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

Peter Bauer

Showing results (201-210 of 585) with videos related to

Pageof 59
Sort By:
European Journal of Human Genetics : EJHG|April 1, 2010
Early onset and slow progression of SCA28, a rare dominant ataxia in a large four-generation family with a novel AFG3L2 mutationUlf Edener, Janine Wöllner, Ute Hehr, et al.
European Heart Journal|August 24, 2004
Suppression of paroxysmal atrial tachyarrhythmias--results of the SOPAT trialMonica Patten, Renke Maas, Peter Bauer, et al.
BMC Public Health|September 3, 2015
Changes in dietary intake during puberty and their determinants: results from the GINIplus birth cohort studyCarla Harris, Claudia Flexeder, Elisabeth Thiering, et al.
European Journal of Human Genetics : EJHG|August 4, 2011
Discrepancies in reporting the CAG repeat lengths for Huntington's diseaseOliver W Quarrell, Olivia Handley, Kirsty O'Donovan, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 25, 2004
Lack of mutations in the epsilon-sarcoglycan gene in patients with different subtypes of primary dystoniasKathrin Grundmann, Ulrike Laubis-Herrmann, Dirk Dressler, et al.
Sleep Medicine|June 20, 2020
Association between objectively assessed physical activity and sleep quality in adolescence. Results from the GINIplus and LISA studiesLaura Negele, Claudia Flexeder, Sibylle Koletzko, et al.
Neuroscience Letters|November 15, 2003
Screening for mutations of the ferritin light and heavy genes in Parkinson's disease patients with hyperechogenicity of the substantia nigraBettina Felletschin, Peter Bauer, Uwe Walter, et al.
Clinical Chemistry|November 26, 2008
Polymorphisms in inflammatory genes and the risk of ischemic stroke and transient ischemic attack: results of a multilocus genotyping assayStefan Greisenegger, Sonja Zehetmayer, Peter Bauer, et al.
Lancet (London, England)|February 5, 2013
Mortality after surgery in Europe - Authors' replyRupert Pearse, Rui P Moreno, Peter Bauer, et al.
Pediatric Pulmonology|June 16, 2015
Peak weight velocity in infancy is negatively associated with lung function in adolescenceFlexeder Claudia, Elisabeth Thiering, Andrea von Berg, et al.
Pageof 59

Showing results (201-210 of 585) with videos related to

Sort By:
Pageof 59
European Journal of Human Genetics : EJHG|April 1, 2010
Early onset and slow progression of SCA28, a rare dominant ataxia in a large four-generation family with a novel AFG3L2 mutationUlf Edener, Janine Wöllner, Ute Hehr, et al.
European Heart Journal|August 24, 2004
Suppression of paroxysmal atrial tachyarrhythmias--results of the SOPAT trialMonica Patten, Renke Maas, Peter Bauer, et al.
BMC Public Health|September 3, 2015
Changes in dietary intake during puberty and their determinants: results from the GINIplus birth cohort studyCarla Harris, Claudia Flexeder, Elisabeth Thiering, et al.
European Journal of Human Genetics : EJHG|August 4, 2011
Discrepancies in reporting the CAG repeat lengths for Huntington's diseaseOliver W Quarrell, Olivia Handley, Kirsty O'Donovan, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 25, 2004
Lack of mutations in the epsilon-sarcoglycan gene in patients with different subtypes of primary dystoniasKathrin Grundmann, Ulrike Laubis-Herrmann, Dirk Dressler, et al.
Sleep Medicine|June 20, 2020
Association between objectively assessed physical activity and sleep quality in adolescence. Results from the GINIplus and LISA studiesLaura Negele, Claudia Flexeder, Sibylle Koletzko, et al.
Neuroscience Letters|November 15, 2003
Screening for mutations of the ferritin light and heavy genes in Parkinson's disease patients with hyperechogenicity of the substantia nigraBettina Felletschin, Peter Bauer, Uwe Walter, et al.
Clinical Chemistry|November 26, 2008
Polymorphisms in inflammatory genes and the risk of ischemic stroke and transient ischemic attack: results of a multilocus genotyping assayStefan Greisenegger, Sonja Zehetmayer, Peter Bauer, et al.
Lancet (London, England)|February 5, 2013
Mortality after surgery in Europe - Authors' replyRupert Pearse, Rui P Moreno, Peter Bauer, et al.
Pediatric Pulmonology|June 16, 2015
Peak weight velocity in infancy is negatively associated with lung function in adolescenceFlexeder Claudia, Elisabeth Thiering, Andrea von Berg, et al.
Pageof 59