Bellini G - Search Results

1

No evidence for association between dyslexia and DYX1C1 functional variants in a group of children and adolescents from Southern Italy.

Bellini G, Bravaccio C, Calamoneri F, Donatella Cocuzza M, Fiorillo P, Gagliano A, Mazzone D, del Giudice EM, Scuccimarra G, Militerni R, Pascotto A. Bellini G, et al. J Mol Neurosci. 2005;27(3):311-4. doi: 10.1385/jmn:27:3:311. J Mol Neurosci. 2005. PMID: 16280601

2

Mutational scanning of potassium, sodium and chloride ion channels in malignant migrating partial seizures in infancy.

Coppola G, Veggiotti P, Del Giudice EM, Bellini G, Longaretti F, Taglialatela M, Pascotto A. Coppola G, et al. Among authors: bellini g. Brain Dev. 2006 Mar;28(2):76-9. doi: 10.1016/j.braindev.2005.05.002. Epub 2005 Sep 15. Brain Dev. 2006. PMID: 16168594

3

A mutation (V260M) in the middle of the M2 pore-lining domain of the glycine receptor causes hereditary hyperekplexia.

del Giudice EM, Coppola G, Bellini G, Cirillo G, Scuccimarra G, Pascotto A. del Giudice EM, et al. Among authors: bellini g. Eur J Hum Genet. 2001 Nov;9(11):873-6. doi: 10.1038/sj.ejhg.5200729. Eur J Hum Genet. 2001. PMID: 11781706

4

The cannabinoid receptor type 2 Q63R variant increases the risk of celiac disease: implication for a novel molecular biomarker and future therapeutic intervention.

Rossi F, Bellini G, Tolone C, Luongo L, Mancusi S, Papparella A, Sturgeon C, Fasano A, Nobili B, Perrone L, Maione S, del Giudice EM. Rossi F, et al. Among authors: bellini g. Pharmacol Res. 2012 Jul;66(1):88-94. doi: 10.1016/j.phrs.2012.03.011. Epub 2012 Mar 24. Pharmacol Res. 2012. PMID: 22465144

5

Benign familial neonatal convulsions (BFNC) resulting from mutation of the KCNQ2 voltage sensor.

Miraglia del Giudice E, Coppola G, Scuccimarra G, Cirillo G, Bellini G, Pascotto A. Miraglia del Giudice E, et al. Among authors: bellini g. Eur J Hum Genet. 2000 Dec;8(12):994-7. doi: 10.1038/sj.ejhg.5200570. Eur J Hum Genet. 2000. PMID: 11175290

6

Neutralization of a unique, negatively-charged residue in the voltage sensor of K V 7.2 subunits in a sporadic case of benign familial neonatal seizures.

Miceli F, Soldovieri MV, Lugli L, Bellini G, Ambrosino P, Migliore M, del Giudice EM, Ferrari F, Pascotto A, Taglialatela M. Miceli F, et al. Among authors: bellini g. Neurobiol Dis. 2009 Jun;34(3):501-10. doi: 10.1016/j.nbd.2009.03.009. Epub 2009 Apr 1. Neurobiol Dis. 2009. PMID: 19344764

7

A novel hyperekplexia-causing mutation in the pre-transmembrane segment 1 of the human glycine receptor alpha1 subunit reduces membrane expression and impairs gating by agonists.

Castaldo P, Stefanoni P, Miceli F, Coppola G, Del Giudice EM, Bellini G, Pascotto A, Trudell JR, Harrison NL, Annunziato L, Taglialatela M. Castaldo P, et al. Among authors: bellini g. J Biol Chem. 2004 Jun 11;279(24):25598-604. doi: 10.1074/jbc.M311021200. Epub 2004 Apr 5. J Biol Chem. 2004. PMID: 15066993 Free article.

8

Familial occurrence of early-onset childhood absence epilepsy.

Titomanlio L, Romano A, Bellini G, Pascotto A, Iuliano R, Miraglia Del Giudice E, Del Giudice E. Titomanlio L, et al. Among authors: bellini g. Eur J Paediatr Neurol. 2007 May;11(3):178-80. doi: 10.1016/j.ejpn.2006.12.005. Epub 2007 Jan 30. Eur J Paediatr Neurol. 2007. PMID: 17267250

9

Atypical gating of M-type potassium channels conferred by mutations in uncharged residues in the S4 region of KCNQ2 causing benign familial neonatal convulsions.

Soldovieri MV, Cilio MR, Miceli F, Bellini G, Miraglia del Giudice E, Castaldo P, Hernandez CC, Shapiro MS, Pascotto A, Annunziato L, Taglialatela M. Soldovieri MV, et al. Among authors: bellini g. J Neurosci. 2007 May 2;27(18):4919-28. doi: 10.1523/JNEUROSCI.0580-07.2007. J Neurosci. 2007. PMID: 17475800 Free PMC article.

10

Correlating the clinical and genetic features of benign familial neonatal seizures (BFNS) with the functional consequences of underlying mutations.

Soldovieri MV, Miceli F, Bellini G, Coppola G, Pascotto A, Taglialatela M. Soldovieri MV, et al. Among authors: bellini g. Channels (Austin). 2007 Jul-Aug;1(4):228-33. doi: 10.4161/chan.4823. Epub 2007 Aug 2. Channels (Austin). 2007. PMID: 18698150 Free article.

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