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Results: 1-12 |
Results: 12
CSF filtration is an effective treatment of Guillain-Barre syndrome - A randomized clinical trial
Authors: Wollinsky, KH Hulser, PJ Brinkmeier, H Aulkemeyer, P Bossenecker, W Huber-Hartmann, KH Rohrbach, P Schreiber, H Weber, F Kron, M Buchele, G Mehrkens, HH Ludolph, AC Rudel, R
Citation: Kh. Wollinsky et al., CSF filtration is an effective treatment of Guillain-Barre syndrome - A randomized clinical trial, NEUROLOGY, 57(5), 2001, pp. 774-780
An endogenous pentapeptide acting as a sodium channel blocker in inflammatory autoimmune disorders of the central nervous system
Authors: Brinkmeier, H Aulkemeyer, P Wollinsky, KH Rudel, R
Citation: H. Brinkmeier et al., An endogenous pentapeptide acting as a sodium channel blocker in inflammatory autoimmune disorders of the central nervous system, NAT MED, 6(7), 2000, pp. 808-811
Anti-GM1 antibodies can block neuronal voltage-gated sodium channels
Authors: Weber, F Rudel, R Aulkemeyer, P Brinkmeier, H
Citation: F. Weber et al., Anti-GM1 antibodies can block neuronal voltage-gated sodium channels, MUSCLE NERV, 23(9), 2000, pp. 1414-1420
Calcium ion in skeletal muscle: Its crucial role for muscle function, plasticity, and disease
Authors: Berchtold, MW Brinkmeier, H Muntener, M
Citation: Mw. Berchtold et al., Calcium ion in skeletal muscle: Its crucial role for muscle function, plasticity, and disease, PHYSIOL REV, 80(3), 2000, pp. 1215-1265
The small sodium-channel blocking factor in the cerebrospinal fluid of multiple sclerosis patients is probably an oligopeptide
Authors: Aulkemeyer, P Hausner, G Brinkmeier, H Weber, F Wurz, A Heidenreich, F Rudel, R
Citation: P. Aulkemeyer et al., The small sodium-channel blocking factor in the cerebrospinal fluid of multiple sclerosis patients is probably an oligopeptide, J NEUR SCI, 172(1), 2000, pp. 49-54
Borna disease virus-related therapy-resistant depression improved after cerebrospinal fluid filtration
Authors: Bechter, K Herzog, S Schreiner, V Brinkmeier, H Aulkemeyer, P Weber, F Wollinsky, KH Schuttler, R
Citation: K. Bechter et al., Borna disease virus-related therapy-resistant depression improved after cerebrospinal fluid filtration, J PSYCH RES, 34(6), 2000, pp. 393-396
Cellular uptake and efficacy of antisense oligonucleotides against RNAs oftwo Na+ channel isoforms
Authors: Keller, H Schu, B Rudel, R Brinkmeier, H
Citation: H. Keller et al., Cellular uptake and efficacy of antisense oligonucleotides against RNAs oftwo Na+ channel isoforms, J PHARM EXP, 295(1), 2000, pp. 367-372
A small sodium channel blacking factor in the cerebrospinal fluid is preferentially found in Guillain-Barre syndrome: a combined cell physiological and HPLC study
Authors: Weber, F Brinkmeier, H Aulkemeyer, P Wollinsky, KH Rudel, R
Citation: F. Weber et al., A small sodium channel blacking factor in the cerebrospinal fluid is preferentially found in Guillain-Barre syndrome: a combined cell physiological and HPLC study, J NEUROL, 246(10), 1999, pp. 955-960
A transient and a persistent calcium release are induced by chlorocresol in cultivated mouse myotubes
Authors: Gschwend, MH Rudel, R Brinkmeier, H Taylor, SR Fohr, KJ
Citation: Mh. Gschwend et al., A transient and a persistent calcium release are induced by chlorocresol in cultivated mouse myotubes, PFLUG ARCH, 438(1), 1999, pp. 101-106
Increased calcium entry into dystrophin-deficient muscle fibres of MDX andADR-MDX mice is reduced by ion channel blockers
Authors: Tutdibi, O Brinkmeier, H Rudel, R Fohr, KJ
Citation: O. Tutdibi et al., Increased calcium entry into dystrophin-deficient muscle fibres of MDX andADR-MDX mice is reduced by ion channel blockers, J PHYSL LON, 515(3), 1999, pp. 859-868
Malignant hyperthermia causing Gly2435Arg mutation of the ryanodine receptor facilitates ryanodine-induced calcium release in myotubes
Authors: Brinkmeier, H Kramer, J Kramer, R Iaizzo, PA Baur, C Lehmann-Horn, F Rudel, R
Citation: H. Brinkmeier et al., Malignant hyperthermia causing Gly2435Arg mutation of the ryanodine receptor facilitates ryanodine-induced calcium release in myotubes, BR J ANAEST, 83(6), 1999, pp. 855-861
Myotonic ADR-MDX mutant mice show less severe muscular dystrophy than MDX mice
Authors: Kramer, R Lochmuller, H Abicht, A Rudel, R Brinkmeier, H
Citation: R. Kramer et al., Myotonic ADR-MDX mutant mice show less severe muscular dystrophy than MDX mice, NEUROMUSC D, 8(8), 1998, pp. 542-550
Risultati: 1-12 |