Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

98 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Spinocerebellar Ataxia Type 1 Characteristics in Patient-Derived Fibroblast and iPSC-Derived Neuronal Cultures.
Buijsen RAM, Hu M, Sáez-González M, Notopoulou S, Mina E, Koning W, Gardiner SL, van der Graaf LM, Daoutsali E, Pepers BA, Mei H, van Dis V, Frimat JP, van den Maagdenberg AMJM, Petrakis S, van Roon-Mom WMC. Buijsen RAM, et al. Among authors: van roon mom wmc. Mov Disord. 2023 Aug;38(8):1428-1442. doi: 10.1002/mds.29446. Epub 2023 Jun 6. Mov Disord. 2023. PMID: 37278528
Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment.
Roux T, Barbier M, Papin M, Davoine CS, Sayah S, Coarelli G, Charles P, Marelli C, Parodi L, Tranchant C, Goizet C, Klebe S, Lohmann E, Van Maldergem L, van Broeckhoven C, Coutelier M, Tesson C, Stevanin G, Duyckaerts C, Brice A, Durr A; SPATAX network. Roux T, et al. Genet Med. 2020 Nov;22(11):1851-1862. doi: 10.1038/s41436-020-0899-x. Epub 2020 Jul 27. Genet Med. 2020. PMID: 32713943 Free article.
TATA-binding protein in neurodegenerative disease.
van Roon-Mom WM, Reid SJ, Faull RL, Snell RG. van Roon-Mom WM, et al. Neuroscience. 2005;133(4):863-72. doi: 10.1016/j.neuroscience.2005.03.024. Neuroscience. 2005. PMID: 15916858 Review.
Amyloid-like inclusions in Huntington's disease.
McGowan DP, van Roon-Mom W, Holloway H, Bates GP, Mangiarini L, Cooper GJ, Faull RL, Snell RG. McGowan DP, et al. Neuroscience. 2000;100(4):677-80. doi: 10.1016/s0306-4522(00)00391-2. Neuroscience. 2000. PMID: 11036200
Human neuroblasts migrate to the olfactory bulb via a lateral ventricular extension.
Curtis MA, Kam M, Nannmark U, Anderson MF, Axell MZ, Wikkelso C, Holtås S, van Roon-Mom WM, Björk-Eriksson T, Nordborg C, Frisén J, Dragunow M, Faull RL, Eriksson PS. Curtis MA, et al. Science. 2007 Mar 2;315(5816):1243-9. doi: 10.1126/science.1136281. Epub 2007 Feb 15. Science. 2007. PMID: 17303719
Striosomes and mood dysfunction in Huntington's disease.
Tippett LJ, Waldvogel HJ, Thomas SJ, Hogg VM, van Roon-Mom W, Synek BJ, Graybiel AM, Faull RL. Tippett LJ, et al. Brain. 2007 Jan;130(Pt 1):206-21. doi: 10.1093/brain/awl243. Epub 2006 Oct 12. Brain. 2007. PMID: 17040921 Clinical Trial.
98 results