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Intravenous immunoglobulin and intravenous methylprednisolone as optimal induction treatment in chronic inflammatory demyelinating polyradiculoneuropathy: protocol of an international, randomised, double-blind, placebo-controlled trial (OPTIC)

Trials, 2021-02, Vol.22 (1), p.155-155, Article 155

2021

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Causality in acute encephalitis: defining aetiologies

Epidemiology and infection, 2010-06, Vol.138 (6), p.783-800

2010

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Frequency of mutations in the genes associated with hereditary sensory and autonomic neuropathy in a UK cohort

Journal of neurology, 2012-08, Vol.259 (8), p.1673-1685

2012

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Localization of major gangliosides in the PNS: implications for immune neuropathies

Brain (London, England : 1878), 2002-11, Vol.125 (11), p.2491-2506

2002

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Chronic inflammatory demyelinating polyradiculoneuropathy: a prevalence study in south east England

Journal of neurology, neurosurgery and psychiatry, 1999-05, Vol.66 (5), p.677-680

1999

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Laboratory biomarkers associated with COVID-19 severity and management

Clinical immunology (Orlando, Fla.), 2020-12, Vol.221, p.108614-108614, Article 108614

2020

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Diagnosis and treatment in inflammatory neuropathies

Journal of neurology, neurosurgery and psychiatry, 2009-08, Vol.85 (1006), p.437-258

2009

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Immunotherapy for IgM anti-myelin-associated glycoprotein paraprotein-associated peripheral neuropathies

Cochrane database of systematic reviews, 2006-04 (2), p.CD002827

2006

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Primary sciatic nerve lymphoma: a case report and review of the literature

Journal of neurology, neurosurgery and psychiatry, 2006-09, Vol.77 (9), p.1087-1089

2006

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GJB1 gene mutations in suspected inflammatory demyelinating neuropathies not responding to treatment

Journal of neurology, neurosurgery and psychiatry, 2009-06, Vol.80 (6), p.699-700

2009

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Plasma cell depletion with bortezomib in the treatment of refractory N‐methyl‐d‐aspartate (NMDA) receptor antibody encephalitis. Rational developments in neuroimmunological treatment

European journal of neurology, 2018-11, Vol.25 (11), p.1384-1388

2018

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209 ‘How rare do we dare’ – hickam’s dictum taken to the extreme

Journal of neurology, neurosurgery and psychiatry, 2019-12, Vol.90 (12), p.e52.4-e53

2019

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Routine blood monitoring in maintenance immunoglobulin treatment of inflammatory neuropathy: Is it clinically relevant?

Journal of the neurological sciences, 2020-01, Vol.408, p.116527-116527, Article 116527

2020

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Therapeutic immunoglobulin should be dosed by clinical outcome rather than by body weight in obese patients

Clinical and experimental immunology, 2015-07, Vol.181 (1), p.179-187

2015

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099 High relapse rate with steroid monotherapy in non-systemic vasculitic neuropathy

Journal of neurology, neurosurgery and psychiatry, 2022-06, Vol.93 (6), p.A42-A42

2022

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Successful treatment of IgM paraproteinaemic neuropathy with fludarabine

Journal of neurology, neurosurgery and psychiatry, 1999-05, Vol.66 (5), p.575-580

1999

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CIDP: mimics and chameleons

Practical Neurology, 2014-12, Vol.14 (6), p.399-408

2014

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Variable phenotypes are associated with PMP22 missense mutations

Neuromuscular disorders : NMD, 2011-02, Vol.21 (2), p.106-114

2011

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Higher frequencies of HLA DQB105:01 and anti-glycosphingolipid antibodies in a cluster of severe Guillain–Barré syndrome

Journal of neurology, 2016-10, Vol.263 (10), p.2105-2113

2016

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Clinical, neuropathological and radiological evidence for a rare complication of rituximab therapy

Neuromuscular disorders : NMD, 2015-07, Vol.25 (7), p.589-592

2015

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P1112: TREATING BING‐NEEL SYNDROME USING A TAILORED APPROACH: EXPERIENCE OF A SPECIALIST NEUROHAEMATOLOGY CLINIC

HemaSphere, 2022-06, Vol.6 (Suppl), p.1002-1003

2022

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Regarding the past, what is the trial you have always been dreaming of in CIDP?

Revue neurologique, 2016-10, Vol.172 (10), p.620-626

2016

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Cochrane 20 years on: The Cochrane Neuromuscular Disease Group

Neuromuscular disorders : NMD, 2013-11, Vol.23 (11), p.871-873

2013

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Rituximab in the treatment of three coexistent neurological autoimmune diseases: chronic inflammatory demyelinating polyradiculoneuropathy, Morvan syndrome and myasthenia gravis

Journal of neurology, neurosurgery and psychiatry, 2011-02, Vol.82 (2), p.230-232

2011

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Hand weakness in Charcot-Marie-Tooth disease 1X

Neuromuscular disorders : NMD, 2012-07, Vol.22 (7), p.622-626

2012

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Intravenous immunoglobulin and intravenous methylprednisolone as optimal induction treatment in chronic inflammatory demyelinating polyradiculoneuropathy: protocol of an international, randomised, double-blind, placebo-controlled trial (OPTIC)

Causality in acute encephalitis: defining aetiologies

Frequency of mutations in the genes associated with hereditary sensory and autonomic neuropathy in a UK cohort

Localization of major gangliosides in the PNS: implications for immune neuropathies

Chronic inflammatory demyelinating polyradiculoneuropathy: a prevalence study in south east England

Laboratory biomarkers associated with COVID-19 severity and management

Diagnosis and treatment in inflammatory neuropathies

Immunotherapy for IgM anti-myelin-associated glycoprotein paraprotein-associated peripheral neuropathies

Primary sciatic nerve lymphoma: a case report and review of the literature

GJB1 gene mutations in suspected inflammatory demyelinating neuropathies not responding to treatment

Plasma cell depletion with bortezomib in the treatment of refractory N‐methyl‐d‐aspartate (NMDA) receptor antibody encephalitis. Rational developments in neuroimmunological treatment

209 ‘How rare do we dare’ – hickam’s dictum taken to the extreme

Routine blood monitoring in maintenance immunoglobulin treatment of inflammatory neuropathy: Is it clinically relevant?

Therapeutic immunoglobulin should be dosed by clinical outcome rather than by body weight in obese patients

099 High relapse rate with steroid monotherapy in non-systemic vasculitic neuropathy

Successful treatment of IgM paraproteinaemic neuropathy with fludarabine

CIDP: mimics and chameleons

Variable phenotypes are associated with PMP22 missense mutations

Higher frequencies of HLA DQB105:01 and anti-glycosphingolipid antibodies in a cluster of severe Guillain–Barré syndrome

Clinical, neuropathological and radiological evidence for a rare complication of rituximab therapy

P1112: TREATING BING‐NEEL SYNDROME USING A TAILORED APPROACH: EXPERIENCE OF A SPECIALIST NEUROHAEMATOLOGY CLINIC

Regarding the past, what is the trial you have always been dreaming of in CIDP?

Cochrane 20 years on: The Cochrane Neuromuscular Disease Group

Rituximab in the treatment of three coexistent neurological autoimmune diseases: chronic inflammatory demyelinating polyradiculoneuropathy, Morvan syndrome and myasthenia gravis

Hand weakness in Charcot-Marie-Tooth disease 1X

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