Malcovati M - Search Results

1

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: malcovati m. J Neurol. 2002 Aug;249(8):967-74. doi: 10.1007/s00415-002-0763-8. J Neurol. 2002. PMID: 12195439

2

Mutational analysis of nicotinic acetylcholine receptor beta2 subunit gene (CHRNB2) in a representative cohort of Italian probands affected by autosomal dominant nocturnal frontal lobe epilepsy.

Duga S, Asselta R, Bonati MT, Malcovati M, Dalprà L, Oldani A, Zucconi M, Ferini-Strambi L, Tenchini ML. Duga S, et al. Among authors: malcovati m. Epilepsia. 2002 Apr;43(4):362-4. doi: 10.1046/j.1528-1157.2002.39001.x. Epilepsia. 2002. PMID: 11952766 Free article.

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. Among authors: malcovati m. 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

In vivo RNA-RNA duplexes from human alpha3 and alpha5 nicotinic receptor subunit mRNAs.

Soldà G, Boi S, Duga S, Fornasari D, Benfante R, Malcovati M, Tenchini ML. Soldà G, et al. Among authors: malcovati m. Gene. 2005 Jan 31;345(2):155-64. doi: 10.1016/j.gene.2004.12.005. Epub 2005 Jan 5. Gene. 2005. PMID: 15716100

5

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. Among authors: malcovati m. Brain Res Bull. 2005 Oct 30;67(4):257-63. doi: 10.1016/j.brainresbull.2005.06.032. Brain Res Bull. 2005. PMID: 16182932

6

Autosomal dominant nocturnal frontal lobe epilepsy. A video-polysomnographic and genetic appraisal of 40 patients and delineation of the epileptic syndrome.

Oldani A, Zucconi M, Asselta R, Modugno M, Bonati MT, Dalprà L, Malcovati M, Tenchini ML, Smirne S, Ferini-Strambi L. Oldani A, et al. Among authors: malcovati m. Brain. 1998 Feb;121 ( Pt 2):205-23. doi: 10.1093/brain/121.2.205. Brain. 1998. PMID: 9549500

7

SER252PHE and 776INS3 mutations in the CHRNA4 gene are rare in the Italian ADNFLE population.

Tenchini ML, Duga S, Bonati MT, Asselta R, Oldani A, Zucconi M, Malcovati M, Dalprà L, Ferini-Strambi L. Tenchini ML, et al. Among authors: malcovati m. Sleep. 1999 Aug 1;22(5):637-9. doi: 10.1093/sleep/22.5.637. Sleep. 1999. PMID: 10450598

8

Refined mapping of CHRNA3/A5/B4 gene cluster and its implications in ADNFLE.

Bonati MT, Asselta R, Duga S, Ferini-Strambi L, Oldani A, Zucconi M, Malcovati M, Dalprà L, Tenchini ML. Bonati MT, et al. Among authors: malcovati m. Neuroreport. 2000 Jul 14;11(10):2097-101. doi: 10.1097/00001756-200007140-00008. Neuroreport. 2000. PMID: 10923651

9

Analysis of Iranian patients allowed the identification of the first truncating mutation in the fibrinogen Bbeta-chain gene causing afibrinogenemia.

Asselta R, Spena S, Duga S, Peyvandi F, Malcovati M, Mannucci PM, Tenchini ML. Asselta R, et al. Among authors: malcovati m. Haematologica. 2002 Aug;87(8):855-9. Haematologica. 2002. PMID: 12161363

10

Arg2074Cys missense mutation in the C2 domain of factor V causing moderately severe factor V deficiency: molecular characterization by expression of the recombinant protein.

Duga S, Montefusco MC, Asselta R, Malcovati M, Peyvandi F, Santagostino E, Mannucci PM, Tenchini ML. Duga S, et al. Among authors: malcovati m. Blood. 2003 Jan 1;101(1):173-7. doi: 10.1182/blood-2002-06-1928. Epub 2002 Aug 15. Blood. 2003. PMID: 12393490 Free article.

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