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November 2013, Vol 70, No. 11, Pages 1337-1461

In This Issue of JAMA Neurology

Highlights

Abstract Full Text
free access
JAMA Neurol. 2013;70(11):1337-1339. doi:10.1001/jamaneurol.2013.2892
Viewpoint

The 11th Revision of the International Classification of Diseases (ICD): The Neurological Perspective

Abstract Full Text
JAMA Neurol. 2013;70(11):1353-1354. doi:10.1001/jamaneurol.2013.4042
Editorial

Structural Variation and the Expanding Genomic Architecture of Parkinson Disease

Abstract Full Text
JAMA Neurol. 2013;70(11):1355-1356. doi:10.1001/jamaneurol.2013.4263

Breastfeeding in Women With Epilepsy

Abstract Full Text
JAMA Neurol. 2013;70(11):1357-1358. doi:10.1001/jamaneurol.2013.4348
Original Investigation

Association Between Early-Onset Parkinson Disease and 22q11.2 Deletion Syndrome: Identification of a Novel Genetic Form of Parkinson Disease and Its Clinical Implications

Abstract Full Text
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JAMA Neurol. 2013;70(11):1359-1366. doi:10.1001/jamaneurol.2013.3646

Butcher et al evaluate a possible association between 22q11.2 deletions and Parkinson disease. Shulman provides commentary in a related editorial.

Early Child Development and Exposure to Antiepileptic Drugs Prenatally and Through Breastfeeding: A Prospective Cohort Study on Children of Women With Epilepsy

Abstract Full Text
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JAMA Neurol. 2013;70(11):1367-1374. doi:10.1001/jamaneurol.2013.4290

Veiby et al determine whether signs of impaired development appear already during the first months of life in children exposed prenatally to antiepileptic drugs, and they explore potential adverse effects of antiepileptic drug exposure through breastfeeding. Van Ness provides commentary in a related editorial.

Longitudinally Extensive Transverse Myelitis With and Without Aquaporin 4 Antibodies

Abstract Full Text
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JAMA Neurol. 2013;70(11):1375-1381. doi:10.1001/jamaneurol.2013.3890

Kitley et al assess if AQP4-Ab–negative patients with LETM share similar disease characteristics with AQP4-Ab–positive patients or whether they have distinct features and alternative diagnoses.

Relationship of Mediterranean Diet and Caloric Intake to Phenoconversion in Huntington Disease

Abstract Full Text
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JAMA Neurol. 2013;70(11):1382-1388. doi:10.1001/jamaneurol.2013.3487

Marder et al attempted to determine whether the MeDi modifies the time to clinical onset of Huntington disease (phenoconversion) in premanifest carriers participating in Prospective Huntington at Risk Observational Study (PHAROS) and to examine the effects of body mass index and caloric intake on time to phenoconversion.

Loss of Fornix White Matter Volume as a Predictor of Cognitive Impairment in Cognitively Normal Elderly Individuals

Abstract Full Text
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JAMA Neurol. 2013;70(11):1389-1395. doi:10.1001/jamaneurol.2013.3263

In a longitudinal cohort study of cognitively normal elderly participants, Fletcher and coauthors examine the involvement of the hippocampus-fornix circuit in the very earliest stages of cognitive impairment and determine whether the volumes of fornix white matter and hippocampal gray matter would be useful markers for understanding the onset of dementia and for clinical intervention.

Incidence of Dementia With Lewy Bodies and Parkinson Disease Dementia

Abstract Full Text
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JAMA Neurol. 2013;70(11):1396-1402. doi:10.1001/jamaneurol.2013.3579

Savica et al investigate the incidence of DLB among residents of Olmsted County, Minnesota, and compare it with the incidence of PDD.

SQSTM1 Mutations in French Patients With Frontotemporal Dementia or Frontotemporal Dementia With Amyotrophic Lateral Sclerosis

Abstract Full Text
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JAMA Neurol. 2013;70(11):1403-1410. doi:10.1001/jamaneurol.2013.3849

Le Ber and coauthors evaluate the exact contribution of SQSTM1 to frontotemporal dementia and frontotemporal dementia with amyotrophic lateral sclerosis in an independent cohort of French patients.

Development and Validation of Pedigree Classification Criteria for Frontotemporal Lobar Degeneration

Abstract Full Text
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JAMA Neurol. 2013;70(11):1411-1417. doi:10.1001/jamaneurol.2013.3956

Wood and coauthors ascertain the frequency of inherited frontotemporal lobar degeneration and develop a validated pedigree classification criteria.

