Monari L[au] - Search Results

Year	Number of Results
1992	3
1993	2
1994	5
1995	2
1997	1
1998	3
2000	3
2001	1
2002	1
2022	0

1

Molecular pathology of fatal familial insomnia.

Parchi P, Petersen RB, Chen SG, Autilio-Gambetti L, Capellari S, Monari L, Cortelli P, Montagna P, Lugaresi E, Gambetti P. Parchi P, et al. Among authors: monari l. Brain Pathol. 1998 Jul;8(3):539-48. doi: 10.1111/j.1750-3639.1998.tb00176.x. Brain Pathol. 1998. PMID: 9669705 Free PMC article. Review.

2

Fatal familial insomnia and the widening spectrum of prion diseases.

Gambetti P, Petersen R, Monari L, Tabaton M, Autilio-Gambetti L, Cortelli P, Montagna P, Lugaresi E. Gambetti P, et al. Among authors: monari l. Br Med Bull. 1993 Oct;49(4):980-94. doi: 10.1093/oxfordjournals.bmb.a072657. Br Med Bull. 1993. PMID: 8137139 Review. No abstract available.

3

A novel mechanism of phenotypic heterogeneity demonstrated by the effect of a polymorphism on a pathogenic mutation in the PRNP (prion protein gene).

Petersen RB, Goldfarb LG, Tabaton M, Brown P, Monari L, Cortelli P, Montagna P, Autilio-Gambetti L, Gajdusek DC, Lugaresi E, et al. Petersen RB, et al. Among authors: monari l. Mol Neurobiol. 1994 Apr-Jun;8(2-3):99-103. doi: 10.1007/BF02780659. Mol Neurobiol. 1994. PMID: 7999319 Review.

4

Equine muscular dystrophy with myotonia.

Montagna P, Liguori R, Monari L, Strong PN, Riva R, Di Stasi V, Gandini G, Cipone M. Montagna P, et al. Among authors: monari l. Clin Neurophysiol. 2001 Feb;112(2):294-9. doi: 10.1016/s1388-2457(00)00511-3. Clin Neurophysiol. 2001. PMID: 11165532

5

31P-magnetic resonance spectroscopy in migraine without aura.

Montagna P, Cortelli P, Monari L, Pierangeli G, Parchi P, Lodi R, Iotti S, Frassineti C, Zaniol P, Lugaresi E, et al. Montagna P, et al. Among authors: monari l. Neurology. 1994 Apr;44(4):666-9. doi: 10.1212/wnl.44.4.666. Neurology. 1994. PMID: 8164822

6

Abnormal platelet mitochondrial function in patients affected by migraine with and without aura.

Sangiorgi S, Mochi M, Riva R, Cortelli P, Monari L, Pierangeli G, Montagna P. Sangiorgi S, et al. Among authors: monari l. Cephalalgia. 1994 Feb;14(1):21-3. doi: 10.1046/j.1468-2982.1994.1401021.x. Cephalalgia. 1994. PMID: 8200018

7

Familial progressive subcortical gliosis: presence of prions and linkage to chromosome 17.

Petersen RB, Tabaton M, Chen SG, Monari L, Richardson SL, Lynch T, Manetto V, Lanska DJ, Markesbery WR, Lynches T [corrected to Lynch T], et al. Petersen RB, et al. Among authors: monari l. Neurology. 1995 Jun;45(6):1062-7. doi: 10.1212/wnl.45.6.1062. Neurology. 1995. PMID: 7783864

8

Abnormal brain and muscle energy metabolism shown by 31P magnetic resonance spectroscopy in patients affected by migraine with aura.

Barbiroli B, Montagna P, Cortelli P, Funicello R, Iotti S, Monari L, Pierangeli G, Zaniol P, Lugaresi E. Barbiroli B, et al. Among authors: monari l. Neurology. 1992 Jun;42(6):1209-14. doi: 10.1212/wnl.42.6.1209. Neurology. 1992. PMID: 1603349

9

Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphism.

Monari L, Chen SG, Brown P, Parchi P, Petersen RB, Mikol J, Gray F, Cortelli P, Montagna P, Ghetti B, et al. Monari L, et al. Proc Natl Acad Sci U S A. 1994 Mar 29;91(7):2839-42. doi: 10.1073/pnas.91.7.2839. Proc Natl Acad Sci U S A. 1994. PMID: 7908444 Free PMC article.

10

Testing models for genetic determination in migraine.

Mochi M, Sangiorgi S, Cortelli P, Carelli V, Scapoli C, Crisci M, Monari L, Pierangeli G, Montagna P. Mochi M, et al. Among authors: monari l. Cephalalgia. 1993 Dec;13(6):389-94. doi: 10.1046/j.1468-2982.1993.1306389.x. Cephalalgia. 1993. PMID: 8313452

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