Brief Communications

• Fukutin-related protein gene mutated in the original kindred limb-girdle MD 2I

  A. Driss, S. Noguchi, R. Amouri, M. Kefi, T. Sasaki, K. Sugie, S. Souilem, Y.K. Hayashi, N. Shimizu, S. Minoshima, J. Kudoh, F. Hentati, I. Nishino

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• Evaluation of essential tremor with multi-voxel magnetic resonance spectroscopy

  Fernando L. Pagan, John A. Butman, James M. Dambrosia, Mark Hallett

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• High rate of constitutional chromosomal rearrangements in apparently sporadic ALS

  T. Meyer, B. Alber, K. Roemer, T. Martin, V.M. Kalscheuer, E. Göttert, K.D. Zang, A.C. Ludolph, H.-H. Ropers, J. Prudlo

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• Carnitine palmitoyltransferase II deficiencyMolecular and biochemical analysis of 32 patients

  T. Wieser, M. Deschauer, K. Olek, T. Hermann, S. Zierz

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• Mutations of ANT1, Twinkle, and POLG1 in sporadic progressive external ophthalmoplegia (PEO)

  A. Agostino, L. Valletta, P.F. Chinnery, G. Ferrari, F. Carrara, R.W. Taylor, A.M. Schaefer, D.M. Turnbull, V. Tiranti, M. Zeviani

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• Late-onset encephalopathy associated with a C11777A mutation of mitochondrial DNA

  M. Deschauer, C. Bamberg, D. Claus, S. Zierz, D.M. Turnbull, R.W. Taylor

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• Outcome of trigeminal nerve section in the treatment of chronic cluster headache

  R.G. Jarrar, D.F. Black, D.W. Dodick, D.H. Davis

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• X-linked myotubular myopathy in a female infant caused by a new MTM1 gene mutation

  Ulrike Schara, Wolfram Kress, Jens Tücke, Wilhelm Mortier

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• Habitual snoring as a risk factor for chronic daily headache

  A.I. Scher, R.B. Lipton, W.F. Stewart

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• Estrogen exposures and memory at midlifeA population-based study of women

  V.W. Henderson, J.R. Guthrie, E.C. Dudley, H.G. Burger, L. Dennerstein

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• Comparison of Alzheimer’s disease risk factors in white and African American families

  D. L. Bachman, R. C. Green, K. S. Benke, L. A. Cupples, L. A. Farrer

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• Mild cognitive impairmentCan FDG-PET predict who is to rapidly convert to Alzheimer’s disease?

  G. Chételat, B. Desgranges, V. de la Sayette, F. Viader, F. Eustache, J.-C. Baron

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• New parkin mutations and atypical phenotypes in families with autosomal recessive parkinsonism

  N. Rawal, M. Periquet, E. Lohmann, C.B. Lücking, H.A. Teive, G. Ambrosio, S. Raskin, S. Lincoln, N. Hattori, J. Guimaraes, M.W.I.M. Horstink, W. Dos Santos Bele, E. Brousolle, A. Destée, Y. Mizuno, M. Farrer, J.-F. Deleuze, G. De Michele, Y. Agid, A. Dürr, A. Brice

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• Benign adult familial myoclonic epilepsyGenetic heterogeneity and allelism with ADCME

  F.A. de Falco, P. Striano, A. de Falco, S. Striano, R. Santangelo, A. Perretti, P. Balbi, M. Cecconi, F. Zara

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• Predict Resident Exam Performance (PREP) Study

  Vern C. Juel, Karen C. Johnston

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• Changes in CSF and plasma HIV-1 RNA and cognition after starting potent antiretroviral therapy

  C.M. Marra, D. Lockhart, J.R. Zunt, M. Perrin, R.W. Coombs, A.C. Collier

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