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Matteo Cassina

Showing results (31-40 of 70) with videos related to

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Reproductive Toxicology (Elmsford, N.Y.)|April 18, 2013
Pregnancy outcome in women exposed to antiepileptic drugs: teratogenic role of maternal epilepsy and its pharmacologic treatmentMatteo Cassina, Arianna Dilaghi, Elena Di Gianantonio, et al.
Clinical Chemistry and Laboratory Medicine|March 18, 2015
Validation of CFTR intronic variants identified during cystic fibrosis population screening by a minigene splicing assayGianpietro Giorgi, Alberto Casarin, Eva Trevisson, et al.
Journal of Pediatric Surgery|April 3, 2019
Prevalence and survival of patients with anorectal malformations: A population-based studyMatteo Cassina, Francesco Fascetti Leon, Michele Ruol, et al.
Cancers|December 24, 2021
Epilepsy in NF1: Epidemiologic, Genetic, and Clinical Features. A Monocentric Retrospective Study in a Cohort of 784 PatientsUgo Sorrentino, Silvia Bellonzi, Chiara Mozzato, et al.
Journal of Clinical and Experimental Neuropsychology|December 30, 2015
Clinical and genetic correlates of decision making in anorexia nervosaElena Tenconi, Daniela Degortes, Maurizio Clementi, et al.
Expert Opinion on Drug Safety|October 17, 2009
Therapy of inflammatory bowel diseases in pregnancy and lactationMatteo Cassina, Luca Fabris, Lajos Okolicsanyi, et al.
Clinical Genetics|June 25, 2023
Severe trichothiodystrophy and cardiac malformation in a newborn carrying a novel GTF2H5 homozygous truncating variantUgo Sorrentino, Caterina Agosto, Franca Benini, et al.
Molecular Genetics & Genomic Medicine|March 8, 2019
The Arg1038Gly missense variant in the NF1 gene causes a mild phenotype without neurofibromasEva Trevisson, Valeria Morbidoni, Monica Forzan, et al.
Cancers|November 20, 2019
Optic Pathway Glioma in Type 1 Neurofibromatosis: Review of Its Pathogenesis, Diagnostic Assessment, and Treatment RecommendationsMatteo Cassina, Luisa Frizziero, Enrico Opocher, et al.
Journal of Assisted Reproduction and Genetics|April 1, 2024
The impact of a second embryo biopsy for preimplantation genetic testing for monogenic diseases (PGT-M) with inconclusive results on pregnancy potential: results from a matched case-control studyCristina Guarneri, Marco Reschini, Monica Pinna, et al.
Pageof 7

Showing results (31-40 of 70) with videos related to

Sort By:
Pageof 7
Reproductive Toxicology (Elmsford, N.Y.)|April 18, 2013
Pregnancy outcome in women exposed to antiepileptic drugs: teratogenic role of maternal epilepsy and its pharmacologic treatmentMatteo Cassina, Arianna Dilaghi, Elena Di Gianantonio, et al.
Clinical Chemistry and Laboratory Medicine|March 18, 2015
Validation of CFTR intronic variants identified during cystic fibrosis population screening by a minigene splicing assayGianpietro Giorgi, Alberto Casarin, Eva Trevisson, et al.
Journal of Pediatric Surgery|April 3, 2019
Prevalence and survival of patients with anorectal malformations: A population-based studyMatteo Cassina, Francesco Fascetti Leon, Michele Ruol, et al.
Cancers|December 24, 2021
Epilepsy in NF1: Epidemiologic, Genetic, and Clinical Features. A Monocentric Retrospective Study in a Cohort of 784 PatientsUgo Sorrentino, Silvia Bellonzi, Chiara Mozzato, et al.
Journal of Clinical and Experimental Neuropsychology|December 30, 2015
Clinical and genetic correlates of decision making in anorexia nervosaElena Tenconi, Daniela Degortes, Maurizio Clementi, et al.
Expert Opinion on Drug Safety|October 17, 2009
Therapy of inflammatory bowel diseases in pregnancy and lactationMatteo Cassina, Luca Fabris, Lajos Okolicsanyi, et al.
Clinical Genetics|June 25, 2023
Severe trichothiodystrophy and cardiac malformation in a newborn carrying a novel GTF2H5 homozygous truncating variantUgo Sorrentino, Caterina Agosto, Franca Benini, et al.
Molecular Genetics & Genomic Medicine|March 8, 2019
The Arg1038Gly missense variant in the NF1 gene causes a mild phenotype without neurofibromasEva Trevisson, Valeria Morbidoni, Monica Forzan, et al.
Cancers|November 20, 2019
Optic Pathway Glioma in Type 1 Neurofibromatosis: Review of Its Pathogenesis, Diagnostic Assessment, and Treatment RecommendationsMatteo Cassina, Luisa Frizziero, Enrico Opocher, et al.
Journal of Assisted Reproduction and Genetics|April 1, 2024
The impact of a second embryo biopsy for preimplantation genetic testing for monogenic diseases (PGT-M) with inconclusive results on pregnancy potential: results from a matched case-control studyCristina Guarneri, Marco Reschini, Monica Pinna, et al.
Pageof 7