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E Flanagan

Showing results (411-420 of 582) with videos related to

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Journal of Huntington'S Disease|October 18, 2017
Neuropathological Comparison of Adult Onset and Juvenile Huntington's Disease with Cerebellar Atrophy: A Report of a Father and SonCaitlin S Latimer, Margaret E Flanagan, Patrick J Cimino, et al.
The Journal of Investigative Dermatology|March 27, 2019
Contribution of STAT3 and RAD23B in Primary Sézary Cells to Histone Deacetylase Inhibitor FK228 ResistanceRosie M Butler, Robert C McKenzie, Christine L Jones, et al.
Ebiomedicine|May 10, 2026
Identification of the ACTB p.Ser348Leu de novo variant in individuals with syndromic neonatal diabetesSuhel Ahmed, Victoria Lewis, James Russ-Silsby, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|February 22, 2025
Human herpesvirus-associated transposable element activation in human aging brains with Alzheimer's diseaseYayan Feng, Shu-Qin Cao, Yi Shi, et al.
The New England Journal of Medicine|January 4, 2023
Multiple Cerebral Hemorrhages in a Patient Receiving Lecanemab and Treated with t-PA for StrokeNicholas J Reish, Pouya Jamshidi, Brian Stamm, et al.
The Journal of Clinical Endocrinology and Metabolism|January 11, 2007
Prevalence of permanent neonatal diabetes in Slovakia and successful replacement of insulin with sulfonylurea therapy in KCNJ11 and ABCC8 mutation carriersJuraj Stanik, Daniela Gasperikova, Magdalena Paskova, et al.
Clinical Endocrinology|November 22, 2008
Mutations in the ABCC8 (SUR1 subunit of the K(ATP) channel) gene are associated with a variable clinical phenotypeTomasz Klupa, Irina Kowalska, Krystyna Wyka, et al.
Ebiomedicine|January 7, 2026
Loss of function variants in the primate-specific gene ZNF808 cause neonatal, transient and adult-onset diabetesJames Russ-Silsby, Kevin Colclough, Matthew B Johnson, et al.
Diabetes|April 10, 2019
Trisomy 21 Is a Cause of Permanent Neonatal Diabetes That Is Autoimmune but Not HLA AssociatedMatthew B Johnson, Elisa De Franco, Siri Atma W Greeley, et al.
American Journal of Obstetrics and Gynecology|July 17, 2010
Mutations in the hepatocyte nuclear factor-1β (HNF1B) gene are common with combined uterine and renal malformations but are not found with isolated uterine malformationsRichard A Oram, Emma L Edghill, Jenny Blackman, et al.
Pageof 59

Showing results (411-420 of 582) with videos related to

Sort By:
Pageof 59
Journal of Huntington'S Disease|October 18, 2017
Neuropathological Comparison of Adult Onset and Juvenile Huntington's Disease with Cerebellar Atrophy: A Report of a Father and SonCaitlin S Latimer, Margaret E Flanagan, Patrick J Cimino, et al.
The Journal of Investigative Dermatology|March 27, 2019
Contribution of STAT3 and RAD23B in Primary Sézary Cells to Histone Deacetylase Inhibitor FK228 ResistanceRosie M Butler, Robert C McKenzie, Christine L Jones, et al.
Ebiomedicine|May 10, 2026
Identification of the ACTB p.Ser348Leu de novo variant in individuals with syndromic neonatal diabetesSuhel Ahmed, Victoria Lewis, James Russ-Silsby, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|February 22, 2025
Human herpesvirus-associated transposable element activation in human aging brains with Alzheimer's diseaseYayan Feng, Shu-Qin Cao, Yi Shi, et al.
The New England Journal of Medicine|January 4, 2023
Multiple Cerebral Hemorrhages in a Patient Receiving Lecanemab and Treated with t-PA for StrokeNicholas J Reish, Pouya Jamshidi, Brian Stamm, et al.
The Journal of Clinical Endocrinology and Metabolism|January 11, 2007
Prevalence of permanent neonatal diabetes in Slovakia and successful replacement of insulin with sulfonylurea therapy in KCNJ11 and ABCC8 mutation carriersJuraj Stanik, Daniela Gasperikova, Magdalena Paskova, et al.
Clinical Endocrinology|November 22, 2008
Mutations in the ABCC8 (SUR1 subunit of the K(ATP) channel) gene are associated with a variable clinical phenotypeTomasz Klupa, Irina Kowalska, Krystyna Wyka, et al.
Ebiomedicine|January 7, 2026
Loss of function variants in the primate-specific gene ZNF808 cause neonatal, transient and adult-onset diabetesJames Russ-Silsby, Kevin Colclough, Matthew B Johnson, et al.
Diabetes|April 10, 2019
Trisomy 21 Is a Cause of Permanent Neonatal Diabetes That Is Autoimmune but Not HLA AssociatedMatthew B Johnson, Elisa De Franco, Siri Atma W Greeley, et al.
American Journal of Obstetrics and Gynecology|July 17, 2010
Mutations in the hepatocyte nuclear factor-1β (HNF1B) gene are common with combined uterine and renal malformations but are not found with isolated uterine malformationsRichard A Oram, Emma L Edghill, Jenny Blackman, et al.
Pageof 59