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Motor overactivity and loss of motor circadian rhythm in fatal familial insomnia: an actigraphic study. [electronic resource] by
- Plazzi, G
- Schutz, Y
- Cortelli, P
- Provini, F
- Avoni, P
- Heikkila, E
- Tinuper, P
- Solieri, L
- Lugaresi, E
- Montagna, P
Producer: 19980219
In:
Sleep vol. 20
Availability: No items available.
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335.
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Lack of vegetative and endocrine circadian rhythms in fatal familial thalamic degeneration. [electronic resource] by
- Lugaresi, A
- Baruzzi, A
- Cacciari, E
- Cortelli, P
- Medori, R
- Montagna, P
- Tinuper, P
- Zucconi, M
- Roiter, I
- Lugaresi, E
Producer: 19871201
In:
Clinical endocrinology vol. 26
Availability: No items available.
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336.
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Defective brain and muscle energy metabolism shown by in vivo 31P magnetic resonance spectroscopy in nonaffected carriers of 11778 mtDNA mutation. [electronic resource] by
- Barbiroli, B
- Montagna, P
- Cortelli, P
- Iotti, S
- Lodi, R
- Barboni, P
- Monari, L
- Lugaresi, E
- Frassineti, C
- Zaniol, P
Producer: 19950824
In:
Neurology vol. 45
Availability: No items available.
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337.
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31P-magnetic resonance spectroscopy in migraine without aura. [electronic resource] by
- Montagna, P
- Cortelli, P
- Monari, L
- Pierangeli, G
- Parchi, P
- Lodi, R
- Iotti, S
- Frassineti, C
- Zaniol, P
- Lugaresi, E
Producer: 19940524
In:
Neurology vol. 44
Availability: No items available.
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338.
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Hypoactive-hypoalert behavior ("psychic akinesia") in intracranial hypotension syndrome. [electronic resource] by
- Vetrugno, R
- Mascalchi, M
- Chierichetti, F
- Gallassi, R
- Alessandria, M
- Guerrini, L
- Vella, A
- Muscas, G
- Lugaresi, E
- Montagna, P
Producer: 20081222
In:
Neurology vol. 71
Availability: No items available.
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339.
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Leber's Hereditary Optic Neuropathy (LHON) with 14484/ND6 mutation in a North African patient. [electronic resource] by
- Carelli, V
- Barboni, P
- Zacchini, A
- Mancini, R
- Monari, L
- Cevoli, S
- Liguori, R
- Sensi, M
- Lugaresi, E
- Montagna, P
Producer: 19990303
In:
Journal of the neurological sciences vol. 160
Availability: No items available.
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340.
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Arylsulfatase A pseudodeficiency and Lafora bodies in a patient with progressive myoclonic epilepsy. [electronic resource] by
- Tinuper, P
- Plazzi, G
- Monari, L
- Sangiorgi, S
- Pellissier, J F
- Cerullo, A
- Provini, F
- Capellari, S
- Baruzzi, A
- Lugaresi, E
Producer: 19940518
In:
Epilepsia vol. 35
Availability: No items available.
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