Study of 962 patients indicates progressive muscular atrophy is a form of ALS von KIM, W.-K, LIU, X, SANDNER, J, PASMANTIER, M, ANDREWS, J, ROWLAND, L. P, MITSUMOTO, H

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The natural history of primary lateral sclerosis von GORDON, P. H, CHENG, B, KATZ, I. B, PINTO, M, HAYS, A. P, MITSUMOTO, H, ROWLAND, L. P

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The ALSFRSr predicts survival time in an ALS clinic population von KAUFMANN, P, LEVY, G, THOMPSON, J. L. P, DELBENE, M. L, BATTISTA, V, GORDON, P. H, ROWLAND, L. P, LEVIN, B, MITSUMOTO, H

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Quantitative objective markers for upper and lower motor neuron dysfunction in ALS von MITSUMOTO, H, ULUG, A. M, MONTES, J, HAYES, S, DASHNAW, S, KAUFMANN, P, GORDON, P. H, HIRSCH, J, LEVIN, B, ROWLAND, L. P, SHUNGU, D. C, PULLMAN, S. L, GOOCH, C. L, CHAN, S, TANG, M.-X, MAO, X, HAYS, A. P, FLOYD, A. G, BATTISTA, V

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Prevalence of depressive disorders and change over time in late-stage ALS von RABKIN, J. G, ALBERT, S. M, DEL BENE, M. L, O'SULLIVAN, I, TIDER, T, ROWLAND, L. P, MITSUMOTO, H

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Premorbid weight, body mass, and varsity athletics in ALS von SCARMEAS, N, SHIH, T, STERN, Y, OTTMAN, R, ROWLAND, L. P

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Wish to die in end-stage ALS von ALBERT, S. M, RABKIN, J. G, DEL BENE, M. L, TIDER, T, O'SULLIVAN, I, ROWLAND, L. P, MITSUMOTO, H

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Clinical features that distinguish PLS, upper motor neuron―dominant ALS, and typical ALS von GORDON, P. H, CHENG, B, KATZ, I. B, MITSUMOTO, H, ROWLAND, L. P

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Transcranial magnetic stimulation in ALS : Utility of central motor conduction tests von FLOYD, A. G, YU, Q. P, PIBOOLNURAK, P, TANG, M. X, FANG, Y, SMITH, W. A, YIM, J, ROWLAND, L. P, MITSUMOTO, H, PULLMAN, S. L

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Objective tests for upper motor neuron involvement in amyotrophic lateral sclerosis (ALS) von KAUFMANN, P, PULLMAN, S. L, SHUNGU, D. C, CHAN, S, HAYS, A. P, DEL BENE, M. L, DOVER, M. A, VUKIC, M, ROWLAND, L. P, MITSUMOTO, H

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Randomized controlled phase II trial of glatiramer acetate in ALS von GORDON, P. H, DOORISH, C, GENDELMAN, H. E, PRZEDBORSKI, S, MITSUMOTO, H, MONTES, J, MOSELY, R. L, DIAMOND, B, MACARTHUR, R. B, WEIMER, L. H, KAUFMANN, P, HAYS, A. P, ROWLAND, L. P

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Myasthenic crisis : Clinical features, mortality, complications, and risk factors for prolonged intubation von THOMAS, C. E, MAYER, S. A, GUNGOR, Y, SWARUP, R, WEBSTER, E. A, CHANG, I, BRANNAGAN, T. H, FINK, M. E, ROWLAND, L. P

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Diagnosis of amyotrophic lateral sclerosis von Rowland, Lewis P

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Inclusion body myositis and myopathies von Griggs, Robert C., Askanas, Valerie, DiMauro, Salvatore, Engel, Andrew, Karpati, George, Mendell, Jerry R., Rowland, Lewis P.

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Challenges and opportunities in clinical trials for spinal muscular atrophy von HIRTZ, D, IANNACCONE, S, HEEMSKERK, J, GWINN-HARDY, K, MOXLEY, R. III, ROWLAND, L. P

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Mitochondrial neurogastrointestinal encephalomyopathy: An autosomal recessive disorder due to thymidine phosphorylase mutations von Nishino, Ichizo, Spinazzola, Antonella, Papadimitriou, Alexandros, Hammans, Simon, Steiner, Israel, Hahn, Cecil D., Connolly, Anne M., Verloes, Alain, Guimarães, João, Maillard, Ivan, Hamano, Hitoshi, Donati, M. Alice, Semrad, Carol E., Russell, James A., Andreu, Antonio L., Hadjigeorgiou, Giorgos M., Vu, Tuan H., Tadesse, Saba, Nygaard, Torbjoern G., Nonaka, Ikuya, Hirano, Ikuo, Bonilla, Eduardo, Rowland, Lewis P., DiMauro, Salvatore, Hirano, Michio

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Impact of spirituality and religiousness on outcomes in patients with ALS von MURPHY, P. L, ALBERT, S. M, WEBER, C. M, DEL BENE, M. L, ROWLAND, L. P

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A prospective study of preferences and actual treatment choices in ALS von ALBERT, S. M, MURPHY, P. L, DEL BENE, M. L, ROWLAND, L. P

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Lymphoproliferative disorders and motor neuron disease: An update von Gordon, P H, Rowland, L P, Younger, D S, Sherman, W H, Hays, A P, Louis, E D, Lange, D J, Trojaborg, W, Lovelace, R E, Murphy, P L, Latov, N

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Prospective study of palliative care in ALS: choice, timing, outcomes von Albert, Steven M., Murphy, Peregrine L., Del Bene, Maura L., Rowland, L.P.

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