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Judit Horvath

Showing results (51-60 of 76) with videos related to

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Journal of Parkinson'S Disease|May 6, 2026
Frontal subcortical executive dysfunction and minor hallucinations in Parkinson's disease are linked to sensitivity to somatomotor conflictsJevita Potheegadoo, Léa F Duong Phan Thanh, Fosco Bernasconi, et al.
Journal of Medical Genetics|April 9, 2013
Evaluating the performance of the breast cancer genetic risk models BOADICEA, IBIS, BRCAPRO and Claus for predicting BRCA1/2 mutation carrier probabilities: a study based on 7352 families from the German Hereditary Breast and Ovarian Cancer ConsortiumChristine Fischer, Karoline Kuchenbäcker, Christoph Engel, et al.
American Journal of Respiratory and Critical Care Medicine|April 22, 2006
DNAH5 mutations are a common cause of primary ciliary dyskinesia with outer dynein arm defectsNada Hornef, Heike Olbrich, Judit Horvath, et al.
Acta Neuropathologica Communications|July 27, 2023
Mitochondrial DNA mutations in MedulloblastomaViktoria L E Funke, Sarah Sandmann, Viktoria Melcher, et al.
American Journal of Human Genetics|October 28, 2008
DNAI2 mutations cause primary ciliary dyskinesia with defects in the outer dynein armNiki Tomas Loges, Heike Olbrich, Lale Fenske, et al.
Breast Care (Basel, Switzerland)|June 15, 2022
Consensus Recommendations of the German Consortium for Hereditary Breast and Ovarian CancerKerstin Rhiem, Bernd Auber, Susanne Briest, et al.
Science Translational Medicine|April 29, 2021
Robot-induced hallucinations in Parkinson's disease depend on altered sensorimotor processing in fronto-temporal networkFosco Bernasconi, Eva Blondiaux, Jevita Potheegadoo, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 12, 2024
Biallelic USP14 variants cause a syndromic neurodevelopmental disorderFrédéric Ebstein, Xenia Latypova, Ka Ying Sharon Hung, et al.
American Journal of Respiratory and Critical Care Medicine|July 22, 2006
Mutations of DNAI1 in primary ciliary dyskinesia: evidence of founder effect in a common mutationMaimoona A Zariwala, Margaret W Leigh, Franck Ceppa, et al.
American Journal of Human Genetics|April 5, 2024
Clustered de novo start-loss variants in GLUL result in a developmental and epileptic encephalopathy via stabilization of glutamine synthetaseAmy G Jones, Matilde Aquilino, Rory J Tinker, et al.
Pageof 8

Showing results (51-60 of 76) with videos related to

Sort By:
Pageof 8
Journal of Parkinson'S Disease|May 6, 2026
Frontal subcortical executive dysfunction and minor hallucinations in Parkinson's disease are linked to sensitivity to somatomotor conflictsJevita Potheegadoo, Léa F Duong Phan Thanh, Fosco Bernasconi, et al.
Journal of Medical Genetics|April 9, 2013
Evaluating the performance of the breast cancer genetic risk models BOADICEA, IBIS, BRCAPRO and Claus for predicting BRCA1/2 mutation carrier probabilities: a study based on 7352 families from the German Hereditary Breast and Ovarian Cancer ConsortiumChristine Fischer, Karoline Kuchenbäcker, Christoph Engel, et al.
American Journal of Respiratory and Critical Care Medicine|April 22, 2006
DNAH5 mutations are a common cause of primary ciliary dyskinesia with outer dynein arm defectsNada Hornef, Heike Olbrich, Judit Horvath, et al.
Acta Neuropathologica Communications|July 27, 2023
Mitochondrial DNA mutations in MedulloblastomaViktoria L E Funke, Sarah Sandmann, Viktoria Melcher, et al.
American Journal of Human Genetics|October 28, 2008
DNAI2 mutations cause primary ciliary dyskinesia with defects in the outer dynein armNiki Tomas Loges, Heike Olbrich, Lale Fenske, et al.
Breast Care (Basel, Switzerland)|June 15, 2022
Consensus Recommendations of the German Consortium for Hereditary Breast and Ovarian CancerKerstin Rhiem, Bernd Auber, Susanne Briest, et al.
Science Translational Medicine|April 29, 2021
Robot-induced hallucinations in Parkinson's disease depend on altered sensorimotor processing in fronto-temporal networkFosco Bernasconi, Eva Blondiaux, Jevita Potheegadoo, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 12, 2024
Biallelic USP14 variants cause a syndromic neurodevelopmental disorderFrédéric Ebstein, Xenia Latypova, Ka Ying Sharon Hung, et al.
American Journal of Respiratory and Critical Care Medicine|July 22, 2006
Mutations of DNAI1 in primary ciliary dyskinesia: evidence of founder effect in a common mutationMaimoona A Zariwala, Margaret W Leigh, Franck Ceppa, et al.
American Journal of Human Genetics|April 5, 2024
Clustered de novo start-loss variants in GLUL result in a developmental and epileptic encephalopathy via stabilization of glutamine synthetaseAmy G Jones, Matilde Aquilino, Rory J Tinker, et al.
Pageof 8