Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Magdalena Mroczek

Showing results (31-40 of 45) with videos related to

Pageof 5
Sort By:
Cancers|February 11, 2023
Genetics, Genomics and Emerging Molecular Therapies of Pancreatic CancerJakub Liu, Magdalena Mroczek, Anna Mach, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|April 18, 2025
AI-assisted identification of disability patterns within identical EDSS gradesMartina Greselin, Po-Jui Lu, Magdalena Mroczek, et al.
Neuropediatrics|December 22, 2020
Three Individuals with PURA Syndrome in a Cohort of Patients with Neuromuscular DiseaseMagdalena Mroczek, Dimitrios Zafeiriou, Juliana Gurgel-Gianetti, et al.
Brain Communications|July 9, 2024
Pathologic <i>RFC1</i> repeat expansions do not contribute to the development of inflammatory neuropathiesSara Nagy, Aisling Carr, Magdalena Mroczek, et al.
Plos One|January 20, 2023
Better safe than sorry-Whole-genome sequencing indicates that missense variants are significant in susceptibility to COVID-19Dawid Słomian, Joanna Szyda, Paula Dobosz, et al.
Frontiers in Oncology|February 27, 2023
The cancer-risk variant frequency among Polish population reported by the first national whole-genome sequencing studyMagdalena Mroczek, Jakub Liu, Mateusz Sypniewski, et al.
International Journal of Molecular Sciences|August 12, 2022
Gene Variants Related to Cardiovascular and Pulmonary Diseases May Correlate with Severe Outcome of COVID-19Mateusz Sypniewski, Zbigniew J Król, Joanna Szyda, et al.
Journal of Medical Genetics|April 8, 2022
<i>FXR1</i>-related congenital myopathy: expansion of the clinical and genetic spectrumMagdalena Mroczek, Cheryl Longman, Maria Elena Farrugia, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|December 20, 2024
Neurostatus-SMARTCARE clinical trial: Enabling health care professionals to assess EDSS for decentralized trials in multiple sclerosisGiulia Mallucci, Andrea Zimmer, Nikolaos Sfikas, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 13, 2020
Sequential targeted exome sequencing of 1001 patients affected by unexplained limb-girdle weaknessAna Töpf, Katherine Johnson, Adam Bates, et al.
Pageof 5

Showing results (31-40 of 45) with videos related to

Sort By:
Pageof 5
Cancers|February 11, 2023
Genetics, Genomics and Emerging Molecular Therapies of Pancreatic CancerJakub Liu, Magdalena Mroczek, Anna Mach, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|April 18, 2025
AI-assisted identification of disability patterns within identical EDSS gradesMartina Greselin, Po-Jui Lu, Magdalena Mroczek, et al.
Neuropediatrics|December 22, 2020
Three Individuals with PURA Syndrome in a Cohort of Patients with Neuromuscular DiseaseMagdalena Mroczek, Dimitrios Zafeiriou, Juliana Gurgel-Gianetti, et al.
Brain Communications|July 9, 2024
Pathologic <i>RFC1</i> repeat expansions do not contribute to the development of inflammatory neuropathiesSara Nagy, Aisling Carr, Magdalena Mroczek, et al.
Plos One|January 20, 2023
Better safe than sorry-Whole-genome sequencing indicates that missense variants are significant in susceptibility to COVID-19Dawid Słomian, Joanna Szyda, Paula Dobosz, et al.
Frontiers in Oncology|February 27, 2023
The cancer-risk variant frequency among Polish population reported by the first national whole-genome sequencing studyMagdalena Mroczek, Jakub Liu, Mateusz Sypniewski, et al.
International Journal of Molecular Sciences|August 12, 2022
Gene Variants Related to Cardiovascular and Pulmonary Diseases May Correlate with Severe Outcome of COVID-19Mateusz Sypniewski, Zbigniew J Król, Joanna Szyda, et al.
Journal of Medical Genetics|April 8, 2022
<i>FXR1</i>-related congenital myopathy: expansion of the clinical and genetic spectrumMagdalena Mroczek, Cheryl Longman, Maria Elena Farrugia, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|December 20, 2024
Neurostatus-SMARTCARE clinical trial: Enabling health care professionals to assess EDSS for decentralized trials in multiple sclerosisGiulia Mallucci, Andrea Zimmer, Nikolaos Sfikas, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 13, 2020
Sequential targeted exome sequencing of 1001 patients affected by unexplained limb-girdle weaknessAna Töpf, Katherine Johnson, Adam Bates, et al.
Pageof 5