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| 1 | Extended Preoperative Chemotherapy Does Not Improve Pathologic Response and Increases Postoperative Liver Insufficiency After Hepatic Resection for Colorectal Liver Metastases显示文摘 | Yoji Kishi MD Daria Zorzi MD Carlo M. Contreras MD Dipen M. Maru MD Scott Kopetz MD Dario Ribero MD Manuela Motta MD Nicoletta Ravarino MD Mauro Risio MD Steven A. Curley MD Eddie K. Abdalla MD Lorenzo Capussotti MD Jean-Nicolas Vauthey MD | 2010 | Annals of Surgical Oncology2010，，11： | 3 |
| 2 | Recombinant PNPLA3 protein shows triglyceride hydrolase activity and its I148M mutation results in loss of function显示文摘 | Piero Pingitore Carlo Pirazzi Rosellina M. Mancina Benedetta M. Motta Cesare Indiveri Arturo Pujia Tiziana Montalcini Kristina Hedfalk Stefano Romeo | 2013 | BBA - Molecular and Cell Biology of Lipids2013，，： | 2 |
| 3 | Delayed inhibition of Nogo-A does not alter injury-induced axonal sprouting but enhances recovery of cognitive function following experimental traumatic brain injury in rats显示文摘 | P.M. Lenzlinger S. Shimizu N. Marklund H.J. Thompson M.E. Schwab K.E. Saatman R.C. Hoover F.M. Bareyre M. Motta A. Luginbuhl R. Pape A.K. Clouse C. Morganti-Kossmann T.K. McIntosh | 2005 | Neuroscience2005，，3： | 1 |
| 4 | Endoscopic ultrasound–fine needle aspiration (EUS–FNA) for pancreatic lesions: Effectiveness in clinical practice显示文摘 | R. Rocca C. De Angelis M. Daperno P. Carucci N. Ravarino M. Bruno L. Crocellà A. Lavagna M. Fracchia D. Pacchioni G. Masoero C. Rigazio E. Ercole R. Sostegni M. Motta G. Bussolati B. Torchio M. Rizzetto A. Pera | 2007 | Digestive and Liver Disease2007，，8： | 1 |
| 5 | Gene expression profile analysis of primary glioblastomas and non-neoplastic brain tissue: identification of potential target genes by oligonucleotide microarray and real-time quantitative PCR显示文摘 | Carlos A. Scrideli Carlos G. Carlotti Oswaldo K. Okamoto Vanessa S. Andrade Maria A. A. Cortez Fábio J. N. Motta Agda K. Lucio-Eterovic Luciano Neder Sérgio Rosemberg Sueli M. Oba-Shinjo Suely K. N. Marie Luíz G. Tone | 2008 | Journal of Neuro - Oncology2008，，3： | 1 |
| 6 | Comparison between 24‐h proteinuria, urinary protein/creatinine ratio and dipstick test in patients with nephropathy: Patterns of proteinuria in dipstick‐negative patients显示文摘 | M. Gai D. Motta S. Giunti F. Fop S. Masini E. Mezza G. P. Segoloni G. Lanfranco | 2006 | Scandinavian Journal of Clinical & Laboratory Investigation2006，，4： | 1 |
| 7 | Evaluation of BTEX and phenol removal from aqueous solution by multi-solute adsorption onto smectite organoclay显示文摘 | M.N. Carvalho M. da Motta M. Benachour D.C.S. Sales C.A.M. Abreu | 2012 | Journal of Hazardous Materials2012，，： | 1 |
| 8 | Longitudinal changes in serum ferritin levels correlate with measures of hepatic stiffness in transfusion-independent patients with β-thalassemia intermedia显示文摘 | Khaled M. Musallam Irene Motta Marta Salvatori Mirella Fraquelli Alessia Marcon Ali T. Taher Maria Domenica Cappellini | 2012 | Blood Cells, Molecules and Diseases . 2012 (3-4)2012，，3： | 1 |
| 9 | A multicenter study of treatment of primary CNS lymphoma显示文摘 | A. J.M. Ferreri M. Reni F. Pasini A. Calderoni U. Tirelli A. Pivnik G. M. Aondio F. Ferrarese H. Gomez M. Ponzoni B. Borisch F. Berger C. Chassagne P. Iuzzolino A. Carbone J. Weis E. Pedrinis T. Motta A. Jouvet T. Barbui F. Cavalli J.Y. Blay | 2002 | Neurology2002，，10： | 1 |
