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S H S Pearce

Showing results (1-10 of 14) with videos related to

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European Thyroid Journal|November 8, 2023
European thyroid journal: passing on the batonS H S Pearce, L Persani
Clinical Endocrinology|August 8, 2014
Rethinking antithyroid drugs in pregnancyC Napier, S H S Pearce
Archives of Disease in Childhood|April 30, 2003
The investigation of hypocalcaemia and ricketsJ Singh, N Moghal, S H S Pearce, et al.
Journal of Molecular Endocrinology|June 16, 2005
A haplotype of the CYP27B1 promoter is associated with autoimmune Addison's disease but not with Graves' disease in a UK populationC E Jennings, C J Owen, V Wilson, et al.
Postgraduate Medical Journal|March 9, 2007
A second corneal arcus?S Vaikkakara, R A James, S H S Pearce, et al.
The Journal of Clinical Endocrinology and Metabolism|October 9, 2014
Role of the X-linked gene GPR174 in autoimmune Addison's diseaseC Napier, A L Mitchell, E Gan, et al.
International Journal of Immunogenetics|February 8, 2007
The role of the IDDM2 locus in the susceptibility of UK APS1 subjects to type 1 diabetes mellitusK A Adamson, T D Cheetham, P Kendall-Taylor, et al.
The Journal of Pathology|January 27, 2004
A comparative study of mRNA and protein expression of the autoimmune regulator gene (Aire) in embryonic and adult murine tissuesK A Adamson, S H S Pearce, J R Lamb, et al.
European Journal of Endocrinology|November 12, 2009
Isolated Addison's disease is unlikely to be caused by mutations in MC2R, MRAP or STAR, three genes responsible for familial glucocorticoid deficiencyR P Dias, L F Chan, L A Metherell, et al.
Clinical Endocrinology|June 5, 2003
CTLA4 gene and Graves' disease: association of Graves' disease with the CTLA4 exon 1 and intron 1 polymorphisms, but not with the promoter polymorphismB Vaidya, E J C Oakes, H Imrie, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
European Thyroid Journal|November 8, 2023
European thyroid journal: passing on the batonS H S Pearce, L Persani
Clinical Endocrinology|August 8, 2014
Rethinking antithyroid drugs in pregnancyC Napier, S H S Pearce
Archives of Disease in Childhood|April 30, 2003
The investigation of hypocalcaemia and ricketsJ Singh, N Moghal, S H S Pearce, et al.
Journal of Molecular Endocrinology|June 16, 2005
A haplotype of the CYP27B1 promoter is associated with autoimmune Addison's disease but not with Graves' disease in a UK populationC E Jennings, C J Owen, V Wilson, et al.
Postgraduate Medical Journal|March 9, 2007
A second corneal arcus?S Vaikkakara, R A James, S H S Pearce, et al.
The Journal of Clinical Endocrinology and Metabolism|October 9, 2014
Role of the X-linked gene GPR174 in autoimmune Addison's diseaseC Napier, A L Mitchell, E Gan, et al.
International Journal of Immunogenetics|February 8, 2007
The role of the IDDM2 locus in the susceptibility of UK APS1 subjects to type 1 diabetes mellitusK A Adamson, T D Cheetham, P Kendall-Taylor, et al.
The Journal of Pathology|January 27, 2004
A comparative study of mRNA and protein expression of the autoimmune regulator gene (Aire) in embryonic and adult murine tissuesK A Adamson, S H S Pearce, J R Lamb, et al.
European Journal of Endocrinology|November 12, 2009
Isolated Addison's disease is unlikely to be caused by mutations in MC2R, MRAP or STAR, three genes responsible for familial glucocorticoid deficiencyR P Dias, L F Chan, L A Metherell, et al.
Clinical Endocrinology|June 5, 2003
CTLA4 gene and Graves' disease: association of Graves' disease with the CTLA4 exon 1 and intron 1 polymorphisms, but not with the promoter polymorphismB Vaidya, E J C Oakes, H Imrie, et al.
Pageof 2