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Christina Nassif

Showing results (11-20 of 24) with videos related to

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American Journal of Human Genetics|April 25, 2017
Dysfunction of the Cerebral Glucose Transporter SLC45A1 in Individuals with Intellectual Disability and EpilepsyMyriam Srour, Noriaki Shimokawa, Fadi F Hamdan, et al.
Lab on a Chip|January 16, 2024
Centrifugal microfluidic system for colorimetric sample-to-answer detection of viral pathogensMatthias Geissler, Daniel Brassard, Nadine Adam, et al.
Materials (Basel, Switzerland)|January 25, 2025
Microfluidic Integration of Magnetically Functionalized Microwires for Flow Cytometry Protein QuantificationLiviu Clime, Catalin Pavel, Lidija Malic, et al.
Lab on a Chip|June 16, 2026
Adeno-associated viral vector purification using a centrifugal microfluidic system: towards workflow automation for low-volume sample processingMatthias Geissler, Lidija Malic, Liviu Clime, et al.
Plos Genetics|October 31, 2014
De novo mutations in moderate or severe intellectual disabilityFadi F Hamdan, Myriam Srour, Jose-Mario Capo-Chichi, et al.
Journal of Medical Genetics|February 5, 2015
Disruption of CLPB is associated with congenital microcephaly, severe encephalopathy and 3-methylglutaconic aciduriaJosé-Mario Capo-Chichi, Sarah Boissel, Edna Brustein, et al.
BMC Medical Genetics|December 20, 2014
Mutations in NFKB2 and potential genetic heterogeneity in patients with DAVID syndrome, having variable endocrine and immune deficienciesThierry Brue, Marie-Hélène Quentien, Konstantin Khetchoumian, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 21, 2017
Genomic study of severe fetal anomalies and discovery of GREB1L mutations in renal agenesisSarah Boissel, Catherine Fallet-Bianco, David Chitayat, et al.
Nature Communications|May 27, 2025
A machine learning and centrifugal microfluidics platform for bedside prediction of sepsisLidija Malic, Peter G Y Zhang, Pamela J Plant, et al.
Journal of Medical Genetics|March 31, 2018
Chitayat-Hall and Schaaf-Yang syndromes:a common aetiology: expanding the phenotype of <i>MAGEL2</i>-related disordersRebekah Jobling, Dimitri James Stavropoulos, Christian R Marshall, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
American Journal of Human Genetics|April 25, 2017
Dysfunction of the Cerebral Glucose Transporter SLC45A1 in Individuals with Intellectual Disability and EpilepsyMyriam Srour, Noriaki Shimokawa, Fadi F Hamdan, et al.
Lab on a Chip|January 16, 2024
Centrifugal microfluidic system for colorimetric sample-to-answer detection of viral pathogensMatthias Geissler, Daniel Brassard, Nadine Adam, et al.
Materials (Basel, Switzerland)|January 25, 2025
Microfluidic Integration of Magnetically Functionalized Microwires for Flow Cytometry Protein QuantificationLiviu Clime, Catalin Pavel, Lidija Malic, et al.
Lab on a Chip|June 16, 2026
Adeno-associated viral vector purification using a centrifugal microfluidic system: towards workflow automation for low-volume sample processingMatthias Geissler, Lidija Malic, Liviu Clime, et al.
Plos Genetics|October 31, 2014
De novo mutations in moderate or severe intellectual disabilityFadi F Hamdan, Myriam Srour, Jose-Mario Capo-Chichi, et al.
Journal of Medical Genetics|February 5, 2015
Disruption of CLPB is associated with congenital microcephaly, severe encephalopathy and 3-methylglutaconic aciduriaJosé-Mario Capo-Chichi, Sarah Boissel, Edna Brustein, et al.
BMC Medical Genetics|December 20, 2014
Mutations in NFKB2 and potential genetic heterogeneity in patients with DAVID syndrome, having variable endocrine and immune deficienciesThierry Brue, Marie-Hélène Quentien, Konstantin Khetchoumian, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 21, 2017
Genomic study of severe fetal anomalies and discovery of GREB1L mutations in renal agenesisSarah Boissel, Catherine Fallet-Bianco, David Chitayat, et al.
Nature Communications|May 27, 2025
A machine learning and centrifugal microfluidics platform for bedside prediction of sepsisLidija Malic, Peter G Y Zhang, Pamela J Plant, et al.
Journal of Medical Genetics|March 31, 2018
Chitayat-Hall and Schaaf-Yang syndromes:a common aetiology: expanding the phenotype of <i>MAGEL2</i>-related disordersRebekah Jobling, Dimitri James Stavropoulos, Christian R Marshall, et al.
Pageof 3