Sfoglia per Titolo  

Opzioni
Vai a: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

Mostrati risultati da 37.588 a 37.607 di 60.038
Titolo Data di pubblicazione Autore(i) File
A Novel High Efficiency Hybrid Power Unit for Hydrogen-Fueled City Transit Bus 1-gen-2019 Ometto, A.; Masciovecchio, C.; Ciancetta, F.; Dovidio, G.
A novel homogenization procedure to model the skin layers in LF numerical dosimetry 1-gen-2016 DE SANTIS, Valerio; Chen, Xi Lin; Cruciani, Silvano; Campi, Tommaso; Feliziani, Mauro
A novel homozygous MFN2 mutation associated with severe and atypical CMT2 phenotype 1-gen-2017 VERROTTI di PIANELLA, Alberto
A novel homozygous splice site mutation in the HPGD gene causes mild primary hypertrophic osteoarthropathy. 1-gen-2010 Sinibaldi, L.; Harifi, G.; Bottillo, I.; Iannicelli, M.; Hassani, Se.; Brancati, F.; Dallapiccola, B.
Novel hydroxyapatite biomaterial covalently linked to raloxifene. 1-gen-2014 Meme, L; Santarelli, A; Marzo, Giuseppe; Emanuelli, M; Nocini, Pf; Bertossi, D; Putignano, A; Dioguardi, M; Lo Muzio, L; Bambini, F.
Novel hypotensive agents from Verbesina caracasana. 8. Synthesis and pharmacology of (3,4-dimethoxycinnamoyl)-N(1) - agmatine and synthetic analogues 1-gen-2001 Carmignani, Marco; Volpe, ANNA RITA; Botta, B; Espinal, R; DE BONNEVAUX, Sc; DE LUCA, C; Botta, M; Corelli, F; Tafi, A; DELLE MONACHE, G.
Novel hypotensive agents from Verbesina caracasana. Synthesis and pharmacology of Caracasanamide 1-gen-1993 Carmignani, Marco; DELLE MONACHE, G.; Botta, B.; DELLE MONACHE, F.; Espinal, R.; DE BONNEVAUX, S. C.; DE LUCA, C.
Novel hypotensive agents from Verbesina Caracasana. Synthesis and pharmacology of caracasandiamide 1-gen-1999 Carmignani, Marco; Volpe, ANNA RITA; DELLE MONACHE, F; Botta, B; Espinal, R; DE BONNEVAUX, S. C.; DE LUCA, C; Botta, M; Corelli, F; Tafi, A; Ripanti, G; DELLE MONACHE, G.
Novel hypotensive agents from Verbesina caracasana: Structure, synthesis and pharmacology 1-gen-2003 Botta, B.; Carmignani, Marco; Volpe, ANNA RITA; Botta, M.; Corelli, F.; DELLE MONACHE, G.
A NOVEL HYPOXIA-REGULATED ALTERNATIVE TRKA SPLICE VARIANT AF POTENTIAL PHYSIOLOGICAL AND PATHOLOGICAL IMPORTANCE 1-gen-2005 Tacconelli, A.; Farina, Antonietta; Cappabianca, L.; Gulino, A.; Mackay, A. R.
Novel infrared-terahertz fusion 3D non-invasive imaging of plant fibre-reinforced polymer composites 1-gen-2022 Hu, J.; Zhang, H.; Sfarra, S.; Santulli, C.; Tian, G.; Maldague, X.
Novel insights in pathophysiology of antiblastic drugs-induced cardiotoxicity and cardioprotection 1-gen-2016 Deidda, Martino; Madonna, Rosalinda; Mango, Ruggiero; Pagliaro, Pasquale; Bassareo, Pier P.; Cugusi, Lucia; Romano, Silvio; Penco, Maria; Romeo, Francesco; Mercuro, Giuseppe
Novel insights on the management of pain: highlights from the 'Science of Relief' meeting 1-gen-2019 Anand, Praveen; Dickenson, Anthony; Finco, Gabriele; Marinangeli, Franco; Polati, Enrico; Romualdi, Patrizia; Tzschentke, Thomas M; Canonico, Pier Luigi
Novel Intramolecular Cyclization of N-Alkynyl Heterocycles Containing Proximate Nucleophiles 1-gen-2003 Abbiati, G.; Arcadi, Antonio; Beccalli, E.; Rossi, E.
Novel Italian family supports clinical and genetic heterogeneity of primary adult-onset torsion dystonia. 1-gen-2002 Brancati, F.; G, Defazio; V, Caputo; Em, Valente; A, Pizzuti; P, Livrea; A, Berardelli; B, Dallapiccola
A novel iterative method to approximate structured singular values 1-gen-2017 Guglielmi, N.; Rehman, M. -. U.; Kressner, D.
Novel kinetic studies on biomass hydrothermal carbonization 1-gen-2018 Gallifuoco, Alberto; DI GIACOMO, Gabriele
A Novel LIPE Nonsense Mutation Found Using Exome Sequencing in Siblings With Late-Onset Familial PartialLipodystrophy 1-gen-2014 Farhan, Sali M. K.; Robinson, John F.; Mcintyre, Adam D.; Marrosu, Maria G.; Ticca, Anna F.; Loddo, Sara; Carboni, Nicola; Brancati, Francesco; Hegele, Robert A.
A novel locus for autosomal dominant cone and cone-rod dystrophies maps to the 6p gene cluster of retinal dystrophies. 1-gen-2005 M, Castori; Em, Valente; M, Clementi; Ap, Tormene; Brancati, F.; V, Caputo; B, Dallapiccola
Novel locus for autosomal dominant pure hereditary spastic paraplegia (SPG19) maps to chromosome 9q33-q34. 1-gen-2002 Em, Valente; Brancati, F.; V, Caputo; E, Bertini; C, Patrono; D, Costanti; B, Dallapiccola
Mostrati risultati da 37.588 a 37.607 di 60.038
Legenda icone

  •  file ad accesso aperto
  •  file disponibili sulla rete interna
  •  file disponibili agli utenti autorizzati
  •  file disponibili solo agli amministratori
  •  file sotto embargo
  •  nessun file disponibile