Myasthenia gravis: an update for the clinician von Sieb, J. P.

Volltext

Fatigue in multiple sclerosis is closely related to sleep disorders: a polysomnographic cross-sectional study von Veauthier, C, Radbruch, H, Gaede, G, Pfueller, CF, Dörr, J, Bellmann-Strobl, J, Wernecke, K-D, Zipp, F, Paul, F, Sieb, JP

Volltext

New Mutations in Acetylcholine Receptor Subunit Genes Reveal Heterogeneity in the Slow-Channel Congenital Myasthenic Syndrome von Engel, Andrew G., Ohno, Kinji, Milone, Margherita, Wang, Hai-Long, Nakano, Satoshi, Bouzat, Cecilia, Pruitt, J. Ned, Hutchinson, David O., Brengman, Joan M., Bren, Nina, Sieb, Joern P., Sine, Steven M.

Volltext

Myasthenia gravis: emerging new therapy options von Sieb, Joern P

Volltext

Severe congenital myasthenic syndrome due to homozygosity of the 1293insG ε-acetylcholine receptor subunit mutation von Sieb, J. P., Kraner, S., Schrank, B., Reitter, B., Goebel, T. H. H., Tzartos, S. J., Steinlein, O. K.

Volltext

Effects of the quinoline derivatives quinine, quinidine, and chloroquine on neuromuscular transmission von Sieb, Jörn P., Milone, Margherita, Engel, Andrew G.

Volltext

Myasthenia gravis and myasthenic syndromes von Marouf, W, Sieb, J P

Volltext

Relapsing alternating ptosis in two siblings von SIEB, J P, HARTMANN, A

Volltext

Congenital myasthenic syndrome of Brahman cattle in South Africa von Thompson, P. N., Steinlein, O. K., Harper, C. K., Kraner, S., Sieb, J. B., Guthrie, A. J.

Volltext

Congenital myasthenic syndromes in two kinships with end-plate acetylcholine receptor and utrophin deficiency von SIEB, J. P, DÖRFLER, P, TZARTOS, S, WEWER, U. M, RÜEGG, M. A, MEYER, D, BAUMANN, I, LINDEMUTH, R, JAKSCHIK, J, RIES, F

Volltext

Recurrent focal myositis von Sieb, Jörn P., Ries, Fernand, Träber, Frank, Keller, Ewald, Block, Wolfgang, Kaminski, Marcel

Volltext

Ephedrine: effects on neuromuscular transmission von Sieb, Jo¨rn P., Engel, Andrew G.

Volltext

Congenital myasthenic syndrome due to heteroallelic nonsense/missense mutations in the acetylcholine receptor epsilon subunit gene von Kraner, S., Burgunder, J.-M., Rösler, K. M., Steinlein, O. K., Sieb, J. P.

Volltext

Fluoroquinolone antibiotics block neuromuscular transmission von Sieb, J P

Volltext

Sporadic adult-onset distal myopathy with rimmed vacuoles, 15–18 nm tubulofilaments and extensive rod formation von Sieb, Jörn P, VonOertzen, Joachim, Tolksdorf, Karen, Dörfler, Petra, Kappes-Horn, Karin, Jerusalem, Felix

Volltext

Intermittent apomorphine injections as rescue therapy for advanced Parkinson's disease. Consensus statement von Trenkwalder, C, Boesch, S, Ceballos-Baumann, A, Dressler, D, Eggert, K, Gasser, T, Honig, H, Müller, T, Reichmann, H, Sieb, J P, Storch, A, Odin, P, Poewe, W

Volltext

Endplate ultrastructure in a case of primary fibromyalgia von Sieb, J P, Dörfler, P, Tolksdorf, K, Jakschik, J

Volltext

Immature end-plates and utrophin deficiency in congenital myasthenic syndrome caused by ε-AChR subunit truncating mutations von SIEB, Jörn P, KRANER, Simone, RAUCH, Michael, STEINLEIN, Ortrud K

Volltext

Occurrence of chloroquine-induced myopathy after low-dose treatment of rheumatoid arthritis for seven years von Haberl, A, Fischer, P, Pongratz, D, Sieb, J P

Volltext

Familial CNS tumors von SIEB, J. B, PULST, S.-M, BUCH, A

Volltext