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Outcomes of Thyroid Dysfunction in People Aged Eighty Years and Older: An Individual Patient Data Meta-Analysis of Four Prospective Studies (Towards Understanding Longitudinal International Older People Studies Consortium).
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- Thyroid, 2021, v. 31, n. 4, p. 552, doi. 10.1089/thy.2020.0567
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- Article
Antigen-Specific Immunotherapy with Thyrotropin Receptor Peptides in Graves' Hyperthyroidism: A Phase I Study.
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- Thyroid, 2019, v. 29, n. 7, p. 1003, doi. 10.1089/thy.2019.0036
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- Article
A novel CLDN16 mutation in a large family with familial hypomagnesaemia with hypercalciuria and nephrocalcinosis.
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- BMC Research Notes, 2013, v. 6, n. 1, p. 1, doi. 10.1186/1756-0500-6-527
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- Article
Left Ventricular Apical Ballooning (Takotsubo Cardiomyopathy) in Thyrotoxicosis.
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- Thyroid, 2007, v. 17, n. 2, p. 181, doi. 10.1089/thy.2006.0102
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- Article
Role of the CD40 Locus in Graves' Disease.
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- Thyroid, 2004, v. 14, n. 7, p. 506
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- Article
Mutational Analysis of the Thyrotropin Receptor Gene in Sporadic and Familial Feline Thyrotoxicosis.
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- Thyroid, 1997, v. 7, n. 6, p. 923, doi. 10.1089/thy.1997.7.923
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- Article
A common molecular basis for three inherited kidney stone diseases.
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- Nature, 1996, v. 379, n. 6564, p. 445, doi. 10.1038/379445a0
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- Article
Phaeochromocytoma and ACTH-dependent cushing's syndrome: tumour crf secretion can mimic pituitary cushing's disease.
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- Clinical Endocrinology, 2016, v. 84, n. 2, p. 177, doi. 10.1111/cen.12960
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- Article
Saving lives of in-patients with adrenal insufficiency: implementation of an alert scheme within the Newcastle-upon-Tyne Hospitals e-Prescribing platform.
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- Clinical Endocrinology, 2014, v. 81, n. 6, p. 937, doi. 10.1111/cen.12457
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- Article
How should I approach standard endocrine evaluation in patients with coeliac disease?
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- Clinical Endocrinology, 2013, v. 79, n. 4, p. 464, doi. 10.1111/cen.12283
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- Article
The cytotoxic T lymphocyte antigen-4 is a major Graves' disease locus.
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- Human Molecular Genetics, 1999, v. 8, n. 7, p. 1195, doi. 10.1093/hmg/8.7.1195
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- Article
Characterisation of Renal Chloride Channel, CLCN5, Mutations in Hypercalciuric Nephrolithiasis (Kidney Stones) Disorders.
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- Human Molecular Genetics, 1997, v. 6, n. 8, p. 1233, doi. 10.1093/hmg/6.8.1233
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- Article
Isolated hypercalciuria with mutation in CLCN5: Relevance to idiopathic hypercalciuria.
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- Kidney International, 2000, v. 57, n. 1, p. 232, doi. 10.1046/j.1523-1755.2000.00774.x
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- Article