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46篇 您的检索式:作者名="Pearce SH"
    题名 作者 年代 出处 被引量
1Diagnostic challenges due to phenocopies:lessons from Multiple Endocrine Neoplasia type1(MEN1)显示文摘Turner JJ Christie PT Pearce SH 2010Hum Mutat2010,31,:1
2Management of hypothyroidism in adults显示文摘Vaidya B Pearce SH 2008BMJ2008,337,:1
3Diagnosis and management of vitaminO Deficiency 显示文摘Pearce SH Cheetham TD 2010BMJ2010,,:1
4Treatment for primary hypothyroi- dism: current approaches and future possibilities 显示文摘Chakem A J Pearce SH Vaidya B 2012Drug Des Devel Ther2012,6,:1
5Spontaneous reporting of adverse reactions to carbimazole and propylthiouracil in the UK显示文摘Pearce SH 0,,05:1
6Subclinical thyroid disorders significance and clinical impact 显示文摘Razvi S Weaver JU Pearce SH 2010J Clin Pathol2010,63,5:1
7Subclinical hypothyroidism and cardiovascular disease-reply 显示文摘Razvi S Pearce SH 2012Arch Intern Med2012,172,19:1
8Treatment for primary hypothy- roidism: current approaches and future possibilities 显示文摘Chakera A J Pearce SH Vaidya B 2012Drug Des Devel Ther2012,6,:1
9Genetics of type 1 diabetes and autoimmune thyroid disease显示文摘Pearce SH Merriman TR 2009Endocrinol Metab Clin North Am2009,38,:1
10The calcium-sensing receptor:Insights into extracellular calcium homuostasis in health and disease显示文摘Pearce SH Thakker RV 1997J Endocrinol1997,154,:1
11Autoimmune Addison' s disease 显示文摘Napier C Pearce SH 2012La Presse Medicale2012,41,12:1
12显示文摘Pearce SH Trump D Wooding C 1996Clin Endocrinol ( Oxf)1996,45,2:1
13The genetics of autoimmune thyroid disease显示文摘Vaidya B Kendall-Taylor P Pearce SH 2002J Clin Endocrinol Metab2002,87,12:1
14Prenatal viral infection in mouse causes differential expression of genes in brains of mouse progeny: a potential animal model for schizophrenia and autism显示文摘Fatemi SH Pearce DA Brooks AI 2005Synapse2005,57,2:1
15Autoimmune Addison disease : patho- physiology and genetic complexity 显示文摘Mitchell AL Pearce SH 2012Nat Rev Endocrinol2012,8,5:1
16Treatment for primary hypothy- roidism: current approaches and future possibilities 显示文摘Chakera AJ Pearce SH Vaidya B 2012Drug Des De- vel Ther2012,6,:1
172013 ETA guideline: management of subclinical hypothyroidism 显示文摘Pearce SH Brabant G Duntas LH 2013Eur Thyroid J2013,2,4:1
18Calcium-sensing receptor mutations in familial benign hypercalcemia and neonatal hyper-parathyroidism显示文摘Pearce SH Trump D Wooding C 1995J Clin Invest1995,96,6:1
19Idiopathic low molecular weight proteinuria associated with hypercalciuric nephrocalcinosis in Japanese children is due to mutations of the renal chloride channel (CLCN5) 显示文摘Lloyd SE Pearce SH Gtinther W 1997J Clin Invest1997,99,5:1
20Characterisation of renal chloride channel,CLCN5 ,mutations in hyperealciuric nephrolithiasis (kidney stones) disorders 显示文摘Lloyd SE Gunther W Pearce SH 1997Hum Mol Genet1997,6,8:1
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