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G Zanni

Showing results (31-40 of 42) with videos related to

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European Urology|May 11, 2006
Bilateral renal mass suggestive of cancer: part 2M Roscigno, R Colombo, M Freschi, et al.
European Urology|February 25, 2006
Bilateral renal mass suggestive of cancerM Roscigno, R Colombo, M Freschi, et al.
New Biotechnology|November 28, 2012
The SNPs in the human genetic blueprint eraS Giampaoli, G Chillemi, F Valeriani, et al.
Frontiers in Pediatrics|July 4, 2025
Case Report: Diagnostic assessment, developmental trajectory and treatment approaches in a case of a complex neurodevelopmental syndrome associated with non- synonymous variants in <i>MECP2</i> (p. R133C) and <i>GABBR1</i>V Napoli, S Guerrera, F Demaria, et al.
Arzneimittel-Forschung|August 1, 1973
New analgesic-anti-inflammatory drugs. 1-Oxo-2-substituted isoindoline derivativesG Nannini, P N Giraldi, G Molgora, et al.
Blood|February 15, 1995
Monoclonal gammopathies and hepatitis C virus infectionC Mussini, M Ghini, M T Mascia, et al.
Clinical Genetics|April 11, 2016
Mutations in the IRBIT domain of ITPR1 are a frequent cause of autosomal dominant nonprogressive congenital ataxiaS Barresi, M Niceta, P Alfieri, et al.
Cerebellum (London, England)|June 5, 2021
PIGQ-Related Glycophosphatidylinositol Deficiency Associated with Nonprogressive Congenital AtaxiaG Zanni, F D'Abrusco, F Nicita, et al.
Neurology|October 14, 2005
Oligophrenin 1 mutations frequently cause X-linked mental retardation with cerebellar hypoplasiaG Zanni, Y Saillour, M Nagara, et al.
Stem Cell Research|May 20, 2025
Production and characterisation of four Joubert syndrome patient-derived induced pluripotent stem cell (iPSC) lines with mutations in either RPGRIP1L or CPLANE1 genesL Pollara, E de Gregorio, V Buonofiglio, et al.
Pageof 5

Showing results (31-40 of 42) with videos related to

Sort By:
Pageof 5
European Urology|May 11, 2006
Bilateral renal mass suggestive of cancer: part 2M Roscigno, R Colombo, M Freschi, et al.
European Urology|February 25, 2006
Bilateral renal mass suggestive of cancerM Roscigno, R Colombo, M Freschi, et al.
New Biotechnology|November 28, 2012
The SNPs in the human genetic blueprint eraS Giampaoli, G Chillemi, F Valeriani, et al.
Frontiers in Pediatrics|July 4, 2025
Case Report: Diagnostic assessment, developmental trajectory and treatment approaches in a case of a complex neurodevelopmental syndrome associated with non- synonymous variants in <i>MECP2</i> (p. R133C) and <i>GABBR1</i>V Napoli, S Guerrera, F Demaria, et al.
Arzneimittel-Forschung|August 1, 1973
New analgesic-anti-inflammatory drugs. 1-Oxo-2-substituted isoindoline derivativesG Nannini, P N Giraldi, G Molgora, et al.
Blood|February 15, 1995
Monoclonal gammopathies and hepatitis C virus infectionC Mussini, M Ghini, M T Mascia, et al.
Clinical Genetics|April 11, 2016
Mutations in the IRBIT domain of ITPR1 are a frequent cause of autosomal dominant nonprogressive congenital ataxiaS Barresi, M Niceta, P Alfieri, et al.
Cerebellum (London, England)|June 5, 2021
PIGQ-Related Glycophosphatidylinositol Deficiency Associated with Nonprogressive Congenital AtaxiaG Zanni, F D'Abrusco, F Nicita, et al.
Neurology|October 14, 2005
Oligophrenin 1 mutations frequently cause X-linked mental retardation with cerebellar hypoplasiaG Zanni, Y Saillour, M Nagara, et al.
Stem Cell Research|May 20, 2025
Production and characterisation of four Joubert syndrome patient-derived induced pluripotent stem cell (iPSC) lines with mutations in either RPGRIP1L or CPLANE1 genesL Pollara, E de Gregorio, V Buonofiglio, et al.
Pageof 5