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1.5 Abstract in rivista: [2371] Home page tipologia

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Prodotti della tipologia (ordinati per Data di deposito in Decrescente ordine): 601 a 620 di 2.371
Titolo Data di pubblicazione Autore(i) File
Upper motor neuron involvement in X-linked recessive bulbospinal muscular atrophy 2006 Terracciano, C; Pachatz, C; Desiato, Mt; Orlacchio, Antonio; Mori, F; Rocchi, C; Bernardi, G; Massa, R.
Cathepsin D, B and L are down-regulated in fibroblasts from Alzheimer’s disease patients 2006 Orlacchio, Antonio; Urbanelli, L; Massini, C; Mencarelli, S; Pelicci, G; Sorbi, S; Hasilik, A; Bernardi, G; Orlacchio, A; Emiliani, C
Association of APOE4 allele with vascular dementia in Italian population 2006 Orlacchio, Antonio; Miele, M; Contino, G; Varlese, M; Babalini, C; Dionisi, L; Moschella, V; Emiliani, C; Orlacchio, A; Bernardi, G; Kawarai, T.
Involvement of lysosomal system in Alzheimer’s disease fibroblasts following vitamin C supplementation 2006 Orlacchio, Antonio; Costanzi, E; Persichetti, E; Bernardi, G; Orlacchio, A; Emiliani, C.
Silver syndrome: clinicogenetic analysis of two Italian pedigrees 2006 Orlacchio, Antonio; Patrono, C; Borreca, A; Babalini, C; Dionisi, L; Moschella, V; Orlacchio, A; Kawarai, T; Bernardi, G.
Clinical and genetic findings of two Italian kindreds with Silver Syndrome 2006 Orlacchio, Antonio; Patrono, C; Borreca, A; Babalini, C; Dionisi, L; Moschella, V; Orlacchio, A; Bernardi, G; Kawarai, T
Silver syndrome variant of hereditary spastic paraplegia: identification of a novel locus 2007 Orlacchio, Antonio; Patrono, C; Gaudiello, F; Moschella, V; Borreca, A; Orlacchio, A; Floris, R; Bernardi, G; Kawarai, T
A new locus for the Silver syndrome type of hereditary spastic paraplegia 2007 Orlacchio, Antonio; Patrono, C; Gaudiello, F; Borreca, A; Moschella, V; Orlacchio, A; Floris, R; Bernardi, G; Kawarai, T.
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.
Prodotti della tipologia (ordinati per Data di deposito in Decrescente ordine): 601 a 620 di 2.371
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Scopri
Tipologia
  • 1 Contributo su Rivista2371
Autore
  • COSTANTINI, Elisabetta256
  • GIANNANTONI, Antonella204
  • IORIO, Alfonso180
  • LIBERATI, Anna Marina164
  • PORENA, Massimo160
  • ORLACCHIO, Antonio133
  • PIRRO, Matteo113
  • FIORUCCI, Stefano98
  • MANNARINO, Elmo92
  • ZUCCHI, ALESSANDRO87
Data di pubblicazione
  • 2020 - 2026108
  • 2010 - 20191001
  • 2000 - 2009960
  • 1990 - 1999256
  • 1980 - 198942
  • 1973 - 19794
Editore
  • Springer Verlag Germany:Tiergarte...11
  • Edizioni Minerva Medica:Corso Bra...5
  • Editore attuale:BLACKWELL PUBLISH...2
  • -Milano: Istituto nazionale per t...1
  • Attuale:OXFORD UNIV PRESS, GREAT ...1
  • BMJ Publishing Group, London1
  • Elsevier Science Limited:Oxford F...1
  • EWRR1
  • Macmillan Magazines Limited:Porte...1
  • Mary Ann Liebert Incorporated:2 M...1
Rivista
  • BLOOD115
  • HAEMATOLOGICA83
  • 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
Lingua
  • eng1615
  • ita153
  • enm1
  • fre1
Accesso al fulltext
  • no fulltext2371