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British Journal of Cancer|June 16, 2005
Pharmacokinetically guided phase I trial of topotecan and etoposide phosphate in recurrent ovarian cancerN C Levitt, D J Propper, S Madhusudan, et al.Diabetic Medicine : a Journal of the British Diabetic Association|January 17, 2013
Biallelic PDX1 (insulin promoter factor 1) mutations causing neonatal diabetes without exocrine pancreatic insufficiencyE De Franco, C Shaw-Smith, S E Flanagan, et al.Diabetologia|April 2, 2016
Successful transfer to sulfonylureas in KCNJ11 neonatal diabetes is determined by the mutation and duration of diabetesTarig Babiker, Natascia Vedovato, Kashyap Patel, et al.Diabetologia|June 18, 2013
Improved genetic testing for monogenic diabetes using targeted next-generation sequencingS Ellard, H Lango Allen, E De Franco, et al.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 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.Pageof 51