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Alessandro Raso

Showing results (11-20 of 43) with videos related to

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Pediatric Blood & Cancer|March 22, 2006
Cerebellar medullomyoblastoma with melanotic tubular structuresPaolo Nozza, Claudia Milanaccio, Gianluca Piatelli, et al.
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.
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.
European Journal of Immunology|October 6, 2007
Both CD133+ and CD133- medulloblastoma cell lines express ligands for triggering NK receptors and are susceptible to NK-mediated cytotoxicityRoberta Castriconi, Alessandra Dondero, Francesca Negri, et al.
Journal of Child Neurology|September 24, 2013
Congenital segmental lymphedema in tuberous sclerosis complex with associated subependymal giant cell astrocytomas treated with Mammalian target of rapamycin inhibitorsGiulia Prato, Maria Margherita Mancardi, Maria Giuseppina Baglietto, 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.
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.
European Journal of Human Genetics : EJHG|April 4, 2003
Reduced folate carrier polymorphism (80A-->G) and neural tube defectsPatrizia De Marco, Maria Grazia Calevo, Anna Moroni, et al.
Neuro-Oncology|September 26, 2015
Diagnostic and prognostic value of 18F-DOPA PET and 1H-MR spectroscopy in pediatric supratentorial infiltrative gliomas: a comparative studyGiovanni Morana, Arnoldo Piccardo, Matteo Puntoni, et al.
Pageof 5

Showing results (11-20 of 43) with videos related to

Sort By:
Pageof 5
Pediatric Blood & Cancer|March 22, 2006
Cerebellar medullomyoblastoma with melanotic tubular structuresPaolo Nozza, Claudia Milanaccio, Gianluca Piatelli, et al.
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.
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.
European Journal of Immunology|October 6, 2007
Both CD133+ and CD133- medulloblastoma cell lines express ligands for triggering NK receptors and are susceptible to NK-mediated cytotoxicityRoberta Castriconi, Alessandra Dondero, Francesca Negri, et al.
Journal of Child Neurology|September 24, 2013
Congenital segmental lymphedema in tuberous sclerosis complex with associated subependymal giant cell astrocytomas treated with Mammalian target of rapamycin inhibitorsGiulia Prato, Maria Margherita Mancardi, Maria Giuseppina Baglietto, 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.
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.
European Journal of Human Genetics : EJHG|April 4, 2003
Reduced folate carrier polymorphism (80A-->G) and neural tube defectsPatrizia De Marco, Maria Grazia Calevo, Anna Moroni, et al.
Neuro-Oncology|September 26, 2015
Diagnostic and prognostic value of 18F-DOPA PET and 1H-MR spectroscopy in pediatric supratentorial infiltrative gliomas: a comparative studyGiovanni Morana, Arnoldo Piccardo, Matteo Puntoni, et al.
Pageof 5