Matrix metalloproteinases and their tissue inhibitors in serum and cerebrospinal fluid of patients with amyotrophic lateral sclerosis von Niebroj-Dobosz, I., Janik, P., Sokołowska, B., Kwiecinski, H.

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Genotype-phenotype correlation of paroxysmal nonkinesigenic dyskinesia von Bruno, M K, Lee, H-Y, Auburger, G W J, Friedman, A, Nielsen, J E, Lang, A E, Bertini, E, Van Bogaert, P, Averyanov, Y, Hallett, M, Gwinn-Hardy, K, Sorenson, B, Pandolfo, M, Kwiecinski, H, Servidei, S, Fu, Y-H, Ptácek, L

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Correlating phenotype and genotype in the periodic paralyses von MILLER, T. M, DIAS DA SILVA, M. R, PETAJAN, J, DALAKAS, M. C, RANUM, L. P. W, FU, Y. H, PTACEK, L. J, MILLER, H. A, KWIECINSKI, H, MENDELL, J. R, TAWIL, R, MCMANIS, P, GRIGGS, R. C, ANGELINI, C, SERVIDEI, S

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Novel VCP mutations in inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia von Watts, GDJ, Thomasova, D, Ramdeen, SK, Fulchiero, EC, Mehta, SG, Drachman, DA, Weihl, CC, Jamrozik, Z, Kwiecinski, H, Kaminska, A, Kimonis, VE

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Hematoma size but not Gcs score on admission predicts in-hospital case fatality in the very elderly. A case control study von Florczak-Rzepka, M, Piechowski-Jozwiak, B, Gocyla, K, Sierdzinski, J, Kwiecinski, H, Kaminska, A

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MuSK-positive myasthenia gravis is rare in the Polish population von Kostera-Pruszczyk, A., Kamińska, A., Dutkiewicz, M., Emeryk-Szajewska, B., Strugalska-Cynowska, M. H., Vincent, A., Kwieciński, H.

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Improvement of motor function in early Parkinson disease by safinamide von STOCCHI, F, ARNOLD, G, FARIELLO, R. G, ONOFRJ, M, KWIECINSKI, H, SZCZUDLIK, A, THOMAS, A, BONUCCELLI, U, VAN DIJK, A, CATTANEO, C, SALA, P

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Erythropoietin concentration in serum and cerebrospinal fluid of patients with amyotrophic lateral sclerosis von Janik, P., Kwiecinski, H., Sokolowska, B., Niebroj-Dobosz, I.

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Changing phenotypic expression in a patient with a mitochondrial encephalopathy due to 13042G>A de novo mutation—a 5 year follow up von Schinwelski, M., Kierdaszuk, B., Dulski, J., Tońska, K., Kodroń, A., Sitek, E. J., Bartnik, E., Kamińska, A., Kwieciński, H., Sławek, J.

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Mutations and polymorphisms of the CLCN2 gene in idiopathic epilepsy von D'AGOSTINO, D, BERTELLI, M, PANDOLFO, M, GALLO, S, CECCHIN, S, ALBIERO, E, GAROFALO, P. G, GAMBARDELLA, A, ST. HILAIRE, J.-M, KWIECINSKI, H, ANDERMANN, E

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Association of apolipoprotein E and myeloperoxidase genotypes to clinical course of familial and sporadic multiple sclerosis von Zakrzewska-Pniewska, B, Styczynska, M, Podlecka, A, Samocka, R, Peplonska, B, Barcikowska, M, Kwiecinski, H

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Randomized Withdrawal Study of Patients With Symptomatic Neurogenic Orthostatic Hypotension Responsive to Droxidopa von Biaggioni, Italo, Freeman, Roy, Mathias, Christopher J, Low, Phillip, Hewitt, L Arthur, Kaufmann, Horacio

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Efficacy and safety of oral fumarate in patients with relapsing-remitting multiple sclerosis: a multicentre, randomised, double-blind, placebo-controlled phase IIb study von Kappos, Ludwig, Prof, Gold, Ralf, Prof, Miller, David H, Prof, MacManus, David G, MSc, Havrdova, Eva, MD, Limmroth, Volker, MD, Polman, Chris H, Prof, Schmierer, Klaus, PhD, Yousry, Tarek A, MD, Yang, Minhua, MS, Eraksoy, Mefkûre, Prof, Meluzinova, Eva, MD, Rektor, Ivan, MD, Dawson, Katherine T, MD, Sandrock, Alfred W, MD, O'Neill, Gilmore N, MB

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Long-term safety and efficacy of teriflunomide: Nine-year follow-up of the randomized TEMSO study von OʼConnor, Paul, Comi, Giancarlo, Freedman, Mark S, Miller, Aaron E, Kappos, Ludwig, Bouchard, Jean-Pierre, Lebrun-Frenay, Christine, Mares, Jan, Benamor, Myriam, Thangavelu, Karthinathan, Liang, Jinjun, Truffinet, Philippe, Lawson, Victoria J, Wolinsky, Jerry S

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CADASIL: new cases and new questions von RAFALOWSKA, J, FIDZIANSKA, A, DZIEWULSKA, D, PODLECKA, A, SZPAK, G. M, KWIECINSKI, H

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Mitoxantrone in progressive multiple sclerosis: a placebo-controlled, double-blind, randomised, multicentre trial von Hartung, Hans-Peter, Gonsette, Richard, Konig, Nikolaus, Kwiecinski, Hubert, Guseo, Andreas, Morrissey, Sean P, Krapf, Hilmar, Zwingers, Thomas

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Dihydropyridine receptor mutations cause hypokalemic periodic paralysis von Ptáček, Louis J., Tawil, Rabi, Griggs, Robert C., Engel, Andrew G., Layzer, Robert B., Kwieciński, Hubert, McManis, Philip G., Santiago, Lorna, Moore, Mary, Fouad, Gameil, Bradley, Paige, Leppert, Mark F.

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Mutations in the human skeletal muscle chloride channel gene (CLCN1) associated with dominant and recessive myotonia congenita von ZHANG, J, GEORGE, A. L, GRIGGS, R. C, FOUAD, G. T, ROBERTS, J, KWIECINSKI, H, CONNOLLY, A. M, PTACEK, L. J

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Weight loss in Huntington disease increases with higher CAG repeat number von AZIZ, N. A, VAN DER BURG, J. M. M, LANDWEHRMEYER, G. B, BRUNDIN, P, STIJNEN, T, ROOS, R. A. C

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European Stroke Initiative Recommendations for Stroke Management – Update 2003 von Olsen, Tom Skyhoj, Langhorne, Peter, Diener, Hans Christoph, Hennerici, Michael, Ferro, Jose, Sivenius, Johani, Wahlgren, Nils Gunnar, Bath, Philip

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