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

M KOENIG

Showing results (401-410 of 524) with videos related to

Pageof 53
Sort By:
Turkish Journal of Anaesthesiology and Reanimation|May 4, 2023
Intraoperative Fraction of Inspired Oxygen and Lung Injury in Coronary Artery Bypass Grafting: Study Protocol for a Randomised Controlled TrialKaicheng Song, Sheng Wang, Jiange Han, et al.
Nature Genetics|November 4, 2000
The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathyP Bomont, L Cavalier, F Blondeau, et al.
Annals of Surgery|January 22, 2015
Circulating Tumor Cells as a Biomarker for Preoperative Prognostic Staging in Patients With Esophageal CancerMatthias Reeh, Katharina E Effenberger, Alexandra M Koenig, et al.
Neurogenetics|March 25, 2000
Homozygosity mapping of giant axonal neuropathy gene to chromosome 16q24.1C Ben Hamida, L Cavalier, S Belal, et al.
The Journal of Arthroplasty|March 1, 2019
Preoperative Patient-Reported Outcomes and Clinical Characteristics as Predictors of 90-Day Cost/Utilization and ComplicationsDaniel J Snyder, Dennis M Bienstock, Aakash Keswani, et al.
Small (Weinheim an Der Bergstrasse, Germany)|October 20, 2023
Nanotube-Like Electronic States in [5,5]-C<sub>90</sub> Fullertube MoleculesÓscar Jover, Alberto Martín-Jiménez, Hannah M Franklin, et al.
Journal of the Neurological Sciences|January 15, 2009
Ataxia with oculomotor apraxia type 2: a clinical and genetic study of 19 patientsM Tazir, L Ali-Pacha, A M'Zahem, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Evidence for a common origin of most Friedreich ataxia chromosomes in the Spanish populationE Monrós, J Cañizares, M D Moltó, et al.
Journal of Neurology|July 19, 2024
Phenotypic variability related to dominant UCHL1 mutations: about three families with optic atrophy and ataxiaC Marelli, F Ramond, C Vignal, et al.
BMC Genomics|August 19, 2016
The beagle dog MicroRNA tissue atlas: identifying translatable biomarkers of organ toxicityErik M Koenig, Craig Fisher, Hugues Bernard, et al.
Pageof 53

Showing results (401-410 of 524) with videos related to

Sort By:
Pageof 53
Turkish Journal of Anaesthesiology and Reanimation|May 4, 2023
Intraoperative Fraction of Inspired Oxygen and Lung Injury in Coronary Artery Bypass Grafting: Study Protocol for a Randomised Controlled TrialKaicheng Song, Sheng Wang, Jiange Han, et al.
Nature Genetics|November 4, 2000
The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathyP Bomont, L Cavalier, F Blondeau, et al.
Annals of Surgery|January 22, 2015
Circulating Tumor Cells as a Biomarker for Preoperative Prognostic Staging in Patients With Esophageal CancerMatthias Reeh, Katharina E Effenberger, Alexandra M Koenig, et al.
Neurogenetics|March 25, 2000
Homozygosity mapping of giant axonal neuropathy gene to chromosome 16q24.1C Ben Hamida, L Cavalier, S Belal, et al.
The Journal of Arthroplasty|March 1, 2019
Preoperative Patient-Reported Outcomes and Clinical Characteristics as Predictors of 90-Day Cost/Utilization and ComplicationsDaniel J Snyder, Dennis M Bienstock, Aakash Keswani, et al.
Small (Weinheim an Der Bergstrasse, Germany)|October 20, 2023
Nanotube-Like Electronic States in [5,5]-C<sub>90</sub> Fullertube MoleculesÓscar Jover, Alberto Martín-Jiménez, Hannah M Franklin, et al.
Journal of the Neurological Sciences|January 15, 2009
Ataxia with oculomotor apraxia type 2: a clinical and genetic study of 19 patientsM Tazir, L Ali-Pacha, A M'Zahem, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Evidence for a common origin of most Friedreich ataxia chromosomes in the Spanish populationE Monrós, J Cañizares, M D Moltó, et al.
Journal of Neurology|July 19, 2024
Phenotypic variability related to dominant UCHL1 mutations: about three families with optic atrophy and ataxiaC Marelli, F Ramond, C Vignal, et al.
BMC Genomics|August 19, 2016
The beagle dog MicroRNA tissue atlas: identifying translatable biomarkers of organ toxicityErik M Koenig, Craig Fisher, Hugues Bernard, et al.
Pageof 53