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Joana Cerqueira

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Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|December 3, 2025
Designing Real-Time EEG and ECG Integration for VR-Based Exposure Therapy: A User StudyAndre Antunes, Joana Cerqueira, Iris Peixoto, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 14, 2011
Intergenerational instability in Huntington disease: extreme repeat changes among 134 transmissionsEliana Marisa Ramos, Joana Cerqueira, Carolina Lemos, et al.
Clinical and Experimental Dental Research|November 6, 2019
Integrating piezoresistive sensors on the embouchure analysis of the lower lip in single reed instrumentalists: implementation of the lip pressure appliance (LPA)Miguel Pais Clemente, Joaquim Mendes, Joana Cerqueira, et al.
Journal of Human Genetics|July 22, 2006
Exclusion of mutations in the PRNP, JPH3, TBP, ATN1, CREBBP, POU3F2 and FTL genes as a cause of disease in Portuguese patients with a Huntington-like phenotypeMaria do Carmo Costa, Andreia Teixeira-Castro, Marco Constante, et al.
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Showing results (1-10 of 4) with videos related to

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Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|December 3, 2025
Designing Real-Time EEG and ECG Integration for VR-Based Exposure Therapy: A User StudyAndre Antunes, Joana Cerqueira, Iris Peixoto, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 14, 2011
Intergenerational instability in Huntington disease: extreme repeat changes among 134 transmissionsEliana Marisa Ramos, Joana Cerqueira, Carolina Lemos, et al.
Clinical and Experimental Dental Research|November 6, 2019
Integrating piezoresistive sensors on the embouchure analysis of the lower lip in single reed instrumentalists: implementation of the lip pressure appliance (LPA)Miguel Pais Clemente, Joaquim Mendes, Joana Cerqueira, et al.
Journal of Human Genetics|July 22, 2006
Exclusion of mutations in the PRNP, JPH3, TBP, ATN1, CREBBP, POU3F2 and FTL genes as a cause of disease in Portuguese patients with a Huntington-like phenotypeMaria do Carmo Costa, Andreia Teixeira-Castro, Marco Constante, et al.
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