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Results of search for 'au:"Müller-Felber, W"', page 3 of 4
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Authors
Abendroth, A
Abendroth, D
Abicht, A
Blaschek, A
Fischer, P
Illner, W D
Land, W
Landgraf, R
Lochmüller, H
Müller-Felber, W
Nusser, J
Pongratz, D
Pongratz, D E
Reilich, P
Reimers, C D
Schara, U
Schlotter, B
Toepfer, M
Wagner, S
Walter, M C
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41.
Tenascin is a useful marker in the diagnosis of inflammatory myopathies.
[electronic resource]
by
Müller-Felber, W
Toepfer, M
Müller, T
Müller-Höcker, J
Fischer, P
Lochmüller, H
Pongratz, D
Producer:
19980824
In:
European journal of medical research
vol. 3
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42.
Markedly different course of Friedreich's ataxia in sib pairs with similar GAA repeat expansions in the frataxin gene.
[electronic resource]
by
Klopstock, T
Chahrokh-Zadeh, S
Holinski-Feder, E
Meindl, A
Gasser, T
Pongratz, D
Müller-Felber, W
Producer:
19990518
In:
Acta neuropathologica
vol. 97
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43.
[50-year-old patient with rapid ataxia onset, generalized paresthesia and myoclonus].
[electronic resource]
by
Toepfer, M
Müller-Felber, W
Huber, R M
Held, E
Wekerle, G
Unger, J
Schlotter, B
Pongratz, D
Producer:
19970707
In:
Der Internist
vol. 38
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44.
Adult-onset glycogen storage disease type 2: clinico-pathological phenotype revisited.
[electronic resource]
by
Schoser, B G H
Müller-Höcker, J
Horvath, R
Gempel, K
Pongratz, D
Lochmüller, H
Müller-Felber, W
Producer:
20071113
In:
Neuropathology and applied neurobiology
vol. 33
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45.
High-dose immunoglobulin therapy in sporadic inclusion body myositis: a double-blind, placebo-controlled study.
[electronic resource]
by
Walter, M C
Lochmüller, H
Toepfer, M
Schlotter, B
Reilich, P
Schröder, M
Müller-Felber, W
Pongratz, D
Producer:
20000327
In:
Journal of neurology
vol. 247
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46.
Consequences of mutations within the C terminus of the FHL1 gene.
[electronic resource]
by
Schoser, B
Goebel, H H
Janisch, I
Quasthoff, S
Rother, J
Bergmann, M
Müller-Felber, W
Windpassinger, C
Producer:
20090918
In:
Neurology
vol. 73
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47.
Delayed colonic transit times in amyotrophic lateral sclerosis assessed with radio-opaque markers.
[electronic resource]
by
Toepfer, M
Schroeder, M
Klauser, A
Lochmüller, H
Hirschmann, M
Riepl, R L
Pongratz, D
Müller-Felber, W
Producer:
19980220
In:
European journal of medical research
vol. 2
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48.
Chronic myopathy in a patient suspected of carrying two malignant hyperthermia susceptibility (MHS) mutations.
[electronic resource]
by
Deufel, T
Müller-Felber, W
Pongratz, D E
Hübner, G
Johnson, K
Iaizzo, P A
Lehmann-Horn, F
Producer:
19930527
In:
Neuromuscular disorders : NMD
vol. 2
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49.
Changes of sonographic, magnetic resonance tomographic, electromyographic, and histopathologic findings within a 2-month period of examinations after experimental muscle denervation.
[electronic resource]
by
Küllmer, K
Sievers, K W
Reimers, C D
Rompe, J D
Müller-Felber, W
Nägele, M
Harland, U
Producer:
19980723
In:
Archives of orthopaedic and trauma surgery
vol. 117
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50.
Congenital myasthenic syndromes: clinical and genetic analysis of 18 patients.
[electronic resource]
by
Abicht, A
Müller-Felber, W
Fischer, P
Jakob, I
Kürz, L
Rudel, R
Mortier, W
Pongratz, D
Lochmüller, H
Producer:
19980310
In:
European journal of medical research
vol. 2
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51.
