Genetic testing in benign familial epilepsies of the first year of life: Clinical and diagnostic significance-Reference-Cited by-同舟云学术

Genetic testing in benign familial epilepsies of the first year of life: Clinical and diagnostic significance

Published:2013-01-29 Issue:3 Volume:54 Page:425-436
ISSN:0013-9580
Container-title:Epilepsia
language:en
Short-container-title:Epilepsia

Author:

Zara Federico¹,Specchio Nicola²,Striano Pasquale,Robbiano Angela¹,Gennaro Elena³,Paravidino Roberta¹,Vanni Nicola¹,Beccaria Francesca⁴,Capovilla Giuseppe⁴,Bianchi Amedeo⁵,Caffi Lorella⁶,Cardilli Viviana⁷,Darra Francesca⁸,Bernardina Bernardo Dalla⁸,Fusco Lucia²,Gaggero Roberto⁹,Giordano Lucio¹⁰,Guerrini Renzo¹¹,Incorpora Gemma¹²,Mastrangelo Massimo¹³,Spaccini Luigina¹³,Laverda Anna Maria¹⁴,Vecchi Marilena¹⁴,Vanadia Francesca¹⁵,Veggiotti Pierangelo¹⁶,Viri Maurizio¹⁷,Occhi Guya¹⁸,Budetta Mauro¹⁹,Taglialatela Maurizio²⁰,Coviello Domenico A.³,Vigevano Federico²,Minetti Carlo

Affiliation:

1. Laboratory of Neurogenetics; Department of Neuroscience; Istituto ‘G. Gaslini’; Genova; Italy

2. Unit of Neurology; Children Hospital “Bambino Gesù”; Roma; Italy

3. Laboratory of Genetics; Hospital Galliera; Genova; Italy

4. Unit of Child Neuropsychiatry; C. Poma Hospital; Mantova; Italy

5. Division of Neurology; Hospital “S. Donato”; Arezzo; Italy

6. Unit of Child Neuropsychiatry; Hospital “Ospedali Riuniti”; Bergamo; Italy

7. Unit of Neonatology; University Hospital “Umberto I”; Roma; Italy

8. Unit of Child Neuropsychiatry; University of Verona; Verona; Italy

9. Unit of Child Neuropsychiatry; ASL2; Savona; Italy

10. Unit of Child Neuropsychiatry; Hospital “Civile”; Brescia; Italy

11. Pediatric Neurology; Hospital A. Meyer; University of Firenze; Firenze; Italy

12. Unit of Pediatrics; Hospital “Civile” Ragusa; Italy

13. Children Hospital “Vittore Buzzi”; Milano; Italy

14. Department of Pediatrics; University Hospital of Padova; Italy

15. Division of Child Neuropsychiatry; Hospital “Civico e Benfratelli”; Palermo; Italy

16. National Neurologic Institute “C. Mondino”; Child Neuropsychiatry Unit; University of Pavia; Pavia; Italy

17. Center for Child Epilepsy; Hospital “Fatebenefratelli e Oftalmico”; Milano; Italy

18. Hospital “Desenzano del Garda”; Desenzano del Garda; Italy

19. Unit of Paediatric Neurology; Hospital “S. Maria Incoronata Dell'Olmo”; Cava de' Tirreni; Italy

20. Department of Health Science; University of Molise; Campobasso; Italy

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/epi.12089/fullpdf

Reference27 articles.

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2. A potassium channel mutation in neonatal human epilepsy;Biervert;Science,1998

3. A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family;Charlier;Nat Genet,1998

4. A novel KCNQ2 K+ channel mutation in benign neonatal convulsions and centrotemporal spikes;Coppola;Neurology,2003

5. Genetics of epilepsy syndromes starting in the first year of life;Deprez;Neurology,2009

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