Hypertrophic olivary degeneration: A clinico-radiologic study

Por Konno, Takuya, Broderick, Daniel F., Tacik, Pawel, Caviness, John N., Wszolek, Zbigniew K.
Publicado no Parkinsonism Relat Disord (2016)

Familial idiopathic basal ganglia calcification: a challenging clinical-pathological correlation

Por Wider, Christian, Dickson, Dennis W., Schweitzer, Katherine J., Broderick, Daniel F., Wszolek, Zbigniew K.
Publicado em 2009

Cerebral Peduncle Angle: Unreliable in Differentiating Progressive Supranuclear Palsy From Other Neurodegenerative Diseases

Por Tipton, Philip W., Konno, Takuya, Broderick, Daniel F., Dickson, Dennis W., Wszolek, Zbigniew K.
Publicado no Parkinsonism Relat Disord (2016)

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...

Por Fujioka, Shinsuke, Broderick, Daniel F., Sundal, Christina, Baker, Matthew C., Rademakers, Rosa, Wszolek, Zbigniew K.
Publicado em 2013

Whole-exome sequencing as a diagnostic tool in a family with episodic ataxia type 1

Por Tacik, Pawel, Guthrie, Kimberly J., Strongosky, Audrey J., Broderick, Daniel F., Riegert-Johnson, Douglas L., Tang, Sha, El-Khechen, Dima, Parker, Alexander S., Ross, Owen A., Wszolek, Zbigniew K.
Publicado no Mayo Clin Proc (2015)

A novel de novo pathogenic mutation in CACNA1A gene

Por Fujioka, Shinsuke, Rayaprolu, Sruti, Sundal, Christina, Broderick, Daniel F., Langley, William A., Shoffner, John, Hyams, Lauren C., Rademakers, Rosa, Graff-Radford, Neill R., Tatum, William, Ross, Owen A., Wszolek, Zbigniew K.
Publicado em 2012

Clinicopathologic variability of the GRN A9D mutation, including amyotrophic lateral sclerosis

Por Cannon, Ashley, Fujioka, Shinsuke, Rutherford, Nicola J., Ferman, Tanis J., Broderick, Daniel F., Boylan, Kevin B., Graff-Radford, Neill R., Uitti, Ryan J., Rademakers, Rosa, Wszolek, Zbigniew K., Dickson, Dennis W.
Publicado em 2013

SLC20A2 and THAP1 deletion in familial basal ganglia calcification with dystonia

Por Baker, Matt, Strongosky, Audrey J., Sanchez-Contreras, Monica Y., Yang, Shan, Ferguson, Will, Calne, Donald B., Calne, Susan, Stoessl, A. Jon, Allanson, Judith E., Broderick, Daniel F., Hutton, Michael L., Dickson, Dennis W., Ross, Owen A., Wszolek, Zbigniew K., Rademakers, Rosa
Publicado em 2013

Mutations in the colony stimulating factor 1 receptor (CSF1R) cause hereditary diffuse leukoencephalopathy with spheroids

Por Rademakers, Rosa, Baker, Matt, Nicholson, Alexandra M., Rutherford, Nicola J., Finch, NiCole, Soto-Ortolaza, Alexandra, Lash, Jennifer, Wider, Christian, Wojtas, Aleksandra, DeJesus-Hernandez, Mariely, Adamson, Jennifer, Kouri, Naomi, Sundal, Christina, Shuster, Elizabeth A., Aasly, Jan, MacKenzie, James, Roeber, Sigrun, Kretzschmar, Hans A., Boeve, Bradley F., Knopman, David S., Petersen, Ronald C., Cairns, Nigel J., Ghetti, Bernardino, Spina, Salvatore, Garbern, James, Tselis, Alexandros C., Uitti, Ryan, Das, Pritam, Van Gerpen, Jay A., Meschia, James F., Levy, Shawn, Broderick, Daniel F., Graff-Radford, Neill, Ross, Owen A., Miller, Bradley B., Swerdlow, Russell H., Dickson, Dennis W., Wszolek, Zbigniew K.
Publicado em 2011