This Issue of JAMA Neurology
January 2014


JAMA Neurol. 2014;71(1):2-3. doi:10.1001/jamaneurol.2013.4126


Dean and colleagues compare magnetic resonance imaging measurements of white matter myelin water fraction and gray matter volume in healthy infant carriers and noncarriers of the APOE ε4 allele, the major susceptibility gene for late-onset Alzheimer disease (AD).

Related Editorial

Hong and coauthors image amyloid deposition in patients with traumatic brain injury (TBI) using carbon 11–labeled Pittsburgh Compound B ([11C]PiB) positron emission tomography and validate these findings using hydrogen 3–labeled Pittsburgh Compound B autoradiography and immunocytochemistry on autopsy-acquired tissue.

Continuing Medical Education

Anthony and coauthors quantify dystrophin messenger RNA and protein expression in patients with DMD deletions treatable by, or mimicking, exon 44 or 45 skipping.

To describe the clinical presentation and progression of a new intermediate variant of glycogen branching enzyme deficiency, Paradas and colleagues performed a clinical, biochemical, morphological, and molecular study of 2 patients with adult acute onset of neurological signs initially diagnosed as multiple sclerosis. Genotype-phenotype correlations are discussed.

Jiao and coauthors determine the aquaporin 4 (AQP4) IgG detection rate using recombinant human APQ4–based assays in sequential serum specimens collected from patients with recurrent longitudinally extensive transverse myelitis (rLETM) categorized as negative by indirect immunofluorescence assay and defined the clinical characteristics and motor disability outcomes in AQP4-IgG–positive rLETM.

Weinstein and colleagues conduct a community-based, prospective cohort study to examine whether higher serum brain-derived neurotrophic factor (BDNF) levels in cognitively healthy adults protect against the future risk for dementia and Alzheimer disease and to identify potential modifiers of this association.

In a cross-sectional study of 44 participants with early-onset Parkinson disease of long duration, Alcalay and colleagues assess cognitive and motor performances, comparing homozygotes and compound heterozygotes who carry 2 PARKIN mutations with noncarriers.

Katz and coauthors define the frequency, timing, and consequences of clinical worsening in patients with diagnosis of reversible cerebral vasoconstriction syndrome.

Grau-Rivera and coauthors determine the frequency of antibodies against neuronal surface antigens in the cerebrospinal fluid of patients with suspected as well as pathologically confirmed Creutzfeldt-Jakob disease.

Clinical Review & Education

Watzlawick and colleagues conduct a systematic review and meta-analysis of RhoA/Rho-associated coiled-coil containing protein kinase blocking approaches to (1) analyze the impact of bias that may lead to inflated effect sizes and (2) determine the normalized effect size of functional locomotor recovery after experimental thoracic spinal cord injury.

Recent studies in both human and animal models strongly suggest that activity in the cortex, especially in motor cortical areas, is directly altered by deep brain stimulation by signals traveling in an antidromic fashion from the subthalamic nucleus. Li and coauthors discuss the evidence for this proposition.

Related Editorial

Continuing Medical Education