Articles

• Olfactory dysfunction in LRRK2 G2019S mutation carriers

  R. Saunders-Pullman, K. Stanley, C. Wang, M. San Luciano, V. Shanker, A. Hunt, L. Severt, D. Raymond, L.J. Ozelius, R.B. Lipton, S.B. Bressman

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• Phenotype in parkinsonian and nonparkinsonian LRRK2 G2019S mutation carriers

  C. Marras, B. Schuele, R.P. Munhoz, E. Rogaeva, J.W. Langston, M. Kasten, C. Meaney, C. Klein, P.M. Wadia, S.-Y. Lim, R.S.-I. Chuang, C. Zadikof, T. Steeves, K.M. Prakash, R.M.A. de Bie, G. Adeli, T. Thomsen, K.K. Johansen, H.A. Teive, A. Asante, W. Reginold, A.E. Lang

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• Late-onset lower motor neuronopathyA new autosomal dominant disorder

  M. Jokela, S. Penttilä, S. Huovinen, P. Hackman, A.M. Saukkonen, J. Toivanen, B. Udd

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• Patient outcomes from symptomatic intracerebral hemorrhage after stroke thrombolysis

  D. Strbian, T. Sairanen, A. Meretoja, J. Pitkäniemi, J. Putaala, O. Salonen, H. Silvennoinen, M. Kaste, T. Tatlisumak, For the Helsinki Stroke Thrombolysis Registry Group

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  CME Course
• Favorable functional outcomes in acute ischemic stroke patients with subclinical hypothyroidism

  Fahimeh H. Akhoundi, Askar Ghorbani, Akbar Soltani, Alipasha Meysamie

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• Cost-effectiveness of disease-modifying therapy for multiple sclerosisA population-based study

  K. Noyes, A. Bajorska, A. Chappel, S.R. Schwid, L.R. Mehta, B. Weinstock-Guttman, R.G. Holloway, A.W. Dick

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• Varicella zoster virus vasculopathyAnalysis of virus-infected arteries

  M.A. Nagel, I. Traktinskiy, Y. Azarkh, B. Kleinschmidt- DeMasters, T. Hedley-Whyte, A. Russman, E.M. VanEgmond, K. Stenmark, M. Frid, R. Mahalingam, M. Wellish, A. Choe, R. Cordery-Cotter, R.J. Cohrs, D. Gilden

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• Current and past Epstein-Barr virus infection in risk of initial CNS demyelination

  R.M. Lucas, A.-L. Ponsonby, K. Dear, P. Valery, M.P. Pender, J.M. Burrows, S.R. Burrows, C. Chapman, A. Coulthard, D.E. Dwyer, T. Dwyer, T. Kilpatrick, M.-L. J. Lay, A.J. McMichael, B.V. Taylor, I.A.F. van der Mei, D. Williams

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• De novo SCN1A mutations in migrating partial seizures of infancy

  D. Carranza Rojo, L. Hamiwka, J.M. McMahon, L.M. Dibbens, T. Arsov, A. Suls, T. Stödberg, K. Kelley, E. Wirrell, B. Appleton, M. Mackay, J.L. Freeman, S.C. Yendle, S.F. Berkovic, T. Bienvenu, P. De Jonghe, D.R. Thorburn, J.C. Mulley, H.C. Mefford, I.E. Scheffer

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• Brain perfusion patterns in familial frontotemporal lobar degeneration

  H. Seelaar, J.M. Papma, G. Garraux, I. de Koning, A.E. Reijs, R. Valkema, A.J.M. Rozemuller, E. Salmon, J.C. van Swieten

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• Trajectories of brain and hippocampal atrophy in FTD with mutations in MAPT or GRN

  J.L. Whitwell, S.D. Weigand, J.L. Gunter, B.F. Boeve, R. Rademakers, M. Baker, D.S. Knopman, Z.K. Wszolek, R.C. Petersen, C.R. Jack, K.A. Josephs

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