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1.

Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies.

Haug, Karsten; Warnstedt, Maike; Alekov, Alexi K; Sander, Thomas; Ramírez, Alfredo; Poser, Barbara; Maljevic, Snezana; Hebeisen, Simon; Kubisch, Christian; Rebstock, Johannes; Horvath, Steve; Hallmann, Kerstin; Dullinger, Joern S; Rau, Birgit; Haverkamp, Fritz; Beyenburg, Stefan; Schulz, Herbert; Janz, Dieter; Giese, Bernd; Müller-Newen, Gerhard; Propping, Peter; Elger, Christian E; Fahlke, Christoph; Lerche, Holger; Heils, Armin.

Nat Genet ; 33(4): 527-32, 2003 Apr.

Artículo en Inglés | MEDLINE | ID: mdl-12612585

2.

Linkage and association analysis of CACNG3 in childhood absence epilepsy.

Everett, Kate V; Chioza, Barry; Aicardi, Jean; Aschauer, Harald; Brouwer, Oebele; Callenbach, Petra; Covanis, Athanasios; Dulac, Olivier; Eeg-Olofsson, Orvar; Feucht, Martha; Friis, Mogens; Goutieres, Françoise; Guerrini, Renzo; Heils, Armin; Kjeldsen, Marianne; Lehesjoki, Anna-Elina; Makoff, Andrew; Nabbout, Rima; Olsson, Ingrid; Sander, Thomas; Sirén, Auli; McKeigue, Paul; Robinson, Robert; Taske, Nichole; Rees, Michele; Gardiner, Mark.

Eur J Hum Genet ; 15(4): 463-72, 2007 Apr.

Artículo en Inglés | MEDLINE | ID: mdl-17264864

3.

Lack of evidence of an allelic association of a functional GABRB3 exon 1a promoter polymorphism with idiopathic generalized epilepsy.

Hempelmann, Anne; Cobilanschi, Joana; Heils, Armin; Muhle, Hiltrud; Stephani, Ulrich; Weber, Yvonne; Lerche, Holger; Sander, Thomas.

Epilepsy Res ; 74(1): 28-32, 2007 Apr.

Artículo en Inglés | MEDLINE | ID: mdl-17215107

4.

Linkage and mutational analysis of CLCN2 in childhood absence epilepsy.

Everett, Kate; Chioza, Barry; Aicardi, Jean; Aschauer, Harald; Brouwer, Oebele; Callenbach, Petra; Covanis, Athanasios; Dooley, Joseph; Dulac, Olivier; Durner, Martina; Eeg-Olofsson, Orvar; Feucht, Martha; Friis, Mogens; Guerrini, Renzo; Heils, Armin; Kjeldsen, Marianne; Nabbout, Rima; Sander, Thomas; Wirrell, Elaine; McKeigue, Paul; Robinson, Robert; Taske, Nichole; Gardiner, Mark.

Epilepsy Res ; 75(2-3): 145-53, 2007 Jul.

Artículo en Inglés | MEDLINE | ID: mdl-17580110

5.

Candidate gene analysis of the succinic semialdehyde dehydrogenase gene (ALDH5A1) in patients with idiopathic generalized epilepsy and photosensitivity.

Lorenz, Susanne; Heils, Armin; Taylor, Kirsten P; Gehrmann, Anne; Muhle, Hiltrud; Gresch, Meike; Becker, Tim; Tauer, Ulrike; Stephani, Ulrich; Sander, Thomas.

Neurosci Lett ; 397(3): 234-9, 2006 Apr 24.

Artículo en Inglés | MEDLINE | ID: mdl-16406321

6.

Confirmatory evidence for an association of the connexin-36 gene with juvenile myoclonic epilepsy.

Hempelmann, Anne; Heils, Armin; Sander, Thomas.

Epilepsy Res ; 71(2-3): 223-8, 2006 Oct.

Artículo en Inglés | MEDLINE | ID: mdl-16876983

7.

Evaluation of CACNA1H in European patients with childhood absence epilepsy.

Chioza, Barry; Everett, Kate; Aschauer, Harald; Brouwer, Oebele; Callenbach, Petra; Covanis, Athanasios; Dulac, Olivier; Durner, Martina; Eeg-Olofsson, Orvar; Feucht, Martha; Friis, Mogens; Heils, Armin; Kjeldsen, Marianne; Larsson, Katrin; Lehesjoki, Anna-Elina; Nabbout, Rima; Olsson, Ingrid; Sander, Thomas; Sirén, Auli; Robinson, Robert; Rees, Michele; Gardiner, R Mark.

Epilepsy Res ; 69(2): 177-81, 2006 May.

Artículo en Inglés | MEDLINE | ID: mdl-16504478

8.

Association analysis of the Arg220His variation of the human gene encoding the GABA delta subunit with idiopathic generalized epilepsy.

Lenzen, Kirsten P; Heils, Armin; Lorenz, Susanne; Hempelmann, Anne; Sander, Thomas.

Epilepsy Res ; 65(1-2): 53-7, 2005 Jun.

Artículo en Inglés | MEDLINE | ID: mdl-16023832

9.

A new EF-hand containing gene EFHC2 on Xp11.4: tentative evidence for association with juvenile myoclonic epilepsy.

Gu, Wenli; Sander, Thomas; Heils, Armin; Lenzen, Kirsten P; Steinlein, Ortrud K.

Epilepsy Res ; 66(1-3): 91-8, 2005.

Artículo en Inglés | MEDLINE | ID: mdl-16112844

10.

A splice-site mutation in GABRG2 associated with childhood absence epilepsy and febrile convulsions.