TDP-43 Pathology, Cognitive Decline, and Dementia in Old Age

Abstract Full Text
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JAMA Neurol. 2013;70(11):1418-1424. doi:10.1001/jamaneurol.2013.3961

Wilson and colleagues conducted a longitudinal clinical-pathologic cohort study to test the hypothesis that transactive response DNA-binding protein 43 (TDP-43) is related to late-life cognitive decline.

Case Report/Case Series

Longitudinal Clinical Follow-up of a Large Family With the R357P Twinkle Mutation

Abstract Full Text
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JAMA Neurol. 2013;70(11):1425-1428. doi:10.1001/jamaneurol.2013.3185

Paradas et al describe the 16-year clinical follow-up of a family with autosomal dominant progressive external ophthalmoplegia due to the p.R357P gene mutation in PEO1.

Orthostatic Tremor, Progressive External Ophthalmoplegia, and Twinkle

Abstract Full Text
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JAMA Neurol. 2013;70(11):1429-1431. doi:10.1001/jamaneurol.2013.3521

Milone et al describe a patient with orthostatic tremor carrying a C10orf2 TWINKLE mutation to highlight the possible association of orthostatic tremor with mitochondrial dysfunction and mutations in the mitochondrial replicative helicase Twinkle.

Macroglossia in Amyotrophic Lateral Sclerosis

Abstract Full Text
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JAMA Neurol. 2013;70(11):1432-1435. doi:10.1001/jamaneurol.2013.3138

McKee and colleagues described 2 patients with amyotrophic lateral sclerosis with tongue enlargement and protrusion outside the oral cavity (macroglossia).

Hypokalemic Periodic Paralysis Induced by Thymic Hyperplasia and Relieved by Thymectomy

Abstract Full Text
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JAMA Neurol. 2013;70(11):1436-1439. doi:10.1001/jamaneurol.2013.3918

Yang et al describe a patient whose hypokalemic weakness attacks were induced by thymic hyperplasia and abolished by thymectomy.

Review

Cerebrospinal Fluid Analysis in the Workup of GLUT1 Deficiency Syndrome: A Systematic Review

Abstract Full Text
JAMA Neurol. 2013;70(11):1440-1444. doi:10.1001/jamaneurol.2013.3090

In a systematic review, Leen and coauthors determine the value of cerebrospinal fluid analysis in the workup for GLUT1 deficiency syndrome.

Clinical Pathologic Conference

Headache and Focal Neurologic Deficits in a 37-Year-Old Woman

Abstract Full Text
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JAMA Neurol. 2013;70(11):1445-1449. doi:10.1001/jamaneurol.2013.3933

Ayodele et al discuss the clinical approach, differential diagnosis, and neuropathological findings in a 37-year-old woman who presented with progressively worsening headache and developed neurologic deficits with multiple cystic lesions in the posterior fossa.

Images in Neurology

Intradural, Extramedullary Anaplastic Astrocytoma Arising From the First Sacral Nerve Root

Abstract Full Text
JAMA Neurol. 2013;70(11):1450-1451. doi:10.1001/2013.jamaneurol.368

Cerebral Microbleeds in Lupus Anticoagulant-Hypoprothrombinemia Syndrome

Abstract Full Text
JAMA Neurol. 2013;70(11):1452-1453. doi:10.1001/2013.jamaneurol.505

Reversible Pure Word Deafness

Abstract Full Text
JAMA Neurol. 2013;70(11):1454-1455. doi:10.1001/2013.jamaneurol.509
Research Letter

Challenges of Making Music: What Causes Musician’s Dystonia?

Abstract Full Text
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JAMA Neurol. 2013;70(11):1456-1459. doi:10.1001/jamaneurol.2013.3931
Comment & Response

Chronic Lymphocytic Inflammation With Pontine Perivascular Enhancement Responsive to Steroids and Fatal B-Cell Lymphoma

Abstract Full Text
JAMA Neurol. 2013;70(11):1459. doi:10.1001/jamaneurol.2013.4074

Chronic Lymphocytic Inflammation With Pontine Perivascular Enhancement Responsive to Steroids and Fatal B-Cell Lymphoma—Reply

Abstract Full Text
JAMA Neurol. 2013;70(11):1459-1460. doi:10.1001/jamaneurol.2013.4757
Book and Media Review

Review of The Biology of Multiple Sclerosis

Abstract Full Text
JAMA Neurol. 2013;70(11):1461. doi:10.1001/jamaneurol.2013.4266
JAMA Neurology Masthead

JAMA Neurology

Abstract Full Text
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JAMA Neurol. 2013;70(11):1348. doi:10.1001/jamaneurol.2013.2890
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