| 10 | Duplication of the short arm of chromosome 9. Analysis of five cases显示文摘 | C. Cuoco G. Gimelli F. Pasquali L. Poloni O. Zuffardi P. Alicata G. Battaglino F. Bernardi R. Cerone M. Cotellessa A. Ghidont S. Motta | 1982 | Human Genetics1982，，1： | 1 |
| 11 | Visceral leishmaniasis in captive wild canids in Brazil显示文摘 | Marcela M. Luppi Marcelo C.C. Malta Teane M.A. Silva Fabiana L. Silva Rafael O.C. Motta Ildikó Miranda Roselene Ecco Renato L. Santos | 2008 | Veterinary Parasitology2008，，1： | 1 |
| 12 | In situ study of hydride precipitation kinetics and re-orientation in Zircaloy using synchrotron radiation显示文摘 | K.B. Colas A.T. Motta J.D. Almer M.R. Daymond M. Kerr A.D. Banchik P. Vizcaino J.R. Santisteban | 2010 | Acta Materialia2010，，20： | 1 |
| 13 | Gela histological scoring system for post‐treatment biopsies of patients with gastric MALT lymphoma is feasible and reliable in routine practice显示文摘 | Christiane Copie‐Bergman Andrew C. Wotherspoon Carlo Capella Teresio Motta Ennio Pedrinis Stefano A. Pileri Francesco Bertoni Annarita Conconi Emanuele Zucca Maurilio Ponzoni Andrés J. M. Ferreri | 2012 | Br J Haematol2012，，1： | 1 |
| 14 | High Diagnostic Accuracy and Interobserver Reliability of Real-Time Elastography in the Evaluation of Thyroid Nodules显示文摘 | Federico Ragazzoni Maurilio Deandrea Alberto Mormile M. Josefina Ramunni Francesca Garino Gabriella Magliona Manuela Motta Bruno Torchio Roberto Garberoglio Paolo Limone | 2012 | Ultrasound in Medicine & Biology2012，，7： | 1 |
| 15 | Purification and Partial Characterization of an Antimicrobial Peptide Produced by a Novel Bacillus sp. Isolated from the Amazon Basin显示文摘 | Amanda S. Motta Daniel M. Lorenzini Adriano Brandelli | 2007 | Current Microbiology2007，，4： | 1 |
| 16 | Effects of silk fibroin fiber incorporation on mechanical properties, endothelial cell colonization and vascularization of PDLLA scaffolds显示文摘 | M. Stoppato H.Y. Stevens E. Carletti C. Migliaresi A. Motta R.E. Guldberg | 2013 | Biomaterials2013，，： | 1 |
| 17 | 病例报道:神经节糖苷GM_1沉积病的胎儿水肿1例显示文摘GM1 gangliosidosis is a rare disorder characterized by de-ficiency of the β-galactosidase enzyme, with the resulting accumulation of glycolipids, oligosaccharides and especially GM1 ganglioside. It can be classified into three clinical types according to the time of onset: infantile, juvenile and adult form. We report a case of GM1 gangliosidosis presenting with fetal hydrops at 24 wk of gestation. The parents were consanguineous; the baby, born at 35 wk of gestation, was dysmorphic and presented severe generalized oedema. The most common cause of fetal hydrops was excluded. A lysosomal storage disease was suspected, and GM1 gangliosidosis was diagnosed. The child developed severe growth and mental retardation and died when she was 21 mo old. Conclusion: We suggest that the possible association between inborn errors of metabolism and antenatal ascites should be considered, in order to offer genetic counselling due to the high recurrence risk and the availability of early antenatal diagnosis. | Sinelli M.T. Motta M. Cattarelli D. G. Chirico 朱新菊 | 2006 | 世界核心医学期刊文摘(儿科学分册)2006，2，6： | 0 |
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