Autosomal dominant cerebellar ataxia type III: a review of the phenotypic and genotypic characteristics

por Fujioka, Shinsuke, Sundal, Christina, Wszolek, Zbigniew K
Publicado 2013

Autosomal dominant cerebellar ataxia type I: A review of the phenotypic and genotypic characteristics

por Whaley, Nathaniel Robb, Fujioka, Shinsuke, Wszolek, Zbigniew K
Publicado 2011

Brain abnormalities, neurodegeneration, and dysosteosclerosis (BANDDOS): new cases, systematic literature review, and associations with CSF1R-ALSP

por Dulski, Jarosław, Souza, Josiane, Santos, Mara Lúcia, Wszolek, Zbigniew K.
Publicado 2023

Neuropsychological profile of CSF1R-related leukoencephalopathy

por Rush, Beth K., Tipton, Philip W., Strongosky, Audrey, Wszolek, Zbigniew K.
Publicado 2023

Genetic architecture of Parkinson’s disease subtypes – Review of the literature

por Dulski, Jarosław, Uitti, Ryan J., Ross, Owen A., Wszolek, Zbigniew K.
Publicado 2022

Microglial replacement therapy: a potential therapeutic strategy for incurable CSF1R-related leukoencephalopathy

por Han, Jinming, Sarlus, Heela, Wszolek, Zbigniew K., Karrenbauer, Virginija Danylaité, Harris, Robert A.
Publicado 2020

Frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17)

por Wszolek, Zbigniew K, Tsuboi, Yoshio, Ghetti, Bernardino, Pickering-Brown, Stuart, Baba, Yasuhiko, Cheshire, William P
Publicado 2006

Crohn’s and Parkinson’s Disease-Associated LRRK2 Mutations Alter Type II Interferon Responses in Human CD14(+) Blood Monocytes Ex Vivo

por Ikezu, Tsuneya, Koro, Lacin, Wolozin, Benjamin, Farraye, Francis A., Strongosky, Audrey J., Wszolek, Zbigniew K.
Publicado 2020

Inhibition of colony stimulating factor-1 receptor (CSF-1R) as a potential therapeutic strategy for neurodegenerative diseases: opportunities and challenges

por Han, Jinming, Chitu, Violeta, Stanley, E. Richard, Wszolek, Zbigniew K., Karrenbauer, Virginija Danylaité, Harris, Robert A.
Publicado 2022

Hematopoietic Stem Cell Transplantation in CSF1R-Related Leukoencephalopathy: Retrospective Study on Predictors of Outcomes

por Dulski, Jarosław, Heckman, Michael G., White, Launia J., Żur-Wyrozumska, Kamila, Lund, Troy C., Wszolek, Zbigniew K.
Publicado 2022

A patient clinically diagnosed as multiple system atrophy harboring LRRK2 p.G2019S

por Ando, Shoichiro, Konno, Takuya, Ishihara, Tomohiko, Hayashi, Hideki, Saito, Natsumi, Nishioka, Kenya, Hattori, Nobutaka, Wszolek, Zbigniew K., Onodera, Osamu
Publicado 2019

Loss of homeostatic microglial phenotype in CSF1R-related Leukoencephalopathy

por Kempthorne, Liam, Yoon, Hyejin, Madore, Charlotte, Smith, Scott, Wszolek, Zbigniew K., Rademakers, Rosa, Kim, Jungsu, Butovsky, Oleg, Dickson, Dennis W.
Publicado 2020

Correction to: Loss of homeostatic microglial phenotype in CSF1R-related Leukoencephalopathy

por Kempthorne, Liam, Yoon, Hyejin, Madore, Charlotte, Smith, Scott, Wszolek, Zbigniew K., Rademakers, Rosa, Kim, Jungsu, Butovsky, Oleg, Dickson, Dennis W.
Publicado 2020

Adult-onset leukodystrophies: a practical guide, recent treatment updates, and future directions

por Muthusamy, Karthik, Sivadasan, Ajith, Dixon, Luke, Sudhakar, Sniya, Thomas, Maya, Danda, Sumita, Wszolek, Zbigniew K., Wierenga, Klaas, Dhamija, Radhika, Gavrilova, Ralitza
Publicado 2023

Defects in Mitochondrial Biogenesis Drive Mitochondrial Alterations in PINK1-deficient Human Dopamine Neurons

por Wang, Hu, Chen, Rong, Xiao, Liming, Kumar, Manoj, Acevedo-Cintrón, Jesús, Siuda, Joanna, Koziorowski, Dariusz, Wszolek, Zbigniew K., Dawson, Valina L., Dawson, Ted M.
Publicado 2023

Neuropathologic basis of frontotemporal dementia in progressive supranuclear palsy

por Sakae, Nobutaka, Josephs, Keith A., Litvan, Irene, Murray, Melissa E., Duara, Ranjan, Uitti, Ryan J., Wszolek, Zbigniew K., Graff‐Radford, Neil R., Dickson, Dennis W.
Publicado 2019

Evaluation of the Role of SNCA Variants in Survival without Neurological Disease

por Heckman, Michael G., Soto-Ortolaza, Alexandra I., Diehl, Nancy N., Carrasquillo, Minerva M., Uitti, Ryan J., Wszolek, Zbigniew K., Graff-Radford, Neill R., Ross, Owen A.
Publicado 2012

When DLB, PD, and PSP masquerade as MSA: An autopsy study of 134 patients

por Koga, Shunsuke, Aoki, Naoya, Uitti, Ryan J., van Gerpen, Jay A., Cheshire, William P., Josephs, Keith A., Wszolek, Zbigniew K., Langston, J. William, Dickson, Dennis W.
Publicado 2015

Slowly progressive dementia caused by MAPT R406W mutations: longitudinal report on a new kindred and systematic review

por Ygland, Emil, van Westen, Danielle, Englund, Elisabet, Rademakers, Rosa, Wszolek, Zbigniew K., Nilsson, Karin, Nilsson, Christer, Landqvist Waldö, Maria, Alafuzoff, Irina, Hansson, Oskar, Gustafson, Lars, Puschmann, Andreas
Publicado 2018

Association of MAPT subhaplotypes with clinical and demographic features in Parkinson’s disease

por Deutschlander, Angela B., Konno, Takuya, Soto‐Beasley, Alexandra I., Walton, Ronald L., van Gerpen, Jay A., Uitti, Ryan J., Heckman, Michael G., Wszolek, Zbigniew K., Ross, Owen A.
Publicado 2020