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1.5 Abstract in rivista: [2363] Home page tipologia

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Prodotti della tipologia (ordinati per Data di deposito in Decrescente ordine): 581 a 600 di 2.363
Titolo Data di pubblicazione Autore(i) File
Clinical and genetic study of a large SPG4 Italian family 2004 Orlacchio, Antonio; Kawarai, T; Totaro, A; St George Hyslop, Ph; Sorbi, S; Bernardi, G.
Expression and processing of cathepsin D in fibroblasts of patients with Alzheimer’s disease 2004 Orlacchio, Antonio; Urbanelli, L; Emiliani, C; Miele, M; Pelicci, G; Sorbi, S; Hasilik, A; Bernardi, G; Orlacchio, A
Impairment of lysosomal system in neurodegenerative diseases 2004 Emiliani, C; Urbanelli, L; Mencarelli, S; Cavalieri, C; Tancini, B; Orlacchio, Antonio; Hasilik, A; Sonnino, S; Orlacchio, A
Ras differentially regulates lysosomal enzymes expression 2004 Emiliani, C; Urbanelli, L; Mencarelli, S; Magini, A; Orlacchio, Antonio; Pelicci, G; Sorbi, S; Bernardi, G; Orlacchio, A
Clinical and genetic study of a large SPG4 Italian family 2005 Orlacchio, Antonio; Kawarai, T; Gaudiello, F; Totaro, A; Schillaci, O; Stefani, A; Floris, R; St George Hyslop, Ph; Sorbi, S; Bernardi, G.
Bone marrow stromal cells as a tool for cell therapy for lysosomal storage disorders with neurologic involvement 2005 Martino, S; Tiribuzi, R; di Girolamo, I; Orlacchio, Antonio; Emiliani, C; Orlacchio, A
Lysosomal proteases cathepsin D, B, and L are down-regulated in fibroblasts from Alzheimer’s disease patients 2005 Urbanelli, L; Emiliani, C; Orlacchio, Antonio; Mencarelli, S; Massini, C; Pelicci, G; Sorbi, S; Hasilik, A; Bernardi, G; Orlacchio, A
Effect of ascorbic acid on lysosomal hydrolases and β-APP processing in Alzheimer’s disease fibroblasts 2005 Costanzi, E; Persichetti, E; Orlacchio, Antonio; Emiliani, C; Orlacchio, A.
New locus for complicated hereditary spastic paraplegia maps to chromosome 1p31.1-1p21.1 2005 Orlacchio, Antonio; Kawarai, T; Gaudiello, F; Floris, R; St George Hyslop, Ph; Bernardi, G.
Novel mutation in the gene SPG3A in hereditary spastic paraplegia 2005 Matsui, M; Kawarai, T; Hase, Y; Tomimoto, H; Iseki, K; Rogaeva, Ea; Orlacchio, Antonio; Bernardi, G; St George Hyslop, Ph; Takahashi, R.
Clinical and genetic study of two Italian families with silver syndrome 2006 Orlacchio, Antonio; Patrono, C; Borreca, A; Babalini, C; Dionisi, L; Moschella, V; Orlacchio, A; Bernardi, G; Kawarai, T.
The HexB gene is up-regulated during the brain development: effect for GM2 gangliosidosis therapy 2006 Martino, S; Tiribuzi, R; di Girolamo, I; Guadalupi, R; D’Angelo, F; Makrypidi, G; Orlacchio, Antonio; Bernardi, G; Orlacchio, A
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.
Prodotti della tipologia (ordinati per Data di deposito in Decrescente ordine): 581 a 600 di 2.363
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Scopri
Tipologia
  • 1 Contributo su Rivista2363
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 - 2025100
  • 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
  • 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
Lingua
  • eng1607
  • ita153
  • enm1
  • fre1
Accesso al fulltext
  • no fulltext2363