The non-dystrophic myotonias: molecular pathogenesis, diagnosis and treatment von Matthews, E., Fialho, D., Tan, S. V., Venance, S. L., Cannon, S. C., Sternberg, D., Fontaine, B., Amato, A. A., Barohn, R. J., Griggs, R. C., Hanna, M. G.

Volltext

Primary episodic ataxias: diagnosis, pathogenesis and treatment von Jen, J.C., Graves, T.D., Hess, E.J., Hanna, M.G., Griggs, R.C., Baloh, R.W.

Volltext

The primary periodic paralyses: diagnosis, pathogenesis and treatment von Venance, S. L., Cannon, S. C., Fialho, D., Fontaine, B., Hanna, M. G., Ptacek, L. J., Tristani-Firouzi, M., Tawil, R., Griggs, R. C.

Volltext

Acetazolamide efficacy in hypokalemic periodic paralysis and the predictive role of genotype von MATTHEWS, E, PORTARO, S, KE, Q, SUD, R, HAWORTH, A, DAVIS, M. B, GRIGGS, R. C, HANNA, M. G

Volltext

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

Volltext

Randomized, double-blind, placebo-controlled trial of albuterol in facioscapulohumeral dystrophy von KISSEL, J. T, MCDERMOTT, M. P, MENDELL, J. R, KING, W. M, PANDYA, S, GRIGGS, R. C, TAWIL, R

Volltext

Andersen's syndrome: A distinct periodic paralysis von Sansone, V., Griggs, R. C., Meola, G., Ptácek, L. J., Barohn, R., Iannaccone, S., Bryan, W., Baker, N., Janas, S. J., Scott, W., Ririe, D., Tawil, R.

Volltext

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

Volltext

A randomized efficacy and safety trial of oxandrolone in the treatment of Duchenne dystrophy von FENICHEL, G. M, GRIGGS, R. C, PANDYA, S, ROBISON, V. D, WANG, H, KISSEL, J, KRAMER, T. I, MENDELL, J. R, MOXLEY, R. T, PESTRONK, A, SHENG, K, FLORENCE, J, KING, W. M

Volltext

A prospective natural history study of inclusion body myositis: implications for clinical trials von ROSE, M. R, MCDERMOTT, M. P, THORNTON, C. A, PALENSKI, C, MARTENS, W. B, GRIGGS, R. C

Volltext

Early and late losses of motor units after poliomyelitis von MCCOMAS, A. J, QUARTLY, C, GRIGGS, R. C

Volltext

Andersen's syndrome: Potassium-sensitive periodic paralysis, ventricular ectopy, and dysmorphic features von Tawil, Rabi, Ptacek, Louis J., Pavlakis, Steven G., DeVivo, Darryl C., Penn, Audrey S., Özdemir, Coskun, Griggs, Robert C.

Volltext

Pilot trial of albuterol in facioscapulohumeral muscular dystrophy von KISSEL, J. T, MCDERMOTT, M. P, NATARAJAN, R, MENDELL, J. R, PANDYA, S, KING, W. M, GRIGGS, R. C, TAWIL, R

Volltext

Multiple mitochondrial DNA deletions in sporadic inclusion body myositis: A study of 56 patients von Santorelli, F. M., Sciacco, M., Tanji, K., Shanske, S., Vu, T. H., Golzi, V., Griggs, R. C., Mendell, J. R., Hays, A. P., Bertorini, T. E., Pestronk, A., Bonilla, E., Dimauro, S.

Volltext

End-plate acetylcholine receptor deficiency due to nonsense mutations in the ε subunit von Engel, Andrew G., Ohno, Kinji, Bouzat, Cecilia, Sine, Steven M., Griggs, Robert C.

Volltext

Myotonic dystrophy with no trinucleotide repeat expansion von Thornton, Charles A., Griggs, Robert C., Moxley III, Richard T.

Volltext

American Academy of Neurology policy on pharmaceutical and device industry support von Hutchins, J C, Rydell, C M, Griggs, R C, Sagsveen, M, Bernat, J L

Volltext

Plasma exchange and intravenous immunoglobulin treatment of neuromuscular disease von Thornton, Charles A., Griggs, Robert C.

Volltext

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

Volltext

Mutations in an S4 segment of the adult skeletal muscle sodium channel cause paramyotonia congenita von Ptáček, Louis J., George, Alfred L., Barchi, Robert L., Griggs, Robert C., Riggs, Jack E., Robertson, Margaret, Leppert, Mark F.

Volltext