Kananura, Colette; Haug, Karsten; Sander, Thomas; Runge, Uwe; Gu, Wenli; Hallmann, Kerstin; Rebstock, Johannes; Heils, Armin; Steinlein, Ortrud K.

Arch Neurol ; 59(7): 1137-41, 2002 Jul.

Artículo en Inglés | MEDLINE | ID: mdl-12117362

11.

Serotonergic gene transcriptional control regions: targets for antidepressant drug development?

Lesch, Klaus Peter; Heils, Armin.

Int J Neuropsychopharmacol ; 3(1): 67-79, 2000 Mar.

Artículo en Inglés | MEDLINE | ID: mdl-11343581

12.

Association analysis between the human interleukin 1beta (-511) gene polymorphism and susceptibility to febrile convulsions.

Tilgen, Nikola; Pfeiffer, Heike; Cobilanschi, Joana; Rau, Birgit; Horvath, Steve; Elger, Christian E; Propping, Peter; Heils, Armin.

Neurosci Lett ; 334(1): 68-70, 2002 Dec 06.

Artículo en Inglés | MEDLINE | ID: mdl-12431777

13.

Failure to replicate an allelic association between an exon 8 polymorphism of the human alpha(1A) calcium channel gene and common syndromes of idiopathic generalized epilepsy.

Sander, Thomas; Toliat, Mohammad R; Heils, Armin; Becker, Christian; Nürnberg, Peter.

Epilepsy Res ; 49(2): 173-7, 2002 Apr.

Artículo en Inglés | MEDLINE | ID: mdl-12049805

14.

Association of the 867Asp variant of the human anion exchanger 3 gene with common subtypes of idiopathic generalized epilepsy.

Sander, Thomas; Toliat, Mohammad Reza; Heils, Armin; Leschik, Gundula; Becker, Christian; Rüschendorf, Franz; Rohde, Klaus; Mundlos, Stefan; Nürnberg, Peter.

Epilepsy Res ; 51(3): 249-55, 2002 Oct.

Artículo en Inglés | MEDLINE | ID: mdl-12399075

15.

Linkage analysis between childhood absence epilepsy and genes encoding GABAA and GABAB receptors, voltage-dependent calcium channels, and the ECA1 region on chromosome 8q.

Robinson, Robert; Taske, Nichole; Sander, Thomas; Heils, Armin; Whitehouse, William; Goutières, Françoise; Aicardi, Jean; Lehesjoki, Anna Elina; Siren, Auli; Laue Friis, Mogens; Kjeldsen, Marianne Juel; Panayiotopoulos, Chrysostomos; Kennedy, Colin; Ferrie, Colin; Rees, Michele; Gardiner, R Mark.

Epilepsy Res ; 48(3): 169-79, 2002 Feb.

Artículo en Inglés | MEDLINE | ID: mdl-11904235

16.

CLCN2 and idiopathic generalized epilepsy.

Heils, Armin.

Adv Neurol ; 95: 265-71, 2005.

Artículo en Inglés | MEDLINE | ID: mdl-15508929

17.

Allelic association of a truncation mutation of the KCNMB3 gene with idiopathic generalized epilepsy.

Lorenz, Susanne; Heils, Armin; Kasper, Johannes M; Sander, Thomas.

Am J Med Genet B Neuropsychiatr Genet ; 144B(1): 10-3, 2007 Jan 05.

Artículo en Inglés | MEDLINE | ID: mdl-16958040

18.

A multicenter study of BRD2 as a risk factor for juvenile myoclonic epilepsy.

Cavalleri, Gianpiero L; Walley, Nicole M; Soranzo, Nicole; Mulley, John; Doherty, Colin P; Kapoor, Ashish; Depondt, Chantal; Lynch, John M; Scheffer, Ingrid E; Heils, Armin; Gehrmann, Anne; Kinirons, Peter; Gandhi, Sonia; Satishchandra, Parthasarathy; Wood, Nicholas W; Anand, Anuranjan; Sander, Thomas; Berkovic, Samuel F; Delanty, Norman; Goldstein, David B; Sisodiya, Sanjay M.

Epilepsia ; 48(4): 706-12, 2007 Apr.

Artículo en Inglés | MEDLINE | ID: mdl-17437413

19.

A mutation in the GABA(A) receptor alpha(1)-subunit is associated with absence epilepsy.

Maljevic, Snezana; Krampfl, Klaus; Cobilanschi, Joana; Tilgen, Nikola; Beyer, Susanne; Weber, Yvonne G; Schlesinger, Friedrich; Ursu, Daniel; Melzer, Werner; Cossette, Patrick; Bufler, Johannes; Lerche, Holger; Heils, Armin.

Ann Neurol ; 59(6): 983-7, 2006 Jun.

Artículo en Inglés | MEDLINE | ID: mdl-16718694

20.

Exploration of the genetic architecture of idiopathic generalized epilepsies.

Hempelmann, Anne; Taylor, Kirsten P; Heils, Armin; Lorenz, Susanne; Prud'homme, Jean-Francois; Nabbout, Rima; Dulac, Olivier; Rudolf, Gabrielle; Zara, Federico; Bianchi, Amedeo; Robinson, Robert; Gardiner, R Mark; Covanis, Athanasios; Lindhout, Dick; Stephani, Ulrich; Elger, Christian E; Weber, Yvonne G; Lerche, Holger; Nürnberg, Peter; Kron, Katherine L; Scheffer, Ingrid E; Mulley, John C; Berkovic, Samuel F; Sander, Thomas.

Epilepsia ; 47(10): 1682-90, 2006 Oct.

Artículo en Inglés | MEDLINE | ID: mdl-17054691

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