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Alexandru Caramizaru

Showing results (1-10 of 6) with videos related to

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Neuropathology and Applied Neurobiology|March 13, 2026
ACTA1-Related Adult-Onset Scapuloperoneal Myopathy With Cores and RodsAlexandru Caramizaru, Marion Onnée, Sergey Nikitin, et al.
International Journal of Molecular Sciences|February 13, 2026
Phenotypic Spectrum in Three Romanian Patients with 8q23-q24 DeletionsAlexandru Caramizaru, Ioana Streata, Andrei Pirvu, et al.
Human Mutation|July 6, 2026
Autosomal Dominant Missense <i>DAG1</i> Variant Linked to Mild-Moderate LGMD R16Edoardo Malfatti, Alexandru Caramizaru, Federica Trentin, et al.
Clinical Genetics|March 17, 2026
Whole Exome Sequencing for Romanian Patients With Neurodevelopmental Disorders Through an International CollaborationAlexandru Caramizaru, Cristina Durac, Andreea Dumitrescu, et al.
Diagnostics (Basel, Switzerland)|December 23, 2022
Pathogenic Copy Number Variations Involved in the Genetic Etiology of Syndromic and Non-Syndromic Intellectual Disability-Data from a Romanian CohortIoana Streață, Alexandru Caramizaru, Anca-Lelia Riza, et al.
Clinical Genetics|February 25, 2025
NEUROMYODredger: Whole Exome Sequencing for the Diagnosis of Neurodevelopmental and Neuromuscular Disorders in Seven CountriesEdoardo Malfatti, Alexandru Caramizaru, Hane Lee, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Neuropathology and Applied Neurobiology|March 13, 2026
ACTA1-Related Adult-Onset Scapuloperoneal Myopathy With Cores and RodsAlexandru Caramizaru, Marion Onnée, Sergey Nikitin, et al.
International Journal of Molecular Sciences|February 13, 2026
Phenotypic Spectrum in Three Romanian Patients with 8q23-q24 DeletionsAlexandru Caramizaru, Ioana Streata, Andrei Pirvu, et al.
Human Mutation|July 6, 2026
Autosomal Dominant Missense <i>DAG1</i> Variant Linked to Mild-Moderate LGMD R16Edoardo Malfatti, Alexandru Caramizaru, Federica Trentin, et al.
Clinical Genetics|March 17, 2026
Whole Exome Sequencing for Romanian Patients With Neurodevelopmental Disorders Through an International CollaborationAlexandru Caramizaru, Cristina Durac, Andreea Dumitrescu, et al.
Diagnostics (Basel, Switzerland)|December 23, 2022
Pathogenic Copy Number Variations Involved in the Genetic Etiology of Syndromic and Non-Syndromic Intellectual Disability-Data from a Romanian CohortIoana Streață, Alexandru Caramizaru, Anca-Lelia Riza, et al.
Clinical Genetics|February 25, 2025
NEUROMYODredger: Whole Exome Sequencing for the Diagnosis of Neurodevelopmental and Neuromuscular Disorders in Seven CountriesEdoardo Malfatti, Alexandru Caramizaru, Hane Lee, et al.
Pageof 1