Lucia Monari
Affiliations: | Università di Bologna, Bologna, Italy |
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"Lucia Monari"Mean distance: 17.19 (cluster 28) | S | N | B | C | P |
Cross-listing: Neuropathology Tree
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Publications
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| Cevoli S, Pierangeli G, Monari L, et al. (2002) Familial hemiplegic migraine: clinical features and probable linkage to chromosome 1 in an Italian family. Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 23: 7-10 |
| Rizzi R, Carelli V, Monari L, et al. (1998) Cerebellar ataxia, hypogonadism and chorioretinopathy: molecular analysis of an Italian family. Italian Journal of Neurological Sciences. 19: 41-4 |
| Carelli V, Barboni P, Zacchini A, et al. (1998) Leber's Hereditary Optic Neuropathy (LHON) with 14484/ND6 mutation in a North African patient. Journal of the Neurological Sciences. 160: 183-8 |
| Parchi P, Petersen RB, Chen SG, et al. (1998) Molecular pathology of fatal familial insomnia. Brain Pathology (Zurich, Switzerland). 8: 539-48 |
| Donati C, Cevoli S, Barboni P, et al. (1997) Respiratory deficient fibroblast-derived cybrid cell clones from a patient with bilateral optic atrophy and secondary lhon mtdna mutations Italian Journal of Neurological Sciences. 18: 59 |
| Petersen RB, Tabaton M, Chen SG, et al. (1995) Familial progressive subcortical gliosis: presence of prions and linkage to chromosome 17. Neurology. 45: 1062-7 |
| Barbiroli B, Montagna P, Cortelli P, et al. (1995) Defective brain and muscle energy metabolism shown by in vivo 31P magnetic resonance spectroscopy in nonaffected carriers of 11778 mtDNA mutation. Neurology. 45: 1364-9 |
| Montagna P, Cortelli P, Monari L, et al. (1994) 31P-magnetic resonance spectroscopy in migraine without aura. Neurology. 44: 666-9 |
| Petersen RB, Goldfarb LG, Tabaton M, et al. (1994) A novel mechanism of phenotypic heterogeneity demonstrated by the effect of a polymorphism on a pathogenic mutation in the PRNP (prion protein gene). Molecular Neurobiology. 8: 99-103 |
| Tinuper P, Plazzi G, Monari L, et al. (1994) Arylsulfatase A pseudodeficiency and Lafora bodies in a patient with progressive myoclonic epilepsy. Epilepsia. 35: 332-5 |