PINESSI, Lorenzo
PINESSI, Lorenzo
NEUROSCIENZE "RITA LEVI MONTALCINI"
A functional polymorphism of the interleukin-6 gene influences the psychiatry comorbidity of migraine
2009-01-01 Rainero I; Rubino E; Negro E; Gallone S; Fenoglio P; Binello E; Gentile S; Vaula G; Pinessi L
A genome-wide linkage scan of a new italian family confirms the presence of several loci influencing migraine without aura
2008-01-01 Rainero I; Rubino E; Pinessi L; Rogaeva E; St.George-Hyslop P
A young boy with a new mutation in lamin A/C gene responsive to treatment with ACHE inhibitors
2011-01-01 Vercelli, L; Benedetti, S; Vittonatto, E; Chiado'-Piat, L; Pilati, E; Pinessi, L; Mongini, T
Abnormal 5-HT1D receptor function in chronic tension-type headache: A neuroendocrine study with sumatriptan
2001-01-01 Rainero I; Valfre' W; Savi L; Rivoiro C; Del Rizzo P; Limone P; Amanzio M; Pollo A; Benedetti F; Pinessi L
Absence of modulation between apolipoprotein E and presenilin 1 genes in Italian families with early-onset Alzheimer's disease
1996-01-01 Nacmias B; Forleo P; Latorraca S; Piacentini S; Amaducci L; Sherrington R; Rogaev E; StGeorgeHyslop P; Rainero I; Pinessi L; Vaula G; Sorbi S
Alzheimer’s disease neurophysiological data - a multimodal investigation
1986-01-01 BIANCO C; BENNA P; COSTA P; TARENZI L; LEOTTA D; SCARZELLA L; RAINERO I; PINESSI L; BERGAMASCO B
Analysis of mutations in two homologous genes causing familial Alzheimer's disease
1996-01-01 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
APOE Gene Polymorphisms and Frontotemporal Dementia: A Meta-Analysis
2009-01-01 Rubino E; Rainero I; Ferrero M; Vaula G; Gentile S; Valfre' W; De Martino P; Negro E; Pinessi L
Aquaporin 4 gene and migraine: an association study
2008-01-01 Rubino E; Rainero I; Gallone S; Valfrè W; Berra E; Pinessi L
Assessing the prevalence of KCNK18 (TRESK) gene mutations in Italian patients with migraine
2012-01-01 Rainero I; Rubino E; Gallone S; Fenoglio P; Zavarise P; Carli D; Boschi S; Pinessi L; Dalla Volta G
Association analyses of genetic variants of the HCTR1 gene in migraine
2009-01-01 Rubino E; Rainero I; Gallone S; Fenoglio P; Negro E; Savi L; Pinessi L
Association between Alzheimer's Disease and the hypocretin receptor 2 gene
2011-01-01 Rainero I; Rubino E; Galimberti D; Gallone S; Fenoglio P; Fenoglio C; Scarpini E; Pinessi L
Association between cluster headache and alcohol dehydrogenase 4 polymorphisms
2008-01-01 Rubino E; Rainero I; Gentile S; Gallone S; Fenoglio P; Gravante E; Crasto F; Pinessi L
Association between interleukin-1α gene polymorphisms and Alzheimer’s Disease: a meta-analytic study
2004-01-01 Rainero I; Valfrè W; Ferrero M; Lo Giudice R; Rivoiro C; Rubino E; Pinessi L
Association between polymorphisms and haplotypes of the HCRTR2 gene and cluster headache
2007-01-01 Rainero I; Gallone S; Rubino E; Valfre' W; Vaula G; Pinessi L
Association between Tumor Necrosis Factor-α and aneurismal subarachnoid hemorrhage
2007-01-01 Rubino E; Fontanella M; Rainero I; Gallone S; Ducati A; Pinessi L
Association of polymorphisms and haplotypes of hypocretin receptor 2 gene with cluster headache
2006-01-01 Rainero I; Gallone S; Rubino E; Ponzo P; Valfre' W; Rivoiro C; Fenoglio P; Pugliese L; Vaula G; Savi L; Gasparini M; Pinessi L
Association study between intracranial aneurysms and polymorphisms of IL-1 alfa, IL-1 beta, IL-1RN genes
2008-01-01 Gallone S; Fontanella M; Fenoglio P; Gravante E; Catro F; Rubino E; Rainero I; Pinessi L
Autosomal dominant adult–onset leukodystrophy (ADLD) without LMNB1 mutations: a new variant?
