Combi R - Search Results

1

Autosomal dominant nocturnal frontal lobe epilepsy--a critical overview.

Combi R, Dalprà L, Tenchini ML, Ferini-Strambi L. Combi R, et al. J Neurol. 2004 Aug;251(8):923-34. doi: 10.1007/s00415-004-0541-x. J Neurol. 2004. PMID: 15316796 Review.

2

Exclusion of linkage of nine neuronal nicotinic acetylcholine receptor subunit genes expressed in brain in autosomal dominant nocturnal frontal lobe epilepsy in four unrelated families.

Bonati MT, Combi R, Asselta R, Duga S, Malcovati M, Oldani A, Zucconi M, Ferini-Strambi L, Dalprà L, Tenchini ML. Bonati MT, et al. Among authors: combi r. J Neurol. 2002 Aug;249(8):967-74. doi: 10.1007/s00415-002-0763-8. J Neurol. 2002. PMID: 12195439

3

Evidence for a fourth locus for autosomal dominant nocturnal frontal lobe epilepsy.

Combi R, Dalprà L, Malcovati M, Oldani A, Tenchini ML, Ferini-Strambi L. Combi R, et al. Brain Res Bull. 2004 Jun 30;63(5):353-9. doi: 10.1016/j.brainresbull.2003.12.007. Brain Res Bull. 2004. PMID: 15245761

4

Two new putative susceptibility loci for ADNFLE.

Combi R, Ferini-Strambi L, Montruccoli A, Bianchi V, Malcovati M, Zucconi M, Dalprà L, Tenchini ML. Combi R, et al. Brain Res Bull. 2005 Oct 30;67(4):257-63. doi: 10.1016/j.brainresbull.2005.06.032. Brain Res Bull. 2005. PMID: 16182932

5

Frontal lobe epilepsy and mutations of the corticotropin-releasing hormone gene.

Combi R, Dalprà L, Ferini-Strambi L, Tenchini ML. Combi R, et al. Ann Neurol. 2005 Dec;58(6):899-904. doi: 10.1002/ana.20660. Ann Neurol. 2005. PMID: 16222669

6

Nocturnal frontal lobe epilepsy and the acetylcholine receptor.

Ferini-Strambi L, Sansoni V, Combi R. Ferini-Strambi L, et al. Among authors: combi r. Neurologist. 2012 Nov;18(6):343-9. doi: 10.1097/NRL.0b013e31826a99b8. Neurologist. 2012. PMID: 23114665 Review.

7

DEPDC5 mutations in families presenting as autosomal dominant nocturnal frontal lobe epilepsy.

Picard F, Makrythanasis P, Navarro V, Ishida S, de Bellescize J, Ville D, Weckhuysen S, Fosselle E, Suls A, De Jonghe P, Vasselon Raina M, Lesca G, Depienne C, An-Gourfinkel I, Vlaicu M, Baulac M, Mundwiller E, Couarch P, Combi R, Ferini-Strambi L, Gambardella A, Antonarakis SE, Leguern E, Steinlein O, Baulac S. Picard F, et al. Among authors: combi r. Neurology. 2014 Jun 10;82(23):2101-6. doi: 10.1212/WNL.0000000000000488. Epub 2014 May 9. Neurology. 2014. PMID: 24814846

8

CHRNA2 mutations are rare in the NFLE population: evaluation of a large cohort of Italian patients.

Combi R, Ferini-Strambi L, Tenchini ML. Combi R, et al. Sleep Med. 2009 Jan;10(1):139-42. doi: 10.1016/j.sleep.2007.11.010. Epub 2008 Jan 28. Sleep Med. 2009. PMID: 18226955

9

Compound heterozygosity with dominance in the Corticotropin Releasing Hormone (CRH) promoter in a case of nocturnal frontal lobe epilepsy.

Combi R, Ferini-Strambi L, Tenchini ML. Combi R, et al. J Sleep Res. 2008 Sep;17(3):361-2. doi: 10.1111/j.1365-2869.2008.00674.x. J Sleep Res. 2008. PMID: 18844820 No abstract available.

10

Clinical and genetic familial study of a large cohort of Italian children with idiopathic epilepsy.

Combi R, Grioni D, Contri M, Redaelli S, Redaelli F, Bassi MT, Barisani D, Lavitrano ML, Tredici G, Tenchini ML, Bertolini M, Dalprà L. Combi R, et al. Brain Res Bull. 2009 Apr 29;79(2):89-96. doi: 10.1016/j.brainresbull.2009.01.008. Epub 2009 Feb 5. Brain Res Bull. 2009. PMID: 19200853

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