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Results: 1-25 | 26-34 |
Results: 26-34/34
New aspects of ALS research: measuring onset and progression 16-18 November 1998, Munich, Germany - Proceedings of a symposium held during the ninth international symposium on ALS/MND - Preface
Authors: Pongratz, D
Citation: D. Pongratz, New aspects of ALS research: measuring onset and progression 16-18 November 1998, Munich, Germany - Proceedings of a symposium held during the ninth international symposium on ALS/MND - Preface, J NEUROL, 246, 1999, pp. NIL_2-NIL_2
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
Open-label trial of riluzole 50 mg b.i.d. in treatment of amyotrophic lateral sclerosis (ALS)
Authors: Pongratz, D Neundorfer, B
Citation: D. Pongratz et B. Neundorfer, Open-label trial of riluzole 50 mg b.i.d. in treatment of amyotrophic lateral sclerosis (ALS), AKT NEUROL, 26(5), 1999, pp. 225-229
Localization of transforming growth factor beta in association with neuromuscular junctions in adult human muscle
Authors: Toepfer, M Fischer, P Abicht, A Lochmuller, H Pongratz, D Muller-Felber, W
Citation: M. Toepfer et al., Localization of transforming growth factor beta in association with neuromuscular junctions in adult human muscle, CELL MOL N, 19(2), 1999, pp. 297-300
A common mutation (epsilon 1267delG) in congenital myasthenic patients of Gypsy ethnic origin
Authors: Abicht, A Stucka, R Karcagi, V Herczegfalvi, A Horvath, R Mortier, W Schara, U Ramaekers, V Jost, W Brunner, J Janssen, G Seidel, U Schlotter, B Muller-Felber, W Pongratz, D Rudel, R Lochmuller, H
Citation: A. Abicht et al., A common mutation (epsilon 1267delG) in congenital myasthenic patients of Gypsy ethnic origin, NEUROLOGY, 53(7), 1999, pp. 1564-1569
The diagnostic process in ALS
Authors: Pongratz, D
Citation: D. Pongratz, The diagnostic process in ALS, J NEUR SCI, 165, 1999, pp. S10-S13
Noninvasive C-13-octanoic acid breath test shows delayed gastric emptying in patients with amyotrophic lateral sclerosis
Authors: Toepfer, M Folwaczny, C Lochmuller, H Schroeder, M Riepl, RL Pongratz, D Muller-Felber, W
Citation: M. Toepfer et al., Noninvasive C-13-octanoic acid breath test shows delayed gastric emptying in patients with amyotrophic lateral sclerosis, DIGESTION, 60(6), 1999, pp. 567-571
Markedly different course of Friedreich's ataxia in sib pairs with similarGAA repeat expansions in the frataxin gene
Authors: Klopstock, T Chahrokh-Zadeh, S Holinski-Feder, E Meindl, A Gasser, T Pongratz, D Muller-Felber, W
Citation: T. Klopstock et al., Markedly different course of Friedreich's ataxia in sib pairs with similarGAA repeat expansions in the frataxin gene, ACT NEUROP, 97(2), 1999, pp. 139-142
Fibromyalgia syndrome and attention deficit hyperactivity disorder: Is there a comorbidity and are there consequences for the therapy of fibromyalgiasyndrome?
Authors: Krause, KH Krause, J Magyarosy, I Ernst, E Pongratz, D
Citation: Kh. Krause et al., Fibromyalgia syndrome and attention deficit hyperactivity disorder: Is there a comorbidity and are there consequences for the therapy of fibromyalgiasyndrome?, J MUSCULO P, 6(4), 1998, pp. 111-116
Risultati: 1-25 | 26-34 |