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Results: 1-25 | 26-32
Results: 1-25/32
Novel approaches to treat muscular dystrophies
Authors: Walter, MC Lochmuller, H
Citation: Mc. Walter et H. Lochmuller, Novel approaches to treat muscular dystrophies, EXPERT OP I, 10(4), 2001, pp. 695-707
When running a stop sign may be a good thing
Authors: Karpati, G Lochmuller, H
Citation: G. Karpati et H. Lochmuller, When running a stop sign may be a good thing, ANN NEUROL, 49(6), 2001, pp. 693-694
Deactivation and desensitization of mouse embryonic- and adult-type nicotinic receptor channel currents
Authors: Jahn, K Mohammadi, B Krampfl, K Abicht, A Lochmuller, H Bufler, J
Citation: K. Jahn et al., Deactivation and desensitization of mouse embryonic- and adult-type nicotinic receptor channel currents, NEUROSCI L, 307(2), 2001, pp. 89-92
The spread of transgene expression at the site of gene construct injection
Authors: O'Hara, AJ Howell, JM Taplin, RH Fletcher, S Lloyd, F Kakulas, B Lochmuller, H Karpati, G
Citation: Aj. O'Hara et al., The spread of transgene expression at the site of gene construct injection, MUSCLE NERV, 24(4), 2001, pp. 488-495
Homozygosity (E140K) in SCO2 causes delayed infantile onset of cardiomyopathy and neuropathy
Authors: Jaksch, M Horvath, R Horn, N Auer, DP Macmillan, C Peters, J Gerbitz, KD Kraegeloh-Mann, I Muntau, A Karcagi, V Kalmanchey, R Lochmuller, H Shoubridge, EA Freisinger, P
Citation: M. Jaksch et al., Homozygosity (E140K) in SCO2 causes delayed infantile onset of cardiomyopathy and neuropathy, NEUROLOGY, 57(8), 2001, pp. 1440-1446
Prion codon 129 homozygosity and sporadic inclusion body myositis
Authors: Lampe, J Gossrau, G Reichmann, H Koch, R Walter, MC Mendel, B Lochmuller, H
Citation: J. Lampe et al., Prion codon 129 homozygosity and sporadic inclusion body myositis, NEUROLOGY, 57(2), 2001, pp. 368-368
Prion codon 129 homozygosity and sporadic inclusion body myositis
Authors: Lampe, J Gossrau, G Reichmann, H Walter, MC Mendel, B Lochmuller, H
Citation: J. Lampe et al., Prion codon 129 homozygosity and sporadic inclusion body myositis, NEUROLOGY, 57(2), 2001, pp. 368-368
A mutation in mt tRNALeu ((UUR)) causing a neuropsychiatric syndrome with depression and cataract
Authors: Jaksch, M Lochmuller, H Schmitt, F Volpel, B Obermaier-Kusser, B Horvath, R
Citation: M. Jaksch et al., A mutation in mt tRNALeu ((UUR)) causing a neuropsychiatric syndrome with depression and cataract, NEUROLOGY, 57(10), 2001, pp. 1930-1931
New insights in pathogenesis and therapy of sporadic inclusion body myositis (s-IBM)
Authors: Walter, MC Lochmuller, H Schlotter, B Reilich, P Muller-Felber, W Pongratz, D
Citation: Mc. Walter et al., New insights in pathogenesis and therapy of sporadic inclusion body myositis (s-IBM), NERVENARZT, 72(2), 2001, pp. 117-121
An agrin minigene rescues dystrophic symptoms in a mouse model for congenital muscular dystrophy
Authors: Moll, J Barzaghi, P Lin, S Bezakova, G Lochmuller, H Engvall, E Muller, U Ruegg, MA
Citation: J. Moll et al., An agrin minigene rescues dystrophic symptoms in a mouse model for congenital muscular dystrophy, NATURE, 413(6853), 2001, pp. 302-307
Muscle-specific overexpression of the adenovirus primary receptor CAR overcomes low efficiency of gene transfer to mature skeletal muscle
Authors: Nalbantoglu, J Larochelle, N Wolf, E Karpati, G Lochmuller, H Holland, PC
Citation: J. Nalbantoglu et al., Muscle-specific overexpression of the adenovirus primary receptor CAR overcomes low efficiency of gene transfer to mature skeletal muscle, J VIROLOGY, 75(9), 2001, pp. 4276-4282
Frequency of mitochondrial transfer RNA mutations and deletions in 225 patients presenting with respiratory chain deficiencies
Authors: Jaksch, M Kleinle, S Scharfe, C Klopstock, T Pongratz, D Muller-Hocker, J Gerbitz, KD Liechti-Gallati, S Lochmuller, H Horvath, R
Citation: M. Jaksch et al., Frequency of mitochondrial transfer RNA mutations and deletions in 225 patients presenting with respiratory chain deficiencies, J MED GENET, 38(10), 2001, pp. 665-673
Characterization of human muscle type cofilin (CFL2) in normal and regenerating muscle
Authors: Thirion, C Stucka, R Mendel, B Gruhler, A Jaksch, M Nowak, KJ Binz, N Laing, NG Lochmuller, H
Citation: C. Thirion et al., Characterization of human muscle type cofilin (CFL2) in normal and regenerating muscle, EUR J BIOCH, 268(12), 2001, pp. 3473-3482
