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E Flanagan

Showing results (391-400 of 582) with videos related to

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Journal of Alzheimer'S Disease : JAD|December 12, 2017
Associations between Use of Specific Analgesics and Concentrations of Amyloid-β 42 or Phospho-Tau in Regions of Human Cerebral CortexMargaret E Flanagan, Eric B Larson, Rod L Walker, et al.
European Journal of Endocrinology|March 8, 2011
The contribution of rapid KATP channel gene mutation analysis to the clinical management of children with congenital hyperinsulinismI Banerjee, M Skae, S E Flanagan, et al.
Psychiatric Services (Washington, D.C.)|April 2, 2016
Comparative Effectiveness of a Burnout Reduction Intervention for Behavioral Health ProvidersAngela L Rollins, Marina Kukla, Gary Morse, et al.
Neurology|January 14, 2021
Memory Resilience in Alzheimer Disease With Primary Progressive AphasiaM-Marsel Mesulam, Christina Coventry, Alan Kuang, et al.
The Journal of Clinical Endocrinology and Metabolism|July 19, 2018
PLIN1 Haploinsufficiency Is Not Associated With LipodystrophyThomas W Laver, Kashyap A Patel, Kevin Colclough, et al.
Diabetes|March 18, 2011
In vitro recovery of ATP-sensitive potassium channels in β-cells from patients with congenital hyperinsulinism of infancyPhilippa D Powell, Christine Bellanné-Chantelot, Sarah E Flanagan, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 21, 2007
Increased ATPase activity produced by mutations at arginine-1380 in nucleotide-binding domain 2 of ABCC8 causes neonatal diabetesHeidi de Wet, Mathew G Rees, Kenju Shimomura, et al.
Infection Control and Hospital Epidemiology|July 1, 2010
Observer bias in hand hygiene compliance reportingSorabh Dhar, Ryan Tansek, Elizabeth A Toftey, et al.
Pediatric Diabetes|June 6, 2009
Incidence of neonatal diabetes in Austria-calculation based on the Austrian Diabetes RegisterBarbara Wiedemann, Edith Schober, Thomas Waldhoer, et al.
Pediatric Diabetes|February 29, 2012
Recessive SLC19A2 mutations are a cause of neonatal diabetes mellitus in thiamine-responsive megaloblastic anaemiaCharles Shaw-Smith, Sarah E Flanagan, Ann-Marie Patch, et al.
Pageof 59

Showing results (391-400 of 582) with videos related to

Sort By:
Pageof 59
Journal of Alzheimer'S Disease : JAD|December 12, 2017
Associations between Use of Specific Analgesics and Concentrations of Amyloid-β 42 or Phospho-Tau in Regions of Human Cerebral CortexMargaret E Flanagan, Eric B Larson, Rod L Walker, et al.
European Journal of Endocrinology|March 8, 2011
The contribution of rapid KATP channel gene mutation analysis to the clinical management of children with congenital hyperinsulinismI Banerjee, M Skae, S E Flanagan, et al.
Psychiatric Services (Washington, D.C.)|April 2, 2016
Comparative Effectiveness of a Burnout Reduction Intervention for Behavioral Health ProvidersAngela L Rollins, Marina Kukla, Gary Morse, et al.
Neurology|January 14, 2021
Memory Resilience in Alzheimer Disease With Primary Progressive AphasiaM-Marsel Mesulam, Christina Coventry, Alan Kuang, et al.
The Journal of Clinical Endocrinology and Metabolism|July 19, 2018
PLIN1 Haploinsufficiency Is Not Associated With LipodystrophyThomas W Laver, Kashyap A Patel, Kevin Colclough, et al.
Diabetes|March 18, 2011
In vitro recovery of ATP-sensitive potassium channels in β-cells from patients with congenital hyperinsulinism of infancyPhilippa D Powell, Christine Bellanné-Chantelot, Sarah E Flanagan, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 21, 2007
Increased ATPase activity produced by mutations at arginine-1380 in nucleotide-binding domain 2 of ABCC8 causes neonatal diabetesHeidi de Wet, Mathew G Rees, Kenju Shimomura, et al.
Infection Control and Hospital Epidemiology|July 1, 2010
Observer bias in hand hygiene compliance reportingSorabh Dhar, Ryan Tansek, Elizabeth A Toftey, et al.
Pediatric Diabetes|June 6, 2009
Incidence of neonatal diabetes in Austria-calculation based on the Austrian Diabetes RegisterBarbara Wiedemann, Edith Schober, Thomas Waldhoer, et al.
Pediatric Diabetes|February 29, 2012
Recessive SLC19A2 mutations are a cause of neonatal diabetes mellitus in thiamine-responsive megaloblastic anaemiaCharles Shaw-Smith, Sarah E Flanagan, Ann-Marie Patch, et al.
Pageof 59