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J Amor

Showing results (331-340 of 430) with videos related to

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Scientific Reports|February 28, 2018
Intragenic DNA methylation in buccal epithelial cells and intellectual functioning in a paediatric cohort of males with fragile XMarta Arpone, Emma K Baker, Lesley Bretherton, et al.
Diabetes Care|August 15, 2018
Erratum. Mediterranean Diet, Retinopathy, Nephropathy, and Microvascular Diabetes Complications: A Post Hoc Analysis of a Randomized Trial. Diabetes Care 2015;38:2134-2141Andrés Díaz-López, Nancy Babio, Miguel A Martínez-González, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|September 19, 2025
Comparing CKD populations with T1D and T2D: a perspective based on the FINE-ONE and FIDELITY populationsHiddo J L Heerspink, Rajiv Agarwal, Antonio J Amor, et al.
Seminars in Reproductive Medicine|June 27, 2022
Setting Preconception Care Priorities in Australia Using a Delphi TechniqueJacqueline A Boyle, Kirsten Black, Edwina Dorney, et al.
Journal of Speech, Language, and Hearing Research : JSLHR|December 5, 2023
Self-Reported Stuttering Severity Is Accurate: Informing Methods for Large-Scale Data Collection in StutteringSarah Horton, Victoria Jackson, Jessica Boyce, et al.
Orphanet Journal of Rare Diseases|March 29, 2014
Expanding the phenotypic spectrum of ARID1B-mediated disorders and identification of altered cell-cycle dynamics due to ARID1B haploinsufficiencyJoe C H Sim, Susan M White, Elizabeth Fitzpatrick, et al.
Transplant International : Official Journal of the European Society for Organ Transplantation|November 19, 2025
Duodenoduodenostomy as an Attractive Option for Exocrine Drainage in Pancreas Transplantation: Insights From a Single-Center CohortAlba Torroella, Rongrong Hu Zhu, Carlos Castillo-Delgado, et al.
Journal of Clinical Medicine|November 23, 2019
Clinical Spectrum and Functional Consequences Associated with Bi-Allelic Pathogenic <i>PNPT1</i> VariantsRocio Rius, Nicole J Van Bergen, Alison G Compton, et al.
Human Molecular Genetics|May 3, 2023
Multi-omics identifies large mitoribosomal subunit instability caused by pathogenic MRPL39 variants as a cause of pediatric onset mitochondrial diseaseSumudu S C Amarasekera, Daniella H Hock, Nicole J Lake, et al.
Annals of Clinical and Translational Neurology|May 23, 2015
Familial cortical dysplasia type IIA caused by a germline mutation in DEPDC5Thomas Scerri, Jessica R Riseley, Greta Gillies, et al.
Pageof 43

Showing results (331-340 of 430) with videos related to

Sort By:
Pageof 43
Scientific Reports|February 28, 2018
Intragenic DNA methylation in buccal epithelial cells and intellectual functioning in a paediatric cohort of males with fragile XMarta Arpone, Emma K Baker, Lesley Bretherton, et al.
Diabetes Care|August 15, 2018
Erratum. Mediterranean Diet, Retinopathy, Nephropathy, and Microvascular Diabetes Complications: A Post Hoc Analysis of a Randomized Trial. Diabetes Care 2015;38:2134-2141Andrés Díaz-López, Nancy Babio, Miguel A Martínez-González, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|September 19, 2025
Comparing CKD populations with T1D and T2D: a perspective based on the FINE-ONE and FIDELITY populationsHiddo J L Heerspink, Rajiv Agarwal, Antonio J Amor, et al.
Seminars in Reproductive Medicine|June 27, 2022
Setting Preconception Care Priorities in Australia Using a Delphi TechniqueJacqueline A Boyle, Kirsten Black, Edwina Dorney, et al.
Journal of Speech, Language, and Hearing Research : JSLHR|December 5, 2023
Self-Reported Stuttering Severity Is Accurate: Informing Methods for Large-Scale Data Collection in StutteringSarah Horton, Victoria Jackson, Jessica Boyce, et al.
Orphanet Journal of Rare Diseases|March 29, 2014
Expanding the phenotypic spectrum of ARID1B-mediated disorders and identification of altered cell-cycle dynamics due to ARID1B haploinsufficiencyJoe C H Sim, Susan M White, Elizabeth Fitzpatrick, et al.
Transplant International : Official Journal of the European Society for Organ Transplantation|November 19, 2025
Duodenoduodenostomy as an Attractive Option for Exocrine Drainage in Pancreas Transplantation: Insights From a Single-Center CohortAlba Torroella, Rongrong Hu Zhu, Carlos Castillo-Delgado, et al.
Journal of Clinical Medicine|November 23, 2019
Clinical Spectrum and Functional Consequences Associated with Bi-Allelic Pathogenic <i>PNPT1</i> VariantsRocio Rius, Nicole J Van Bergen, Alison G Compton, et al.
Human Molecular Genetics|May 3, 2023
Multi-omics identifies large mitoribosomal subunit instability caused by pathogenic MRPL39 variants as a cause of pediatric onset mitochondrial diseaseSumudu S C Amarasekera, Daniella H Hock, Nicole J Lake, et al.
Annals of Clinical and Translational Neurology|May 23, 2015
Familial cortical dysplasia type IIA caused by a germline mutation in DEPDC5Thomas Scerri, Jessica R Riseley, Greta Gillies, et al.
Pageof 43