Literature DB >> 9853443

Anticipation in familial cavernous angioma: a study of 52 families from International Familial Cavernous Angioma Study. IFCAS Group.

A M Siegel, E Andermann, A Badhwar, G A Rouleau, G L Wolford, F Andermann, K Hess.   

Abstract

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Year:  1998        PMID： 9853443     DOI： 10.1016/s0140-6736(05)61447-x

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


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  10 in total

Review 1.  Familial occurrence of brain arteriovenous malformations: a systematic review.

Authors:  J van Beijnum; H B van der Worp; H M Schippers; O van Nieuwenhuizen; L J Kappelle; G J E Rinkel; J W Berkelbach van der Sprenkel; C J M Klijn
Journal:  J Neurol Neurosurg Psychiatry       Date:  2007-01-26       Impact factor: 10.154

Review 2.  Cerebrovascular disorders associated with genetic lesions.

Authors:  Philipp Karschnia; Sayoko Nishimura; Angeliki Louvi
Journal:  Cell Mol Life Sci       Date:  2018-10-16       Impact factor: 9.261

Review 3.  Cerebral Cavernous Malformations: An Update on Prevalence, Molecular Genetic Analyses, and Genetic Counselling.

Authors:  Stefanie Spiegler; Matthias Rath; Christin Paperlein; Ute Felbor
Journal:  Mol Syndromol       Date:  2018-01-25

4.  A Novel CCM1/KRIT1 Heterozygous Nonsense Mutation (c.1864C>T) Associated with Familial Cerebral Cavernous Malformation: a Genetic Insight from an 8-Year Continuous Observational Study.

Authors:  Chenlong Yang; Van Halm-Lutterodt Nicholas; Jizong Zhao; Bingquan Wu; Haohao Zhong; Yan Li; Yulun Xu
Journal:  J Mol Neurosci       Date:  2017-03-02       Impact factor: 3.444

5.  [Familial cavernous malformations of the central nervous system. A clinical and genetic study of 15 German families].

Authors:  A M Siegel; H Bertalanffy; J J Dichgans; C E Elger; H Hopf; N Hopf; M Keidel; A Kleider; G Nowak; R A Pfeiffer; J Schramm; S Spuck; H Stefan; U Sure; C R Baumann; G A Rouleau; D J Verlaan; E Andermann; F Andermann
Journal:  Nervenarzt       Date:  2005-02       Impact factor: 1.214

6.  Inherited cavernous malformations of the central nervous system: clinical and genetic features in 19 Swiss families.

Authors:  C Graeni; F Stepper; M Sturzenegger; A Merlo; D J Verlaan; F Andermann; C R Baumann; F Bonassin; D Georgiadis; R W Baumgartner; G A Rouleau; A M Siegel
Journal:  Neurosurg Rev       Date:  2009-09-17       Impact factor: 3.042

7.  Small deletion at the 7q21.2 locus in a CCM family detected by real-time quantitative PCR.

Authors:  Lucia Anna Muscarella; Vito Guarnieri; Michelina Coco; Serena Belli; Paola Parrella; Giuseppe Pulcrano; Domenico Catapano; Vincenzo A D'Angelo; Leopoldo Zelante; Leonardo D'Agruma
Journal:  J Biomed Biotechnol       Date:  2010-07-27

8.  Factors associated with epileptic seizure of cavernous malformations in the central nervous system in West China.

Authors:  Cheng Huang; Ming-Wan Chen; Yang Si; Jin-Mei Li; Dong Zhou
Journal:  Pak J Med Sci       Date:  2013-09       Impact factor: 1.088

9.  Familial Multiple Cavernous Malformation Syndrome: MR Features in This Uncommon but Silent Threat.

Authors:  Marc Mespreuve; Filip Vanhoenacker; Marc Lemmerling
Journal:  J Belg Soc Radiol       Date:  2016-03-21       Impact factor: 1.894

10.  KRIT1 Gene in Patients with Cerebral Cavernous Malformations: Clinical Features and Molecular Characterization of Novel Variants.

Authors:  Claudia Ricci; Alfonso Cerase; Giulia Riolo; Giuditta Manasse; Stefania Battistini
Journal:  J Mol Neurosci       Date:  2021-03-02       Impact factor: 3.444
  10 in total

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