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E Flanagan

Showing results (381-390 of 582) with videos related to

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The Journal of Pathology. Clinical Research|October 3, 2019
Unravelling the genetic causes of mosaic islet morphology in congenital hyperinsulinismJayne Al Houghton, Indraneel Banerjee, Guftar Shaikh, et al.
Diabetes Care|June 17, 2008
Coincidence of a novel KCNJ11 missense variant R365H with a paternally inherited 6q24 duplication in a patient with transient neonatal diabetesJuraj Staník, Mark Lethby, Sarah E Flanagan, et al.
Science Advances|December 5, 2020
Oligodendroglial glycolytic stress triggers inflammasome activation and neuropathology in Alzheimer's diseaseXinwen Zhang, Rihua Wang, Di Hu, et al.
Histopathology|August 18, 2017
Application of the condensed protocol for the NIA-AA guidelines for the neuropathological assessment of Alzheimer's disease in an academic clinical practiceRajnish Bharadwaj, Patrick J Cimino, Margaret E Flanagan, et al.
Journal of Burn Care & Research : Official Publication of the American Burn Association|July 26, 2011
The results of a national survey regarding nutritional care of obese burn patientsJennifer R Coen, Annette M Carpenter, Jeffrey W Shupp, et al.
The Journal of Clinical Endocrinology and Metabolism|October 14, 2022
Hyperinsulinemic Hypoglycemia Diagnosed in Childhood Can Be MonogenicJasmin J Hopkins, Alexandra J Childs, Jayne A L Houghton, et al.
Indian Pediatrics|January 7, 2022
Molecular Characterization and Management of Congenital Hyperinsulinism: A Tertiary Centre ExperienceRajni Sharma, Kakali Roy, Amit Kumar Satapathy, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|February 8, 2012
Clinical characteristics of recessive and dominant congenital hyperinsulinism due to mutation(s) in the ABCC8/KCNJ11 genes encoding the ATP-sensitive potasium channel in the pancreatic beta cellGönül Oçal, Sarah E Flanagan, Bülent Hacihamdioğlu, et al.
Journal of Clinical Research in Pediatric Endocrinology|July 1, 2017
An <i>ABCC8</i> Nonsense Mutation Causing Neonatal Diabetes Through Altered Transcript ExpressionSarah E Flanagan, Vũ Chí Dũng, Jayne A L Houghton, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|November 29, 2017
Monogenic Diabetes Not Caused By Mutations in Mody Genes: A Very Heterogenous Group of DiabetesZeynep Şıklar, Elisa de Franco, Matthew B Johnson, et al.
Pageof 59

Showing results (381-390 of 582) with videos related to

Sort By:
Pageof 59
The Journal of Pathology. Clinical Research|October 3, 2019
Unravelling the genetic causes of mosaic islet morphology in congenital hyperinsulinismJayne Al Houghton, Indraneel Banerjee, Guftar Shaikh, et al.
Diabetes Care|June 17, 2008
Coincidence of a novel KCNJ11 missense variant R365H with a paternally inherited 6q24 duplication in a patient with transient neonatal diabetesJuraj Staník, Mark Lethby, Sarah E Flanagan, et al.
Science Advances|December 5, 2020
Oligodendroglial glycolytic stress triggers inflammasome activation and neuropathology in Alzheimer's diseaseXinwen Zhang, Rihua Wang, Di Hu, et al.
Histopathology|August 18, 2017
Application of the condensed protocol for the NIA-AA guidelines for the neuropathological assessment of Alzheimer's disease in an academic clinical practiceRajnish Bharadwaj, Patrick J Cimino, Margaret E Flanagan, et al.
Journal of Burn Care & Research : Official Publication of the American Burn Association|July 26, 2011
The results of a national survey regarding nutritional care of obese burn patientsJennifer R Coen, Annette M Carpenter, Jeffrey W Shupp, et al.
The Journal of Clinical Endocrinology and Metabolism|October 14, 2022
Hyperinsulinemic Hypoglycemia Diagnosed in Childhood Can Be MonogenicJasmin J Hopkins, Alexandra J Childs, Jayne A L Houghton, et al.
Indian Pediatrics|January 7, 2022
Molecular Characterization and Management of Congenital Hyperinsulinism: A Tertiary Centre ExperienceRajni Sharma, Kakali Roy, Amit Kumar Satapathy, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|February 8, 2012
Clinical characteristics of recessive and dominant congenital hyperinsulinism due to mutation(s) in the ABCC8/KCNJ11 genes encoding the ATP-sensitive potasium channel in the pancreatic beta cellGönül Oçal, Sarah E Flanagan, Bülent Hacihamdioğlu, et al.
Journal of Clinical Research in Pediatric Endocrinology|July 1, 2017
An <i>ABCC8</i> Nonsense Mutation Causing Neonatal Diabetes Through Altered Transcript ExpressionSarah E Flanagan, Vũ Chí Dũng, Jayne A L Houghton, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|November 29, 2017
Monogenic Diabetes Not Caused By Mutations in Mody Genes: A Very Heterogenous Group of DiabetesZeynep Şıklar, Elisa de Franco, Matthew B Johnson, et al.
Pageof 59