Associate Professor, Neurology, Mayo Medical School
Neurology
Dr. Christopher J. Klein, MD
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Christopher J. Klein practices Neurology. He graduated from University of Toledo College of Medicine. Christopher J. Klein is also published. He has 58 publications published. The lastest publication: "Defects of mutant DNMT1 are linked to a spectrum of neurological disorders.' Doctor Christopher J. Klein, MD is registered with Medicare.
Publications
- Defects of mutant DNMT1 are linked to a spectrum of neurological Disorders.
- Retrospective study of a TTR FAP cohort to modify NIS+7 for therapeutic trials.
- Cryoglobulinemic vasculitis in a patient with CREST syndrome.
- Application of whole exome sequencing in undiagnosed inherited polyneuropathies.
- Proficiency of Nerve conduction using standard methods and reference values (Cl. NPhys Trial 4).
- Progressive Multifocal Leukoencephalopathy: a rare infectious complication following allogeneic hematopoietic cell transplantation (HCT).
- Inherited neuropathies: Clinical overview and update.
- Novel SOD1 mutation Discovered in atypical ALS by whole exome sequencing.
- A multicenter trial of the proficiency of smart quantitative sensation tests.
- MRI Findings in Autoimmune Voltage-Gated Potassium Channel Complex Encephalitis with Seizures: One Potential Etiology for Mesial Temporal Sclerosis.
- Peripheral neuropathy incidence in inflammatory bowel Disease: a population-based study.
- Reply: Surgical and postpartum hereditary brachial Plexus attacks and prophylactic immunotherapy.
- Striational antibodies in a paraneoplastic context.
- DNMT1 mutation hot spot causes varied phenotypes of HSAN1 with Dementia and hearing loss.
- A trial of proficiency of Nerve conduction: Greater standardization still needed.
- Infrequent SCN9A mutations in congenital insensitivity to pain and erythromelalgia.
- Mass spectrometry analysis reveals non-mutated apolipoprotein a1 lumbosacral radiculoPlexus amyloidoma.
- Surgical and postpartum hereditary brachial Plexus attacks and prophylactic immunotherapy.
- IgM-monoclonal gammopathy neuropathy and Tremor: A first epidemiologic case control study.
- Batch effect correction for genome-wide methylation data with Illumina Infinium platform.
- Neuronal intracellular transport and neurodegenerative Disease.
- Meralgia paresthetica: Relation to obesity, advanced age, and diabetes mellitus.
- Large kindred evaluation of mitofusin 2 novel mutation, extremes of neurologic presentations, and preserved Nerve mitochondria.
- Psychiatric manifestations of voltage-gated potassium-channel complex autoimmunity.
- Purkinje Cell Cytoplasmic Autoantibody Type 1 Accompaniments: The Cerebellum and Beyond.
- Mutations in DNMT1 cause hereditary sensory neuropathy with Dementia and hearing loss.
- A case of sensory Ataxia as the presenting manifestation of neurosarcoidosis.
- Mass spectrometric-based proteomic analysis of amyloid Neuropathy type in nerve tissue.
- Hypertrophic Nerves producing myelopathy in fulminant CIDP.
- Scapuloperoneal spinal muscular atrophy and CMT2C are allelic Disorders caused by alterations in TRPV4.
- SEPT9 mutations and a conserved 17q25 sequence in sporadic and hereditary brachial plexus Neuropathy.
- T-cell neurolymphomatosis involving cauda equina and sciatic Nerves.
- Voltage-gated potassium channel autoimmunity mimicking creutzfeldt-jakob Disease.
- Antibodies to myelin-associated glycoprotein (anti-Mag) in IgM amyloidosis may influence expression of Neuropathy in rare patients.
- Disseminated sporotrichosis presenting with granulomatous Inflammatory multiple mononeuropathies.
- Does impaired glucose metabolism cause Polyneuropathy? Review of previous studies and design of a prospective controlled population-based study.
- Lenalidomide therapy in a patient with POEMS syndrome.
- The inherited neuropathies.
- Isolated amyloidosis presenting with lumbosacral radiculoplexopathy: description of two cases and pathogenic review.
- Modeling chronic glycemic exposure variables as correlates and predictors of microvascular complications of diabetes.
- Later-onset Fabry Disease: an adult variant presenting with the cramp-fasciculation syndrome.
- Monotonicity of nerve tests in diabetes: subclinical nerve dysfunction precedes diagnosis of Polyneuropathy.
- Genetic testing in inherited Peripheral neuropathies.
- Identification of transthyretin variants by sequential proteomic and genomic analysis.
- Bulbospinal muscular atrophy: Kennedy's Disease.
- Adult polyglucosan body Disease: case description of an expanding genetic and clinical syndrome.
- Indifference rather than insensitivity to pain.
- Imaging features of copper deficiency myelopathy: a study of 25 cases.
- Elevated creatine kinase and transaminases in asymptomatic SBMA.
- Impaired Glycemia and Diabetic Polyneuropathy: The OC IG Survey.
- Novel myelin protein zero mutation (Arg36Trp) in a patient with acute onset painful Neuropathy.
- Case of mononeuritis multiplex onset with rituximab therapy for Waldenström's macroglobulinemia.
- Pathology and molecular genetics of inherited Neuropathy.
- The neuropathies of Waldenström's macroglobulinemia (WM) and IgM-MGUS.
- Post-surgical Inflammatory neuropathy.
- Neurologic course, endocrine dysfunction and triplet repeat size in Spinal bulbar muscular atrophy.
- Signs and symptoms versus nerve conduction studies to diagnose Diabetic sensorimotor polyneuropathy: Cl vs. NPhys trial.
Schools
Med Coll Of Ohio
Procedures Preformed
- EEG (Electroencephalogram)
- EMG (Electromyography)
Conditions Treated
- Acoustic Neuroma
- Alzheimer's Disease
- Ataxia
- Autonomic Disorders
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Doctors Specialties
- Clinical Neurophysiology
- Neurology
Accepted Insurances
Education
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Johns Hopkins University -
Mayo School of Graduate Medical Education -
University of Toledo College of Medicine
Hospital
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Mayo Clinic - Rochester, Minnesota
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1780658377 |
| Last Name Of The Provider | KLEIN |
| First Name Of The Provider | CHRISTOPHER |
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