Silver syndrome variant of hereditary spastic paraplegia: new locus maps to chromosome 4p16-p15 and allelism with SPG4
2007 Orlacchio, Antonio; Patrono, C; Gaudiello, F; Rocchi, C; Moschella, V; Floris, R; Bernardi, G; Kawarai, T.
CSF biomarkers, impairment of cerebral hemodynamics and degree of cognitive decline: An overview in different dementia subtypes
2007 Stefani, A; Diomedi, M; Orlacchio, Antonio; Galati, S; Martorana, A; Bernardini, S
Absence of association between APOA1 polymorphism and Alzheimer’s disease
2008 Varlese, Ml; Babalini, C; Patrono, C; Borreca, A; Montieri, P; Esposito, Z; Sancesario, G; Orlacchio, Antonio; Bernardi, G; Kawarai, T; Orlacchio, A.
CSCE-based mutation analysis of NIPA1 gene revealed no mutations in Italian patients with autosomal dominant hereditary spastic paraplegia
2008 Borreca, A; Patrono, C; Babalini, C; Montieri, P; Varlese, Ml; Moschella, V; Bernardi, G; Kawarai, T; Orlacchio, Antonio
Autosomal recessive juvenile ALS associated with SPATACSIN mutations
2008 Orlacchio, Antonio; Borreca, A; Patrono, C; Babalini, C; Mercuri, Nb; Bernardi, G; Kawarai, T.
Identification of biochemical markers for the diagnosis of Alzheimer’s disease in patients affected by type II diabetes
2008 Orlacchio, Antonio; Massini, C; Tiribuzi, R; Costanzi, E; Makrypidi, G; Mattoli, F; Esposito, Z; Patrono, C; Miele, Ml; Maiotti, M; Sancesario, G; Zampolini, M; Orlacchio, A; Martino, Sabata
Association study of the APOA1 gene in an Italian population with Alzheimer’s disease
2008 Orlacchio, Antonio; Babalini, C; Varlese, Ml; Patrono, C; Borreca, A; Esposito, Z; Sancesario, G; Orlacchio, A; Kawarai, T; Bernardi, G.
ALS phenotypes with mutations in SPG11
2009 Orlacchio, Antonio; Babalini, C; Patrono, C; Montieri, P; Varlese, Ml; Borreca, A; Moschella, V; Mercuri, Nb; Bernardi, G; Kawarai, T
Spatacsin mutations in autosomal recessive juvenile ALS
2009 Orlacchio, Antonio; Babalini, C; Borreca, A; Patrono, C; Moschella, V; Mercuri, Nb; Yilmaz, S; Munhoz, R; Rogaeva, Ea; St George Hyslop, Ph; Bernardi, G; Kawarai, T.
Epidemiological, clinical, and genetic study in a large cohort of patients with spastic paraplegia
2016 Pedace, L; Montecchiani, C; Casella, A; Gaudiello, F; Miele, M; Massa, R; Caltagirone, C; Munhoz, Rp; Pedroso, Jl; Barsottini, Ogp; Kawarai, T; Orlacchio, Antonio
HSP-SPG3A: unusual clinical characteristics in a black South-African family
2011 Orlacchio, Antonio; Montieri, P; Babalini, C; Gaudiello, F; Bernardi, G; Kawarai, T.
Reticulon mutations in Hereditary Spastic Paraplegia
2011 Orlacchio, Antonio; Rebelo, A; Montenegro, G; Connell, J; Allison, R; Huang, J; Babalini, C; Bernardi, G; Pericak Vance, M; Reid, E; Züchner, S.
Lysosomal enzymes in Alzheimer’s and type 2 diabetes mellitus patients
2011 Tiribuzi, R; Orlacchio, Antonio; Crispoltoni, L; D’Angelo, F; Datti, A; Martino, S; Orlacchio, A
miR128 up-regulation correlates with impaired Amyloid-β42 degradation in monocytes of patients with sporadic Alzheimer’s disease
2013 Tiribuzi, R; Crispoltoni, L; Porcellati, S; Mearini, M; Di Lullo, M; Florenzano, F; Pirro, M; Bagaglia, F; Palmerini, Ca; Miele, M; Kawarai, T; Zampolini, M; Orlacchio, Antonio; Orlacchio, A
Crocus sativus stigma extract improves amyloid-β degradation in monocytes from Alzheimer’s Disease patients
2014 Orlacchio, Antonio; Tiribuzi, R; Crispoltoni, L; Porcellati, S; Del Pino, Am; Di Lullo, M; Lo Giudice, T; Miele, M; Kawarai, T; Orlacchio, A.
