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ALYSSA PAETAU, MD
MD
Surgery Physician
NPI: 1851530216Individual
Specialties, Licenses & Credentials
Surgery PhysicianPrimary
Surgery
Code: 208600000X
ME102450(FL)
Research & Publications (20)
Ectopic recurrence of craniopharyngioma along the surgical route: case report and literature review.
PMID 19499168·Acta Neurochir (Wien)·2010
5-case
A novel mutation of the GAA gene in a Finnish late-onset Pompe disease patient: clinical phenotype and follow-up with enzyme replacement therapy.
PMID 19472353·Muscle Nerve·2009
5-case
Combined use of non-invasive techniques for improved functional localization for a selected group of epilepsy surgery candidates.
PMID 19159694·Neuroimage·2009
5-case
Cathepsin D expression level affects alpha-synuclein processing, aggregation, and toxicity in vivo.
PMID 19203374·Mol Brain·2009
7-preclinical
Neuropathologic findings of dementia with lewy bodies (DLB) in a population-based Vantaa 85+ study.
PMID 19625740·J Alzheimers Dis·2009
8-other
Neuronal caspase-3 and PARP-1 correlate differentially with apoptosis and necrosis in ischemic human stroke.
PMID 19529948·Acta Neuropathol·2009
8-other
Senile systemic amyloidosis affects 25% of the very aged and associates with genetic variation in alpha2-macroglobulin and tau: a population-based autopsy study.
PMID 18382889·Ann Med·2008
8-other
PET amyloid ligand [11C]PIB uptake shows predominantly striatal increase in variant Alzheimer's disease.
PMID 18583368·Brain·2008
5-case
Hydrolethalus syndrome: neuropathology of 21 cases confirmed by HYLS1 gene mutation analysis.
PMID 18648327·J Neuropathol Exp Neurol·2008
8-other
Neurofibrillary tau pathology modulated by genetic variation of alpha-synuclein.
PMID 18661559·Ann Neurol·2008
8-other
Thymidine kinase 2 defects can cause multi-tissue mtDNA depletion syndrome.
PMID 18819985·Brain·2008
5-case
Stem cell protein BMI-1 is an independent marker for poor prognosis in oligodendroglial tumours.
PMID 18346113·Neuropathol Appl Neurobiol·2008
8-other
Infantile-onset spinocerebellar ataxia and mitochondrial recessive ataxia syndrome are associated with neuronal complex I defect and mtDNA depletion.
PMID 18775955·Hum Mol Genet·2008
8-other
Panel review of anaplastic oligodendroglioma from European Organization For Research and Treatment of Cancer Trial 26951: assessment of consensus in diagnosis, influence of 1p/19q loss, and correlations with outcome.
PMID 17549014·J Neuropathol Exp Neurol·2007
3-trial
Reappraisal of a consecutive autopsy series of patients with primary degenerative dementia: Lewy-related pathology.
PMID 17614849·APMIS·2007
8-other
Hypomyelination with atrophy of the basal ganglia and cerebellum: follow-up and pathology.
PMID 17620549·Neurology·2007
8-other
Recessive Twinkle mutations in early onset encephalopathy with mtDNA depletion.
PMID 17921179·Brain·2007
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 14540 OLD SAINT AUGUSTINE RD, SUITE 2571
JACKSONVILLE, FL 32258 - Phone
- (904) 886-2251
Quick Facts
- NPI
- 1851530216
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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