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Matteo Cassina

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Endocrine Connections|August 27, 2025
Optimising diagnosis in children with Short Stature: an integrated clinical and NGS approachLaura Guazzarotti, Chiara Mozzato, Silvia Zoletto, et al.
Expert Opinion on Drug Safety|July 29, 2010
Migraine therapy during pregnancy and lactationMatteo Cassina, Elena Di Gianantonio, Irene Toldo, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|December 13, 2017
Prenatal detection of trisomy 8 mosaicism: Pregnancy outcome and follow up of a series of 17 consecutive casesMatteo Cassina, Annapaola Calò, Leonardo Salviati, et al.
Fetal and Pediatric Pathology|March 15, 2012
Congenital pulmonary airway malformation (CPAM) [congenital cystic adenomatoid malformation] associated with tracheoesophageal fistula and agensesis of the corpus callosumMarco Pizzi, Matteo Fassan, Kathrin Ludwig, et al.
Journal of Nephrology|June 5, 2021
Genotype-phenotype correlation in Gordon's syndrome: report of two cases carrying novel heterozygous mutationsFranca Anglani, Leonardo Salviati, Matteo Cassina, et al.
Molecular Syndromology|August 16, 2014
Genetics of coenzyme q10 deficiencyMara Doimo, Maria A Desbats, Cristina Cerqua, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 17, 2024
Characterization of Two Novel PNKP Splice-Site Variants in a Proband With Microcephaly, Intellectual Disability, and Multiple MalformationsUgo Sorrentino, Elisa Baschiera, Maria Andrea Desbats, et al.
The Journal of Clinical Endocrinology and Metabolism|July 30, 2010
Treatment of hyperthyroidism in pregnancy and birth defectsMaurizio Clementi, Elena Di Gianantonio, Matteo Cassina, et al.
European Journal of Human Genetics : EJHG|December 15, 2016
A synonymous splicing mutation in the SF3B4 gene segregates in a family with highly variable Nager syndromeMatteo Cassina, Cristina Cerqua, Silvia Rossi, et al.
Genes|March 29, 2023
Homozygous <i>TNNI3</i> Mutations and Severe Early Onset Dilated Cardiomyopathy: Patient Report and Review of the LiteratureUgo Sorrentino, Ilaria Gabbiato, Chiara Canciani, et al.
Pageof 7

Showing results (11-20 of 70) with videos related to

Sort By:
Pageof 7
Endocrine Connections|August 27, 2025
Optimising diagnosis in children with Short Stature: an integrated clinical and NGS approachLaura Guazzarotti, Chiara Mozzato, Silvia Zoletto, et al.
Expert Opinion on Drug Safety|July 29, 2010
Migraine therapy during pregnancy and lactationMatteo Cassina, Elena Di Gianantonio, Irene Toldo, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|December 13, 2017
Prenatal detection of trisomy 8 mosaicism: Pregnancy outcome and follow up of a series of 17 consecutive casesMatteo Cassina, Annapaola Calò, Leonardo Salviati, et al.
Fetal and Pediatric Pathology|March 15, 2012
Congenital pulmonary airway malformation (CPAM) [congenital cystic adenomatoid malformation] associated with tracheoesophageal fistula and agensesis of the corpus callosumMarco Pizzi, Matteo Fassan, Kathrin Ludwig, et al.
Journal of Nephrology|June 5, 2021
Genotype-phenotype correlation in Gordon's syndrome: report of two cases carrying novel heterozygous mutationsFranca Anglani, Leonardo Salviati, Matteo Cassina, et al.
Molecular Syndromology|August 16, 2014
Genetics of coenzyme q10 deficiencyMara Doimo, Maria A Desbats, Cristina Cerqua, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 17, 2024
Characterization of Two Novel PNKP Splice-Site Variants in a Proband With Microcephaly, Intellectual Disability, and Multiple MalformationsUgo Sorrentino, Elisa Baschiera, Maria Andrea Desbats, et al.
The Journal of Clinical Endocrinology and Metabolism|July 30, 2010
Treatment of hyperthyroidism in pregnancy and birth defectsMaurizio Clementi, Elena Di Gianantonio, Matteo Cassina, et al.
European Journal of Human Genetics : EJHG|December 15, 2016
A synonymous splicing mutation in the SF3B4 gene segregates in a family with highly variable Nager syndromeMatteo Cassina, Cristina Cerqua, Silvia Rossi, et al.
Genes|March 29, 2023
Homozygous <i>TNNI3</i> Mutations and Severe Early Onset Dilated Cardiomyopathy: Patient Report and Review of the LiteratureUgo Sorrentino, Ilaria Gabbiato, Chiara Canciani, et al.
Pageof 7