about
Effectiveness of interventions to reduce ordering of thyroid function tests: a systematic reviewPremature birth and low birth weight associated with nonautoimmune hyperthyroidism due to an activating thyrotropin receptor gene mutationThyroid research: stepping forward.Pituitary apoplexy: a review of clinical presentation, management and outcome in 45 cases.2014 European thyroid association guidelines for the management of subclinical hypothyroidism in pregnancy and in children.Recent advances in the molecular genetics of congenital and acquired primary adrenocortical failure.Five-year follow-up for women with subclinical hypothyroidism in pregnancy.Investigating hyperkalaemia in adults.Management of Hyperthyroidism in Pregnancy: Results of a Survey among Members of the European Thyroid AssociationA meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid functionTelephone consultations in place of face to face out-patient consultations for patients discharged from hospital following surgery: a systematic review.Management of hypothyroidism in adults.A meta-analysis of the associations between common variation in the PDE8B gene and thyroid hormone parameters, including assessment of longitudinal stability of associations over time and effect of thyroid hormone replacement.Common variation in the DIO2 gene predicts baseline psychological well-being and response to combination thyroxine plus triiodothyronine therapy in hypothyroid patients.Fetal thyroid hormone level at birth is associated with fetal growth.The genetics of autoimmune thyroid disease.Identification of novel genetic Loci associated with thyroid peroxidase antibodies and clinical thyroid disease.Side effects of anti-thyroid drugs and their impact on the choice of treatment for thyrotoxicosis in pregnancySuspected Spontaneous Reports of Birth Defects in the UK Associated with the Use of Carbimazole and Propylthiouracil in Pregnancy.Linkage Analysis in Autoimmune Addison's Disease: NFATC1 as a Potential Novel Susceptibility Locus.Orbital decompression for Graves' orbitopathy in EnglandAdrenal steroidogenesis after B lymphocyte depletion therapy in new-onset Addison's diseaseMaternal hypothyroxinaemia in pregnancy is associated with obesity and adverse maternal metabolic parameters.Adrenocorticotropin-secreting carcinoid tumour identified and treated 12 years after presentation with Cushing's syndromeA common variation in deiodinase 1 gene DIO1 is associated with the relative levels of free thyroxine and triiodothyronine.2012 European thyroid association guidelines for the management of familial and persistent sporadic non-autoimmune hyperthyroidism caused by thyroid-stimulating hormone receptor germline mutations.A preconsultation web-based tool to generate an agenda for discussion in diabetes outpatient clinics to improve patient outcomes (DIAT): a feasibility study.Carbimazole embryopathy: implications for the choice of antithyroid drugs in pregnancy.Quality of life in thyroid eye disease: impact of quality of care.Diagnosis of Graves' orbitopathy (DiaGO): results of a pilot study to assess the utility of an office tool for practicing endocrinologists.Management of thyroid eye disease in the United Kingdom: A multi-centre thyroid eye disease audit.Iodine deficiency amongst pregnant women in South-West England.A Follow-Up Study of the Prevalence of Valvular Heart Abnormalities in Hyperprolactinemic Patients Treated With Cabergoline.TSH levels and risk of miscarriage in women on long-term levothyroxine: a community-based study.Iodine supplementation in pregnancy - is it time?Exploring reasons for variation in ordering thyroid function tests in primary care: a qualitative study.An international survey of screening and management of hypothyroidism during pregnancy in Latin America.Impact of month of birth on the development of autoimmune thyroid disease in the United Kingdom and Europe.Further evidence for a susceptibility locus on chromosome 20q13.11 in families with dominant transmission of Graves disease.Correction: Linkage Analysis in Autoimmune Addison's Disease: NFATC1 as a Potential Novel Susceptibility Locus.
P50
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P50
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հետազոտող
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Bijay Vaidya
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Bijay Vaidya
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Bijay Vaidya
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Bijay Vaidya
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Bijay Vaidya
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Bijay Vaidya
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Bijay Vaidya
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Bijay Vaidya
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Bijay Vaidya
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Bijay Vaidya
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Bijay Vaidya
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Bijay Vaidya
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Bijay Vaidya
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Bijay Vaidya
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Bijay Vaidya
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P2798
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P496
0000-0002-2223-0494