Bonati MT - Search Results

1

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: bonati mt. Brain. 1998 Feb;121 ( Pt 2):205-23. doi: 10.1093/brain/121.2.205. Brain. 1998. PMID: 9549500

2

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: bonati mt. Sleep. 1999 Aug 1;22(5):637-9. doi: 10.1093/sleep/22.5.637. Sleep. 1999. PMID: 10450598

3

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. Neuroreport. 2000 Jul 14;11(10):2097-101. doi: 10.1097/00001756-200007140-00008. Neuroreport. 2000. PMID: 10923651

4

A new biallelic polymorphism in intron 1 of the CHRNA4 gene may cause erroneous genotyping of a closely linked CA repeat marker.

Bonati MT, Duga S, Asselta R, Ferini-Strambi L, Oldani A, Zucconi M, Malcovati M, Dalprà L, Tenchini ML. Bonati MT, et al. Mol Cell Probes. 2000 Dec;14(6):373-80. doi: 10.1006/mcpr.2000.0327. Mol Cell Probes. 2000. PMID: 11090267

5

Characterization of the genomic structure of the human neuronal nicotinic acetylcholine receptor CHRNA5/A3/B4 gene cluster and identification of novel intragenic polymorphisms.

Duga S, Soldà G, Asselta R, Bonati MT, Dalprà L, Malcovati M, Tenchini ML. Duga S, et al. Among authors: bonati mt. J Hum Genet. 2001;46(11):640-8. doi: 10.1007/s100380170015. J Hum Genet. 2001. PMID: 11721883

6

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: bonati mt. Epilepsia. 2002 Apr;43(4):362-4. doi: 10.1046/j.1528-1157.2002.39001.x. Epilepsia. 2002. PMID: 11952766 Free article.

7

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

8

Autosomal dominant restless legs syndrome maps on chromosome 14q.

Bonati MT, Ferini-Strambi L, Aridon P, Oldani A, Zucconi M, Casari G. Bonati MT, et al. Brain. 2003 Jun;126(Pt 6):1485-92. doi: 10.1093/brain/awg137. Brain. 2003. PMID: 12764067

9

Genetics in restless legs syndrome.

Ferini-Strambi L, Bonati MT, Oldani A, Aridon P, Zucconi M, Casari G. Ferini-Strambi L, et al. Among authors: bonati mt. Sleep Med. 2004 May;5(3):301-4. doi: 10.1016/j.sleep.2004.01.005. Sleep Med. 2004. PMID: 15165539 Review.

10

A familial t(4;8) translocation segregates with epilepsy and migraine with aura.

Crippa M, Malatesta P, Bonati MT, Trapasso F, Fortunato F, Annesi G, Larizza L, Labate A, Finelli P, Perrotti N, Gambardella A. Crippa M, et al. Among authors: bonati mt. Ann Clin Transl Neurol. 2020 May;7(5):855-859. doi: 10.1002/acn3.51040. Epub 2020 Apr 21. Ann Clin Transl Neurol. 2020. PMID: 32315120 Free PMC article.

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