Showing results (11-20 of 42) with videos related to

Sort By:
Pageof 5
Pediatric Radiology|January 1, 1990
Radiographic findings in hereditary multiple exostoses and a new theory of the pathogenesis of exostosesU E Pazzaglia, L Pedrotti, G Beluffi, et al.
Physical Review Letters|January 15, 2011
Quantum plasmonics with quantum dot-metal nanoparticle molecules: influence of the Fano effect on photon statisticsA Ridolfo, O Di Stefano, N Fina, et al.
Journal of Physics. Condensed Matter : an Institute of Physics Journal|March 15, 2011
Calculation of the local optical density of states in absorbing and gain mediaO Di Stefano, N Fina, S Savasta, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|March 29, 2008
Pai syndrome: a further report of a case with bifid nose, lipoma, and agenesis of the corpus callosumS Savasta, S Chiapedi, S Perrini, et al.
Physical Review Letters|August 29, 2014
Spontaneous conversion from virtual to real photons in the ultrastrong-coupling regimeR Stassi, A Ridolfo, O Di Stefano, et al.
Acta Paediatrica (Oslo, Norway : 1992)|September 1, 1995
Recurrent chest pain as the presenting manifestation of spinal meningiomaG L Marseglia, S Savasta, A Ravelli, et al.
Pediatric Radiology|January 1, 1989
Thalamic hemorrhage in a 4-year-old child induced by nephro-vascular hypertensionE Bianchi, S Savasta, F Torcetta, et al.
American Journal of Medical Genetics|December 18, 2001
FISH characterization of a supernumerary r(1)(::cen-->q22::q22-->sq21::) chromosome associated with multiple anomalies and bilateral cataractsP Finelli, P Cavalli, D Giardino, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|June 1, 1992
Muscle phosphofructokinase deficiency in a myopathic child with severe mental retardation and aplasia of cerebellar vermisO Pastoris, M Dossena, L Vercesi, et al.
Immunogenetics|June 17, 1999
Genomic organization of the HSET locus and the possible association of HLA-linked genes with immotile cilia syndrome (ICS)K Janitz, A Wild, S Beck, et al.
Pageof 5