Low penetrance of autosomal dominant lateral temporal epilepsy in Italian families withoutLGI1mutations

Author:

Michelucci Roberto1,Pasini Elena1,Malacrida Sandro2,Striano Pasquale3,Bonaventura Carlo Di4,Pulitano Patrizia5,Bisulli Francesca6,Egeo Gabriella4,Santulli Lia7,Sofia Vito8,Gambardella Antonio9,Elia Maurizio10,de Falco Arturo11,Neve Angela la12,Banfi Paola13,Coppola Giangennaro14,Avoni Patrizia6,Binelli Simona15,Boniver Clementina16,Pisano Tiziana17,Marchini Marco18,Dazzo Emanuela19,Fanciulli Manuela20,Bartolini Yerma1,Riguzzi Patrizia1,Volpi Lilia1,de Falco Fabrizio A.11,Giallonardo Anna Teresa4,Mecarelli Oriano5,Striano Salvatore7,Tinuper Paolo6,Nobile Carlo19

Affiliation:

1. Unit of Neurology; IRCCS Institute of Neurological Sciences of Bologna; Bellaria Hospital; Bologna Italy

2. Department of Biology; University of Padua; Padova Italy

3. Muscular and Neurodegenerative Disease Unit; Institute “G. Gaslini”; University of Genova; Genova Italy

4. Department of Neurological Sciences; University of Rome “Sapienza”; Roma Italy

5. Department of Neurology and Psychiatry; Sapienza University; Umberto 1° Hospital; Roma Italy

6. Neurological Clinic; Bellaria Hospital IRCCS Institute of Neurological Sciences of Bologna and Department of Biomedical and Neuromotor Sciences; University of Bologna; Bologna Italy

7. Department of Neurological Sciences; Federico II University; Napoli Italy

8. Department of Neurosciences; University of Catania; Catania Italy

9. Institute of Neurology; University “Magna Graecia”; Catanzaro Italy

10. Oasi Institute for Research on Mental Retardation and Brain Aging (IRCCS); Troina Italy

11. Division of Neurology New; Loreto Hospital; Napoli Italy

12. Neurology Clinic; University of Bari; Bari Italy

13. Unit of Neurology; Circolo Hospital; Varese Italy

14. Child and Adolescent Neuropsychiatry; Medical School; University of Salerno; Salerno Italy

15. C. Besta Foundation Neurological Institute; Milano Italy

16. Department of Pediatrics; Clinical Neurophysiology; Padova Italy

17. A. Meyer Children's Hospital - University of Florence, Pediatric Neurology; Firenze Italy

18. Division of Neurology; “C. Poma” Hospital; Mantova Italy

19. Section of Padua; CNR-Institute of Neurosciences; Padova Italy

20. Porto Conte Researches; Alghero Italy

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference36 articles.

1. On the use of familial aggregation in population-based case probands for calculating penetrance;Begg;J Natl Cancer Inst,2002

2. LGI1 mutations in temporal lobe epilepsies;Berkovic;Neurology,2004

3. Partial epilepsy with prominent auditory symptoms not linked to chromosome 10q;Bisulli;Epileptic Disord,2002

4. Idiopathic partial epilepsy with auditory features (IPEAF): a clinical and genetic study of 53 sporadic cases;Bisulli;Brain,2004a

5. A de novo LGI1 mutation in sporadic partial epilepsy with auditory features;Bisulli;Ann Neurol,2004b

Cited by 31 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3