Aggregation of Mutant Cu/Zn Superoxide Dismutase Proteins in a Culture Model of ALS von DURHAM, H D, ROY, J, DONG, L, FIGLEWICZ, D A

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Paraoxonase gene polymorphisms and sporadic ALS von SLOWIK, A, TOMIK, B, WOLKOW, P. P, PARTYKA, D, TURAJ, W, MALECKI, M. T, PERA, J, DZIEDZIC, T, SZCZUDLIK, A, FIGLEWICZ, D. A

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DD genotype of ACE gene is a risk factor for intracerebral hemorrhage von SLOWIK, A, TURAJ, W, DZIEDZIC, T, HAEFELE, A, PERA, J, MALECKI, M. T, GLODZIK-SOBANSKA, L, SZERMER, P, FIGLEWICZ, D. A, SZCZUDLIK, A

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Up‐Regulation of Protein Chaperones Preserves Viability of Cells Expressing Toxic Cu/Zn‐Superoxide Dismutase Mutants Associated with Amyotrophic Lateral Sclerosis von Bruening, Wendy, Roy, Josée, Giasson, Benoit, Figlewicz, Denise A, Mushynski, Walter E, Durham, Heather D

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Intramuscular grafts of myoblasts genetically modified to secrete glial cell line-derived neurotrophic factor prevent motoneuron loss and disease progression in a mouse model of fa... von HASAN MOHAJERI, M, FIGLEWICZ, D. A, BOHN, M. C

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Variants of the heavy neurofilament subunit are associated with the development of amyotrophic lateral sclerosis von Figlewicz, Denise A., Krizus, Aldis, Martinoli, Maria G., Meininger, Vincent, Dib, Michel, Rouleau, Guy A., Julien, Jean-Pierre

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Spinobulbar muscular atrophy can mimic ALS: The importance of genetic testing in male patients with atypical ALS von PARBOOSINGH, J. S, FIGLEWICZ, D. A, KRIZUS, A, MEININGER, V, AZAD, N. A, NEWMAN, D. S, ROULEAU, G. A

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Definitive molecular diagnosis of facioscapulohumeral dystrophy von ORRELL, R. W, TAWIL, R, FORRESTER, J, KISSEL, J. T, MENDELL, J. R, FIGLEWICZ, D. A

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Hereditary Spastic Paraplegia: Advances in Genetic Research von Fink, J K, Heiman-Patterson, T, Bird, T, Cambi, F, Dube, M.-P, Figlewicz, D A, Fink, J K, Haines, J L, Hentati, A, Pericak-Vance, M A, Raskind, W, Rouleau, G A, Siddique, T

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A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2 von Hadano, Shinji, Hand, Collette K., Osuga, Hitoshi, Yanagisawa, Yoshiko, Otomo, Asako, Devon, Rebecca S., Miyamoto, Natsuki, Showguchi-Miyata, Junko, Okada, Yoshinori, Singaraja, Roshni, Figlewicz, Denise A., Kwiatkowski, Thomas, Hosler, Betsy A., Sagie, Tally, Skaug, Jennifer, Nasir, Jamal, Brown, Robert H., Scherer, Stephen W., Rouleau, Guy A., Hayden, Michael R., Ikeda, Joh-E

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Identification of new mutations of the Cu/Zn superoxide dismutase gene of patients with familial amyotrophic lateral sclerosis von PRAMATAROVA, A, FIGLEWICZ, D. A, KRIZUS, A, HAN, F. Y, CEBALLOS-PICOT, I, NICOLE, A, DIB, M, MEININGER, V, BROWN, R. H, ROULEAU, G. A

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Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33–q35 von Hentati, Afif, Bejaoui, Khemissa, Pericak-Vance, Margaret A., Hentati, Faycal, Speer, Marcy C., Hung, Wu-Yen, Figlewicz, Denise A., Haines, Jonathan, Rimmler, Jackie, Ben Hamida, Christiane, Ben Hamida, Mongi, Brown, Robert H., Siddique, Teepu

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Selective Loss of α Motoneurons Innervating the Medial Gastrocnemius Muscle in a Mouse Model of Amyotrophic Lateral Sclerosis von Mohajeri, M.Hasan, Figlewicz, Denise A., Bohn, Martha C.

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Paraoxonase-1 Q192R polymorphism and risk of sporadic amyotrophic lateral sclerosis von Slowik, A, Tomik, B, Partyka, D, Turaj, W, Pera, J, Dziedzic, T, Szermer, P, Figlewicz, DA, Szczudlik, A

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Glutamate Potentiates the Toxicity of Mutant Cu/Zn-Superoxide Dismutase in Motor Neurons by Postsynaptic Calcium-Dependent Mechanisms von Roy, Josee, Minotti, Sandra, Dong, Lichun, Figlewicz, Denise A, Durham, Heather D

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LACK OF ASSOCIATION BETWEEN VEGF GENE POLYMORPHISMS AND PLASMA VEGF LEVELS AND SPORADIC ALS von GOLENIA, A, TOMIK, B, ZAWISLAK, D, WOLKOW, P, DZIUBEK, A, SADO, M, SZCZUDLIK, A, FIGLEWICZ, D. A, SLOWIK, A

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"Pure" hereditary spastic paraplegias: the story becomes complicated von Figlewicz, D A, Bird, T D

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Coexistence of Huntington's disease and familial amyotrophic lateral sclerosis : case presentation von RUBIO, A, STEINBERG, K, FIGLEWICZ, D. A, MACDONALD, M. E, GREENAMYRE, T, HAMILL, R, SHOULSON, I, POWERS, J. M

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Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis von Rosen, Daniel R., Siddique, Teepu, Patterson, David, Figlewicz, Denise A., Sapp, Peter, Hentati, Afif, Donaldson, Deirdre, Goto, Jun, O'Regan, Jeremiah P., Deng, Han-Xiang, Rahmani, Zohra, Krizus, Aldis, McKenna-Yasek, Diane, Cayabyab, Annarueber, Gaston, Sandra M., Berger, Ralph, Tanzi, Rudolph E., Halperin, John J., Herzfeldt, Brian, Van den Bergh, Raymond, Hung, Wu-Yen, Bird, Thomas, Deng, Gang, Mulder, Donald W., Smyth, Celestine, Laing, Nigel G., Soriano, Edwin, Pericak–Vance, Margaret A., Haines, Jonathan, Rouleau, Guy A., Gusella, James S., Horvitz, H. Robert, Brown, Robert H.

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A two basepair deletion in the SOD 1 gene causes familial amyotrophic lateral sclerosis von PRAMATAROVA, A, GOTO, J, NANBA, E, NAKASHIMA, K, TAKAHASHI, K, TAKAGI, A, KANAZAWA, I, FIGLEWICZ, D. A, ROULEAU, G. A

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