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Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association
|
May 8, 2007
Cytotoxic T-lymphocyte-associated antigen-4 single nucleotide polymorphisms and haplotypes in primary biliary cirrhosis
Peter Donaldson, Sivakumar Veeramani, Anna Baragiotta, et al.
Clinical Endocrinology
|
August 20, 2008
The tryptophan 620 allele of the lymphoid tyrosine phosphatase (PTPN22) gene predisposes to autoimmune Addison's disease
Matthew Roycroft, Marta Fichna, David McDonald, et al.
European Journal of Endocrinology
|
January 14, 2021
Vitamin D status and pathway genes in five European autoimmune Addison's disease cohorts
Marissa Penna-Martinez, Gesine Meyer, Anette Boe Wolff, et al.
BMJ Open
|
January 24, 2019
Adjuvant rituximab, a potential treatment for the young patient with Graves' hyperthyroidism (RiGD): study protocol for a single-arm, single-stage, phase II trial
Michael Cole, Ann Marie Hynes, Denise Howel, et al.
BMC Musculoskeletal Disorders
|
August 7, 2007
Refining animal models in fracture research: seeking consensus in optimising both animal welfare and scientific validity for appropriate biomedical use
Jorg A Auer, Allen Goodship, Steven Arnoczky, et al.
The Lancet. Psychiatry
|
January 5, 2016
Antidepressant augmentation with metyrapone for treatment-resistant depression (the ADD study): a double-blind, randomised, placebo-controlled trial
R Hamish McAllister-Williams, Ian M Anderson, Andreas Finkelmeyer, et al.
Plant Physiology
|
July 17, 2013
Transcriptional dynamics of two seed compartments with opposing roles in Arabidopsis seed germination
Bas J W Dekkers, Simon Pearce, R P van Bolderen-Veldkamp, et al.
The Journal of Clinical Endocrinology and Metabolism
|
June 19, 2008
Mutations in prokineticin 2 and prokineticin receptor 2 genes in human gonadotrophin-releasing hormone deficiency: molecular genetics and clinical spectrum
Lindsay W Cole, Yisrael Sidis, ChengKang Zhang, et al.
The Journal of Clinical Investigation
|
January 20, 2007
Digenic mutations account for variable phenotypes in idiopathic hypogonadotropic hypogonadism
Nelly Pitteloud, Richard Quinton, Simon Pearce, et al.
European Journal of Endocrinology
|
February 27, 2008
Consensus statement of the European Group on Graves' orbitopathy (EUGOGO) on management of GO
Luigi Bartalena, Lelio Baldeschi, Alison Dickinson, et al.
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of 5
Search research articles
Search
Showing results (31-40 of 43) with videos related to
Sort By:
Page
of 5
Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association
|
May 8, 2007
Cytotoxic T-lymphocyte-associated antigen-4 single nucleotide polymorphisms and haplotypes in primary biliary cirrhosis
Peter Donaldson, Sivakumar Veeramani, Anna Baragiotta, et al.
Clinical Endocrinology
|
August 20, 2008
The tryptophan 620 allele of the lymphoid tyrosine phosphatase (PTPN22) gene predisposes to autoimmune Addison's disease
Matthew Roycroft, Marta Fichna, David McDonald, et al.
European Journal of Endocrinology
|
January 14, 2021
Vitamin D status and pathway genes in five European autoimmune Addison's disease cohorts
Marissa Penna-Martinez, Gesine Meyer, Anette Boe Wolff, et al.
BMJ Open
|
January 24, 2019
Adjuvant rituximab, a potential treatment for the young patient with Graves' hyperthyroidism (RiGD): study protocol for a single-arm, single-stage, phase II trial
Michael Cole, Ann Marie Hynes, Denise Howel, et al.
BMC Musculoskeletal Disorders
|
August 7, 2007
Refining animal models in fracture research: seeking consensus in optimising both animal welfare and scientific validity for appropriate biomedical use
Jorg A Auer, Allen Goodship, Steven Arnoczky, et al.
The Lancet. Psychiatry
|
January 5, 2016
Antidepressant augmentation with metyrapone for treatment-resistant depression (the ADD study): a double-blind, randomised, placebo-controlled trial
R Hamish McAllister-Williams, Ian M Anderson, Andreas Finkelmeyer, et al.
Plant Physiology
|
July 17, 2013
Transcriptional dynamics of two seed compartments with opposing roles in Arabidopsis seed germination
Bas J W Dekkers, Simon Pearce, R P van Bolderen-Veldkamp, et al.
The Journal of Clinical Endocrinology and Metabolism
|
June 19, 2008
Mutations in prokineticin 2 and prokineticin receptor 2 genes in human gonadotrophin-releasing hormone deficiency: molecular genetics and clinical spectrum
Lindsay W Cole, Yisrael Sidis, ChengKang Zhang, et al.
The Journal of Clinical Investigation
|
January 20, 2007
Digenic mutations account for variable phenotypes in idiopathic hypogonadotropic hypogonadism
Nelly Pitteloud, Richard Quinton, Simon Pearce, et al.
European Journal of Endocrinology
|
February 27, 2008
Consensus statement of the European Group on Graves' orbitopathy (EUGOGO) on management of GO
Luigi Bartalena, Lelio Baldeschi, Alison Dickinson, et al.
Page
of 5