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 Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

1,187 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Correction: The effect of NOTCH3 pathogenic variant position on CADASIL disease severity: NOTCH3 EGFr 1-6 pathogenic variant are associated with a more severe phenotype and lower survival compared with EGFr 7-34 pathogenic variant.
Rutten JW, Van Eijsden BJ, Duering M, Jouvent E, Opherk C, Pantoni L, Federico A, Dichgans M, Markus HS, Chabriat H, Oberstein SAJL. Rutten JW, et al. Among authors: federico a. Genet Med. 2019 Aug;21(8):1895. doi: 10.1038/s41436-018-0306-z. Genet Med. 2019. PMID: 30237574 Free PMC article.
The effect of NOTCH3 pathogenic variant position on CADASIL disease severity: NOTCH3 EGFr 1-6 pathogenic variant are associated with a more severe phenotype and lower survival compared with EGFr 7-34 pathogenic variant.
Rutten JW, Van Eijsden BJ, Duering M, Jouvent E, Opherk C, Pantoni L, Federico A, Dichgans M, Markus HS, Chabriat H, Lesnik Oberstein SAJ. Rutten JW, et al. Among authors: federico a. Genet Med. 2019 Mar;21(3):676-682. doi: 10.1038/s41436-018-0088-3. Epub 2018 Jul 22. Genet Med. 2019. PMID: 30032161 Free PMC article.
Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) as a model of small vessel disease: update on clinical, diagnostic, and management aspects.
Di Donato I, Bianchi S, De Stefano N, Dichgans M, Dotti MT, Duering M, Jouvent E, Korczyn AD, Lesnik-Oberstein SA, Malandrini A, Markus HS, Pantoni L, Penco S, Rufa A, Sinanović O, Stojanov D, Federico A. Di Donato I, et al. Among authors: federico a. BMC Med. 2017 Feb 24;15(1):41. doi: 10.1186/s12916-017-0778-8. BMC Med. 2017. PMID: 28231783 Free PMC article. Review.
Genome-wide genotyping demonstrates a polygenic risk score associated with white matter hyperintensity volume in CADASIL.
Opherk C, Gonik M, Duering M, Malik R, Jouvent E, Hervé D, Adib-Samii P, Bevan S, Pianese L, Silvestri S, Dotti MT, De Stefano N, Liem M, Boon EM, Pescini F, Pachai C, Bracoud L, Müller-Myhsok B, Meitinger T, Rost N, Pantoni L, Lesnik Oberstein S, Federico A, Ragno M, Markus HS, Tournier-Lasserve E, Rosand J, Chabriat H, Dichgans M. Opherk C, et al. Among authors: federico a. Stroke. 2014 Apr;45(4):968-72. doi: 10.1161/STROKEAHA.113.004461. Epub 2014 Feb 27. Stroke. 2014. PMID: 24578207 Free article.
Gene symbol: Notch3. Disease: CADASIL.
Bianchi S, Scali O, Dotti MT, Pantoni L, Parnetti L, Inzitari D, Federico A. Bianchi S, et al. Among authors: federico a. Hum Genet. 2005 Dec;118(3-4):546. Hum Genet. 2005. PMID: 16521299 No abstract available.
Correction to: Heritable and non-heritable uncommon causes of stroke.
Bersano A, Kraemer M, Burlina A, Mancuso M, Finsterer J, Sacco S, Salvarani C, Caputi L, Chabriat H, Oberstein SL, Federico A, Tournier-Lasserve E, Hunt D, Dichgans M, Arnold M, Debette S, Markus HS. Bersano A, et al. Among authors: federico a. J Neurol. 2021 Aug;268(8):2808-2809. doi: 10.1007/s00415-020-09948-4. J Neurol. 2021. PMID: 32556534 No abstract available.
APOE ɛ2 is associated with white matter hyperintensity volume in CADASIL.
Gesierich B, Opherk C, Rosand J, Gonik M, Malik R, Jouvent E, Hervé D, Adib-Samii P, Bevan S, Pianese L, Silvestri S, Dotti MT, De Stefano N, van der Grond J, Boon EM, Pescini F, Rost N, Pantoni L, Oberstein SA, Federico A, Ragno M, Markus HS, Tournier-Lasserve E, Chabriat H, Dichgans M, Duering M, Ewers M. Gesierich B, et al. Among authors: federico a. J Cereb Blood Flow Metab. 2016 Jan;36(1):199-203. doi: 10.1038/jcbfm.2015.85. J Cereb Blood Flow Metab. 2016. PMID: 25920955 Free PMC article.
Gene symbol: NOTCH3. Disease: CADASIL.
Bianchi S, Scali O, Dotti MT, Pantoni L, Parnetti L, Inzitari D, Federico A. Bianchi S, et al. Among authors: federico a. Hum Genet. 2005 Dec;118(3-4):534. Hum Genet. 2005. PMID: 16521241 No abstract available.
Gene symbol: NOTCH3. Disease: CADASIL.
Bianchi S, Scali O, Dotti MT, Pantoni L, Parnetti L, Inzitari D, Federico A. Bianchi S, et al. Among authors: federico a. Hum Genet. 2005 Dec;118(3-4):535. Hum Genet. 2005. PMID: 16521242 No abstract available.
1,187 results