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Peter Bauer

Showing results (381-390 of 585) with videos related to

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Human Molecular Genetics|June 19, 2013
Genetic screening for Niemann-Pick disease type C in adults with neurological and psychiatric symptoms: findings from the ZOOM studyPeter Bauer, David J Balding, Hans H Klünemann, et al.
European Journal of Human Genetics : EJHG|June 22, 2024
Facing the challenges to shorten the diagnostic odyssey: first Whole Genome Sequencing experience of a Colombian cohort with suspected rare diseasesHarvy Mauricio Velasco, Aida Bertoli-Avella, Carolina Jaramillo Jaramillo, et al.
European Journal of Anaesthesiology|May 23, 2015
Nonelective surgery at night and in-hospital mortality: Prospective observational data from the European Surgical Outcomes StudyBas van Zaane, Wilton A van Klei, Wolfgang F Buhre, et al.
Neurogenetics|May 4, 2012
A high-throughput resequencing microarray for autosomal dominant spastic paraplegia genesClaudia Dufke, Nina Schlipf, Rebecca Schüle, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 12, 2018
Utility and implications of exome sequencing in early-onset Parkinson's diseaseJoanne Trinh, Katja Lohmann, Hauke Baumann, et al.
Medrxiv : the Preprint Server for Health Sciences|January 2, 2026
How many do we miss? - Evaluation of age at onset and family history as selection criteria for genetic testing in Parkinson's diseaseAlexander Balck, Eva-Juliane Vollstedt, Ana Westenberger, et al.
The Journal of Allergy and Clinical Immunology|May 16, 2015
Prediction and prevention of allergic rhinitis: A birth cohort study of 20 yearsLinus B Grabenhenrich, Thomas Keil, Andreas Reich, et al.
Annals of Neurology|September 30, 2005
New mutations in protein kinase Cgamma associated with spinocerebellar ataxia type 14Stephan Klebe, Alexandra Durr, Alexander Rentschler, et al.
JAMA Neurology|May 11, 2026
Genetic Testing by Age at Onset in Parkinson DiseaseAlexander Balck, Eva-Juliane Vollstedt, Ana Westenberger, et al.
European Journal of Human Genetics : EJHG|June 23, 2005
PINK1, Parkin, and DJ-1 mutations in Italian patients with early-onset parkinsonismChristine Klein, Ana Djarmati, Katja Hedrich, et al.
Pageof 59

Showing results (381-390 of 585) with videos related to

Sort By:
Pageof 59
Human Molecular Genetics|June 19, 2013
Genetic screening for Niemann-Pick disease type C in adults with neurological and psychiatric symptoms: findings from the ZOOM studyPeter Bauer, David J Balding, Hans H Klünemann, et al.
European Journal of Human Genetics : EJHG|June 22, 2024
Facing the challenges to shorten the diagnostic odyssey: first Whole Genome Sequencing experience of a Colombian cohort with suspected rare diseasesHarvy Mauricio Velasco, Aida Bertoli-Avella, Carolina Jaramillo Jaramillo, et al.
European Journal of Anaesthesiology|May 23, 2015
Nonelective surgery at night and in-hospital mortality: Prospective observational data from the European Surgical Outcomes StudyBas van Zaane, Wilton A van Klei, Wolfgang F Buhre, et al.
Neurogenetics|May 4, 2012
A high-throughput resequencing microarray for autosomal dominant spastic paraplegia genesClaudia Dufke, Nina Schlipf, Rebecca Schüle, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 12, 2018
Utility and implications of exome sequencing in early-onset Parkinson's diseaseJoanne Trinh, Katja Lohmann, Hauke Baumann, et al.
Medrxiv : the Preprint Server for Health Sciences|January 2, 2026
How many do we miss? - Evaluation of age at onset and family history as selection criteria for genetic testing in Parkinson's diseaseAlexander Balck, Eva-Juliane Vollstedt, Ana Westenberger, et al.
The Journal of Allergy and Clinical Immunology|May 16, 2015
Prediction and prevention of allergic rhinitis: A birth cohort study of 20 yearsLinus B Grabenhenrich, Thomas Keil, Andreas Reich, et al.
Annals of Neurology|September 30, 2005
New mutations in protein kinase Cgamma associated with spinocerebellar ataxia type 14Stephan Klebe, Alexandra Durr, Alexander Rentschler, et al.
JAMA Neurology|May 11, 2026
Genetic Testing by Age at Onset in Parkinson DiseaseAlexander Balck, Eva-Juliane Vollstedt, Ana Westenberger, et al.
European Journal of Human Genetics : EJHG|June 23, 2005
PINK1, Parkin, and DJ-1 mutations in Italian patients with early-onset parkinsonismChristine Klein, Ana Djarmati, Katja Hedrich, et al.
Pageof 59