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What proportion of AQP4-IgG-negative NMO spectrum disorder patients are MOG-IgG positive? A cross sectional study of 132 patients
by
Mutch, Kerry
, Jacob, Anu
, Hamid, Shahd H. M.
, Das, Kumar
, Linaker, Samantha
, Whittam, Daniel
, Solomon, Tom
, Bhojak, Maneesh
in
Adolescent
/ Adult
/ Antibodies
/ Aquaporin 4
/ Aquaporin 4 - immunology
/ Aquaporins
/ Clinical trials
/ Cross-Sectional Studies
/ Demyelinating Diseases - blood
/ Demyelinating Diseases - immunology
/ Demyelination
/ Female
/ Glycoproteins
/ Humans
/ Immunoglobulin G
/ Immunoglobulin G - blood
/ Immunosuppressive Agents - therapeutic use
/ Magnetic resonance imaging
/ Male
/ Medicine
/ Medicine & Public Health
/ Middle Aged
/ Myelin
/ Myelin-Oligodendrocyte Glycoprotein - immunology
/ Neurology
/ Neuromyelitis
/ Neuromyelitis Optica - blood
/ Neuromyelitis Optica - drug therapy
/ Neuromyelitis Optica - epidemiology
/ Neuromyelitis Optica - immunology
/ Neuroradiology
/ Neurosciences
/ Oligodendrocyte-myelin glycoprotein
/ Original Communication
/ Patients
/ Young Adult
2017
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What proportion of AQP4-IgG-negative NMO spectrum disorder patients are MOG-IgG positive? A cross sectional study of 132 patients
by
Mutch, Kerry
, Jacob, Anu
, Hamid, Shahd H. M.
, Das, Kumar
, Linaker, Samantha
, Whittam, Daniel
, Solomon, Tom
, Bhojak, Maneesh
in
Adolescent
/ Adult
/ Antibodies
/ Aquaporin 4
/ Aquaporin 4 - immunology
/ Aquaporins
/ Clinical trials
/ Cross-Sectional Studies
/ Demyelinating Diseases - blood
/ Demyelinating Diseases - immunology
/ Demyelination
/ Female
/ Glycoproteins
/ Humans
/ Immunoglobulin G
/ Immunoglobulin G - blood
/ Immunosuppressive Agents - therapeutic use
/ Magnetic resonance imaging
/ Male
/ Medicine
/ Medicine & Public Health
/ Middle Aged
/ Myelin
/ Myelin-Oligodendrocyte Glycoprotein - immunology
/ Neurology
/ Neuromyelitis
/ Neuromyelitis Optica - blood
/ Neuromyelitis Optica - drug therapy
/ Neuromyelitis Optica - epidemiology
/ Neuromyelitis Optica - immunology
/ Neuroradiology
/ Neurosciences
/ Oligodendrocyte-myelin glycoprotein
/ Original Communication
/ Patients
/ Young Adult
2017
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What proportion of AQP4-IgG-negative NMO spectrum disorder patients are MOG-IgG positive? A cross sectional study of 132 patients
by
Mutch, Kerry
, Jacob, Anu
, Hamid, Shahd H. M.
, Das, Kumar
, Linaker, Samantha
, Whittam, Daniel
, Solomon, Tom
, Bhojak, Maneesh
in
Adolescent
/ Adult
/ Antibodies
/ Aquaporin 4
/ Aquaporin 4 - immunology
/ Aquaporins
/ Clinical trials
/ Cross-Sectional Studies
/ Demyelinating Diseases - blood
/ Demyelinating Diseases - immunology
/ Demyelination
/ Female
/ Glycoproteins
/ Humans
/ Immunoglobulin G
/ Immunoglobulin G - blood
/ Immunosuppressive Agents - therapeutic use
/ Magnetic resonance imaging
/ Male
/ Medicine
/ Medicine & Public Health
/ Middle Aged
/ Myelin
/ Myelin-Oligodendrocyte Glycoprotein - immunology
/ Neurology
/ Neuromyelitis
/ Neuromyelitis Optica - blood
/ Neuromyelitis Optica - drug therapy
/ Neuromyelitis Optica - epidemiology
/ Neuromyelitis Optica - immunology
/ Neuroradiology
/ Neurosciences
/ Oligodendrocyte-myelin glycoprotein
/ Original Communication
/ Patients
/ Young Adult
2017
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What proportion of AQP4-IgG-negative NMO spectrum disorder patients are MOG-IgG positive? A cross sectional study of 132 patients
Journal Article
What proportion of AQP4-IgG-negative NMO spectrum disorder patients are MOG-IgG positive? A cross sectional study of 132 patients
2017
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Overview
Antibodies to myelin oligodendrocyte glycoprotein (MOG-IgG) have been described in patients with neuromyelitis optica spectrum disorders (NMOSD) without aquaporin-4 antibodies (AQP4-IgG). We aimed to identify the proportion of AQP4-IgG-negative NMOSD patients who are seropositive for MOG-IgG. In a cross sectional study, we reviewed all patients seen in the National NMO clinic over the last 4 years (after the availability of MOG-IgG testing), including clinical information, MRI, and antibody tests. 261 unique patients were identified. 132 cases satisfied the 2015 NMOSD diagnostic criteria. Of these, 96 (73%) were AQP4-IgG positive and 36 (27%) were AQP4-IgG negative. These 36 patients were tested for MOG-IgG and 15/36 (42%) tested positive. 20% (25/125) of the patients who did not satisfy NMOSD criteria had MOG-IgG. Approximately half of seronegative NMOSD is MOG-Ig seropositive and one in five of non-NMOSD/non-MS demyelination is MOG-IgG positive. Since MOG-associated demyelinating disease is likely different from AQP4-IgG disease in terms of underlying disease mechanisms, relapse risk and possibly treatment, testing for MOG-IgG in patients with AQP4-IgG-negative NMOSD and other non-MS demyelination may have significant implications to management and clinical trials.
Publisher
Springer Berlin Heidelberg,Springer Nature B.V
Subject
/ Adult
/ Demyelinating Diseases - blood
/ Demyelinating Diseases - immunology
/ Female
/ Humans
/ Immunosuppressive Agents - therapeutic use
/ Male
/ Medicine
/ Myelin
/ Myelin-Oligodendrocyte Glycoprotein - immunology
/ Neuromyelitis Optica - blood
/ Neuromyelitis Optica - drug therapy
/ Neuromyelitis Optica - epidemiology
/ Neuromyelitis Optica - immunology
/ Oligodendrocyte-myelin glycoprotein
/ Patients
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