PRKAR1B mutations are a rare cause of FUS negative neuronal intermediate filament inclusion disease

por Pottier, Cyril, Baker, Matt, Dickson, Dennis W., Rademakers, Rosa
Publicado en Brain (2015)

A new subtype of frontotemporal lobar degeneration with FUS pathology

por Neumann, Manuela, Rademakers, Rosa, Roeber, Sigrun, Baker, Matt, Kretzschmar, Hans A., Mackenzie, Ian R. A.
Publicado 2009

Abundant FUS-immunoreactive pathology in neuronal intermediate filament inclusion disease

por Neumann, Manuela, Roeber, Sigrun, Kretzschmar, Hans A., Rademakers, Rosa, Baker, Matt, Mackenzie, Ian R. A.
Publicado 2009

Diffuse leukoencephalopathy with spheroids presenting as primary progressive aphasia

por Oboudiyat, Carly, Bigio, Eileen H., Bonakdarpour, Borna, Baker, Matt C., Rademakers, Rosa, Weintraub, Sandra, Mesulam, M.-Marsel
Publicado en Neurology (2015)

Gene Expression Study on Peripheral Blood Identifies Progranulin Mutations

por Coppola, Giovanni, Karydas, Anna, Rademakers, Rosa, Wang, Qing, Baker, Matt, Hutton, Mike, Miller, Bruce L., Geschwind, Daniel H.
Publicado 2008

Psychosis and Hallucinations in FTD with C9ORF72 mutation: A detailed clinical cohort

por Kertesz, Andrew, Ang, Lee Cyn, Jesso, Sarah, MacKinley, Julia, Baker, Matt, Brown, Patricia, Shoesmith, Christen, Rademakers, Rosa, Finger, Elizabeth C.
Publicado 2013

Coexistence of Progressive Supranuclear Palsy With Pontocerebellar Atrophy and Myotonic Dystrophy Type 1

por Koga, Shunsuke, Eric Ahlskog, J, DeTure, Michael A, Baker, Matt, Roemer, Shanu F, Konno, Takuya, Rademakers, Rosa, Ross, Owen A, Dickson, Dennis W
Publicado en J Neuropathol Exp Neurol (2019)

Pathological heterogeneity in amyotrophic lateral sclerosis with FUS mutations: two distinct patterns correlating with disease severity and mutation

por Mackenzie, Ian R. A., Ansorge, Olaf, Strong, Michael, Bilbao, Juan, Zinman, Lorne, Ang, Lee-Cyn, Baker, Matt, Stewart, Heather, Eisen, Andrew, Rademakers, Rosa, Neumann, Manuela
Publicado 2011

ALS-FTD complex disorder due to C9ORF72 gene mutation – description of first Polish family

por Siuda, Joanna, Lewicka, Tatiana, Bujak, Malgorzata, Opala, Grzegorz, Golenia, Aleksandra, Slowik, Agnieszka, van Blitterswijk, Marka, Baker, Matt, Ertekin-Taner, Nilufer, Wszolek, Zbigniew K., Rademakers, Rosa
Publicado 2014

C9ORF72 hexanucleotide repeat expansions in patients with ALS from the Coriell Cell Repository

por Rutherford, Nicola J., DeJesus- Hernandez, Mariely, Baker, Matt C., Kryston, Thomas B., Brown, Patricia E., Lomen-Hoerth, Catherine, Boylan, Kevin, Wszolek, Zbigniew K., Rademakers, Rosa
Publicado 2012

C9ORF72 repeat expansions and other FTD gene mutations in a clinical AD patient series from Mayo Clinic

por Wojtas, Aleksandra, Heggeli, Kristin A, Finch, NiCole, Baker, Matt, DeJesus-Hernandez, Mariely, Younkin, Steven G, Dickson, Dennis W, Graff-Radford, Neill R, Rademakers, Rosa
Publicado 2012

Frontotemporal dementia and parkinsonism linked to chromosome 17 - the first Polish family

por Narożańska, Ewa, Jasińska-Myga, Barbara, Sitek, Emilia J., Robowski, Piotr, Brockhuis, Bogna, Lass, Piotr, Dubaniewicz, Mirosława, Wieczorek, Dariusz, Baker, Matt, Rademakers, Rosa, Wszolek, Zbigniew K., Sławek, Jarosław
Publicado 2011

