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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 Registry
Clare 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 populations
Steve 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 gout
Viola 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 countries
T 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 Discrepancy
Oriana 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 UK
Federica Buonocore, Avinaash Maharaj, Younus Qamar, et al.
Plos One
|
December 24, 2015
A Transcriptional Signature of Fatigue Derived from Patients with Primary Sjögren's Syndrome
Katherine James, Shereen Al-Ali, Jessica Tarn, et al.
Wellcome Open Research
|
June 8, 2021
SARS-CoV-2 detection by a clinical diagnostic RT-LAMP assay
Michael 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 Missplicing
Avinaash 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 deficiency
Nils Krone, Nicole Reisch, Jan Idkowiak, et al.
Page
of 71
Search research articles
Search
Showing results (691-700 of 703) with videos related to
Sort By:
Page
of 71
Rheumatology (Oxford, England)
|
October 30, 2015
Eligibility for clinical trials in primary Sjögren's syndrome: lessons from the UK Primary Sjögren's Syndrome Registry
Clare 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 populations
Steve 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 gout
Viola 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 countries
T 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 Discrepancy
Oriana 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 UK
Federica Buonocore, Avinaash Maharaj, Younus Qamar, et al.
Plos One
|
December 24, 2015
A Transcriptional Signature of Fatigue Derived from Patients with Primary Sjögren's Syndrome
Katherine James, Shereen Al-Ali, Jessica Tarn, et al.
Wellcome Open Research
|
June 8, 2021
SARS-CoV-2 detection by a clinical diagnostic RT-LAMP assay
Michael 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 Missplicing
Avinaash 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 deficiency
Nils Krone, Nicole Reisch, Jan Idkowiak, et al.
Page
of 71