Zobrazeno 1 - 10
of 291
pro vyhledávání: '"R, Biancheri"'
Autor:
R. Biancheri
Publikováno v:
The Journal of Sport and Anatomy. :37-40
Autor:
C Marchal, D D McIntire, M Massoud, F Lazzini, N Linder, D Levine, C Gutiérrez-Márquez, L A Bailão, G L Hedlund, G C Meyberg-Solomayer, G G Colleoni, A Benachi, T R de Haan, L Quartulli, P M Jayaram, G F Eich, L W Averill, A Vorsselmans, F Bonilla-Musoles, A Vossough, M S van der Knaap, L Geerts, F Dhombres, D Kidron, M L Watt-Morse, F Peyron, J Pardo, J Nijman, J Amir, J E Sanín-Blair, N P Deasy, H Werner, J Atias, M de Santis, M T Whitehead, P T Levy, P Tomà, M Vouga, S Friszer, A Buenerd, B Tatli, G Malm, G Duarte, B Weisz, H Buxmann, G Hartnoll, A Perolo, P Bonasoni, S Stagno, B Tseng, Y J Crow, R Biancheri, T Lerman-Sagie, K Dewar, M A Verboon-Maciolek, D O'Rourke, O Picone, M A al Thagafi, J T Parer, M L Rossi, S Lipitz, M Mohlo, F Brunelle, L Schuler-Faccini, J L Anderson, O A Glenn, R Wright, D Lev, M Uriel, D M Twickler, L R Pistorius, M Wien, L M Hill, F Piersigilli, B Maugey-Laulom, R F Pass, C E Lindan, A Beke, Y Murakami, H Gunardi, B Guerra, R Salmaso, E Martin, V Wiwanitkit, G Sournies, D Warren, A Yuksel, M L Kulkarni, G R Nagy, Y Mogami, K Latkóczy, A Carletti, J C Rodriguez Leonel, Y Suzuki, A Zerem, N Teissier, Y Yinon, G Cloud, L S de Vries, C A Alford, I Simon, B Suarez, P Mezzano, P Pinaud, C Soussotte, A A Karparov, M C Maberry, P Soares de Oliveira-Szejnfeld, G M Magnano, A L White, T Drier de Laforte, A G Cordier, M Besnard, S al Shahwan, P W Callen, M D King, F H Carvalho, L J Salomon, Y Akyol, A S Melo, D Nadal, M I Steinlin, E Araujo Júnior, M L Daniel, C Cluver, C R Wake, K Yanagihara, M Nishioka, I H Kalelioglu, Ashley J. Robinson, A Rossi, E Done, C Auriti, D Pugash, Y Toribe, J Gunkel, A C Regenstein, W K Oliveira, P Maurice, J F Bale, F Gay-Andrieu, N M Mehta, K B Fowler, G M Schauer, L A Ramenghi, L A Bok, M M Cannie, C Parazzini, R Has, S A Laifer, A Righini, A J Barkovich, P Sonigo, M Epelman, M Feldmann, M Tamarkin, A M Kulkarni, Y Ville, E J Boltshauser, S Domizio, A Yildirim, B Feldman, W Bonacci, S Sigaudy, S Ryan, N Farkas, G A Vorona, J Garcia-Flores, E Schiff, E Cristina, C Y Ho, A U Stücker, S N Bryant, S Parisot, V V Kandula, J M Jarosz, B J Freij, C Gire, J M Jouannic, K B Leonard, P S Dimova, G J Demmler, N G Osborne, L Sanapo, L Guibaud, M R De Gasperis, P Guillemette-Artur, L Ben-Sira, S Baskar, T C Cox, C P Dunham, T Matsuishi, M Recio, S M Lanni, E M Korhonen, B Joob, M M Amorim, Y Dogan, G V França, M Motobayashi, L Tychsen, P G Barth, D Baud, C L Ong, P Marty, T C Bailão, M Nishikawa, D Carles, L Bradley, P Droulle, N Girard, D M Money, S Stivaros, M W Rac, D A Herrera, W J Britt, M Severino, J H Livingston, I Muller-Hansen, N Zahalka, M C Rizzi, M. Ashraf Ederies, E H Gröndahl, M Cagneaux, T J Boll, J Pialat, J R Marquis, C Garel, F S Cole, R Franco, J Perlman, J Attia-Sobol, N Oosterom, M Leyder, J L Sever, D Prayer, T Fehm, D Eyrolle-Guignot, R S Aguiar, D J Bonthius, G Malinger, M Tepperberg-Dikawa, F Groenendaal, G Serra, H Odendaal, A Reitter, G Seganti, G Tonni, C Doneda, C Hoffmann, L Ben Sira, C D Smyser, F Jacquemard, Y Yamashita, G Sabatino, G Simonazzi, A D Bardeguez, R Meyer, J P Crino, E Hughes, J Courtier, R W Driggers, Y Inaba, F Diard, R Devlieger, I Lewensohn-Fuchs, G Hendson, M L Engman, J Smal, G Benoist