Fibre type specific expression of Leu19-antigen and N-CAM in skeletal muscle in various stages after experimental denervation.
[electronic resource]
by
Müller-Felber, W
Küllmer, K
Fischer, P
Reimers, C D
Wagner, S
Harland, U
Schmidt-Achert, M
Pongratz, D
Producer:
19930706
In:
Virchows Archiv. A, Pathological anatomy and histopathology
vol. 422
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52.
[Splints in birth-related brachial plexus injuries].
[electronic resource]
by
Schenck, T L
Bayer, T
Enders, A
Marton, M-A
Machens, H-G
Müller-Felber, W
Giunta, R E
Producer:
20110824
In:
Handchirurgie, Mikrochirurgie, plastische Chirurgie : Organ der Deutschsprachigen Arbeitsgemeinschaft fur Handchirurgie : Organ der Deutschsprachigen Arbeitsgemeinschaft fur Mikrochirurgie der Peripheren Nerven und Gefasse : Organ der V
vol. 43
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53.
Immunosuppressive treatment of rippling muscles in patients with myasthenia gravis.
[electronic resource]
by
Müller-Felber, W
Ansevin, C F
Ricker, K
Müller-Jenssen, A
Töpfer, M
Goebel, H H
Pongratz, D E
Producer:
20000214
In:
Neuromuscular disorders : NMD
vol. 9
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54.
Mitochondrial DNA depletion and fatal infantile hepatic failure due to mutations in the mitochondrial polymerase γ (POLG) gene: a combined morphological/enzyme histochemical and immunocytochemical/biochemical and molecular genetic study.
[electronic resource]
by
Müller-Höcker, J
Horvath, R
Schäfer, S
Hessel, H
Müller-Felber, W
Kühr, J
Copeland, W C
Seibel, P
Producer:
20120416
In:
Journal of cellular and molecular medicine
vol. 15
Online resources:
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55.
[Spinal muscular atrophy : Time for newborn screening?]
[electronic resource]
by
Vill, K
Blaschek, A
Schara, U
Kölbel, H
Hohenfellner, K
Harms, E
Olgemöller, B
Walter, Maggie C
Müller-Felber, W
Producer:
20190327
In:
Der Nervenarzt
vol. 88
Online resources:
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56.
Genetic identity of Marinesco-Sjögren/myoglobinuria and CCFDN syndromes.
[electronic resource]
by
Merlini, L
Gooding, R
Lochmüller, H
Müller-Felber, W
Walter, M C
Angelicheva, D
Talim, B
Hallmayer, J
Kalaydjieva, L
Producer:
20020402
In:
Neurology
vol. 58
Online resources:
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57.
Duct occlusion-induced vascularized islet grafts are not associated with progressive long-term dysfunction.
[electronic resource]
by
Illner, W D
Schneeberger, H
Hofmann, G
Piehlmeier, W
Mojto, J
Scheuer, R
Müller-Felber, W
Landgraf, R
Land, W
Producer:
19950405
In:
Transplantation proceedings
vol. 27
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58.
Creatine monohydrate in muscular dystrophies: A double-blind, placebo-controlled clinical study.
[electronic resource]
by
Walter, M C
Lochmüller, H
Reilich, P
Klopstock, T
Huber, R
Hartard, M
Hennig, M
Pongratz, D
Müller-Felber, W
Producer:
20000530
In:
Neurology
vol. 54
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59.
Early white matter changes in childhood multiple sclerosis: a diffusion tensor imaging study.
[electronic resource]
by
Blaschek, A
Keeser, D
Müller, S
Koerte, I K
Sebastian Schröder, A
Müller-Felber, W
Heinen, F
Ertl-Wagner, B
Producer:
20140527
In:
AJNR. American journal of neuroradiology
vol. 34
Online resources:
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60.
Prediction of response to IVIg treatment in patients with lower motor neurone disorders.
[electronic resource]
by
Strigl-Pill, N
König, A
Schröder, M
Beranek, H
Schoser, B G H
Spaeth, M
Pongratz, D
Müller-Felber, W
Producer:
20060509
In:
European journal of neurology
vol. 13
Online resources:
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