Dual eligible patients are not the same: How social risk may impact quality measurement's ability to reduce inequities

door Alberti, Philip M., Baker, Matthew C.
Gepubliceerd in Medicine (Baltimore) (2020)

Comparison of Adverse Events Among Home- vs Facility-Administered Biologic Infusions, 2007-2017

door Baker, Matthew C., Weng, Yingjie, Fairchild, Robert, Ahuja, Neera, Rohatgi, Nidhi
Gepubliceerd in JAMA Netw Open (2021)

Osteoarthritis risk is reduced after treatment with ticagrelor compared to clopidogrel: a propensity score matching analysis

door Baker, Matthew C., Weng, Yingjie, Robinson, William H., Ahuja, Neera, Rohatgi, Nidhi
Gepubliceerd in Arthritis Rheumatol (2020)

An adult-onset leukoencephalopathy with axonal spheroids and pigmented glia accompanied by brain calcifications: A case report and a literature review of brain calcifications disor...

door Fujioka, Shinsuke, Broderick, Daniel F., Sundal, Christina, Baker, Matthew C., Rademakers, Rosa, Wszolek, Zbigniew K.
Gepubliceerd in 2013

TNF-alpha Inhibition for the Treatment of Cardiac Sarcoidosis

door Baker, Matthew C., Sheth, Khushboo, Witteles, Ronald, Genovese, Mark C., Shoor, Stanford, Simard, Julia F.
Gepubliceerd in Semin Arthritis Rheum (2019)

Expanded C9ORF72 Hexanucleotide Repeat in Depressive Pseudodementia

door Bieniek, Kevin F., van Blitterswijk, Marka, Baker, Matthew C., Petrucelli, Leonard, Rademakers, Rosa, Dickson, Dennis W.
Gepubliceerd in 2014

Enhancement of DNA tumor vaccine efficacy by gene gun–mediated codelivery of threshold amounts of plasmid-encoded helper antigen

door Leitner, Wolfgang W., Baker, Matthew C., Berenberg, Thomas L., Lu, Michael C., Yannie, P. Josef, Udey, Mark C.
Gepubliceerd in 2009

PREFERENTIAL DISRUPTION OF AUDITORY WORD REPRESENTATIONS IN PRIMARY PROGRESSIVE APHASIA WITH THE NEUROPATHOLOGY OF FTLD-TDP TYPE A

door Mesulam, Marek-Marsel, Nelson, Matthew J, Hyun, JungMoon, Rader, Benjamin, Hurley, Robert S, Rademakers, Rosa, Baker, Matthew C, Bigio, Eileen H., Weintraub, Sandra
Gepubliceerd in Cogn Behav Neurol (2019)

CD52 Is Elevated on B cells of SLE Patients and Regulates B Cell Function

door Bhamidipati, Kartik, Silberstein, John L., Chaichian, Yashaar, Baker, Matthew C., Lanz, Tobias V., Zia, Amin, Rasheed, Yusuf S., Cochran, Jennifer R., Robinson, William H.
Gepubliceerd in Front Immunol (2021)

Genetic screening and functional characterization of PDGFRB mutations associated with Basal Ganglia Calcification of Unknown Etiology

door Sanchez-Contreras, Monica, Baker, Matthew C., Finch, NiCole A., Nicholson, Alexandra, Wojtas, Aleksandra, Wszolek, Zbigniew K., Ross, Owen A., Dickson, Dennis W., Rademakers, Rosa
Gepubliceerd in 2014

Dominant Frontotemporal Dementia Mutations in 140 Cases of Primary Progressive Aphasia and Speech Apraxia

door Flanagan, Eoin P., Baker, Matthew C., Perkerson, Ralph B., Duffy, Joseph R., Strand, Edythe A., Whitwell, Jennifer L., Machulda, Mary M., Rademakers, Rosa, Josephs, Keith A.
Gepubliceerd in Dement Geriatr Cogn Disord (2015)

Symmetrical Corticobasal Syndrome Caused by a Novel c.314dup Progranulin Mutation

door Dopper, Elise G. P., Seelaar, Harro, Chiu, Wang Zheng, de Koning, Inge, van Minkelen, Rick, Baker, Matthew C., Rozemuller, Annemieke J. M., Rademakers, Rosa, van Swieten, John C.
Gepubliceerd in 2011

