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J H Smith

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Proceedings of the American Thoracic Society|September 11, 2009
Developmental aspects of the upper airway: report from an NHLBI Workshop, March 5-6, 2009Carole L Marcus, Richard J H Smith, Leila A Mankarious, et al.
Annals of Clinical and Translational Neurology|September 5, 2015
PRIMA1 mutation: a new cause of nocturnal frontal lobe epilepsyMichael S Hildebrand, Rick Tankard, Elena V Gazina, et al.
The Journal of Chemical Physics|July 3, 2024
Force Field X: A computational microscope to study genetic variation and organic crystals using theory and experimentRose A Gogal, Aaron J Nessler, Andrew C Thiel, et al.
Anaesthesia|November 3, 2023
Organisation of UK hospitals and anaesthetic departments in the treatment of peri-operative cardiac arrest: an analysis from the 7th National Audit Project (NAP7) local co-ordinator baseline surveyE Kursumovic, J Soar, J P Nolan, et al.
Anaesthesia|November 9, 2023
The incidence of potentially serious complications during non-obstetric anaesthetic practice in the United Kingdom: an analysis from the 7th National Audit Project (NAP7) activity surveyA D Kane, T M Cook, R A Armstrong, et al.
Anaesthesia|March 1, 2023
Patient characteristics, anaesthetic workload and techniques in the UK: an analysis from the 7th National Audit Project (NAP7) activity surveyA D Kane, J Soar, R A Armstrong, et al.
International Journal of Pediatric Otorhinolaryngology|May 20, 2019
International Pediatric Otolaryngology Group (IPOG) consensus recommendations: Diagnosis, pre-operative, operative and post-operative pediatric choanal atresia careEric Moreddu, Mark Rizzi, Eelam Adil, et al.
Human Genetics|January 26, 2021
A biallelic variant in CLRN2 causes non-syndromic hearing loss in humansBarbara Vona, Neda Mazaheri, Sheng-Jia Lin, et al.
Nature Genetics|July 5, 2016
Genetic dissection of the α-globin super-enhancer in vivoDeborah Hay, Jim R Hughes, Christian Babbs, et al.
Kidney International|August 22, 2024
An expert discussion on the atypical hemolytic uremic syndrome nomenclature-identifying a road map to precision: a report of a National Kidney Foundation Working GroupCarla M Nester, David L Feldman, Richard Burwick, et al.
Pageof 59

Showing results (551-560 of 588) with videos related to

Sort By:
Pageof 59
Proceedings of the American Thoracic Society|September 11, 2009
Developmental aspects of the upper airway: report from an NHLBI Workshop, March 5-6, 2009Carole L Marcus, Richard J H Smith, Leila A Mankarious, et al.
Annals of Clinical and Translational Neurology|September 5, 2015
PRIMA1 mutation: a new cause of nocturnal frontal lobe epilepsyMichael S Hildebrand, Rick Tankard, Elena V Gazina, et al.
The Journal of Chemical Physics|July 3, 2024
Force Field X: A computational microscope to study genetic variation and organic crystals using theory and experimentRose A Gogal, Aaron J Nessler, Andrew C Thiel, et al.
Anaesthesia|November 3, 2023
Organisation of UK hospitals and anaesthetic departments in the treatment of peri-operative cardiac arrest: an analysis from the 7th National Audit Project (NAP7) local co-ordinator baseline surveyE Kursumovic, J Soar, J P Nolan, et al.
Anaesthesia|November 9, 2023
The incidence of potentially serious complications during non-obstetric anaesthetic practice in the United Kingdom: an analysis from the 7th National Audit Project (NAP7) activity surveyA D Kane, T M Cook, R A Armstrong, et al.
Anaesthesia|March 1, 2023
Patient characteristics, anaesthetic workload and techniques in the UK: an analysis from the 7th National Audit Project (NAP7) activity surveyA D Kane, J Soar, R A Armstrong, et al.
International Journal of Pediatric Otorhinolaryngology|May 20, 2019
International Pediatric Otolaryngology Group (IPOG) consensus recommendations: Diagnosis, pre-operative, operative and post-operative pediatric choanal atresia careEric Moreddu, Mark Rizzi, Eelam Adil, et al.
Human Genetics|January 26, 2021
A biallelic variant in CLRN2 causes non-syndromic hearing loss in humansBarbara Vona, Neda Mazaheri, Sheng-Jia Lin, et al.
Nature Genetics|July 5, 2016
Genetic dissection of the α-globin super-enhancer in vivoDeborah Hay, Jim R Hughes, Christian Babbs, et al.
Kidney International|August 22, 2024
An expert discussion on the atypical hemolytic uremic syndrome nomenclature-identifying a road map to precision: a report of a National Kidney Foundation Working GroupCarla M Nester, David L Feldman, Richard Burwick, et al.
Pageof 59