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Showing results (431-440 of 866) with videos related to

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Archives of Gynecology and Obstetrics|June 19, 2016
Acute-phase proteins in prediction of preeclampsia in patients with abnormal midtrimester uterine Doppler velocimetryJohannes Stubert, Torsten Kleber, Michael Bolz, et al.
The Journal of Arthroplasty|May 1, 2016
The Physician as the Provider at Risk: Rolling the DiceStephen B Murphy, Nicholas J Bolz, David P Terry, et al.
Ophthalmology. Retina|March 10, 2020
Peripapillary Sparing in Autosomal Recessive BestrophinopathyJohannes Birtel, Martin Gliem, Philipp Herrmann, et al.
Frontiers in Genetics|October 12, 2017
Recurrent and Prolonged Infections in a Child with a Homozygous <i>IFIH1</i> Nonsense MutationMaha Zaki, Michaela Thoenes, Amit Kawalia, et al.
The American Journal of Cardiology|September 15, 1993
Digital dipyridamole stress echocardiography in silent ischemia after coronary artery bypass grafting and/or after healing of acute myocardial infarctionK Bjoernstad, S Aakhus, J Lundbom, et al.
European Journal of Human Genetics : EJHG|July 31, 2008
An USH2A founder mutation is the major cause of Usher syndrome type 2 in Canadians of French origin and confirms common roots of Quebecois and AcadiansInga Ebermann, Robert K Koenekoop, Irma Lopez, et al.
Genome Biology|April 5, 2007
Deafblindness in French Canadians from Quebec: a predominant founder mutation in the USH1C gene provides the first genetic link with the Acadian populationInga Ebermann, Irma Lopez, Maria Bitner-Glindzicz, et al.
Clinical Genetics|April 4, 2017
Genome-wide linkage and sequence analysis challenge CCDC66 as a human retinal dystrophy candidate gene and support a distinct NMNAT1-related fundus phenotypeA O Khan, B S Budde, P Nürnberg, et al.
The Journal of Arthroplasty|June 3, 2024
Short-Term (90 Days) Clinical Outcomes Following the Day of Surgery Conversion of Inpatient to Same-Day Hip and Knee ArthroplastyBrynn P Charron, Nicholas J Bolz, Brent A Lanting, et al.
Plos One|January 13, 2022
Blindness and visual impairment in Central EuropeMarlene Glatz, Regina Riedl, Wilfried Glatz, et al.
Pageof 87

Showing results (431-440 of 866) with videos related to

Sort By:
Pageof 87
Archives of Gynecology and Obstetrics|June 19, 2016
Acute-phase proteins in prediction of preeclampsia in patients with abnormal midtrimester uterine Doppler velocimetryJohannes Stubert, Torsten Kleber, Michael Bolz, et al.
The Journal of Arthroplasty|May 1, 2016
The Physician as the Provider at Risk: Rolling the DiceStephen B Murphy, Nicholas J Bolz, David P Terry, et al.
Ophthalmology. Retina|March 10, 2020
Peripapillary Sparing in Autosomal Recessive BestrophinopathyJohannes Birtel, Martin Gliem, Philipp Herrmann, et al.
Frontiers in Genetics|October 12, 2017
Recurrent and Prolonged Infections in a Child with a Homozygous <i>IFIH1</i> Nonsense MutationMaha Zaki, Michaela Thoenes, Amit Kawalia, et al.
The American Journal of Cardiology|September 15, 1993
Digital dipyridamole stress echocardiography in silent ischemia after coronary artery bypass grafting and/or after healing of acute myocardial infarctionK Bjoernstad, S Aakhus, J Lundbom, et al.
European Journal of Human Genetics : EJHG|July 31, 2008
An USH2A founder mutation is the major cause of Usher syndrome type 2 in Canadians of French origin and confirms common roots of Quebecois and AcadiansInga Ebermann, Robert K Koenekoop, Irma Lopez, et al.
Genome Biology|April 5, 2007
Deafblindness in French Canadians from Quebec: a predominant founder mutation in the USH1C gene provides the first genetic link with the Acadian populationInga Ebermann, Irma Lopez, Maria Bitner-Glindzicz, et al.
Clinical Genetics|April 4, 2017
Genome-wide linkage and sequence analysis challenge CCDC66 as a human retinal dystrophy candidate gene and support a distinct NMNAT1-related fundus phenotypeA O Khan, B S Budde, P Nürnberg, et al.
The Journal of Arthroplasty|June 3, 2024
Short-Term (90 Days) Clinical Outcomes Following the Day of Surgery Conversion of Inpatient to Same-Day Hip and Knee ArthroplastyBrynn P Charron, Nicholas J Bolz, Brent A Lanting, et al.
Plos One|January 13, 2022
Blindness and visual impairment in Central EuropeMarlene Glatz, Regina Riedl, Wilfried Glatz, et al.
Pageof 87