Pages that link to "Q43590701"
Jump to navigation
Jump to search
The following pages link to Genetic and Clinical Features of 42 Kindreds with Resistance to Thyroid Hormone: The National Institutes of Health Prospective Study (Q43590701):
Displaying 50 items.
- Approach to the patient with resistance to thyroid hormone and pregnancy (Q24624754) (← links)
- The diagnosis and management of hyperthyroidism in Korea: consensus report of the korean thyroid association (Q26823622) (← links)
- The syndromes of reduced sensitivity to thyroid hormone (Q27006848) (← links)
- Homozygous thyroid hormone receptor β-gene mutations in resistance to thyroid hormone: three new cases and review of the literature. (Q27693183) (← links)
- Thyroid hormone receptor beta is essential for development of auditory function (Q28510090) (← links)
- Guidelines for the treatment of hypothyroidism: prepared by the american thyroid association task force on thyroid hormone replacement (Q28649731) (← links)
- A dominant-negative thyroid hormone receptor blocks amphibian metamorphosis by retaining corepressors at target genes. (Q30452390) (← links)
- Thyroid hormone receptors control developmental maturation of the middle ear and the size of the ossicular bones (Q30457720) (← links)
- Aberrant Monoaminergic System in Thyroid Hormone Receptor-β Deficient Mice as a Model of Attention-Deficit/Hyperactivity Disorder (Q30661604) (← links)
- An Outline of Inherited Disorders of the Thyroid Hormone Generating System (Q34269861) (← links)
- Clinical, metabolic, and organ-specific indices of thyroid function (Q34303018) (← links)
- Thyroid hormone resistance syndrome (Q34378604) (← links)
- Resistance to thyroid hormone (Q34435743) (← links)
- The spectrum of thyroid diseases in childhood and its evolution during transition to adulthood: natural history, diagnosis, differential diagnosis and management (Q34444307) (← links)
- Adult ADHD and Comorbid Somatic Disease: A Systematic Literature Review (Q34541036) (← links)
- Hyperactivity and learning deficits in transgenic mice bearing a human mutant thyroid hormone beta1 receptor gene (Q35039106) (← links)
- Pituitary tumor endocrinopathies and their endocrine evaluation (Q35105409) (← links)
- An intronic SNP in the thyroid hormone receptor β gene is associated with pituitary cell-specific over-expression of a mutant thyroid hormone receptor β2 (R338W) in the index case of pituitary-selective resistance to thyroid hormone (Q35206200) (← links)
- Molecular basis of resistance to thyroid hormone. (Q35208690) (← links)
- Germline and somatic thyroid hormone receptor mutations in man. (Q35605651) (← links)
- Impaired adipogenesis caused by a mutated thyroid hormone alpha1 receptor (Q35676227) (← links)
- Resistance to thyroid hormone--an incidental finding (Q35863617) (← links)
- A Case of Resistance to Thyroid Hormone with Chronic Thyroiditis: Discovery of a Novel Mutation (I54V) (Q36168837) (← links)
- Syndromes of thyroid hormone resistance. (Q36179255) (← links)
- A two-day-old hyperthyroid neonate with thyroid hormone resistance born to a mother with well-controlled Graves' disease: a case report (Q36237795) (← links)
- Transgenic mice bearing a human mutant thyroid hormone beta 1 receptor manifest thyroid function anomalies, weight reduction, and hyperactivity. (Q36437755) (← links)
- Role of TSH in the spontaneous development of asymmetrical thyroid carcinoma in mice with a targeted mutation in a single allele of the thyroid hormone-β receptor (Q36439404) (← links)
- Role of Thyroid Hormones in Skeletal Development and Bone Maintenance (Q36773018) (← links)
- Newborn thyroxine levels and childhood ADHD (Q36793752) (← links)
- One Novel and Two Recurrent THRB Mutations Associated with Resistance to Thyroid Hormone: Structure-based Computational Mutation Prediction (Q36943151) (← links)
- Resistance to thyroid hormone with missense mutation (V349M) in the thyroid hormone receptor beta gene (Q37203565) (← links)
- Transgenic mouse models for ADHD. (Q37203801) (← links)
- Another story of mice and men: the types of RTH. (Q37224116) (← links)
- A thyroid hormone receptor mutation that dissociates thyroid hormone regulation of gene expression in vivo (Q37224312) (← links)
- Recruitment of N-CoR/SMRT-TBLR1 corepressor complex by unliganded thyroid hormone receptor for gene repression during frog development (Q37277846) (← links)
- A rare thyroid hormone receptor beta (THRβ) gene mutation in a 15-year-old girl with thyroid hormone resistance syndrome: a case report (Q37513746) (← links)
- Resistance to Thyroid Hormone Complicated with Type 2 Diabetes and Cardiomyopathy in a Patient with a TRβ Mutation (Q37521133) (← links)
- Multiple Hürthle cell adenomas in a patient with thyroid hormone resistance (Q37662277) (← links)
- Thyroid hormone resistance syndrome caused by heterozygous A317T mutation in thyroid hormone receptor β gene: Report of one Chinese pedigree and review of the literature (Q37726676) (← links)
- Is there a role for inherited TRβ mutation in human carcinogenesis? [corrected]. (Q37998339) (← links)
- Iodine deficiency, thyroid function and hearing deficit: a review (Q38113895) (← links)
- The multiple effects of thyroid disorders on bone and mineral metabolism (Q38244163) (← links)
- Label-free quantitative mass spectrometry reveals novel pathways involved in LL-37 expression. (Q38311118) (← links)
- Exploring the Validity of Proposed Transgenic Animal Models of Attention-Deficit Hyperactivity Disorder (ADHD). (Q39324205) (← links)
- Resistance to thyroid hormone is associated with raised energy expenditure, muscle mitochondrial uncoupling, and hyperphagia (Q39812091) (← links)
- Effect of thyroid hormone on growth. Lessons from the syndrome of resistance to thyroid hormone (Q41175270) (← links)
- Resistance To Thyroid Hormone: Implications for Neurodevelopmental Research On the Effects of Thyroid Hormone Disruptors (Q41699303) (← links)
- Central hyperthyroidism (Q41735089) (← links)
- Nuclear receptors: structure, function and involvement in disease (Q41756427) (← links)
- Thyroid disease mediated by molecular defects in cell surface and nuclear receptors (Q42465892) (← links)