Paraneoplastic neurological disorders (PND) are due to immune-mediated damage of the nervous system, and the immune response is believed to be triggered as anti-tumor immunity. Early recognition of PND facilitates prompt detection of underlying tumors. Detection of paraneoplastic neuronal autoantibodies facilitates early diagnosis of PND. A novel paraneoplastic neuronal antibody, anti-neuronal nuclear antibody type 3 (ANNA-3) was identified in eleven patients, the majority had SCLC and diverse neurological manifestations. Autoimmune myasthenia gravis (MG) is due to impaired neuromuscular transmission predominantly due to pathogenic acetylcholine receptor (AChR) autoantibodies. Muscle-specific tyrosine kinase (MuSK) autoantibodies are detected in some AChR autoantibodies-negative generalized MG patients. Among 562 Mayo Clinic patients with adult- onset generalized MG based on clinical and electrophysiological criteria, AChR autoantibodies seronegativity rate was 8.2% and MuSK autoantibodies was detected in 38% of AChR autoantibodies-negative patients. The seronegativity rate in adult-onset generalized MG is ~5%.
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Paraneoplastic neurological disorders (PND) are due to immune-mediated damage of the nervous system, and the immune response is believed to be triggered as anti-tumor immunity. Early recognition of PND facilitates prompt detection of underlying tumors. Detection of paraneoplastic neuronal autoantibodies facilitates early diagnosis of PND. A novel paraneoplastic neuronal antibody, anti-neuronal nuclear antibody type 3 (ANNA-3) was identified in eleven patients, the majority had SCLC and diverse neurological manifestations. Autoimmune myasthenia gravis (MG) is due to impaired neuromuscular transmission predominantly due to pathogenic acetylcholine receptor (AChR) autoantibodies. Muscle-specific tyrosine kinase (MuSK) autoantibodies are detected in some AChR autoantibodies-negative generalized MG patients. Among 562 Mayo Clinic patients with adult- onset generalized MG based on clinical and electrophysiological criteria, AChR autoantibodies seronegativity rate was 8.2% and MuSK autoantibodies was detected in 38% of AChR autoantibodies-negative patients. The seronegativity rate in adult-onset generalized MG is ~5%.
The author graduated from the Faculty of Medicine, the University of Hong Kong, and started neurology training in the Department of Medicine, University of Hong Kong. He spent one year in 2000-2001 on neuroimmunology research in Mayo CLinic Rochester under the supervision of Professor Vanda A Lennon, a great teacher, scientist and friend.
Les informations fournies dans la section « A propos du livre » peuvent faire référence à une autre édition de ce titre.
Vendeur : BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, Allemagne
Taschenbuch. Etat : Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Paraneoplastic neurological disorders (PND) are due to immune-mediated damage of the nervous system, and the immune response is believed to be triggered as anti-tumor immunity. Early recognition of PND facilitates prompt detection of underlying tumors. Detection of paraneoplastic neuronal autoantibodies facilitates early diagnosis of PND. A novel paraneoplastic neuronal antibody, anti-neuronal nuclear antibody type 3 (ANNA-3) was identified in eleven patients, the majority had SCLC and diverse neurological manifestations. Autoimmune myasthenia gravis (MG) is due to impaired neuromuscular transmission predominantly due to pathogenic acetylcholine receptor (AChR) autoantibodies. Muscle-specific tyrosine kinase (MuSK) autoantibodies are detected in some AChR autoantibodies-negative generalized MG patients. Among 562 Mayo Clinic patients with adult- onset generalized MG based on clinical and electrophysiological criteria, AChR autoantibodies seronegativity rate was 8.2% and MuSK autoantibodies was detected in 38% of AChR autoantibodies-negative patients. The seronegativity rate in adult-onset generalized MG is ~5%. 256 pp. Englisch. N° de réf. du vendeur 9783838382203
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Etat : New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: CHAN Koon HoThe author graduated from the Faculty of Medicine, the University of Hong Kong, and started neurology training in the Department of Medicine, University of Hong Kong. He spent one year in 2000-2001 on neuroimmunology r. N° de réf. du vendeur 5418484
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Vendeur : preigu, Osnabrück, Allemagne
Taschenbuch. Etat : Neu. Autoantibodies in Neurological Disorders | Neuronal and Muscle Autoantibodies in Paraneoplastic Neurological Disorders and Autoimmune Myasthenia Gravis | Koon Ho Chan | Taschenbuch | 256 S. | Englisch | 2010 | LAP LAMBERT Academic Publishing | EAN 9783838382203 | Verantwortliche Person für die EU: preigu GmbH & Co. KG, Lengericher Landstr. 19, 49078 Osnabrück, mail[at]preigu[dot]de | Anbieter: preigu. N° de réf. du vendeur 107438957
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Taschenbuch. Etat : Neu. This item is printed on demand - Print on Demand Titel. Neuware -Paraneoplastic neurological disorders (PND) are due to immune-mediated damage of the nervous system, and the immune response is believed to be triggered as anti-tumor immunity. Early recognition of PND facilitates prompt detection of underlying tumors. Detection of paraneoplastic neuronal autoantibodies facilitates early diagnosis of PND. A novel paraneoplastic neuronal antibody, anti-neuronal nuclear antibody type 3 (ANNA-3) was identified in eleven patients, the majority had SCLC and diverse neurological manifestations. Autoimmune myasthenia gravis (MG) is due to impaired neuromuscular transmission predominantly due to pathogenic acetylcholine receptor (AChR) autoantibodies. Muscle-specific tyrosine kinase (MuSK) autoantibodies are detected in some AChR autoantibodies-negative generalized MG patients. Among 562 Mayo Clinic patients with adult- onset generalized MG based on clinical and electrophysiological criteria, AChR autoantibodies seronegativity rate was 8.2% and MuSK autoantibodies was detected in 38% of AChR autoantibodies-negative patients. The seronegativity rate in adult-onset generalized MG is ~5%.VDM Verlag, Dudweiler Landstraße 99, 66123 Saarbrücken 256 pp. Englisch. N° de réf. du vendeur 9783838382203
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Taschenbuch. Etat : Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Paraneoplastic neurological disorders (PND) are due to immune-mediated damage of the nervous system, and the immune response is believed to be triggered as anti-tumor immunity. Early recognition of PND facilitates prompt detection of underlying tumors. Detection of paraneoplastic neuronal autoantibodies facilitates early diagnosis of PND. A novel paraneoplastic neuronal antibody, anti-neuronal nuclear antibody type 3 (ANNA-3) was identified in eleven patients, the majority had SCLC and diverse neurological manifestations. Autoimmune myasthenia gravis (MG) is due to impaired neuromuscular transmission predominantly due to pathogenic acetylcholine receptor (AChR) autoantibodies. Muscle-specific tyrosine kinase (MuSK) autoantibodies are detected in some AChR autoantibodies-negative generalized MG patients. Among 562 Mayo Clinic patients with adult- onset generalized MG based on clinical and electrophysiological criteria, AChR autoantibodies seronegativity rate was 8.2% and MuSK autoantibodies was detected in 38% of AChR autoantibodies-negative patients. The seronegativity rate in adult-onset generalized MG is ~5%. N° de réf. du vendeur 9783838382203
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