Valentino ML - Search Results

1

High frequency of migraine-only patients negative for the 3243 A>G tRNALeu mtDNA mutation in two MELAS families.

Cevoli S, Pallotti F, La Morgia C, Valentino ML, Pierangeli G, Cortelli P, Baruzzi A, Montagna P, Carelli V. Cevoli S, et al. Among authors: valentino ml. Cephalalgia. 2010 Aug;30(8):919-27. doi: 10.1177/0333102409354654. Epub 2010 Mar 12. Cephalalgia. 2010. PMID: 20656703

2

A null allele for the Afm175xg3 marker at locus D17S795 caused by a primer binding failure.

Mochi M, Valentino ML, Montagna P. Mochi M, et al. Among authors: valentino ml. Int J Legal Med. 1996;109(2):104-6. doi: 10.1007/BF01355528. Int J Legal Med. 1996. PMID: 8912059

3

Searching for migraine genes: exclusion of 290 cM out of the whole human genome.

Monari L, Mochi M, Valentino ML, Arnaldi C, Cortelli P, De Monte A, Pierangeli G, Prologo G, Scapoli C, Soriani S, Montagna P. Monari L, et al. Among authors: valentino ml. Ital J Neurol Sci. 1997 Oct;18(5):277-82. doi: 10.1007/BF02083304. Ital J Neurol Sci. 1997. PMID: 9412851

4

Acquired neuromyotonia after bone marrow transplantation.

Liguori R, Vincent A, Avoni P, Valentino ML, D'Alessandro R, Zaccaria A, Bandini G, Montagna P. Liguori R, et al. Among authors: valentino ml. Neurology. 2000 Mar 28;54(6):1390-1. doi: 10.1212/wnl.54.6.1390. Neurology. 2000. PMID: 10746621 No abstract available.

5

Focal myoclonus and propriospinal propagation.

Vetrugno R, Provini F, Plazzi G, Valentino ML, Liguori R, Lugaresi E, Montagna P. Vetrugno R, et al. Among authors: valentino ml. Clin Neurophysiol. 2000 Dec;111(12):2175-9. doi: 10.1016/s1388-2457(00)00471-5. Clin Neurophysiol. 2000. PMID: 11090769

6

Leber's hereditary optic neuropathy (LHON/11778) with myoclonus: report of two cases.

Carelli V, Valentino ML, Liguori R, Meletti S, Vetrugno R, Provini F, Mancardi GL, Bandini F, Baruzzi A, Montagna P. Carelli V, et al. Among authors: valentino ml. J Neurol Neurosurg Psychiatry. 2001 Dec;71(6):813-6. doi: 10.1136/jnnp.71.6.813. J Neurol Neurosurg Psychiatry. 2001. PMID: 11723211 Free PMC article.

7

Biochemical-clinical correlation in patients with different loads of the mitochondrial DNA T8993G mutation.

Carelli V, Baracca A, Barogi S, Pallotti F, Valentino ML, Montagna P, Zeviani M, Pini A, Lenaz G, Baruzzi A, Solaini G. Carelli V, et al. Among authors: valentino ml. Arch Neurol. 2002 Feb;59(2):264-70. doi: 10.1001/archneur.59.2.264. Arch Neurol. 2002. PMID: 11843698

8

Phosphorus MR spectroscopy shows a tissue specific in vivo distribution of biochemical expression of the G3460A mutation in Leber's hereditary optic neuropathy.

Lodi R, Carelli V, Cortelli P, Iotti S, Valentino ML, Barboni P, Pallotti F, Montagna P, Barbiroli B. Lodi R, et al. Among authors: valentino ml. J Neurol Neurosurg Psychiatry. 2002 Jun;72(6):805-7. doi: 10.1136/jnnp.72.6.805. J Neurol Neurosurg Psychiatry. 2002. PMID: 12023431 Free PMC article.

9

Familial hemiplegic migraine: clinical features and probable linkage to chromosome 1 in an Italian family.

Cevoli S, Pierangeli G, Monari L, Valentino ML, Bernardoni P, Mochi M, Cortelli P, Montagna P. Cevoli S, et al. Among authors: valentino ml. Neurol Sci. 2002 Apr;23(1):7-10. doi: 10.1007/s100720200016. Neurol Sci. 2002. PMID: 12111614

10

Mitochondrial DNA nucleotide changes C14482G and C14482A in the ND6 gene are pathogenic for Leber's hereditary optic neuropathy.

Valentino ML, Avoni P, Barboni P, Pallotti F, Rengo C, Torroni A, Bellan M, Baruzzi A, Carelli V. Valentino ML, et al. Ann Neurol. 2002 Jun;51(6):774-8. doi: 10.1002/ana.10193. Ann Neurol. 2002. PMID: 12112086

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