In This Issue
Editorials
- An important first stepA standard curriculum for the neurology clerkshipRobert C. Griggs, David C. Anderson
Articles
- Neuropsychological and psychiatric sequelae of pallidotomy for PDClinical trial findingsJ. Green, W. M. McDonald, J. L. Vitek, M. Haber, H. Barnhart, R. A.E. Bakay, M. Evatt, A. Freeman, N. Wahlay, S. Triche, B. Sirockman, M. R. DeLong
- Evidence for widespread movement-associated functional MRI changes in patients with PPMSM. A. Rocca, P. M. Matthews, D. Caputo, A. Ghezzi, A. Falini, G. Scotti, G. Comi, M. Filippi
- Ciguatera fish poisoningA double-blind randomized trial of mannitol therapyHans Schnorf, M. Taurarii, T. Cundy
- Association of homozygous 7048G7049 variant in the intron six of Nurr1 gene with Parkinson’s diseaseP.-Y. Xu, R. Liang, J. Jankovic, C. Hunter, Y.-X. Zeng, T. Ashizawa, D. Lai, W.-D. Le
- Migraine in the United StatesEpidemiology and patterns of health care useR. B. Lipton, A. I. Scher, K. Kolodner, J. Liberman, T. J. Steiner, W. F. Stewart
- Expression of JC virus T-antigen in a patient with MS and glioblastoma multiformeL. Del Valle, S. Delbue, J. Gordon, S. Enam, S. Croul, P. Ferrante, K. Khalili
- Proton MR spectroscopic imaging predicts lesion progression on MRI in X-linked adrenoleukodystrophyF. S. Eichler, P. B. Barker, C. Cox, D. Edwin, A. M. Ulug, H. W. Moser, G. V. Raymond
- Increased familial risk of the psychotic phenotype of Alzheimer diseaseR. A. Sweet, V. L. Nimgaonkar, B. Devlin, O. L. Lopez, S. T. DeKosky
- Prevalence and clinical importance of sleep apnea in the first night after cerebral infarctionA. Iranzo, J. Santamaría, J. Berenguer, M. Sánchez, A. Chamorro
- Familial periventricular heterotopiaMissense and distal truncating mutations of the FLN1 geneF. Moro, R. Carrozzo, P. Veggiotti, G. Tortorella, D. Toniolo, A. Volzone, R. Guerrini
- Early onset autosomal dominant dementia with ataxia, extrapyramidal features, and epilepsyA. Filla, G. De Michele, S. Cocozza, A. Patrignani, G. Volpe, I. Castaldo, G. Ruggiero, V. Bonavita, C. Masters, G. Casari, A. Bruni
- Selective reduction of N-acetylaspartate in medial temporal and parietal lobes in ADN. Schuff, A. A. Capizzano, A. T. Du, D. L. Amend, J. O’Neill, D. Norman, J. Kramer, W. Jagust, B. Miller, O. M. Wolkowitz, K. Yaffe, M. W. Weiner
- The value of sleep deprivation as a diagnostic tool in adult sleepwalkersSteve Joncas, Antonio Zadra, Jean Paquet, Jacques Montplaisir
- Absence of linkage to 8q24 in a European family with familial adult myoclonic epilepsy (FAME)P. Labauge, L. O. Amer, M. Simonetta-Moreau, F. Attané, C. Tannier, M. Clanet, G. Castelnovo, I. An-Gourfinkel, Y. Agid, A. Brice, A. Ducros, E. LeGuern
- Normobaric hyperoxia reduces MRI diffusion abnormalities and infarct size in experimental strokeAneesh B. Singhal, Rick M. Dijkhuizen, Bruce R. Rosen, Eng H. Lo
Special Article
- The neurology clerkship core curriculumD.J. Gelb, C.H. Gunderson, K.A. Henry, H.S. Kirshner, R.F. Józefowicz
Views & Reviews
- Cerebral cavernous malformationsMutations in Krit1D. J. Verlaan, W. J. Davenport, H. Stefan, U. Sure, A. M. Siegel, G. A. Rouleau
Medical Hypothesis
- Cycad neurotoxins, consumption of flying foxes, and ALS-PDC disease in GuamPaul Alan Cox, Oliver W. Sacks
Clinical/Scientific Notes
- Spinocerebellar ataxia type 10 is rare in populations other than MexicansT. Matsuura, L. P.W. Ranum, V. Volpini, M. Pandolfo, H. Sasaki, K. Tashiro, K. Watase, H. Y. Zoghbi, T. Ashizawa
- Multifocal myoclonus due to verapamil overdoseLata Vadlamudi, Eelco F.M. Wijdicks
- Isolated weakness of index finger due to small cortical infarctionJong S. Kim, Jong P. Chung, Sang W. Ha
NeuroImages
- Intraluminal carotid thrombusMarkus Busch, Randolf Klingebiel, Georg Bohner, Florian Masuhr
Correspondence
- Ring chromosome 20 epilepsy syndrome in children: Electroclinical featuresPedro Jesús Serrano-Castro
Corrections
Calendar
Filler
Historical Neurology
- The mystery of the Doctor’s son, or the riddle of West syndromePaul Eling, Willy O. Renier, Joern Pomper, Tallie Z. Baram
Brief Communications
- “Economy Class” stroke syndrome?Y. Isayev, R. K.T. Chan, P. M. Pullicino
- Progressive bulbospinal amyotrophy in Triple A syndrome with AAAS gene mutationC. Goizet, B. Catargi, F. Tison, A. Tullio-Pelet, S. Hadj-Rabia, F. Pujol, A. Lagueny, S. Lyonnet, D. Lacombe
- CAG/CTG repeat expansions at the Huntington’s disease–like 2 locus are rare in Huntington’s disease patientsG. Stevanin, A. Camuzat, S. E. Holmes, C. Julien, R. Sahloul, C. Dodé, V. Hahn-Barma, C. A. Ross, R. L. Margolis, A. Durr, A. Brice
- The cerebellum may be directly involved in cognitive functionsM. Vokaer, J. C. Bier, S. Elincx, T. Claes, P. Paquier, S. Goldman, E. J. Bartholomé, M. Pandolfo
- Midbrain deafness with normal brainstem auditory evoked potentialsE. Vitte, F. Tankéré, I. Bernat, A. Zouaoui, G. Lamas, J. Soudant
- HLA-A2 homozygosity but not heterozygosity is associated with Alzheimer diseaseS. Zareparsi, D. M. James, J. A. Kaye, T. D. Bird, G. D. Schellenberg, H. Payami
- fMRI/EEG in paroxysmal activity elicited by elimination of central vision and fixationG. D. Iannetti, C. Di Bonaventura, P. Pantano, A. T. Giallonardo, P. L. Romanelli, L. Bozzao, M. Manfredi, G. B. Ricci
- Chronic inflammatory demyelinating polyneuropathy presenting with features of GBSK. Mori, N. Hattori, M. Sugiura, H. Koike, K. Misu, M. Ichimura, M. Hirayama, G. Sobue
Changes, People, Comments