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Hindmarsh

Showing results (691-700 of 703) with videos related to

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Rheumatology (Oxford, England)|October 30, 2015
Eligibility for clinical trials in primary Sjögren's syndrome: lessons from the UK Primary Sjögren's Syndrome RegistryClare Oni, Sheryl Mitchell, Katherine James, et al.
Journal of Epidemiology and Community Health|April 13, 2022
Household income, fetal size and birth weight: an analysis of eight populationsSteve Turner, Anke G Posthumus, Eric A P Steegers, et al.
Annals of the Rheumatic Diseases|March 2, 2020
Rare genetic variants in interleukin-37 link this anti-inflammatory cytokine to the pathogenesis and treatment of goutViola Klück, Rosanne C van Deuren, Giulio Cavalli, et al.
Diabetologia|July 2, 2008
Establishing glycaemic control with continuous subcutaneous insulin infusion in children and adolescents with type 1 diabetes: experience of the PedPump Study in 17 countriesT Danne, T Battelino, P Jarosz-Chobot, et al.
Arthritis Care & Research|December 20, 2016
Subjective and Objective Measures of Dryness Symptoms in Primary Sjögren's Syndrome: Capturing the DiscrepancyOriana M Bezzina, Peter Gallagher, Sheryl Mitchell, et al.
Journal of the Endocrine Society|July 14, 2021
Genetic Analysis of Pediatric Primary Adrenal Insufficiency of Unknown Etiology: 25 Years' Experience in the UKFederica Buonocore, Avinaash Maharaj, Younus Qamar, et al.
Plos One|December 24, 2015
A Transcriptional Signature of Fatigue Derived from Patients with Primary Sjögren's SyndromeKatherine James, Shereen Al-Ali, Jessica Tarn, et al.
Wellcome Open Research|June 8, 2021
SARS-CoV-2 detection by a clinical diagnostic RT-LAMP assayMichael D Buck, Enzo Z Poirier, Ana Cardoso, et al.
Journal of the Endocrine Society|January 9, 2019
Predicted Benign and Synonymous Variants in <i>CYP11A1</i> Cause Primary Adrenal Insufficiency Through MissplicingAvinaash Maharaj, Federica Buonocore, Eirini Meimaridou, et al.
The Journal of Clinical Endocrinology and Metabolism|December 14, 2011
Genotype-phenotype analysis in congenital adrenal hyperplasia due to P450 oxidoreductase deficiencyNils Krone, Nicole Reisch, Jan Idkowiak, et al.
Pageof 71

Showing results (691-700 of 703) with videos related to

Sort By:
Pageof 71
Rheumatology (Oxford, England)|October 30, 2015
Eligibility for clinical trials in primary Sjögren's syndrome: lessons from the UK Primary Sjögren's Syndrome RegistryClare Oni, Sheryl Mitchell, Katherine James, et al.
Journal of Epidemiology and Community Health|April 13, 2022
Household income, fetal size and birth weight: an analysis of eight populationsSteve Turner, Anke G Posthumus, Eric A P Steegers, et al.
Annals of the Rheumatic Diseases|March 2, 2020
Rare genetic variants in interleukin-37 link this anti-inflammatory cytokine to the pathogenesis and treatment of goutViola Klück, Rosanne C van Deuren, Giulio Cavalli, et al.
Diabetologia|July 2, 2008
Establishing glycaemic control with continuous subcutaneous insulin infusion in children and adolescents with type 1 diabetes: experience of the PedPump Study in 17 countriesT Danne, T Battelino, P Jarosz-Chobot, et al.
Arthritis Care & Research|December 20, 2016
Subjective and Objective Measures of Dryness Symptoms in Primary Sjögren's Syndrome: Capturing the DiscrepancyOriana M Bezzina, Peter Gallagher, Sheryl Mitchell, et al.
Journal of the Endocrine Society|July 14, 2021
Genetic Analysis of Pediatric Primary Adrenal Insufficiency of Unknown Etiology: 25 Years' Experience in the UKFederica Buonocore, Avinaash Maharaj, Younus Qamar, et al.
Plos One|December 24, 2015
A Transcriptional Signature of Fatigue Derived from Patients with Primary Sjögren's SyndromeKatherine James, Shereen Al-Ali, Jessica Tarn, et al.
Wellcome Open Research|June 8, 2021
SARS-CoV-2 detection by a clinical diagnostic RT-LAMP assayMichael D Buck, Enzo Z Poirier, Ana Cardoso, et al.
Journal of the Endocrine Society|January 9, 2019
Predicted Benign and Synonymous Variants in <i>CYP11A1</i> Cause Primary Adrenal Insufficiency Through MissplicingAvinaash Maharaj, Federica Buonocore, Eirini Meimaridou, et al.
The Journal of Clinical Endocrinology and Metabolism|December 14, 2011
Genotype-phenotype analysis in congenital adrenal hyperplasia due to P450 oxidoreductase deficiencyNils Krone, Nicole Reisch, Jan Idkowiak, et al.
Pageof 71