| Year |
Citation |
Score |
| 2002 |
Cevoli S, Pierangeli G, Monari L, Valentino ML, Bernardoni P, Mochi M, Cortelli P, Montagna P. 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. PMID 12111614 DOI: 10.1007/S100720200016 |
0.353 |
|
| 1998 |
Rizzi R, Carelli V, Monari L, Mochi M, Liguori R, Sensi M, Cocozza S, Filla A, Montagna P. Cerebellar ataxia, hypogonadism and chorioretinopathy: molecular analysis of an Italian family. Italian Journal of Neurological Sciences. 19: 41-4. PMID 10935859 DOI: 10.1007/Bf03028811 |
0.395 |
|
| 1998 |
Carelli V, Barboni P, Zacchini A, Mancini R, Monari L, Cevoli S, Liguori R, Sensi M, Lugaresi E, Montagna P. Leber's Hereditary Optic Neuropathy (LHON) with 14484/ND6 mutation in a North African patient. Journal of the Neurological Sciences. 160: 183-8. PMID 9849804 DOI: 10.1016/S0022-510X(98)00239-1 |
0.537 |
|
| 1998 |
Parchi P, Petersen RB, Chen SG, Autilio-Gambetti L, Capellari S, Monari L, Cortelli P, Montagna P, Lugaresi E, Gambetti P. Molecular pathology of fatal familial insomnia. Brain Pathology (Zurich, Switzerland). 8: 539-48. PMID 9669705 DOI: 10.1111/J.1750-3639.1998.Tb00176.X |
0.705 |
|
| 1997 |
Donati C, Cevoli S, Barboni P, Montagna P, Lugaresi E, Ga S, Valentine ML, Monari L, Martinuza M, Carelli V. 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. |
0.465 |
|
| 1995 |
Petersen RB, Tabaton M, Chen SG, Monari L, Richardson SL, Lynch T, Manetto V, Lanska DJ, Markesbery WR, Lynches T [corrected to Lynch T]. Familial progressive subcortical gliosis: presence of prions and linkage to chromosome 17. Neurology. 45: 1062-7. PMID 7783864 DOI: 10.1212/Wnl.45.6.1062 |
0.688 |
|
| 1995 |
Barbiroli B, Montagna P, Cortelli P, Iotti S, Lodi R, Barboni P, Monari L, Lugaresi E, Frassineti C, Zaniol P. 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. PMID 7617199 DOI: 10.1212/Wnl.45.7.1364 |
0.548 |
|
| 1994 |
Montagna P, Cortelli P, Monari L, Pierangeli G, Parchi P, Lodi R, Iotti S, Frassineti C, Zaniol P, Lugaresi E. 31P-magnetic resonance spectroscopy in migraine without aura. Neurology. 44: 666-9. PMID 8164822 DOI: 10.1212/Wnl.44.4.666 |
0.578 |
|
| 1994 |
Petersen RB, Goldfarb LG, Tabaton M, Brown P, Monari L, Cortelli P, Montagna P, Autilio-Gambetti L, Gajdusek DC, Lugaresi E. 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. PMID 7999319 DOI: 10.1007/Bf02780659 |
0.667 |
|
| 1994 |
Tinuper P, Plazzi G, Monari L, Sangiorgi S, Pellissier JF, Cerullo A, Provini F, Capellari S, Baruzzi A, Lugaresi E. Arylsulfatase A pseudodeficiency and Lafora bodies in a patient with progressive myoclonic epilepsy. Epilepsia. 35: 332-5. PMID 7908874 DOI: 10.1111/J.1528-1157.1994.Tb02440.X |
0.609 |
|
| 1994 |
Monari L, Chen SG, Brown P, Parchi P, Petersen RB, Mikol J, Gray F, Cortelli P, Montagna P, Ghetti B. Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphism. Proceedings of the National Academy of Sciences of the United States of America. 91: 2839-42. PMID 7908444 DOI: 10.1073/Pnas.91.7.2839 |
0.576 |
|
| 1993 |
Gambetti P, Petersen R, Monari L, Tabaton M, Autilio-Gambetti L, Cortelli P, Montagna P, Lugaresi E. Fatal familial insomnia and the widening spectrum of prion diseases. British Medical Bulletin. 49: 980-94. PMID 8137139 DOI: 10.1093/Oxfordjournals.Bmb.A072657 |
0.606 |
|
| 1993 |
Monari L, Petersen RB, Chen SG, Cortelli P, Montagna P, Berg L, Julien J, Lugaresi E, Autilio-Gambetti L, Gambetti P. Detection of prion protein in fibroblasts from two Fatal Familial Insomnia kindred Journal of Neuropathology and Experimental Neurology. 52: 293. DOI: 10.1097/00005072-199305000-00133 |
0.454 |
|
| 1993 |
Petersen RB, Goldfarb L, Tabaton M, Brown P, LeBlanc A, Montagna P, Cortelli P, Monari L, Autilio-Gambetti L, Gajdusek DC, Lugaresi E, Gambetti P. Effect of a Polymorphism on the Pathogenic 178Asn Mutation in the Prion Protein Gene Journal of Neuropathology and Experimental Neurology. 52: 293. DOI: 10.1097/00005072-199305000-00131 |
0.621 |
|
| 1992 |
Barbiroli B, Montagna P, Cortelli P, Funicello R, Iotti S, Monari L, Pierangeli G, Zaniol P, Lugaresi E. Abnormal brain and muscle energy metabolism shown by 31P magnetic resonance spectroscopy in patients affected by migraine with aura. Neurology. 42: 1209-14. PMID 1603349 DOI: 10.1212/Wnl.42.6.1209 |
0.495 |
|
| 1992 |
Montagna P, Gabellini AS, Monari L, Lugaresi E. Parkinsonian syndrome after long-term treatment with clebopride. Movement Disorders : Official Journal of the Movement Disorder Society. 7: 89-90. PMID 1557073 DOI: 10.1002/Mds.870070120 |
0.357 |
|
| 1992 |
Montagna P, Cortelli P, Avoni P, Marchello LP, Monari L, Tinuper P, Gambetti P, Lugaresi E. Abnormal sympathetic skin responses in thalamic lesions. Electroencephalography and Clinical Neurophysiology. 85: 225-7. PMID 1376682 DOI: 10.1016/0168-5597(92)90137-Z |
0.569 |
|
| 1992 |
Plazzi G, Tinuper P, Monari L, Capellari S, Sangiorgi S, Montagna P, Provini F, Cerullo A, Pellissier JF, Baruzzi A, Lugaresi E. Arylsulphatase A (ASA) pseudodeficiency (PD) and Lafora bodies (LB) in a patient with non progressive myoclonic epilepsy | EPILESSIA MIOCLONICA NON PROGRESSIVA CON CORPI DI LAFORA E PSEUDODEFICIENZA DI ARILSULFATASI A Bollettino - Lega Italiana Contro L'Epilessia. 195-196. |
0.551 |
|
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