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Fetal Loss Associated With Excess Thyroid Hormone Exposure
João Anselmo · JAMA
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Research needs in allergy: an EAACI position paper, in collaboration with EFA
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A Large Family with Carney Complex Caused by the S147G PRKAR1A Mutation Shows a Unique Spectrum of Disease Including Adrenocortical Cancer
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Self‐medication of anaphylactic reactions due to Hymenoptera stings—an EAACI Task Force Consensus Statement
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Diagnosis of Human Leptospirosis in a Clinical Setting: Real-Time PCR High Resolution Melting Analysis for Detection of Leptospira at the Onset of Disease
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Report of the Brazilian Chronic Dialysis Census 2012
Ricardo Sesso, Antônio Alberto Lopes, Fernando Saldanha Thomé et al. · Brazilian Journal of Nephrology
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Juvenile idiopathic arthritis in adulthood: fulfilment of classification criteria for adult rheumatic diseases, long-term outcomes and predictors of inactive disease, functional status and damage
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Standard endovascular aneurysm repair in patients with wide infrarenal aneurysm necks is associated with increased risk of adverse events
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Patients with large neck diameter have a higher risk of type IA endoleaks and aneurysm rupture after standard endovascular aneurysm repair
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Increased Hepatic Fat Content in Patients with Resistance to Thyroid Hormone Beta
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MECP2 coding sequence and 3′UTR variation in 172 unrelated autistic patients
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Risk Factors, Dynamics, and Clinical Consequences of Aortic Neck Dilatation after Standard Endovascular Aneurysm Repair
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Oxidative stress and mitochondrial dysfunction play a role in myelodysplastic syndrome development, diagnosis, and prognosis: A pilot study
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Serum copper as a novel biomarker for resistance to thyroid hormone
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Control of Allergic Rhinitis and Asthma Test (CARAT) can be used to assess individual patients over time
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A case of choking phobia: towards a conceptual approach
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Alveolar Soft-part Sarcoma of the Urinary Bladder With Urethral Recurrence: A Unique Case With Emphasis on Differential Diagnoses and Diagnostic Utility of an Immunohistochemical Panel Including TFE3
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Regression of a Large Goiter in a Patient with Resistance to Thyroid Hormone by Every Other Day Treatment with Triiodothyronine
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Molecular study of congenital erythrocytosis in 70 unrelated patients revealed a potential causal mutation in less than half of the cases (Where is/are the missing gene(s)?)
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17 Jul 2013 |
47 |
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A New PAX8 Mutation Causing Congenital Hypothyroidism in Three Generations of a Family Is Associated with Abnormalities in the Urogenital Tract
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Iliac Seal Zone Dynamics and Clinical Consequences After Endovascular Aneurysm Repair
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Deletion of CFTR Translation Start Site Reveals Functional Isoforms of the Protein in CF Patients
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Validation of Control of Allergic Rhinitis and Asthma Test for Children (CARATKids) – a prospective multicenter study
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