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

36 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Mutations in a gene encoding a novel protein containing a phosphotyrosine-binding domain cause type 2 cerebral cavernous malformations.
Liquori CL, Berg MJ, Siegel AM, Huang E, Zawistowski JS, Stoffer T, Verlaan D, Balogun F, Hughes L, Leedom TP, Plummer NW, Cannella M, Maglione V, Squitieri F, Johnson EW, Rouleau GA, Ptacek L, Marchuk DA. Liquori CL, et al. Among authors: verlaan d. Am J Hum Genet. 2003 Dec;73(6):1459-64. doi: 10.1086/380314. Epub 2003 Nov 17. Am J Hum Genet. 2003. PMID: 14624391 Free PMC article.
Cerebral cavernous malformations: mutations in Krit1.
Verlaan DJ, Davenport WJ, Stefan H, Sure U, Siegel AM, Rouleau GA. Verlaan DJ, et al. Neurology. 2002 Mar 26;58(6):853-7. doi: 10.1212/wnl.58.6.853. Neurology. 2002. PMID: 11914398 Review.
[Familial cavernous malformations of the central nervous system. A clinical and genetic study of 15 German families].
Siegel AM, Bertalanffy H, Dichgans JJ, Elger CE, Hopf H, Hopf N, Keidel M, Kleider A, Nowak G, Pfeiffer RA, Schramm J, Spuck S, Stefan H, Sure U, Baumann CR, Rouleau GA, Verlaan DJ, Andermann E, Andermann F. Siegel AM, et al. Among authors: verlaan dj. Nervenarzt. 2005 Feb;76(2):175-80. doi: 10.1007/s00115-004-1779-3. Nervenarzt. 2005. PMID: 15702360 German.
No CCM2 mutations in a cohort of 31 sporadic cases.
Verlaan DJ, Laurent SB, Rouleau GA, Siegel AM. Verlaan DJ, et al. Neurology. 2004 Nov 23;63(10):1979. doi: 10.1212/01.wnl.0000144195.55540.9d. Neurology. 2004. PMID: 15557534 No abstract available.
36 results