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S H Pearce

Showing results (41-50 of 48) with videos related to

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Journal of Internal Medicine|December 17, 2013
Consensus statement on the diagnosis, treatment and follow-up of patients with primary adrenal insufficiencyE S Husebye, B Allolio, W Arlt, et al.
American Journal of Human Genetics|December 5, 1998
A common and recurrent 13-bp deletion in the autoimmune regulator gene in British kindreds with autoimmune polyendocrinopathy type 1S H Pearce, T Cheetham, H Imrie, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|October 16, 2015
Serum 25-hydroxyvitamin D concentration and its determinants in the very old: the Newcastle 85+ StudyT R Hill, A Granic, K Davies, et al.
Kidney International|January 5, 2000
Isolated hypercalciuria with mutation in CLCN5: relevance to idiopathic hypercalciuriaS J Scheinman, J P Cox, S E Lloyd, et al.
Nature|February 1, 1996
A common molecular basis for three inherited kidney stone diseasesS E Lloyd, S H Pearce, S E Fisher, et al.
The Journal of Clinical Endocrinology and Metabolism|February 26, 2000
Association analysis of the cytotoxic T lymphocyte antigen-4 (CTLA-4) and autoimmune regulator-1 (AIRE-1) genes in sporadic autoimmune Addison's diseaseB Vaidya, H Imrie, D R Geatch, et al.
Clinical Genetics|March 13, 2016
Expanding the genotypic spectrum of Perrault syndromeL A M Demain, J E Urquhart, J O'Sullivan, et al.
Journal of Endocrinological Investigation|June 1, 2020
Asymmetry indicates more severe and active disease in Graves' orbitopathy: results from a prospective cross-sectional multicentre studyP Perros, M P Žarković, G C Panagiotou, et al.
Pageof 5

Showing results (41-50 of 48) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 48 results.
Journal of Internal Medicine|December 17, 2013
Consensus statement on the diagnosis, treatment and follow-up of patients with primary adrenal insufficiencyE S Husebye, B Allolio, W Arlt, et al.
American Journal of Human Genetics|December 5, 1998
A common and recurrent 13-bp deletion in the autoimmune regulator gene in British kindreds with autoimmune polyendocrinopathy type 1S H Pearce, T Cheetham, H Imrie, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|October 16, 2015
Serum 25-hydroxyvitamin D concentration and its determinants in the very old: the Newcastle 85+ StudyT R Hill, A Granic, K Davies, et al.
Kidney International|January 5, 2000
Isolated hypercalciuria with mutation in CLCN5: relevance to idiopathic hypercalciuriaS J Scheinman, J P Cox, S E Lloyd, et al.
Nature|February 1, 1996
A common molecular basis for three inherited kidney stone diseasesS E Lloyd, S H Pearce, S E Fisher, et al.
The Journal of Clinical Endocrinology and Metabolism|February 26, 2000
Association analysis of the cytotoxic T lymphocyte antigen-4 (CTLA-4) and autoimmune regulator-1 (AIRE-1) genes in sporadic autoimmune Addison's diseaseB Vaidya, H Imrie, D R Geatch, et al.
Clinical Genetics|March 13, 2016
Expanding the genotypic spectrum of Perrault syndromeL A M Demain, J E Urquhart, J O'Sullivan, et al.
Journal of Endocrinological Investigation|June 1, 2020
Asymmetry indicates more severe and active disease in Graves' orbitopathy: results from a prospective cross-sectional multicentre studyP Perros, M P Žarković, G C Panagiotou, et al.
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