Showing results (41-50 of 94) with videos related to
Sort By:
Pageof 10
Birth Defects Research. Part A, Clinical and Molecular Teratology|November 5, 2004
Molecular genetic analysis of human homologs of Caenorhabditis elegans mab-21-like 1 gene in patients with neural tube defectsElisa Merello, Patrizia De Marco, Anna Moroni, et al.Neurosurgery|March 11, 2006
Spectrum of nonterminal myelocystocelesAndrea Rossi, Gianluca Piatelli, Carlo Gandolfo, et al.World Neurosurgery|February 23, 2016
Idiopathic Cervical Hematomyelia in an Infant: Spinal Cord Injury without Radiographic Abnormality Caused by a Trivial Trauma? Case Report and Review of the LiteraturePietro Fiaschi, Mariasavina Severino, Giuseppe Marcello Ravegnani, et al.Journal of Molecular Neuroscience : MN|August 27, 2016
Genetic Screening of Pediatric Cavernous MalformationsElisa Merello, Marco Pavanello, Alessandro Consales, et al.Birth Defects Research. Part A, Clinical and Molecular Teratology|February 8, 2006
Mutational screening of the CYP26A1 gene in patients with caudal regression syndromePatrizia De Marco, Elisa Merello, Samantha Mascelli, et al.Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|May 27, 2010
Detection of transplacental melanoma metastasis using quantitative PCRAlessandro Raso, Samantha Mascelli, Paolo Nozza, et al.Neuroradiology|February 1, 2011
Magnetic resonance imaging spectrum of medulloblastomaJulia Fruehwald-Pallamar, Stefan B Puchner, Andrea Rossi, et al.International Journal of Cancer|May 10, 2005
Subtype-specific expression and genetic alterations of the chemokinereceptor gene CXCR4 in medulloblastomasUlrich Schüller, Arend Koch, Wolfgang Hartmann, et al.Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|March 22, 2014
Value of 18F-3,4-dihydroxyphenylalanine PET/MR image fusion in pediatric supratentorial infiltrative astrocytomas: a prospective pilot studyGiovanni Morana, Arnoldo Piccardo, Claudia Milanaccio, et al.Birth Defects Research. Part A, Clinical and Molecular Teratology|February 25, 2006
HLXB9 homeobox gene and caudal regression syndromeElisa Merello, Patrizia De Marco, Samantha Mascelli, et al.Pageof 10