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E Flanagan

Showing results (431-440 of 582) with videos related to

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Diabetologia|March 2, 2026
Systematic analysis of loss-of-function variants across MODY genes demonstrates gene-specific effects and expands the spectrum of INS variants causing MODYThomas W Laver, Aparajita Sriram, Matthew N Wakeling, et al.
Brain Pathology (Zurich, Switzerland)|April 26, 2026
Data-driven thresholds for standardized classification of severe Alzheimer's disease neuropathology using digital neuropathologyRyan K Shahidehpour, Allison M Neltner, Mitchell A Klusty, et al.
Journal of Autism and Developmental Disorders|April 4, 2015
Stability and Change in the Cognitive and Adaptive Behaviour Scores of Preschoolers with Autism Spectrum DisorderHelen E Flanagan, Isabel M Smith, Tracy Vaillancourt, et al.
Journal of the American Medical Informatics Association : JAMIA|September 5, 2013
You and me and the computer makes three: variations in exam room use of the electronic health recordJason J Saleem, Mindy E Flanagan, Alissa L Russ, et al.
Diabetes|June 11, 2016
Isolated Pancreatic Aplasia Due to a Hypomorphic PTF1A MutationJayne A L Houghton, Galvin H Swift, Charles Shaw-Smith, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|February 25, 2025
The Nun Study: Insights from 30 years of aging and dementia researchKyra M Clarke, Shahroo Etemadmoghadam, Benjamin Danner, et al.
The Journal of Investigative Dermatology|August 4, 2019
Frequent and Persistent PLCG1 Mutations in Sézary Cells Directly Enhance PLCγ1 Activity and Stimulate NFκB, AP-1, and NFAT SignalingVarsha M Patel, Charlotte E Flanagan, Marta Martins, et al.
Diabetologia|February 7, 2013
Clinical presentation of 6q24 transient neonatal diabetes mellitus (6q24 TNDM) and genotype-phenotype correlation in an international cohort of patientsL E Docherty, S Kabwama, A Lehmann, et al.
The Journal of Pediatrics|December 3, 2014
Increased plasma incretin concentrations identifies a subset of patients with persistent congenital hyperinsulinism without KATP channel gene defectsYanqin Shi, Hima B Avatapalle, Mars S Skae, et al.
Journal of Medical Genetics|March 31, 2026
Long-read sequencing enables trio-assisted phasing of <i>de novo</i> variants in the imprinted gene <i>MAGEL2</i>Thomas W Laver, Preeah Sangha, Lucy Mallin, et al.
Pageof 59

Showing results (431-440 of 582) with videos related to

Sort By:
Pageof 59
Diabetologia|March 2, 2026
Systematic analysis of loss-of-function variants across MODY genes demonstrates gene-specific effects and expands the spectrum of INS variants causing MODYThomas W Laver, Aparajita Sriram, Matthew N Wakeling, et al.
Brain Pathology (Zurich, Switzerland)|April 26, 2026
Data-driven thresholds for standardized classification of severe Alzheimer's disease neuropathology using digital neuropathologyRyan K Shahidehpour, Allison M Neltner, Mitchell A Klusty, et al.
Journal of Autism and Developmental Disorders|April 4, 2015
Stability and Change in the Cognitive and Adaptive Behaviour Scores of Preschoolers with Autism Spectrum DisorderHelen E Flanagan, Isabel M Smith, Tracy Vaillancourt, et al.
Journal of the American Medical Informatics Association : JAMIA|September 5, 2013
You and me and the computer makes three: variations in exam room use of the electronic health recordJason J Saleem, Mindy E Flanagan, Alissa L Russ, et al.
Diabetes|June 11, 2016
Isolated Pancreatic Aplasia Due to a Hypomorphic PTF1A MutationJayne A L Houghton, Galvin H Swift, Charles Shaw-Smith, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|February 25, 2025
The Nun Study: Insights from 30 years of aging and dementia researchKyra M Clarke, Shahroo Etemadmoghadam, Benjamin Danner, et al.
The Journal of Investigative Dermatology|August 4, 2019
Frequent and Persistent PLCG1 Mutations in Sézary Cells Directly Enhance PLCγ1 Activity and Stimulate NFκB, AP-1, and NFAT SignalingVarsha M Patel, Charlotte E Flanagan, Marta Martins, et al.
Diabetologia|February 7, 2013
Clinical presentation of 6q24 transient neonatal diabetes mellitus (6q24 TNDM) and genotype-phenotype correlation in an international cohort of patientsL E Docherty, S Kabwama, A Lehmann, et al.
The Journal of Pediatrics|December 3, 2014
Increased plasma incretin concentrations identifies a subset of patients with persistent congenital hyperinsulinism without KATP channel gene defectsYanqin Shi, Hima B Avatapalle, Mars S Skae, et al.
Journal of Medical Genetics|March 31, 2026
Long-read sequencing enables trio-assisted phasing of <i>de novo</i> variants in the imprinted gene <i>MAGEL2</i>Thomas W Laver, Preeah Sangha, Lucy Mallin, et al.
Pageof 59