Koon Ho Chan (61 results)

Paperback. Condition: Brand New. 116 pages. 8.66x5.91x0.27 inches. In Stock.

Taschenbuch. Condition: Neu. Diagnosis and Treatments of Neuromyelitis Optica Spectrum Disorders | Autoimmune central nervous system inflammatory demyelinating disorders more common in Asians seropositive for AQP4-IgG | Koon Ho Chan | Taschenbuch | 116 S. | Englisch | 2017 | LAP LAMBERT Academic Publishing | EAN 9783330005945 | Verantwortliche Person für die EU: preigu GmbH & Co. KG, Lengericher Landstr. 19, 49078 Osnabrück, mail[at]preigu[dot]de | Anbieter: preigu.…

Taschenbuch. Condition: 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.…

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Taschenbuch. Condition: Neu. Diagnostic et traitements des troubles du spectre de la neuromyélite optique | Troubles inflammatoires démyélinisants auto-immuns du système nerveux central plus fréquents chez les Asiatiques séropositifs pour l'AQP4-IgG | Koon Ho Chan | Taschenbuch | Französisch | 2025 | Editions Notre Savoir | EAN 9786202456517 | Verantwortliche Person für die EU: SIA OmniScriptum Publishing, Brivibas Gatve 197, 1039 RIGA, LETTLAND, customerservice[at]vdm-vsg[dot]de | Anbieter: preigu.…

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Taschenbuch. Condition: Neu. Diagnosi e trattamenti dei disturbi dello spettro della neuromielite ottica | Disturbi infiammatori demielinizzanti del sistema nervoso centrale autoimmuni più comuni negli asiatici sieropositivi per AQP4-IgG | Koon Ho Chan | Taschenbuch | Italienisch | 2025 | Edizioni Sapienza | EAN 9786202456524 | Verantwortliche Person für die EU: SIA OmniScriptum Publishing, Brivibas Gatve 197, 1039 RIGA, LETTLAND, customerservice[at]vdm-vsg[dot]de | Anbieter: preigu.…

Taschenbuch. Condition: Neu. Diagnose und Behandlung von Neuromyelitis-optica-Spektrum-Erkrankungen | Autoimmunbedingte entzündliche Demyelinisierungserkrankungen des Zentralnervensystems, die häufiger bei Asiaten mit AQP4-IgG-Seropositivität auftreten | Koon Ho Chan | Taschenbuch | 92 S. | Deutsch | 2025 | Verlag Unser Wissen | EAN 9786202456494 | Verantwortliche Person für die EU: SIA OmniScriptum Publishing, Brivibas Gatve 197, 1039 RIGA, LETTLAND, customerservice[at]vdm-vsg[dot]de | Anbieter: preigu.…

Taschenbuch. Condition: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Neuromyelitis optica (NMO) is a treatable central nervous system inflammatory demyelinating disorders characterized by acute myelitis and optic neuritis, especially clinically severe longitudinally extensive transverse myelitis (LETM) and simultaneous bilateral ON. NMO is likely autoimmune in nature as a significant proportion of patients are seropositive for aquaporin-4 (AQP4) IgG autoantibodies. I studied the clinical features of Chinese NMOSD patients and their AQP4-IgG seropositivity rates of by tissued-based immunofluorescence. I also studied a cell-based immunofluorescence assay using transfected human embryonic kidney cells overexpressing human AQP4 on cell membrane and found that cell-based assay has higher sensitivity than tissue-based assay in detection of AQP4 autoantibodies in NMO (78% versus 61%). I further studied the clinical and neuroradiological characteristics of Chinese NMOSD patients with brain involvement. I found that 59% of NMOSD patients have clinical and/or radiological evidence of brain involvement. Importantly, brainstem is the most frequently affected brain region and 24% of NMOSD patients had clinical manifestation of brainstem encephalitis. 116 pp. Englisch.…

Taschenbuch. Condition: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware 92 pp. Spanisch.

