In This Issue
Editorials
- What’s in a name?Lumping or splitting ALS, PLS, PMA, and the other motor neuron diseasesJeffrey Rosenfeld, Michael Swash
- Futility studiesSpending a little to save a lotSteven R. Schwid, Gary R. Cutter
Articles
- Haptoglobin and the development of cerebral artery vasospasm after subarachnoid hemorrhageM. Borsody, A. Burke, W. Coplin, R. Miller-Lotan, A. Levy
- Recurrent stroke and cardiac risks after first ischemic strokeThe Northern Manhattan StudyM. S. Dhamoon, R. R. Sciacca, T. Rundek, R. L. Sacco, M.S.V. Elkind
- The natural history of primary lateral sclerosisP. H. Gordon, B. Cheng, I. B. Katz, M. Pinto, A. P. Hays, H. Mitsumoto, L. P. Rowland
- Mutation analysis of the paraplegin gene (SPG7) in patients with hereditary spastic paraplegiaN. Elleuch, C. Depienne, A. Benomar, A. M. Ouvrard Hernandez, X. Ferrer, B. Fontaine, D. Grid, C.M.E. Tallaksen, R. Zemmouri, G. Stevanin, A. Durr, A. Brice
- A two-stage design for a phase II clinical trial of coenzyme Q10 in ALSG. Levy, P. Kaufmann, R. Buchsbaum, J. Montes, A. Barsdorf, R. Arbing, V. Battista, X. Zhou, H. Mitsumoto, B. Levin, J.L.P. Thompson
- Topiramate in essential tremorA double-blind, placebo-controlled trialW. G. Ondo, J. Jankovic, G. S. Connor, R. Pahwa, R. Elble, M. A. Stacy, W. C. Koller, L. Schwarzman, S. -C. Wu, J. F. Hulihan
- Gray and white matter brain atrophy and neuropsychological impairment in multiple sclerosisMichael P. Sanfilipo, Ralph H.B. Benedict, Bianca Weinstock-Guttman, Rohit Bakshi
- Ventricular enlargement in MSOne-year change at various stages of diseaseC. M. Dalton, K. A. Miszkiel, P. W. O’Connor, G. T. Plant, G.P.A. Rice, D. H. Miller
- Memory fMRI in left hippocampal sclerosisOptimizing the approach to predicting postsurgical memoryMark P. Richardson, Bryan A. Strange, John S. Duncan, Raymond J. Dolan
- Nystagmus while recumbent in horizontal canal benign paroxysmal positional vertigoByung In Han, Hui Jong Oh, Ji Soo Kim
- Functional imaging of allodynia in complex regional pain syndromeChristian Maihöfner, Hermann O. Handwerker, Frank Birklein
- MRS shows abnormalities before symptoms in familial Alzheimer diseaseA. K. Godbolt, A. D. Waldman, D. G. MacManus, J. M. Schott, C. Frost, L. Cipolotti, N. C. Fox, M. N. Rossor
Views & Reviews
- Optimizing the ongoing search for new treatments for Parkinson diseaseUsing futility designsB. C. Tilley, Y. Y. Palesch, K. Kieburtz, B. Ravina, P. Huang, J. J. Elm, K. Shannon, G. F. Wooten, C. M. Tanner, G. C. Goetz
Clinical/Scientific Notes
- Age-related electrical status epilepticus during sleep and epileptic negative myoclonus in DRPLAK. Kobayashi, H. Hata, M. Oka, M. Ito, H. Yoshinaga, K. Kashihara, Y. Ohtsuka
- Hiccups associated with dopamine agonists in Parkinson diseaseParikshat Sharma, John C. Morgan, Kapil D. Sethi
- Hippocampal sclerosis in Alzheimer disease and other dementiasJohannes Attems, Kurt A. Jellinger
- Three sites of high-flow CSF leakage in spontaneous intracranial hypotensionK. Hüfner, W. Koch, M. Ständer, J. -C. Tonn, K. Tatsch, T. Meindl, R. Brüning, T. Brandt, M. Strupp
- Perils of the prozone reaction: Neurosyphilis presenting as an RPR-negative subacute dementiaStephanie Lessig, Evelyn Tecoma
Reflections: Neurology and the Humanities
NeuroImages
- Asymptomatic huge calcified subdural hematoma in a patient on oral anticoagulant therapyA. Kavčič, B. Meglič, N. Pečarič Meglič, D. B. Vodušek, A. Mesec
- Extensive peri-lesional connectivity in congenital hemiparesisM. Staudt, M. Erb, C. Braun, C. Gerloff, W. Grodd, I. Krägeloh-Mann
