Hypertrophic olivary degeneration: A clinico-radiologic study

由 Konno, Takuya, Broderick, Daniel F., Tacik, Pawel, Caviness, John N., Wszolek, Zbigniew K.
發表在 Parkinsonism Relat Disord (2016)

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

由 Wider, Christian, Dickson, Dennis W., Schweitzer, Katherine J., Broderick, Daniel F., Wszolek, Zbigniew K.
出版 2009

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

由 Tipton, Philip W., Konno, Takuya, Broderick, Daniel F., Dickson, Dennis W., Wszolek, Zbigniew K.
發表在 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...

由 Fujioka, Shinsuke, Broderick, Daniel F., Sundal, Christina, Baker, Matthew C., Rademakers, Rosa, Wszolek, Zbigniew K.
出版 2013

Acquisition of Apoptotic Resistance in Cadmium-Transformed Human Prostate Epithelial Cells: Bcl-2 Overexpression Blocks the Activation of JNK Signal Transduction Pathway

由 Qu, Wei, Ke, Hengning, Pi, Jingbo, Broderick, Daniel, French, John E., Webber, Mukta M., Waalkes, Michael P.
出版 2007

Hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS): a misdiagnosed disease entity

由 Sundal, Christina, Lash, Jennifer, Aasly, Jan, ygarden, Sarka Ø, Roeber, Sigrun, Kretzschman, Hans, Garbern, James Y., Tselis, Alex, Rademakers, Rosa, Dickson, Dennis W., Broderick, Daniel, Wszolek, Zbigniew K.
出版 2011

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

由 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.
發表在 Mayo Clin Proc (2015)

Characterization of a Pathogenic Variant in the ABCD1 Gene Through Protein Molecular Modeling

由 Richter Jr., John E., Vadlamudi, Charitha, Macklin, Sarah K., Samreen, Ayesha, Helmi, Haytham, Broderick, Daniel, Mohammad, Ahmed N., Hines, Stephanie L., VanGerpen, Jay A., Atwal, Paldeep S., Caulfield, Thomas R.
發表在 Case Rep Genet (2020)

A novel de novo pathogenic mutation in CACNA1A gene

由 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.
出版 2012

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

由 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.
出版 2013

SLC20A2 and THAP1 deletion in familial basal ganglia calcification with dystonia

由 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
出版 2013

MRI characteristics and scoring in HDLS due to CSF1R gene mutations

由 Sundal, Christina, Van Gerpen, Jay A., Nicholson, Alexandra M., Wider, Christian, Shuster, Elizabeth A., Aasly, Jan, Spina, Salvatore, Ghetti, Bernardino, Roeber, Sigrun, Garbern, James, Borjesson-Hanson, Anne, Tselis, Alex, Swerdlow, Russell H., Miller, Bradley B., Fujioka, Shinsuke, Heckman, Michael G., Uitti, Ryan J., Josephs, Keith A., Baker, Matt, Andersen, Oluf, Rademakers, Rosa, Dickson, Dennis W., Broderick, Daniel, Wszolek, Zbigniew K.
出版 2012

Parkinsonian features in hereditary diffuse leukoencephalopathy with spheroids (HDLS) and CSF1R mutations

由 Sundal, Christina, Fujioka, Shinsuke, Van Gerpen, Jay A., Wider, Christian, Nicholson, Alexandra M., Baker, Matt, Shuster, Elizabeth A., Aasly, Jan, Spina, Salvatore, Ghetti, Bernardino, Roeber, Sigrun, Garbern, James, Tselis, Alex, Swerdlow, Russell H., Miller, Bradley B., Borjesson-Hanson, Anne, Uitti, Ryan J., Ross, Owen, Stoessl, John A., Rademakers, Rosa, Josephs, Keith A., Dickson, Dennis W., Broderick, Daniel, Wszolek, Zbigniew K.
出版 2013

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

由 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.
出版 2011