Taschenbuch. Condition: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Neuromyelitis optica (NMO) is a treatable central nervous system inflammatory demyelinating disorders characterized by acute myelitis and optic neuritis, especially clinically severe longitudinally extensive transverse myelitis (LETM) and simultaneous bilateral ON. NMO is likely autoimmune in nature as a significant proportion of patients are seropositive for aquaporin-4 (AQP4) IgG autoantibodies. I studied the clinical features of Chinese NMOSD patients and their AQP4-IgG seropositivity rates of by tissued-based immunofluorescence. I also studied a cell-based immunofluorescence assay using transfected human embryonic kidney cells overexpressing human AQP4 on cell membrane and found that cell-based assay has higher sensitivity than tissue-based assay in detection of AQP4 autoantibodies in NMO (78% versus 61%). I further studied the clinical and neuroradiological characteristics of Chinese NMOSD patients with brain involvement. I found that 59% of NMOSD patients have clinical and/or radiological evidence of brain involvement. Importantly, brainstem is the most frequently affected brain region and 24% of NMOSD patients had clinical manifestation of brainstem encephalitis.…

Condition: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: CHAN Koon HoDr. Koon-Ho CHAN graduated from the University of Hong Kong. He studied neuronal autoantibodies in paraneoplastic neurological disorders under the mentorship of Professor Vanda Lennon during elective study in Mayo Clinic..…

Taschenbuch. Condition: 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.…

Taschenbuch. Condition: Neu. This item is printed on demand - Print on Demand Titel. Neuware -Neuromyelitis optica (NMO) is a treatable central nervous system inflammatory demyelinating disorders characterized by acute myelitis and optic neuritis, especially clinically severe longitudinally extensive transverse myelitis (LETM) and simultaneous bilateral ON. NMO is likely autoimmune in nature as a significant proportion of patients are seropositive for aquaporin-4 (AQP4) IgG autoantibodies. I studied the clinical features of Chinese NMOSD patients and their AQP4-IgG seropositivity rates of by tissued-based immunofluorescence. I also studied a cell-based immunofluorescence assay using transfected human embryonic kidney cells overexpressing human AQP4 on cell membrane and found that cell-based assay has higher sensitivity than tissue-based assay in detection of AQP4 autoantibodies in NMO (78% versus 61%). I further studied the clinical and neuroradiological characteristics of Chinese NMOSD patients with brain involvement. I found that 59% of NMOSD patients have clinical and/or radiological evidence of brain involvement. Importantly, brainstem is the most frequently affected brain region and 24% of NMOSD patients had clinical manifestation of brainstem encephalitis.VDM Verlag, Dudweiler Landstraße 99, 66123 Saarbrücken 116 pp. Englisch.…

Condition: 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.…

Taschenbuch. Condition: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware 96 pp. Französisch.

PAP. Condition: New. New Book. Shipped from UK. THIS BOOK IS PRINTED ON DEMAND. Established seller since 2000.

PAP. Condition: New. New Book. Shipped from UK. THIS BOOK IS PRINTED ON DEMAND. Established seller since 2000.

PAP. Condition: New. New Book. Shipped from UK. THIS BOOK IS PRINTED ON DEMAND. Established seller since 2000.

PAP. Condition: New. New Book. Shipped from UK. THIS BOOK IS PRINTED ON DEMAND. Established seller since 2000.

Taschenbuch. Condition: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - La neuromielitis óptica (NMO) es un trastorno inflamatorio desmielinizante del sistema nervioso central tratable que se caracteriza por mielitis aguda y neuritis óptica, especialmente mielitis transversa longitudinal extensa (LETM) clínicamente grave y ON bilateral simultánea. La NMO es probablemente de naturaleza autoinmune, ya que una proporción significativa de pacientes son seropositivos para autoanticuerpos IgG contra la acuaporina-4 (AQP4). Estudié las características clínicas de pacientes chinos con NMOSD y sus tasas de seropositividad para AQP4-IgG mediante inmunofluorescencia tisular. También estudié un ensayo de inmunofluorescencia celular utilizando células renales embrionarias humanas transfectadas que sobreexpresan AQP4 humana en la membrana celular y descubrí que el ensayo celular tiene una mayor sensibilidad que el ensayo tisular en la detección de autoanticuerpos AQP4 en la NMO (78 % frente a 61 %). Además, estudié las características clínicas y neurorradiológicas de pacientes chinos con NMOSD con afectación cerebral. Descubrí que el 59 % de los pacientes con NMOSD presentan evidencia clínica y/o radiológica de afectación cerebral. Es importante destacar que el tronco encefálico es la región cerebral más frecuentemente afectada y que el 24 % de los pacientes con NMOSD presentaban manifestaciones clínicas de encefalitis del tronco encefálico.…

Taschenbuch. Condition: 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%.…

PAP. Condition: New. New Book. Delivered from our UK warehouse in 4 to 14 business days. THIS BOOK IS PRINTED ON DEMAND. Established seller since 2000.