Correspondence
- New and reliable MRI diagnosis for progressive supranuclear palsyZ. K. Wszolek, J. Slowinski, A. Imamura, Y. Tsuboi, D. F. Broderick
- Spontaneous CSF leak treated with percutaneous CT-guided fibrin glueM. Savoiardo, T. De Simone, A. Franzini, G. Broggi, L. Chiapparini
- Encephalopathy and peripheral neuropathy following diethylene glycol ingestionG. Patrick Daubert, Abhishek Katiyar, John Wilson, Lydia Baltarowich
- Ventriculoperitoneal shunt in patients with leptomeningeal metastasisMarc C. Chamberlain, Michael Glantz
DEPARTMENTS
Resident and Fellow Page
- Teaching NeuroImage: Horner syndrome due to internal carotid artery dissectionSara Mazzucco, Nicolò Rizzuto
Brief Communications
- Figuring out drawing-induced epilepsyKuan H. Kho, Walter M. van den Bergh, Willy P.J. Spetgens, Frans S.S. Leijten
- Cerebrovascular reactivity and vasospasm after subarachnoid hemorrhage: A pilot studyJ. A. Frontera, T. Rundek, J. M. Schmidt, J. Claassen, A. Parra, K. E. Wartenberg, R. E. Temes, S. A. Mayer, J. P. Mohr, R. S. Marshall
- Increasing the specificity of diagnostic criteria for schwannomatosisMichael E. Baser, J. M. Friedman, D. Gareth R. Evans
- Proteomic profiling distinguishes astrocytomas and identifies differential tumor markersJ. Li, Z. Zhuang, H. Okamoto, A. O. Vortmeyer, D. M. Park, M. Furuta, Y. S. Lee, E. H. Oldfield, W. Zeng, R. J. Weil
- Neuropsychological deficits in long-term frequent cannabis usersLambros Messinis, Anthoula Kyprianidou, Sonia Malefaki, Panagiotis Papathanasopoulos
- Memory impairment in now abstinent MDMA users and continued users: A longitudinal follow-upKonstantine K. Zakzanis, Zachariah Campbell
- High-dose rituximab and anti-MAG–associated polyneuropathyS. Renaud, P. Fuhr, M. Gregor, K. Schweikert, D. Lorenz, C. Daniels, G. Deuschl, A. Gratwohl, A. J. Steck
- Charcot–Marie–Tooth type 4F disease caused by S399fsx410 mutation in the PRX geneD. Kabzińska, H. Drac, D. L. Sherman, A. Kostera-Pruszczyk, P. J. Brophy, A. Kochański, I. Hausmanowa-Petrusewicz
- Novel mutations in the HSN2 gene causing hereditary sensory and autonomic neuropathy type IIK. Coen, D. Pareyson, M. Auer-Grumbach, G. Buyse, N. Goemans, K. G. Claeys, N. Verpoorten, M. Laurà, V. Scaioli, W. Salmhofer, T. R. Pieber, E. Nelis, P. De Jonghe, V. Timmerman
- Coexistence of CMT-2D and distal SMA-V phenotypes in an Italian family with a GARS gene mutationR. Del Bo, F. Locatelli, S. Corti, M. Scarlato, S. Ghezzi, A. Prelle, G. Fagiolari, M. Moggio, M. Carpo, N. Bresolin, G. P. Comi
- NCAM is hyposialylated in hereditary inclusion body myopathy due to GNE mutationsE. Ricci, A. Broccolini, T. Gidaro, R. Morosetti, C. Gliubizzi, R. Frusciante, G. M. Di Lella, P. A. Tonali, M. Mirabella
- Phenotype-genotype correlation in Dutch patients with myoclonus-dystoniaM.C.F. Gerrits, E. M.J. Foncke, R. de Haan, K. Hedrich, Y. L.C. van de Leemput, F. Baas, L. J. Ozelius, J. D. Speelman, C. Klein, M. A.J. Tijssen
- Somatosensory cortical atrophy after spinal cord injury: A voxel-based morphometry studyM. T. Jurkiewicz, A. P. Crawley, M. C. Verrier, M. G. Fehlings, D. J. Mikulis
- Different degrees of right-to-left shunting predict migraine and stroke: Data from 420 patientsGian Paolo Anzola, Eva Morandi, Francesco Casilli, Eustaquio Onorato
- Thrombolytic therapy of acute ischemic stroke during pregnancyA. Murugappan, W. M. Coplin, A. N. Al-Sadat, K. J. McAllen, L. H. Schwamm, L. R. Wechsler, C. S. Kidwell, J. L. Saver, S. Starkman, Y. P. Gobin, G. Duckwiler, M. Krueger, G. Rordorf, J. P. Broderick, G. E. Tietjen, S. R. Levine