2009-01-01 G. Vaula; A. Brussino; M. Seri; E. Di Gregorio; S. Leombruni; D. Daniele; G.B. Bradac; L. Pinessi; A. Brusco
Basement membrane-small vessel disease and leukoencephalopathy: evidence for genetic eterogeneity?
2010-01-01 Vaula G; Rizzu P; Calcia A; Brusco A; Brussino A; Rainero I; Cerrato P; Soardo F; Gallo G; Pinessi L
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
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 | |
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 | |
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 | |
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 | |
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 | |
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 | |
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 | |
APOE Gene Polymorphisms and Frontotemporal Dementia: A Meta-Analysis | 2009 | Rubino E; Rainero I; Ferrero M; Vaula G; Gentile S; Valfre' W; De Martino P; Negro E; Pinessi L | |
Aquaporin 4 gene and migraine: an association study | 2008 | Rubino E; Rainero I; Gallone S; Valfrè W; Berra E; Pinessi L | |
Assessing the prevalence of KCNK18 (TRESK) gene mutations in Italian patients with migraine | 2012 | Rainero I; Rubino E; Gallone S; Fenoglio P; Zavarise P; Carli D; Boschi S; Pinessi L; Dalla Volta G | |
Association analyses of genetic variants of the HCTR1 gene in migraine | 2009 | Rubino E; Rainero I; Gallone S; Fenoglio P; Negro E; Savi L; Pinessi L | |
Association between Alzheimer's Disease and the hypocretin receptor 2 gene | 2011 | Rainero I; Rubino E; Galimberti D; Gallone S; Fenoglio P; Fenoglio C; Scarpini E; Pinessi L | |
Association between cluster headache and alcohol dehydrogenase 4 polymorphisms | 2008 | Rubino E; Rainero I; Gentile S; Gallone S; Fenoglio P; Gravante E; Crasto F; Pinessi L | |
Association between interleukin-1α gene polymorphisms and Alzheimer’s Disease: a meta-analytic study | 2004 | Rainero I; Valfrè W; Ferrero M; Lo Giudice R; Rivoiro C; Rubino E; Pinessi L | |
Association between polymorphisms and haplotypes of the HCRTR2 gene and cluster headache | 2007 | Rainero I; Gallone S; Rubino E; Valfre' W; Vaula G; Pinessi L | |
Association between Tumor Necrosis Factor-α and aneurismal subarachnoid hemorrhage | 2007 | Rubino E; Fontanella M; Rainero I; Gallone S; Ducati A; Pinessi L | |
Association of polymorphisms and haplotypes of hypocretin receptor 2 gene with cluster headache | 2006 | Rainero I; Gallone S; Rubino E; Ponzo P; Valfre' W; Rivoiro C; Fenoglio P; Pugliese L; Vaula G; Savi L; Gasparini M; Pinessi L | |
Association study between intracranial aneurysms and polymorphisms of IL-1 alfa, IL-1 beta, IL-1RN genes | 2008 | Gallone S; Fontanella M; Fenoglio P; Gravante E; Catro F; Rubino E; Rainero I; Pinessi L | |
Autosomal dominant adult–onset leukodystrophy (ADLD) without LMNB1 mutations: a new variant? | 2009 | G. Vaula; A. Brussino; M. Seri; E. Di Gregorio; S. Leombruni; D. Daniele; G.B. Bradac; L. Pinessi; A. Brusco | |
Basement membrane-small vessel disease and leukoencephalopathy: evidence for genetic eterogeneity? | 2010 | Vaula G; Rizzu P; Calcia A; Brusco A; Brussino A; Rainero I; Cerrato P; Soardo F; Gallo G; Pinessi L |