Publikováno v:
Journal of Pediatric Neurology. 15:192-200
Infection during pregnancy is common and the developing fetal brain is vulnerable to vertical transmission due to immaturity of the fetal immune system. Infection is a major cause of multiple organ abnormalities, including the neuraxis, due to the ne
Publikováno v:
Neuromuscular Disorders. 28:S118
Autor:
Eugenio Mercuri, Filippo M. Santorelli, Carla Uggetti, Antonella Pini, Laura Farina, Marina Mora, Elena Pegoraro, C Boito, Carlo P. Trevisan, Alessandra Ruggieri, Sonia Messina, Gaetano Tortorella, Isabella Moroni, Tiziana Mongini, Raffaele Pezzani, Carmela Scuderi, Chiara Aiello, Enzo Ricci, Marika Pane, Antonio Toscano, Enrico Bertini, Simona Saredi, Angela Berardinelli, Anna Pichiecchio, Claudio Bruno, Alessandra Tessa, Lucia Morandi, R. Biancheri, Adele D'Amico
Publikováno v:
Neuromuscular Disorders. 18:565-571
Mutations in POMT1 and POMT2 genes were originally identified in Walker–Warburg syndrome (WWS) and subsequently reported in patients with milder phenotypes characterised by mental retardation with or without brain abnormalities and without ocular m
Autor:
M. Di Rocco, Chiara Panicucci, Stefania Assereto, Denise Cassandrini, R. Biancheri, Thomas Sander, A. Rossi, Angela Robbiano, Elisabetta Gazzerro, Carlo Minetti, Holger Trucks, Claudio Bruno, Federico Zara, G. Brigati
Publikováno v:
Clinical Genetics. 86:99-101
Autor:
Andrea Rossi, Paolo Tortori-Donati, Maura Faraci, Concetta Micalizzi, Edoardo Lanino, Riccardo Haupt, R. Biancheri
Publikováno v:
Scopus-Elsevier
Hemolymphoproliferative diseases (HLD) are among the most common causes of morbidity and mortality in children. In the past few years, the increased effectiveness of treatment modalities has significantly increased overall survival, but has also disc
Publikováno v:
Giornale italiano di medicina del lavoro ed ergonomia. 34
Recent legislation has made mandatory to perform the risk assessment taking into account gender differences. This should imply to consider not only the simple differences due to biologic difference between male and female workers, but also what is mo
Autor:
M. G. Alpigiani, Mariasavina Severino, Paola Feraco, M. Di Rocco, R. Biancheri, Marisol Mirabelli-Badenier, Andrea Rossi
Publikováno v:
AJNR Am J Neuroradiol
SUMMARY: CDG-1a is an early-onset neurodegenerative disease with selective hindbrain involvement and highly variable clinical presentation. We retrospectively reviewed the clinical records and MR imaging studies of 5 children (3 boys and 2 girls aged
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c7342220c53f71660fd3b1da5a4c8a3
http://hdl.handle.net/11585/656811
http://hdl.handle.net/11585/656811
Autor:
Denise Cassandrini, Filippo M. Santorelli, Marianna Ciccolella, R. Biancheri, Alessandra Tessa, Andrea Rossi, Carlo Minetti
Publikováno v:
Neuromuscular disorders : NMD. 19(1)
Hereditary spastic paraplegias (HSPs) are relatively frequent disorders presenting great genetic heterogeneity. The recent identification of mutations in SPG5/CYP7B1 in six autosomal recessive kindred linked to the SPG5 locus on chromosome 8q prompte
Publikováno v:
The neuroradiology journal. 20(4)