Pages that link to "Q34249342"

The following pages link to Familial dysalbuminemic hyperthyroxinemia: a syndrome that can be confused with thyrotoxicosis (Q34249342):

Displaying 37 items.

• An Outline of Inherited Disorders of the Thyroid Hormone Generating System (Q34269861) (← links)
• Evaluation of the patient with a suspected thyroid disorder (Q34295539) (← links)
• Detection of familial dysalbuminaemic hyperthyroxinaemia (Q34492032) (← links)
• Role of serum carrier proteins in the peripheral metabolism and tissue distribution of thyroid hormones in familial dysalbuminemic hyperthyroxinemia and congenital elevation of thyroxine-binding globulin (Q35577492) (← links)
• A point mutation in transthyretin increases affinity for thyroxine and produces euthyroid hyperthyroxinemia (Q35817997) (← links)
• Familial dysalbuminaemic hyperthyroxinaemia (Q36721169) (← links)
• One Novel and Two Recurrent THRB Mutations Associated with Resistance to Thyroid Hormone: Structure-based Computational Mutation Prediction (Q36943151) (← links)
• Molecular genetics of human serum albumin: restriction enzyme fragment length polymorphisms and analbuminemia (Q37515245) (← links)
• Structure and function of thyroid hormone plasma membrane transporters (Q38299941) (← links)
• A point mutation in the human serum albumin gene results in familial dysalbuminaemic hyperthyroxinaemia (Q38308581) (← links)
• Diseases of the thyroid gland. (Q39376304) (← links)
• Thyroid dysfunction. (Q39558025) (← links)
• Thyroid function tests in thyroid and nonthyroid disease (Q40212082) (← links)
• Familial euthyroid hyperthyroxinemia secondary to pituitary and peripheral resistance to thyroid hormones (Q42506696) (← links)
• Coexistence of familial dysalbuminemic hyperthyroxinemia with familial hypercholesterolemia and multiple lipoprotein type hyperlipidemia (Q44084771) (← links)
• Familial dysalbuminemic hyperthyroxinemia in a 4-year-old girl with hyperactivity, palpitations and advanced dental age: how gold standard assays may be misleading. (Q47825510) (← links)
• Elevated thyroxine levels in a euthyroid patient (Q50009334) (← links)
• Familial dysalbuminaemic hyperthyroxinaemia: a review (Q68127240) (← links)
• A new type of albumin with predominantly increased binding affinity for 3,3',5-triiodothyronine in a patient with Graves' disease (Q69027241) (← links)
• Congenital hypothyroidism and partial thyroid hormone unresponsiveness of the pituitary in a patient with congenital thyroxine binding albumin elevation (Q69255207) (← links)
• [Euthyroid hyperthyroxinemias] (Q69501340) (← links)
• Clinical and laboratory assessment of thyroid abnormalities (Q69914622) (← links)
• Euthyroid hyperthyroxinemia (Q69936888) (← links)
• Hyperthyroidism. Causes, clinical features, and diagnosis (Q69970342) (← links)
• Studies of thyroxine binding to plasma proteins in health and disease (Q70280058) (← links)
• Euthyroid hyperthyroxinemia (Q70332927) (← links)
• A four generation study of familial dysalbuminemic hyperthyroxinemia: diagnosis in the presence of an acquired excess of thyroxine-binding globulin (Q70345269) (← links)
• Familial dysalbuminemic hyperthyroxinemia (FDH): inadequacy of the "analog" methods for assaying free-T4 levels (Q71426632) (← links)
• Hyperthyroxinemia associated with high thyroxine binding to albumin in euthyroid subjects (Q71646722) (← links)
• Hyperthyroxinaemia: does it mean hyperthyroidism? (Q72526715) (← links)
• Kaposi sarcoma in homosexual men: Is it a new disease? (Q72528416) (← links)
• Hyperthyroxinaemia: does it mean hyperthyroidism? (Q72528421) (← links)
• Abnormal free thyroxine levels with analogue methods (Q72544320) (← links)
• Resistance to thyroid hormone (Q72561670) (← links)
• Specific thyroxine binding albumin is a constituent of normal human serum (Q72569405) (← links)
• Homozygous Mutation in Human Serum Albumin and Its Implication on Thyroid Tests (Q88419119) (← links)
• FAMILIAL DYSALBUMINAEMIC HYPERTHYROXINEMIA INTERFERES WITH CURRENT FREE THYROID HORMONE IMMUNOASSAY METHODS (Q90661050) (← links)