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Elisa Cattaneo

Showing results (1-10 of 33) with videos related to

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European Journal of Medical Genetics|December 25, 2015
Rare interstitial deletion of chromosome 2p11.2p12. Report of a new patient with developmental delay and unusual clinical featuresRosamaria Silipigni, Elisa Cattaneo, Marco Baccarin, et al.
Neuropediatrics|November 29, 2021
Progressive Clinical and Neuroradiological Findings in a Child with BCL11B Missense Mutation: Expanding the Phenotypic Spectrum of Related DisorderEnrico Alfei, Elisa Cattaneo, Luigina Spaccini, et al.
International Journal of Molecular Sciences|April 17, 2025
Advancing Forensic Human Chronological Age Estimation: Biochemical, Genetic, and Epigenetic Approaches from the Last 15 Years: A Systematic ReviewBeatrice Marcante, Laura Marino, Narjis Elisa Cattaneo, et al.
Journal of Biomolecular Techniques : JBT|April 2, 2010
Laser-capture microdissection impairs activity-based protein profiles for serine hydrolase in human lung adenocarcinomaStéphane Collaud, Thomas Wiedl, Elisa Cattaneo, et al.
Italian Journal of Pediatrics|June 5, 2016
Moebius syndrome: clinical features, diagnosis, management and early interventionOdoardo Picciolini, Matteo Porro, Elisa Cattaneo, et al.
International Journal of Environmental Research and Public Health|August 27, 2021
Autosomal Dominant Hypophosphatemic Rickets: A Case Report and Review of the LiteratureChiara Mameli, Arianna Sangiorgio, Valeria Colombo, et al.
Italian Journal of Pediatrics|May 27, 2018
Currarino syndrome and microcephaly due to a rare 7q36.2 microdeletion: a case reportLucia Cococcioni, Susanna Paccagnini, Elena Pozzi, et al.
Neurogenetics|September 9, 2020
Cerebellar dysplasia related to PIK3CA mutation: a three-case seriesMartina Di Stasi, Giana Izzo, Elisa Cattaneo, et al.
Case Reports in Endocrinology|December 15, 2025
Concomitant Mutations in the Thyroglobulin and SLC26A4 Genes Leading to Fetal Goiter and Congenital Hypothyroidism in a Patient With Pendred SyndromeValeria Calcaterra, Mariano Lanna, Elisa Ligato, et al.
Molecular Cancer|December 18, 2009
The protein tyrosine phosphatase receptor type R gene is an early and frequent target of silencing in human colorectal tumorigenesisMirco Menigatti, Elisa Cattaneo, Jacob Sabates-Bellver, et al.
Pageof 4

Showing results (1-10 of 33) with videos related to

Sort By:
Pageof 4
European Journal of Medical Genetics|December 25, 2015
Rare interstitial deletion of chromosome 2p11.2p12. Report of a new patient with developmental delay and unusual clinical featuresRosamaria Silipigni, Elisa Cattaneo, Marco Baccarin, et al.
Neuropediatrics|November 29, 2021
Progressive Clinical and Neuroradiological Findings in a Child with BCL11B Missense Mutation: Expanding the Phenotypic Spectrum of Related DisorderEnrico Alfei, Elisa Cattaneo, Luigina Spaccini, et al.
International Journal of Molecular Sciences|April 17, 2025
Advancing Forensic Human Chronological Age Estimation: Biochemical, Genetic, and Epigenetic Approaches from the Last 15 Years: A Systematic ReviewBeatrice Marcante, Laura Marino, Narjis Elisa Cattaneo, et al.
Journal of Biomolecular Techniques : JBT|April 2, 2010
Laser-capture microdissection impairs activity-based protein profiles for serine hydrolase in human lung adenocarcinomaStéphane Collaud, Thomas Wiedl, Elisa Cattaneo, et al.
Italian Journal of Pediatrics|June 5, 2016
Moebius syndrome: clinical features, diagnosis, management and early interventionOdoardo Picciolini, Matteo Porro, Elisa Cattaneo, et al.
International Journal of Environmental Research and Public Health|August 27, 2021
Autosomal Dominant Hypophosphatemic Rickets: A Case Report and Review of the LiteratureChiara Mameli, Arianna Sangiorgio, Valeria Colombo, et al.
Italian Journal of Pediatrics|May 27, 2018
Currarino syndrome and microcephaly due to a rare 7q36.2 microdeletion: a case reportLucia Cococcioni, Susanna Paccagnini, Elena Pozzi, et al.
Neurogenetics|September 9, 2020
Cerebellar dysplasia related to PIK3CA mutation: a three-case seriesMartina Di Stasi, Giana Izzo, Elisa Cattaneo, et al.
Case Reports in Endocrinology|December 15, 2025
Concomitant Mutations in the Thyroglobulin and SLC26A4 Genes Leading to Fetal Goiter and Congenital Hypothyroidism in a Patient With Pendred SyndromeValeria Calcaterra, Mariano Lanna, Elisa Ligato, et al.
Molecular Cancer|December 18, 2009
The protein tyrosine phosphatase receptor type R gene is an early and frequent target of silencing in human colorectal tumorigenesisMirco Menigatti, Elisa Cattaneo, Jacob Sabates-Bellver, et al.
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