Professor, Neurology, UCSF School of Medicine
Neurology
Dr. Michael D. Geschwind, MD
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Michael D. Geschwind is an expert in the field of Neurology. He researched medicine at Albert Einstein College of Medicine of Yeshiva University. He received awards:"CMS Meaningful Use Stage 1 Certification". Dr. Michael D. Geschwind is a published MD. He has 69 papers published. The most current publication "Cerebellar top-of-the-basilar syndrome." Michael D. Geschwind, MD accepts all Medicare patients.
Publications
- Creutzfeldt-Jakob Disease-Like Periodic Sharp Wave Complexes in Voltage-Gated Potassium Channel-Complex Antibodies Encephalitis: A Case Report.
- A clinical approach to diagnosis of autoimmune encephalitis.
- White matter involvement in sporadic Creutzfeldt-Jakob Disease.
- Episodic bradycardia as neurocardiac prodrome to voltage-gated potassium channel complex/leucine-rich, glioma inactivated 1 antibody encephalitis.
- Ascertainment bias causes false signal of anticipation in genetic prion Disease.
- More than memory impairment in voltage-gated potassium channel complex encephalopathy.
- Effect of Rituximab in Patients With Leucine-Rich, Glioma-Inactivated 1 Antibody-Associated Encephalopathy.
- Quantitative 7T Phase Imaging in Premanifest Huntington Disease.
- An epigenetic signature in Peripheral blood associated with the haplotype on 17q21.31, a risk factor for neurodegenerative tauopathy.
- Doxycycline for Creutzfeldt-Jakob Disease: a failure, but a step in the right direction.
- Preimplantation Genetic Diagnosis (PGD) for Genetic Prion Disorder Due to F198S Mutation in the PRNP Gene.
- Executive functions in premanifest Huntington's Disease.
- Whipple's Disease Masquerades as Dementia With Lewy Bodies.
- Seizures and Epileptiform Activity in the Early Stages of Alzheimer Disease.
- Ethics in prion Disease.
- Neurodegenerative Disease Phenotypes in Carriers of MAPT p.A152T, A Risk Factor for Frontotemporal Dementia Spectrum Disorders and Alzheimer Disease.
- Diagnosis and treatment of rapidly progressive Dementias.
- Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's Diseases.
- Clinical Overlap between Jakob-Creutzfeldt Disease and Lewy Body Disease.
- Clinicopathological correlations in Corticobasal degeneration.
- Pathologic evidence that the T188R mutation in PRNP is associated with prion Disease.
- Are you related to "the Geschwind?".
- Adult-onset drug-refractory seizure disorder associated with anti-voltage-gated potassium-channel antibody.
- Immunologically mediated Dementias.
- Prion proteins in subpopulations of white blood cells from patients with sporadic Creutzfeldt-Jakob Disease.
- AMPA receptor antibodies in limbic encephalitis alter synaptic receptor location.
- Correlating DWI MRI with pathologic and other features of Jakob-Creutzfeldt Disease.
- Voltage-gated potassium channel autoimmunity mimicking creutzfeldt-jakob Disease.
- Neuroimaging in Dementia.
- Creutzfeldt-Jakob Disease in recipients of corneal transplants.
- Rapidly progressive Dementia.
- A 54-year-old man with slowness of movement and confusion.
- The diagnostic utility of brain biopsy procedures in patients with rapidly deteriorating neurological conditions or Dementia.
- Human prions and plasma lipoproteins.
- Human growth hormone-related iatrogenic Creutzfeldt-Jakob Disease with abnormal imaging.
- Patterns of brain atrophy that differentiate Corticobasal degeneration syndrome from progressive supranuclear palsy.
- Diffusion-weighted and fluid-attenuated inversion recovery imaging in Creutzfeldt-Jakob Disease: high sensitivity and specificity for diagnosis.
- Diagnosis of human prion Disease.
- When sporadic Disease is not sporadic: the potential for genetic etiology.
