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Aleksandra Landowska

Showing results (1-10 of 12) with videos related to

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Developmental Period Medicine|April 12, 2018
[Fragile X syndrome and FMR1-dependent diseases - diagnostic scheme based on own experience .]Aleksandra Landowska, Sylwia Rzońca, Jerzy Bal, et al.
Developmental Period Medicine|April 12, 2018
[Fragile X syndrome and FMR1-dependent diseases - clinical presentation, epidemiology and molecular background]Aleksandra Landowska, Sylwia Rzońca, Jerzy Bal, et al.
Frontiers in Human Neuroscience|November 17, 2018
Within- and Between-Session Prefrontal Cortex Response to Virtual Reality Exposure Therapy for AcrophobiaAleksandra Landowska, David Roberts, Peter Eachus, et al.
JMIR Serious Games|June 20, 2022
Perceptions of Cognitive Training Games and Assessment Technologies for Dementia: Acceptability Study With Patient and Public Involvement WorkshopsKyle Harrington, Michael P Craven, Max L Wilson, et al.
Frontiers in Neuroergonomics|January 18, 2024
Benchmarking framework for machine learning classification from fNIRS dataJohann Benerradi, Jeremie Clos, Aleksandra Landowska, et al.
American Journal of Medical Genetics. Part A|May 26, 2018
MAP2K2 mutation as a cause of cardio-facio-cutaneous syndrome in an infant with a severe and fatal course of the diseaseMonika Gos, Robert Smigiel, Teresa Kaczan, et al.
Scientific Reports|December 28, 2024
Performance metrics outperform physiological indicators in robotic teleoperation workload assessmentGift Odoh, Aleksandra Landowska, Emily M Crowe, et al.
Genes|December 23, 2023
Research on the Pathogenesis of Cognitive and Neurofunctional Impairments in Patients with Noonan Syndrome: The Role of Rat Sarcoma-Mitogen Activated Protein Kinase Signaling Pathway Gene DisturbancesNatalia Braun-Walicka, Agnieszka Pluta, Tomasz Wolak, et al.
Genes|September 7, 2016
Towards a Better Molecular Diagnosis of FMR1-Related Disorders-A Multiyear Experience from a Reference LabSylwia Olimpia Rzońca, Monika Gos, Daniel Szopa, et al.
Molecular Genetics and Metabolism|January 25, 2026
A rare GCH1 p.Arg170Gly variant shows impaired enzymatic activity and co-occurs with a novel NEXMIF p.Asp155GlnfsTer2 leading to a complex neurological phenotype: functional studies and clinical aspectsKlaudia Ślusarczyk, Julia Zuzanna Kamińska, Katarzyna Kuśmierska, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Developmental Period Medicine|April 12, 2018
[Fragile X syndrome and FMR1-dependent diseases - diagnostic scheme based on own experience .]Aleksandra Landowska, Sylwia Rzońca, Jerzy Bal, et al.
Developmental Period Medicine|April 12, 2018
[Fragile X syndrome and FMR1-dependent diseases - clinical presentation, epidemiology and molecular background]Aleksandra Landowska, Sylwia Rzońca, Jerzy Bal, et al.
Frontiers in Human Neuroscience|November 17, 2018
Within- and Between-Session Prefrontal Cortex Response to Virtual Reality Exposure Therapy for AcrophobiaAleksandra Landowska, David Roberts, Peter Eachus, et al.
JMIR Serious Games|June 20, 2022
Perceptions of Cognitive Training Games and Assessment Technologies for Dementia: Acceptability Study With Patient and Public Involvement WorkshopsKyle Harrington, Michael P Craven, Max L Wilson, et al.
Frontiers in Neuroergonomics|January 18, 2024
Benchmarking framework for machine learning classification from fNIRS dataJohann Benerradi, Jeremie Clos, Aleksandra Landowska, et al.
American Journal of Medical Genetics. Part A|May 26, 2018
MAP2K2 mutation as a cause of cardio-facio-cutaneous syndrome in an infant with a severe and fatal course of the diseaseMonika Gos, Robert Smigiel, Teresa Kaczan, et al.
Scientific Reports|December 28, 2024
Performance metrics outperform physiological indicators in robotic teleoperation workload assessmentGift Odoh, Aleksandra Landowska, Emily M Crowe, et al.
Genes|December 23, 2023
Research on the Pathogenesis of Cognitive and Neurofunctional Impairments in Patients with Noonan Syndrome: The Role of Rat Sarcoma-Mitogen Activated Protein Kinase Signaling Pathway Gene DisturbancesNatalia Braun-Walicka, Agnieszka Pluta, Tomasz Wolak, et al.
Genes|September 7, 2016
Towards a Better Molecular Diagnosis of FMR1-Related Disorders-A Multiyear Experience from a Reference LabSylwia Olimpia Rzońca, Monika Gos, Daniel Szopa, et al.
Molecular Genetics and Metabolism|January 25, 2026
A rare GCH1 p.Arg170Gly variant shows impaired enzymatic activity and co-occurs with a novel NEXMIF p.Asp155GlnfsTer2 leading to a complex neurological phenotype: functional studies and clinical aspectsKlaudia Ślusarczyk, Julia Zuzanna Kamińska, Katarzyna Kuśmierska, et al.
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