Lucia Monari

Affiliations: 
Università di Bologna, Bologna, Italy 
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"Lucia Monari"
Mean distance: 17.19 (cluster 28)
 
SNBCP
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
Montagna P, Liguori R, Monari L, et al. (2001) Equine muscular dystrophy with myotonia. Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology. 112: 294-9
Parmeggiani A, Posar A, De Giorgi LB, et al. (2000) Sneddon syndrome, arylsulfatase A pseudodeficiency and impairment of cerebral white matter. Brain & Development. 22: 390-3
Donadio V, Bonsi P, Zele I, et al. (2000) Myoglobinuria after ingestion of extracts of guarana, Ginkgo biloba and kava. Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 21: 124
Avoni P, Monari L, Carelli V, et al. (2000) Congenital encephalomyopathy with epilepsy, chorioretinitis, basal ganglia involvement, and muscle minicores. Annals of Neurology. 47: 395-9
Cevoli S, Monari L, Valentino ML, et al. (2000) Familial hemiplegic migraine: Probable linkage to chromosome 1 and genetic heterogeneity | Emicrania emiplegica famigliare: Probabile linkage al cromosoma 1 ed eterogeneità genetica Confinia Cephalalgica. 9: 117-121
Mochi M, Valentino ML, Monari L, et al. (2000) Genetics of migraine with and without aura: Linkage analysis and association studies | Genetica della emicrania con e senza aura: Analisi di linkage e studi di associazione Confinia Cephalalgica. 9: 123-128
Riguzzi P, D'Orsi G, Meletti S, et al. (1999) Late onset myoclonic epilepsy in a patient with mitochondrial encephalomyopathy: A clinical, polygraphic and biochemical study | Epilessia mioclonica a esordio tardivo in un caso di encefalopatia mitocondriale: Studio clinico, poligrafico e biochimico Bollettino - Lega Italiana Contro L'Epilessia. 249-250
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
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