Professor, Neurology, Mayo Medical School
Neurology
Dr. Sean J. Pittock, MD
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Sean J. Pittock practices Neurology. He over the years received 1 awards: "Regional Top Doctor". Doctor Sean J. Pittock, MD is a published doctor and has 90 publications published. The lastest was: 'Neuromyelitis optica spectrum initially diagnosed as antiphospholipid antibody myelitis.' He accepts Medicare payments and is registered with Medicare.gov.
Publications
- Neuromyelitis Optica spectrum initially diagnosed as antiphospholipid antibody myelitis.
- SRP-IgG detected incidentally associates with autoimmune myopathy.
- Monitoring oligoclonal immunoglobulins in cerebral Spinal fluid using microLC-ESI-Q-TOF mass spectrometry.
- Status of diagnostic approaches to AQP4-IgG seronegative NMO and NMO/MS overlap Syndromes.
- Responses to and Outcomes of Treatment of Autoimmune Cerebellar Ataxia in Adults.
- Diagnostic utility of aquaporin-4 in the analysis of active demyelinating lesions.
- Short Myelitis Lesions in Aquaporin-4-IgG-Positive Neuromyelitis Optica Spectrum Disorders.
- Seroprevalence of Aquaporin-4-IgG in a Northern California Population Representative Cohort of Multiple Sclerosis.
- Investigation of the KIR4.1 potassium channel as a putative antigen in patients with Multiple sclerosis: a comparative study.
- Immunotherapy trial as diagnostic test in evaluating patients with presumed autoimmune gastrointestinal dysmotility.
- Autoimmune Aquaporin-4 Myopathy in Neuromyelitis Optica Spectrum.
- Hydrocephalus in neuromyelitis Optica.
- Paraneoplastic neuromyelitis Optica spectrum disorder associated with metastatic carcinoid expressing aquaporin-4.
- Aquaporin 4 IgG Serostatus and Outcome in Recurrent Longitudinally Extensive Transverse Myelitis.
- Childhood Onset of Stiff-Man Syndrome.
- MRI Findings in Autoimmune Voltage-Gated Potassium Channel Complex Encephalitis with Seizures: One Potential Etiology for Mesial Temporal Sclerosis.
- Individualized Rituximab Treatment for Neuromyelitis Optica Spectrum Disorders.
- Teaching NeuroImages: diagnostic utility of FDG-PET in neurolymphomatosis.
- Eculizumab in AQP4-IgG-positive relapsing neuromyelitis optica spectrum Disorders: an open-label pilot study.
- Striational antibodies in a paraneoplastic context.
- Autoimmune chorea in adults.
- Intractable Nausea and Vomiting from Autoantibodies Against a Brain Water Channel.
- Paraneoplastic lower motor neuronopathy associated with Hodgkin lymphoma.
- Astrocytic autoantibody of neuromyelitis Optica (NMO-IgG) binds to aquaporin-4 extracellular loops, monomers, tetramers and high order arrays.
- Large kindred evaluation of mitofusin 2 novel mutation, extremes of neurologic presentations, and preserved Nerve mitochondria.
- Optic neuritis in an ethnically diverse population: Higher risk of atypical cases in patients of African or African-Caribbean heritage.
- Statin therapy and Multiple sclerosis disability in a population-based cohort.
- Psychiatric manifestations of voltage-gated potassium-channel complex autoimmunity.
- Purkinje Cell Cytoplasmic Autoantibody Type 1 Accompaniments: The Cerebellum and Beyond.
- Sleep manifestations of voltage-gated potassium channel complex autoimmunity.
- Extratemporal EEG and MRI findings in ANNA-1 (anti-Hu) encephalitis.
- Neural autoantibody evaluation in functional gastrointestinal Disorders: a population-based case-control study.
- Neuronal voltage-gated potassium channel complex autoimmunity in children.
- CSF complements serum for evaluating paraneoplastic antibodies and NMO-IgG.
- Beneficial Plasma Exchange Response in Central Nervous System Inflammatory Demyelination.
- Failure of Autologous Hematopoietic Stem Cell Transplantation to Prevent Relapse of Neuromyelitis Optica.
- Reply to Duprez et al. and List et al. regarding chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids.
- Intractable vomiting as the initial presentation of neuromyelitis Optica.
- Isolated sympathetic failure with autoimmune Autonomic ganglionopathy.
- Autoimmune dementia: clinical course and predictors of immunotherapy response.
- Paraneoplastic jaw Dystonia and laryngospasm with antineuronal nuclear autoantibody type 2 (anti-Ri).
- Eliminating false-positive results in serum tests for neuromuscular autoimmunity.
- Positron emission tomography-computed tomography in paraneoplastic neurologic Disorders: systematic analysis and review.
- Neural autoantibody profile of primary achalasia.
- Humoral pattern II Multiple sclerosis pathology not associated with neuromyelitis Optica IgG.