Beneficial effect of Crocus sativus stigma extract in amyloid-beta degradation by monocytes from sporadic Alzheimer's disease patients
2014 Crispoltoni, L; Tiribuzi, R; Porcellati, S; Palmerini, Ca; Del Pino, Am; Di Lullo, M; Lo Giudice, T; Miele, M; Kawarai, T; Rende, M; Orlacchio, A; Orlacchio, Antonio
Hereditary Spastic Paraplegia: a novel mutation and expansion of the phenotype variability in SPG10
2014 Lo Giudice, T; Carosi, L; Di Lullo, M; Lombardi, F; Babalini, C; Gaudiello, F; Marfia, Ga; Massa, R; Kawarai, T; Orlacchio, Antonio
Crocus sativus L. stigma extract improves amyloid-β degradation mediated by Cathepsin B in monocytes from Alzheimer’s Disease patients
2014 Crispoltoni, L; Tiribuzi, R; Porcellati, S; DEL PINO, Alberto Marco; Di Lullo, M; Lo Giudice, T; Miele, M; Kawarai, T; Palmerini, Ca; Orlacchio, Antonio; Orlacchio, A
SPG11 mutations cause autosomal recessive axonal Charcot-Marie-Tooth disease
2015 Lo Giudice, T; Montecchiani, C; Di Lullo, M; Mearini, M; Casella, A; Gaudiello, F; Terracciano, C; Massa, R; Rogaeva, E; St George-Hyslop, Ph; Pedroso, Jl; Barsottini, Ogp; Kawarai, T; Orlacchio, Antonio
Clinical and genetic study of a large SPG4 Italian family with hereditary spastic paraplegia and early-onset familial Alzheimer’s disease
2015 Lo Giudice, T; Casella, A; Mearini, M; Montecchiani, C; Miele, M; Kawarai, T; Orlacchio, Antonio
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Silver syndrome variant of hereditary spastic paraplegia: new locus maps to chromosome 4p16-p15 and allelism with SPG4 | 2007 | Orlacchio, Antonio; Patrono, C; Gaudiello, F; Rocchi, C; Moschella, V; Floris, R; Bernardi, G; Kawarai, T. | |
| CSF biomarkers, impairment of cerebral hemodynamics and degree of cognitive decline: An overview in different dementia subtypes | 2007 | Stefani, A; Diomedi, M; Orlacchio, Antonio; Galati, S; Martorana, A; Bernardini, S | |
| Absence of association between APOA1 polymorphism and Alzheimer’s disease | 2008 | Varlese, Ml; Babalini, C; Patrono, C; Borreca, A; Montieri, P; Esposito, Z; Sancesario, G; Orlacchio, Antonio; Bernardi, G; Kawarai, T; Orlacchio, A. | |
| CSCE-based mutation analysis of NIPA1 gene revealed no mutations in Italian patients with autosomal dominant hereditary spastic paraplegia | 2008 | Borreca, A; Patrono, C; Babalini, C; Montieri, P; Varlese, Ml; Moschella, V; Bernardi, G; Kawarai, T; Orlacchio, Antonio | |
| Autosomal recessive juvenile ALS associated with SPATACSIN mutations | 2008 | Orlacchio, Antonio; Borreca, A; Patrono, C; Babalini, C; Mercuri, Nb; Bernardi, G; Kawarai, T. | |
| Identification of biochemical markers for the diagnosis of Alzheimer’s disease in patients affected by type II diabetes | 2008 | Orlacchio, Antonio; Massini, C; Tiribuzi, R; Costanzi, E; Makrypidi, G; Mattoli, F; Esposito, Z; Patrono, C; Miele, Ml; Maiotti, M; Sancesario, G; Zampolini, M; Orlacchio, A; Martino, Sabata | |
| Association study of the APOA1 gene in an Italian population with Alzheimer’s disease | 2008 | Orlacchio, Antonio; Babalini, C; Varlese, Ml; Patrono, C; Borreca, A; Esposito, Z; Sancesario, G; Orlacchio, A; Kawarai, T; Bernardi, G. | |
| ALS phenotypes with mutations in SPG11 | 2009 | Orlacchio, Antonio; Babalini, C; Patrono, C; Montieri, P; Varlese, Ml; Borreca, A; Moschella, V; Mercuri, Nb; Bernardi, G; Kawarai, T | |
| Spatacsin mutations in autosomal recessive juvenile ALS | 2009 | Orlacchio, Antonio; Babalini, C; Borreca, A; Patrono, C; Moschella, V; Mercuri, Nb; Yilmaz, S; Munhoz, R; Rogaeva, Ea; St George Hyslop, Ph; Bernardi, G; Kawarai, T. | |
