The Genetics and Neuropathology of Neurodegenerative Disorders: Perspectives and Implications for Research and Clinical Practice

Por Van Deerlin, Vivianna M.
Publicado em 2012

Alzheimer’s Disease and Frontotemporal Dementia: The Current State of Genetics and Genetic Testing Since the Advent of Next-Generation Sequencing

Por Goldman, Jill S., Van Deerlin, Vivianna M.
Publicado no Mol Diagn Ther (2018)

Validation of a Long-Read PCR Assay for Sensitive Detection and Sizing of C9orf72 Hexanucleotide Repeat Expansions

Por Suh, EunRan, Grando, Kaitlyn, Van Deerlin, Vivianna M.
Publicado no J Mol Diagn (2018)

Prenatal healthcare providers’ Gaucher disease carrier screening practices

Por Falcone, Dana, Wood, Elisabeth McCarty, Mennuti, Michael, Xie, Sharon X., Van Deerlin, Vivianna M.
Publicado em 2012

An evaluation of tyramide signal amplification and archived fixed and frozen tissue in microarray gene expression analysis

Por Karsten, Stanislav L., Van Deerlin, Vivianna M. D., Sabatti, Chiara, Gill, Lisa H., Geschwind, Daniel H.
Publicado em 2002

Genetic Testing and Parkinson Disease: Assessment of Patient Knowledge, Attitudes, and Interest

Por Falcone, Dana Clay, Wood, Elisabeth McCarty, Xie, Sharon X., Siderowf, Andrew, Van Deerlin, Vivianna M.
Publicado em 2011

Clinical and Pathological Characteristics of Patients with Leucine-Rich Repeat Kinase-2 Mutations

Por Covy, Jason P., Yuan, Wuxing, Waxman, Elisa A., Hurtig, Howard I., Van Deerlin, Vivianna M., Giasson, Benoit I
Publicado em 2009

Poly-A binding protein-1 localization to a subset of TAR DNA-binding protein of 43 kDa inclusions in amyotrophic lateral sclerosis occurs more frequently in patients harboring an e...

Por McGurk, Leeanne, Lee, Virginia, M., Trojanowksi, John Q., Van Deerlin, Vivianna M., Lee, Edward B., Bonini, Nancy M.
Publicado em 2014

Microglial Activation Correlates with Disease Progression and Upper Motor Neuron Clinical Symptoms in Amyotrophic Lateral Sclerosis

Por Brettschneider, Johannes, Toledo, Jon B., Van Deerlin, Vivianna M., Elman, Lauren, McCluskey, Leo, Lee, Virginia M.-Y., Trojanowski, John Q.
Publicado em 2012

Longitudinal structural gray matter and white matter MRI changes in presymptomatic progranulin mutation carriers

Por Olm, Christopher A., McMillan, Corey T., Irwin, David J., Van Deerlin, Vivianna M., Cook, Philip A., Gee, James C., Grossman, Murray
Publicado no Neuroimage Clin (2018)

TDP-43 Pathology in a Case of Hereditary Spastic Paraplegia with a NIPA1/SPG6 Mutation

Por Martinez-Lage, Maria, Molina-Porcel, Laura, Falcone, Dana, McCluskey, Leo, Lee, Virginia M.-Y., Van Deerlin, Vivianna M., Trojanowski, John Q.
Publicado em 2012

Atypical Alzheimer’s disease in an elderly US resident with amyotrophic lateral sclerosis and pathological tau in spinal motor neurons

Por MCCLUSKEY, LEO F., GESER, FELIX, ELMAN, LAUREN B., VAN DEERLIN, VIVIANNA M., ROBINSON, JOHN L., LEE, VIRGINIA M.-Y., TROJANOWSKI, JOHN Q.
Publicado em 2014

TDP-43 skeins show properties of amyloid in a subset of ALS cases

Por Robinson, John L., Geser, Felix, Stieber, Anna, Umoh, Mfon, Kwong, Linda K., Van Deerlin, Vivianna M., Lee, Virginia M.-Y., Trojanowski, John Q.
Publicado em 2012

PRION PROTEIN CODON 129 POLYMORPHISM MODIFIES AGE AT ONSET OF FRONTOTEMPORAL DEMENTIA WITH THE C.709-1G>A PROGRANULIN MUTATION

Por Moreno, Fermín, Alzualde, Ainhoa, Camblor, Pablo Martínez, Barandiaran, Myriam, Van Deerlin, Vivianna M., Gabilondo, Alazne, Martí Massó, José F., de Munain, Adolfo López, Indakoetxea, Begoña
Publicado em 2011

Expression of TMEM106B, the frontotemporal lobar degeneration-associated protein, in normal and diseased human brain

Por Busch, Johanna I, Martinez-Lage, Maria, Ashbridge, Emily, Grossman, Murray, Van Deerlin, Vivianna M, Hu, Fenghua, Lee, Virginia MY, Trojanowski, John Q, Chen-Plotkin, Alice S
Publicado em 2013

C9orf72 hypermethylation protects against repeat expansion-associated pathology in ALS/FTD

Por Liu, Elaine Y., Russ, Jenny, Wu, Kathryn, Neal, Donald, Suh, Eunran, McNally, Anna G., Irwin, David J., Van Deerlin, Vivianna M., Lee, Edward B.
Publicado em 2014

Frontotemporal Lobar Degeneration: Defining Phenotypic Diversity Through Personalized Medicine

Por Irwin, David J, Cairns, Nigel J., Grossman, Murray, McMillan, Corey T., Lee, Edward B., Van Deerlin, Vivianna M., Lee, Virginia M.-Y., Trojanowski, John Q.
Publicado no Acta Neuropathol (2014)

Can MRI screen for CSF biomarkers in neurodegenerative disease?

Por McMillan, Corey T., Avants, Brian, Irwin, David J., Toledo, Jon B., Wolk, David A., Van Deerlin, Vivianna M., Shaw, Leslie M., Trojanoswki, John Q., Grossman, Murray
Publicado em 2013

Acetylated Tau Neuropathology in Sporadic and Hereditary Tauopathies

Por Irwin, David J., Cohen, Todd J., Grossman, Murray, Arnold, Steven E., McCarty-Wood, Elisabeth, Van Deerlin, Vivianna M., Lee, Virginia M.-Y., Trojanowski, John Q.
Publicado em 2013

Development and Validation of Pedigree Classification Criteria for Frontotemporal Lobar Degeneration

Por Wood, Elisabeth M., Falcone, Dana, Suh, EunRan, Irwin, David J., Chen-Plotkin, Alice S., Lee, Edward B., Xie, Sharon X., Van Deerlin, Vivianna M., Grossman, Murray
Publicado em 2013