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ItalianoPINESSI, Lorenzo
Pubblicazioni
Risultati 1 - 20 di 330 (tempo di esecuzione: 0.001 secondi).
| Titolo | Data di pubblicazione | Autore(i) | |
|---|---|---|---|
| 1 | A comparison of familial and sporadic migraine in a headache clinic population | 2002 | RAINERO I; VALFRÈ W; GENTILE S; LO GIUDICE R; FERRERO M; SAVI L; PINESSI L |
| 2 | A double-blind, randomized, multicenter, Italian study of frovatriptan versus rizatriptan for the acute treatment of migraine. | 2011 | Savi L; Omboni S; Lisotto C; Zanchin G; Ferrari MD; Zava D; Pinessi L |
| 3 | A family with autosomal dominant leukodystrophy linked to 5q23.2-q23.3 without lamin B1 mutations | 2010 | Brussino A; Vaula G; Cagnoli C; Panza E; Seri M; Di Gregorio E; Scappaticci S; Camanini S; Daniele D; Bradac GB; Pinessi L; Cavalieri S; Grosso E; Migone N; Brusco A |
| 4 | A functional polymorphism of the interleukin-6 gene influences the psychiatry comorbidity of migraine | 2009 | Rainero I; Rubino E; Negro E; Gallone S; Fenoglio P; Binello E; Gentile S; Vaula G; Pinessi L |
| 5 | A genome-wide linkage scan of a new italian family confirms the presence of several loci influencing migraine without aura | 2008 | Rainero I; Rubino E; Pinessi L; Rogaeva E; St.George-Hyslop P |
| 6 | A new Italian pedigree with early-onset Alzheimer's disease | 1994 | RAINERO I; BERGAMINI L; BRUNI AC ;FERINI-STRAMBI L; FONCIN JF; GEI G; MACCIARDI F; MONTESI MP; PINESSI L; VAULA G |
| 7 | A polymorphism in the interleukin-1α gene influences the clinical features of migraine | 2002 | RAINERO I; PINESSI L; SALANI G; VALFRÈ W; RIVOIRO C; SAVI L; GENTILE S; GIUDICE RL; GRIMALDI LM |
| 8 | A polymorphism of the hypocretin receptor 2 gene is associated with cluster headache | 2004 | RAINERO I; GALLONE S; VALFRÈ W; FERRERO M; ANGILELLA G; RIVOIRO C; RUBINO E; DE MARTINO P; SAVI L; FERRONE M; PINESSI L |
| 9 | A young boy with a new mutation in lamin A/C gene responsive to treatment with ACHE inhibitors | 2011 | Vercelli, L; Benedetti, S; Vittonatto, E; Chiado'-Piat, L; Pilati, E; Pinessi, L; Mongini, T |
| 10 | Abdominal pain associated with musical hallucinations: a case report | 2007 | GENTILE S; FERRERO M; GIUDICE RL; RAINERO I; PINESSI L |
| 11 | Abnormal 5-HT1D receptor function in chronic tension-type headache: A neuroendocrine study with sumatriptan | 2001 | Rainero I; Valfre' W; Savi L; Rivoiro C; Del Rizzo P; Limone P; Amanzio M; Pollo A; Benedetti F; Pinessi L |
| 12 | Abnormal 5-HT1D receptor function in cluster headache: A neuroendocrine study with sumatriptan | 2003 | PINESSI L; RAINERO I; VALFRE' W; LO GIUDICE R; FERRERO M; RIVOIRO C; ARVAT E; GIANOTTI L; DEL RIZZO P; LIMONE P |
| 13 | Absence of linkage between the interleukin-6 gene (-174 G/C) polymorphism and migraine | 2003 | RAINERO I; SALANI G; VALFRÈ W; SAVI L; RIVOIRO C; FERRERO M; PINESSI L; GRIMALDI LM |
| 14 | Absence of modulation between apolipoprotein E and presenilin 1 genes in Italian families with early-onset Alzheimer's disease | 1996 | Nacmias B; Forleo P; Latorraca S; Piacentini S; Amaducci L; Sherrington R; Rogaev E; StGeorgeHyslop P; Rainero I; Pinessi L; Vaula G; Sorbi S |
| 15 | Absence of TARDBP Gene Mutations in an Italian Series of Patients with Frontotemporal Lobar Degeneration | 2009 | Salvatore Gallone; Maria Teresa Giordana; Elio Scarpini; Innocenzo Rainero; Elisa Rubino; Pierpaola Fenoglio; Daniela Galimberti; Silvia Grifoni; Eliana Venturelli; Pier Luigi Acutis; Silvia Peletto; Maria Grazia Maniaci; Patrizia Ferrero; Michela Zotta; Lorenzo Pinessi |
| 16 | Adrenergic regulation of alpha-MSH secretion in man: evidence for a stimulatory role of beta-receptors | 1993 | LIMONE P ;D'ALESSANDRO V ;RAINERO I ;AMBROGIO C ;PINESSI L ;DE GENNARO T ;MOLINATTI GM |
| 17 | Age of Onset of Mood Disorders and Complexity of Personality Traits | 2013 | L. Ostacoli;M. Zuffranieri;M. Cavallo;A. Zennaro;I. Rainero;L. Pinessi;M. V. Pacchiana Parravicini;E. Ladisa;P. M. Furlan;R. L. Picci |
| 18 | Alpha-MSH and Parkinson disease | 1988 | RAINERO I; PINESSI L |
| 19 | Alzheimer’s disease neurophysiological data - a multimodal investigation | 1986 | BIANCO C; BENNA P; COSTA P; TARENZI L; LEOTTA D; SCARZELLA L; RAINERO I; PINESSI L; BERGAMASCO B |
| 20 | Analysis of mutations in two homologous genes causing familial Alzheimer's disease | 1996 | StGeorgeHyslop PH; Sherrington R; Rogaev E; Tsuda T; Ikeda M; Pollen D; Roses A; PericakVance M; Nee L; Polinsky R; Rainero I; Pinessi L; Vaula G; Sorbi S; Amaducci L; Bruni A; Montesi M; Foncin JF; Abe K; Aoki M; Shoji M; Hirai S; Watanabe M; Lannfelt L |
Dettaglio
PINESSI, Lorenzo
NEUROSCIENZE "RITA LEVI MONTALCINI"
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