| Epidemiological, clinical, and genetic study in a large cohort of patients with spastic paraplegia | 2016 | Pedace, L; Montecchiani, C; Casella, A; Gaudiello, F; Miele, M; Massa, R; Caltagirone, C; Munhoz, Rp; Pedroso, Jl; Barsottini, Ogp; Kawarai, T; Orlacchio, Antonio | |
| HSP-SPG3A: unusual clinical characteristics in a black South-African family | 2011 | Orlacchio, Antonio; Montieri, P; Babalini, C; Gaudiello, F; Bernardi, G; Kawarai, T. | |
| Reticulon mutations in Hereditary Spastic Paraplegia | 2011 | Orlacchio, Antonio; Rebelo, A; Montenegro, G; Connell, J; Allison, R; Huang, J; Babalini, C; Bernardi, G; Pericak Vance, M; Reid, E; Züchner, S. | |
| Lysosomal enzymes in Alzheimer’s and type 2 diabetes mellitus patients | 2011 | Tiribuzi, R; Orlacchio, Antonio; Crispoltoni, L; D’Angelo, F; Datti, A; Martino, S; Orlacchio, A | |
| miR128 up-regulation correlates with impaired Amyloid-β42 degradation in monocytes of patients with sporadic Alzheimer’s disease | 2013 | Tiribuzi, R; Crispoltoni, L; Porcellati, S; Mearini, M; Di Lullo, M; Florenzano, F; Pirro, M; Bagaglia, F; Palmerini, Ca; Miele, M; Kawarai, T; Zampolini, M; Orlacchio, Antonio; Orlacchio, A | |
| Crocus sativus stigma extract improves amyloid-β degradation in monocytes from Alzheimer’s Disease patients | 2014 | Orlacchio, Antonio; Tiribuzi, R; Crispoltoni, L; Porcellati, S; Del Pino, Am; Di Lullo, M; Lo Giudice, T; Miele, M; Kawarai, T; Orlacchio, A. | |
| Beneficial effect of Crocus sativus stigma extract in amyloid-beta degradation by monocytes from sporadic Alzheimer's disease patients | 2014 | Crispoltoni, L; Tiribuzi, R; Porcellati, S; Palmerini, Ca; Del Pino, Am; Di Lullo, M; Lo Giudice, T; Miele, M; Kawarai, T; Rende, M; Orlacchio, A; Orlacchio, Antonio | |
| Hereditary Spastic Paraplegia: a novel mutation and expansion of the phenotype variability in SPG10 | 2014 | Lo Giudice, T; Carosi, L; Di Lullo, M; Lombardi, F; Babalini, C; Gaudiello, F; Marfia, Ga; Massa, R; Kawarai, T; Orlacchio, Antonio | |
| Crocus sativus L. stigma extract improves amyloid-β degradation mediated by Cathepsin B in monocytes from Alzheimer’s Disease patients | 2014 | Crispoltoni, L; Tiribuzi, R; Porcellati, S; DEL PINO, Alberto Marco; Di Lullo, M; Lo Giudice, T; Miele, M; Kawarai, T; Palmerini, Ca; Orlacchio, Antonio; Orlacchio, A | |
| SPG11 mutations cause autosomal recessive axonal Charcot-Marie-Tooth disease | 2015 | Lo Giudice, T; Montecchiani, C; Di Lullo, M; Mearini, M; Casella, A; Gaudiello, F; Terracciano, C; Massa, R; Rogaeva, E; St George-Hyslop, Ph; Pedroso, Jl; Barsottini, Ogp; Kawarai, T; Orlacchio, Antonio | |
| Clinical and genetic study of a large SPG4 Italian family with hereditary spastic paraplegia and early-onset familial Alzheimer’s disease | 2015 | Lo Giudice, T; Casella, A; Mearini, M; Montecchiani, C; Miele, M; Kawarai, T; Orlacchio, Antonio |
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- 1 Contributo su Rivista2363
Data di pubblicazione
- 2020 - 2025100
- 2010 - 20191001
- 2000 - 2009960
- 1990 - 1999256
- 1980 - 198942
- 1973 - 19794
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- Springer Verlag Germany:Tiergarte...11
- Edizioni Minerva Medica:Corso Bra...5
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- HAEMATOLOGICA81
- NEUROUROLOGY AND URODYNAMICS80
- EUROPEAN UROLOGY. SUPPLEMENTS75
- GASTROENTEROLOGY75
- THE JOURNAL OF UROLOGY66
- URODINAMICA64
- JOURNAL OF PLANT PATHOLOGY45
- ANNALS OF THE RHEUMATIC DISEASES43
- BLOOD TRANSFUSION40
Keyword
- female urology32
- urinary incontinence30
- urodynamics28
- surgery27
- pelvic organ prolapse18
- stress urinary incontinence15
- voiding dysfunction13
- botulinum a toxin12
- resiniferatoxin12
- prostate cancer11
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