- Challenging the clinical utility of the 14-3-3 protein for the diagnosis of sporadic Creutzfeldt-Jakob Disease.
- Psychiatric and neuroimaging findings in Creutzfeldt-Jakob Disease.
- Sporadic Creutzfeldt-Jakob Disease mimicking variant Creutzfeldt-Jakob Disease.
- Application of quantitative DTI metrics in sporadic CJD.
- Genetic CJD with a novel E200G mutation in the prion protein gene and comparison with E200K mutation cases.
- Expression of Nerve growth factor in vivo from a defective herpes simplex virus 1 vector prevents effects of axotomy on sympathetic ganglia.
- De novo prions.
- Variably protease-sensitive prionopathy: a new sporadic Disease of the prion protein.
- Familial Creutzfeldt-Jakob Disease with V180I mutation.
- Diffusion-weighted MRI hyperintensity patterns differentiate CJD from other rapid Dementias.
- Thorough work-up and new diagnostic criteria needed for CJD.
- Exome sequencing identifies ACSF3 as a cause of combined malonic and methylmalonic aciduria.
- Amyloid imaging in distinguishing atypical prion Disease from Alzheimer Disease.
- Autoimmune encephalopathies.
- A case of enteroviral meningoencephalitis presenting as rapidly progressive Dementia.
- Phenotypic heterogeneity and genetic modification of P102L inherited prion Disease in an international series.
- Clinical trials for prion Disease: difficult challenges, but hope for the future.
- A randomized, placebo-controlled trial of latrepirdine in Huntington Disease.
- First symptom in sporadic Creutzfeldt-Jakob Disease.
- Anti-GAD antibody cerebellar ataxia mimicking Creutzfeldt-Jakob Disease.
- Transfer of the Nerve growth factor gene into cell lines and cultured neurons using a defective herpes simplex virus vector. Transfer of the NGF gene into cells by a H...
- Expression of bcl-2 from a defective herpes simplex virus-1 vector limits neuronal death in focal Cerebral ischemia.
- Presenile Dementia syndromes: an update on taxonomy and diagnosis.
- The relative contributions of HAART and alpha-interferon for therapy of Progressive multifocal leukoencephalopathy in AIDS.
- Cerebellar top-of-the-basilar Syndrome.
- Defective HSV-1 vector expressing BDNF in auditory ganglia elicits neurite outgrowth: model for treatment of neuron loss following cochlear Degeneration.
- Regulated release and polarized localization of brain-derived neurotrophic factor in hippocampal neurons.
- Localized gene transfer into organotypic hippocampal slice cultures and acute hippocampal slices.
- The care of the teeth as dealt with in "ladies' books".
Schools
Albert Einstein College of Medicine of Yeshiva University
UCLA Med Center
John39S Hopkins School Of Med
Ucsf Med Center
Conditions Treated
- Alzheimer's Disease
- Ataxia
- Central Nervous System Lymphoma
- Cerebral Artery Thrombosis
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Doctors Specialties
- Neurology
Accepted Insurances
Awards
- CMS Meaningful Use Stage 1 Certification
Education
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Johns Hopkins University -
UCLA Medical Center -
Albert Einstein College of Medicine of Yeshiva University
Hospital
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San Francisco General Hospital and Trauma Center -
UCSF Medical Center
Drug Facts
| NPI NUMBER | 1700813565 | |
| NPPES Provider LastName | GESCHWIND | |
| NPPES Provider FirstName | MICHAEL | |
| NPPES Provider ZIPCode | 941430001 | |
| NPPES Provider State | CA | |
| Specialty Description | Neurology | |
| Total Claim Count | 110.0 | |
| Distinct Opioid Count | 0.0 | |
| Opioid Claim Count | 0.0 | |
| Percent Opioid Claims | 0.0 |
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1700813565 |
| Last Name Of The Provider | GESCHWIND |
| First Name Of The Provider | MICHAEL |
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