Tau Pathology in Frontotemporal Lobar Degeneration with C9ORF72 Hexanucleotide Repeat Expansion

door Bieniek, Kevin F., Murray, Melissa E., Rutherford, Nicola J., Castanedes-Casey, Monica, DeJesus-Hernandez, Mariely, Liesinger, Amanda M., Baker, Matthew C., Boylan, Kevin B., Rademakers, Rosa, Dickson, Dennis W.
Gepubliceerd in 2012

Microglia in frontotemporal lobar degeneration with progranulin or C9ORF72 mutations

door Sakae, Nobutaka, Roemer, Shanu F., Bieniek, Kevin F., Murray, Melissa E., Baker, Matthew C., Kasanuki, Koji, Graff‐Radford, Neill R., Petrucelli, Leonard, Van Blitterswijk, Marka, Rademakers, Rosa, Dickson, Dennis W.
Gepubliceerd in Ann Clin Transl Neurol (2019)

Progranulin-associated PiB-negative logopenic primary progressive aphasia

door Josephs, Keith A., Duffy, Joseph R., Strand, Edythe A., Machulda, Mary M., Vemuri, Prashanthi, Senjem, Matthew L., Perkerson, Ralph B., Baker, Matthew C., Lowe, Val, Jack, Clifford R., Rademakers, Rosa, Whitwell, Jennifer L.
Gepubliceerd in 2014

Frontotemporal dementia in a Brazilian Caucasian kindred with the C9orf72 mutation

door Takada, Leonel T., Pimentel, Maria Lucia V., DeJesus-Hernandez, Mariely, Fong, Jamie C., Yokoyama, Jennifer S., Karydas, Anna, Thibodeau, Marie-Pierre, Rutherford, Nicola J., Baker, Matthew C., Lomen-Hoerth, Catherine, Rademakers, Rosa, Miller, Bruce L.
Gepubliceerd in 2012

Reduced C9orf72 gene expression in c9FTD/ALS is caused by histone trimethylation, an epigenetic event detectable in blood

door Belzil, Veronique V., Bauer, Peter O., Prudencio, Mercedes, Gendron, Tania F., Stetler, Caroline T., Yan, Irene K., Pregent, Luc, Daughrity, Lillian, Baker, Matthew C., Rademakers, Rosa, Boylan, Kevin, Patel, Tushar C., Dickson, Dennis W., Petrucelli, Leonard
Gepubliceerd in 2013

Profilin-1 mutations are rare in patients with amyotrophic lateral sclerosis and frontotemporal dementia

door van Blitterswijk, Marka, Baker, Matthew C., Bieniek, Kevin F., Knopman, David S., Josephs, Keith A., Boeve, Bradley, Caselli, Richard, Wszolek, Zbigniew K., Petersen, Ronald, Graff-Radford, Neill R., Boylan, Kevin B., Dickson, Dennis W., Rademakers, Rosa
Gepubliceerd in 2013

A truncating SOD1 mutation, p.Gly141X, is associated with clinical and pathologic heterogeneity, including frontotemporal lobar degeneration

door Nakamura, Masataka, Bieniek, Kevin F., Lin, Wen-Lang, Graff-Radford, Neill R., Murray, Melissa E., Castanedes-Casey, Monica, Desaro, Pamela, Baker, Matthew C., Rutherford, Nicola J., Robertson, Janice, Rademakers, Rosa, Dickson, Dennis W., Boylan, Kevin B.
Gepubliceerd in Acta Neuropathol (2015)

Cognitive impairment in progressive supranuclear palsy is associated with tau burden

door Koga, Shunsuke, Parks, Adam, Kasanuki, Koji, Sanchez-Contreras, Monica, Baker, Matthew C., Josephs, Keith A., Ahlskog, J. Eric, Uitti, Ryan J., Graff-Radford, Neill, van Gerpen, Jay A., Wszolek, Zbigniew K., Rademakers, Rosa, Dickson, Dennis W.
Gepubliceerd in Mov Disord (2017)