Decreased aminoacylation of mutant tRNAs in MELAS but not in MERRF patients
Authors: Borner, GV Zeviani, M Tiranti, V Carrara, F Hoffmann, S Gerbitz, KD Lochmuller, H Pongratz, D Klopstock, T Melberg, A Holme, E Paabo, S
Citation: Gv. Borner et al., Decreased aminoacylation of mutant tRNAs in MELAS but not in MERRF patients, HUM MOL GEN, 9(4), 2000, pp. 467-475
A modified alignment of human and rodent 5 ' untranslated sequences of theacetylcholine receptor epsilon subunit gene reveals additional regions of high homology
Authors: Stucka, R Abicht, A Song, IH Bonsch, D Deufel, T Lochmuller, H
Citation: R. Stucka et al., A modified alignment of human and rodent 5 ' untranslated sequences of theacetylcholine receptor epsilon subunit gene reveals additional regions of high homology, NEUROMUSC D, 10(3), 2000, pp. 213-214
High-dose immunoglobulin therapy in sporadic inclusion body myositis: a double-blind, placebo-controlled study
Authors: Walter, MC Lochmuller, H Toepfer, M Schlotter, B Reilich, P Schroder, M Muller-Felber, W Pongratz, D
Citation: Mc. Walter et al., High-dose immunoglobulin therapy in sporadic inclusion body myositis: a double-blind, placebo-controlled study, J NEUROL, 247(1), 2000, pp. 22-28
Leber's hereditary optic neuropathy presenting as multiple sclerosis-like disease of the CNS
Authors: Horvath, R Abicht, A Shoubridge, EA Karcagi, V Rozsa, C Komoly, S Lochmuller, H
Citation: R. Horvath et al., Leber's hereditary optic neuropathy presenting as multiple sclerosis-like disease of the CNS, J NEUROL, 247(1), 2000, pp. 65-67
Successful management of polyneuropathy associated with IgM gammopathy of undetermined significance with antibody-based immunoadsorption
Authors: Toepfer, M Schroeder, M Muller-Felber, W Lochmuller, H Sitter, T Pongratz, D Schiffl, H
Citation: M. Toepfer et al., Successful management of polyneuropathy associated with IgM gammopathy of undetermined significance with antibody-based immunoadsorption, CLIN NEPHR, 53(5), 2000, pp. 404-407
Nemaline cardiomyopathy in a young adult: An ultraimmunohistochemical study and review of the literature
Authors: Muller-Hocker, J Schafer, S Mendel, B Lochmuller, H Pongratz, D
Citation: J. Muller-hocker et al., Nemaline cardiomyopathy in a young adult: An ultraimmunohistochemical study and review of the literature, ULTRA PATH, 24(6), 2000, pp. 407-416
Creatine monohydrate in muscular dystrophies: A double-blind, placebo-controlled clinical study
Authors: Walter, MC Lochmuller, H Reilich, P Klopstock, T Huber, R Hartard, M Hennig, M Pongratz, D Muller-Felber, W
Citation: Mc. Walter et al., Creatine monohydrate in muscular dystrophies: A double-blind, placebo-controlled clinical study, NEUROLOGY, 54(9), 2000, pp. 1848-1850
Characterization of human SCO1 and COX17 genes in mitochondrial cytochrome-c-oxidase deficiency
Authors: Horvath, R Lochmuller, H Stucka, R Yao, JB Shoubridge, EA Kim, SH Gerbitz, KD Jaksch, M
Citation: R. Horvath et al., Characterization of human SCO1 and COX17 genes in mitochondrial cytochrome-c-oxidase deficiency, BIOC BIOP R, 276(2), 2000, pp. 530-533
Intracerebral adenovirus-mediated p53 tumor suppressor gene therapy for experimental human glioma
Authors: Li, HW Alonso-Vanegas, M Colicos, MA Jung, SS Lochmuller, H Sadikot, AF Snipes, GJ Seth, P Karpati, G Nalbantoglu, J
Citation: Hw. Li et al., Intracerebral adenovirus-mediated p53 tumor suppressor gene therapy for experimental human glioma, CLIN CANC R, 5(3), 1999, pp. 637-642
Myopathy with trabecular muscle fibers
Authors: Weller, B Carpenter, S Lochmuller, H Karpati, G
Citation: B. Weller et al., Myopathy with trabecular muscle fibers, NEUROMUSC D, 9(4), 1999, pp. 208-214
Prospects of gene therapy for muscular dystrophy
Authors: Lochmuller, H
Citation: H. Lochmuller, Prospects of gene therapy for muscular dystrophy, NERVENHEILK, 18(1), 1999, pp. 14-16
Neuromyotonia, myocloni, sensory neuropathy and cerebellar symptoms in a patient with antibodies to neuronal nucleoproteins (anti-Hu-antibodies)
Authors: Toepfer, M Schroeder, M Unger, JW Lochmuller, H Pongratz, D Muller-Felber, W
Citation: M. Toepfer et al., Neuromyotonia, myocloni, sensory neuropathy and cerebellar symptoms in a patient with antibodies to neuronal nucleoproteins (anti-Hu-antibodies), CLIN NEUROL, 101(3), 1999, pp. 207-209
Risultati: 1-25 | 26-32