MRS in Early and Presymptomatic Carriers of a Novel Octapeptide Repeat Insertion in the Prion Protein Gene

por McDade, Eric M, Boeve, Bradley F., Fields, Julie A, Kumar, Neeraj, Rademakers, Rosa, Baker, Matt C., Knopman, David S., Petersen, Ronald C., Jack, Clifford R., Kantarci, Kejal
Publicado 2012

Clinicopathologic Correlations in a Family with a TBK1 Mutation Presenting as Primary Progressive Aphasia and Primary Lateral Sclerosis.

por Hirsch-Reinshagen, Veronica, Alfaify, Omar A., Hsiung, Ging-Yuek R., Pottier, Cyril, Baker, Matt, Perkerson, Ralph B., Rademakers, Rosa, Briemberg, Hanna, Foti, Dean J., Mackenzie, Ian R.
Publicado en Amyotroph Lateral Scler Frontotemporal Degener (2019)

Clinical and pathological features of amyotrophic lateral sclerosis caused by mutation in the C9ORF72 gene on chromosome 9p

por Stewart, Heather, Rutherford, Nicola J., Briemberg, Hannah, Krieger, Charles, Cashman, Neil, Fabros, Marife, Baker, Matt, Fok, Alice, DeJesus-Hernandez, Mariely, Eisen, Andrew, Rademakers, Rosa, Mackenzie, Ian R. A.
Publicado 2012

Frontotemporal Lobar Degeneration with TDP-43 Proteinopathy and Chromosome 9p Repeat Expansion in C9ORF72: Clinicopathologic Correlation

por Bigio, Eileen H., Weintraub, Sandra, Rademakers, Rosa, Baker, Matt, Ahmadian, Saman S., Rademaker, Alfred, Weitner, Bing Bing, Mao, Qinwen, Lee, Kyung-Hwa, Mishra, Manjari, Ganti, Rakhee A., Mesulam, M-Marsel
Publicado 2012

FDG-PET in presymptomatic C9orf72 mutation carriers

por Popuri, Karteek, Beg, Mirza Faisal, Lee, Hyunwoo, Balachandar, Rakesh, Wang, Lei, Sossi, Vesna, Jacova, Claudia, Baker, Matt, Shahinfard, Elham, Rademakers, Rosa, Mackenzie, Ian R.A., Hsiung, Ging-Yuek R.
Publicado en Neuroimage Clin (2021)

Hereditary Diffuse Leukoencephalopathy with Spheroids with Phenotype of Primary Progressive MS

por Sundal, Christina, Baker, Matt, Karrenbauer, Virginija, Gustavsen, Marte, Bedri, Sahl, Glaser, Anna, Myhr, Kjell-Morten, Haugarvoll, Kristoffer, Zetterberg, Henrik, Harbo, Hanne, Kockum, Ingrid, Hillert, Jan, Wszolek, Zbigniew, Rademakers, Rosa, Andersen, Oluf
Publicado en Eur J Neurol (2014)

De Novo Truncating FUS Gene Mutation as a Cause of Sporadic Amyotrophic Lateral Sclerosis

por DeJesus-Hernandez, Mariely, Kocerha, Jannet, Finch, NiCole, Crook, Richard, Baker, Matt, Desaro, Pamela, Johnston, Amelia, Rutherford, Nicola, Wojtas, Aleksandra, Kennelly, Kathleen, Wszolek, Zbigniew K., Graff-Radford, Neill, Boylan, Kevin, Rademakers, Rosa
Publicado 2010

A familial form of parkinsonism, dementia, and motor neuron disease: a longitudinal study

por Fujioka, Shinsuke, Boeve, Bradley F., Parisi, Joseph E., Tacik, Pawel, Aoki, Naoya, Strongosky, Audrey J., Baker, Matt, Ross, Owen A., Rademakers, Rosa, Sossi, Vesna, Dickson, Dennis W., Stoessl, A. Jon, Wszolek, Zbigniew K.
Publicado en Parkinsonism Relat Disord (2014)