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VIVIANNA VAN DEERLIN, MD
MD
Clinical Pathology/Laboratory Medicine Physician
NPI: 1013951979IndividualAccepts Medicare
Specialties, Licenses & Credentials
Clinical Pathology/Laboratory Medicine PhysicianPrimary
Pathology — Clinical Pathology/Laboratory Medicine
Code: 207ZP0105X
MD062112L(PA)
CMS Specialties
PrimaryPATHOLOGY
Education
WASHINGTON UNIVERSITY SCHOOL OF MEDICINE
Class of 1994
Research & Publications (20)
TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysis.
PMID 18396105·Lancet Neurol·2008
8-other
Biochemical and pathological characterization of frontotemporal dementia due to a Leu266Val mutation in microtubule-associated protein tau in an African American individual.
PMID 17072625·Acta Neuropathol·2007
5-case
Clinical, genetic, and pathologic characteristics of patients with frontotemporal dementia and progranulin mutations.
PMID 17698705·Arch Neurol·2007
8-other
Familial frontotemporal dementia: from gene discovery to clinical molecular diagnostics.
PMID 14500612·Clin Chem·2003
6-review
Optimizing gene expression analysis in archival brain tissue.
PMID 12462400·Neurochem Res·2002
8-other
Bone marrow engraftment analysis after allogeneic bone marrow transplantation.
PMID 10702903·Clin Lab Med·2000
6-review
Brain progranulin expression in GRN-associated frontotemporal lobar degeneration.
PMID 19649643·Acta Neuropathol·2010
8-other
Amyotrophic lateral sclerosis-plus syndrome with TAR DNA-binding protein-43 pathology.
PMID 19139310·Arch Neurol·2009
5-case
Recommended principles and practices for validating clinical molecular pathology tests.
PMID 19415949·Arch Pathol Lab Med·2009
6-review
Clinical and pathological continuum of multisystem TDP-43 proteinopathies.
PMID 19204154·Arch Neurol·2009
8-other
Clinical and pathological characteristics of patients with leucine-rich repeat kinase-2 mutations.
PMID 19006185·Mov Disord·2009
4-observational
Two German kindreds with familial amyotrophic lateral sclerosis due to TARDBP mutations.
PMID 18779421·Arch Neurol·2008
8-other
A90V TDP-43 variant results in the aberrant localization of TDP-43 in vitro.
PMID 18505686·FEBS Lett·2008
8-other
Sudden extramedullary T-lymphoblastic blast crisis in chronic myelogenous leukemia: a nonrandom event associated with imatinib?
PMID 18343792·Am J Clin Pathol·2008
5-case
Variations in the progranulin gene affect global gene expression in frontotemporal lobar degeneration.
PMID 18223198·Hum Mol Genet·2008
8-other
Corticobasal syndrome and primary progressive aphasia as manifestations of LRRK2 gene mutations.
PMID 17914064·Neurology·2008
8-other
Factors associated with survival probability in autopsy-proven frontotemporal lobar degeneration.
PMID 17615171·J Neurol Neurosurg Psychiatry·2008
8-other
Clinicopathological concordance and discordance in three monozygotic twin pairs with familial Alzheimer's disease.
PMID 17615170·J Neurol Neurosurg Psychiatry·2007
4-observational
Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiative.
PMID 17826340·Lancet Neurol·2007
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 3400 SPRUCE STREET, 7.103 FOUNDERS PAVILLION
PHILADELPHIA, PA 19104 - Phone
- (215) 662-6550
Quick Facts
- NPI
- 1013951979
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 32
- Publications
- 20
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