- Polymyoclonus, laryngospasm, and cerebellar Ataxia associated with adenocarcinoma and multiple neural cation channel autoantibodies.
- Prediction of neuromyelitis Optica attack severity by quantitation of complement-mediated injury to aquaporin-4-expressing cells.
- Diagnosis of neuromyelitis spectrum Disorders: comparative sensitivities and specificities of immunohistochemical and immunoprecipitation assays.
- Treatment of neuromyelitis Optica with mycophenolate mofetil: retrospective analysis of 24 patients.
- Neuromyelitis optica IgG serostatus in fulminant central nervous system inflammatory demyelinating Disease.
- Ganglionic acetylcholine receptor autoantibody: oncological, neurological, and serological accompaniments.
- AQP4-IgG immunoprecipitation assay optimization.
- Reversible extralimbic paraneoplastic encephalopathies with large abnormalities on magnetic resonance images.
- Posterior reversible encephalopathy syndrome in neuromyelitis optica spectrum Disorders.
- Coexistence of myasthenia gravis and serological markers of neurological autoimmunity in neuromyelitis Optica.
- Aquaporin-4-binding autoantibodies in patients with neuromyelitis Optica impair glutamate transport by down-regulating EAAT2.
- Voltage-gated potassium channel autoimmunity mimicking creutzfeldt-jakob Disease.
- Serologic profiles aiding the diagnosis of autoimmune gastrointestinal dysmotility.
- Aquaporin-4 autoantibodies in a paraneoplastic context.
- Autoimmune Myelopathy associated with collapsin response-mediator protein-5 immunoglobulin G.
- Neuromyelitis Optica: a new perspective.
- Neuromyelitis Optica and non organ-specific autoimmunity.
- Whole-body tremulousness: isolated generalized polymyoclonus.
- Heterogeneity of presentation and outcome in the Irish rapid-onset Dystonia-parkinsonism kindred.
- The pathology of MS: new insights and potential clinical applications.
- Does benign Multiple sclerosis today imply benign Multiple sclerosis tomorrow?: implications for treatment.
- Neuromyelitis Optica IgG status in acute partial transverse myelitis.
- Glutamic acid decarboxylase autoimmunity with brainstem, extrapyramidal, and Spinal cord dysfunction.
- Neuromyelitis Optica brain lesions localized at sites of high aquaporin 4 expression.
- Not every patient with Multiple sclerosis should be treated at time of diagnosis.
- Brain abnormalities in neuromyelitis Optica.
- Neuromyelitis Optica IgG predicts relapse after longitudinally extensive transverse myelitis.
- Therapeutic decision making in MS: impact of a slower disability progression.
- IgG marker of optic-spinal Multiple sclerosis binds to the aquaporin-4 water channel.
- Amphiphysin autoimmunity: paraneoplastic accompaniments.
- Prevalence of tremor in Multiple sclerosis and associated disability in the Olmsted County population.
- Paraneoplastic antibodies coexist and predict cancer, not neurological Syndrome.
- Clinical implications of benign Multiple sclerosis: a 20-year population-based follow-up study.
- Neuropathology of primary Restless leg syndrome: absence of specific tau- and alpha-synuclein pathology.
- From parallel to perpendicular: getting "straightened out" with levodopa therapy.
- Quality of life is favorable for most patients with Multiple sclerosis: a population-based cohort study.
- Bright red nuclei.
- The Orpington Prognostic Scale within the first 48 hours of admission as a predictor of outcome in ischemic stroke.
- Anti-neuronal nuclear autoantibody type 2: paraneoplastic accompaniments.
- OKT3 neuroToxicity presenting as akinetic mutism.
- The Oxfordshire Community Stroke Project classification: correlation with imaging, associated complications, and prediction of outcome in acute ischemic stroke.
- The "spray can" sign: validation of a clinical observation in chronic inflammatory demyelinating Polyneuropathy.
- Unilateral osteoarthritis--"the working hand".
- Reversible Myelopathy in a 34-year-old man with vitamin B12 deficiency.
Conditions Treated
- Anterior Horn Disease
- Ataxia
- Autonomic Disorders
- Convulsions
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Doctors Specialties
- Neurology
Accepted Insurances
Awards
- Regional Top Doctor
Education
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Mayo School of Graduate Medical Education -
University College of Dublin National Univ SOM
Hospital
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Mayo Clinic - Rochester, Minnesota
Drug Facts
| NPI NUMBER | 1154395358 | |
| NPPES Provider LastName | PITTOCK | |
| NPPES Provider FirstName | SEAN | |
| NPPES Provider ZIPCode | 559050001 | |
| NPPES Provider State | MN | |
| Specialty Description | Neurology | |
| Total Claim Count | 126.0 | |
| Distinct Opioid Count | 0.0 | |
| Opioid Claim Count | 0.0 | |
| Percent Opioid Claims | 0.0 |
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1154395358 |
| Last Name Of The Provider | PITTOCK |
| First Name Of The Provider | SEAN |
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