139 results on '"Knobel,Meyer"'
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2. Low-level laser in the treatment of patients with hypothyroidism induced by chronic autoimmune thyroiditis: a randomized, placebo-controlled clinical trial
3. An outline concerning the potential use of recombinant human thyrotropin for improving radioiodine therapy of multinodular goiter
4. Cardiovascular assessment of hyperthyroid patients with multinodular goiter before and after radioiodine treatment preceded by stimulation with recombinant human TSH
5. PREOPERATIVE ASSESSMENT OF THYROID NODULES: ROLE OF ULTRASONOGRAPHY AND FINE NEEDLE ASPIRATION BIOPSY FOLLOWED BY CYTOLOGY
6. Contributors
7. Iodine Deficiency Disorders
8. PREVALENCE OF CHRONIC AUTOIMMUNE THYROIDITIS IN THE URBAN AREA NEIGHBORING A PETROCHEMICAL COMPLEX AND A CONTROL AREA IN SAO PAULO, BRAZIL
9. Pediatric Aspects of Thyroid Function and Iodine
10. Pathological findings in dyshormonogenetic goiter with defective lodide transport
11. The p.A2215D Thyroglobulin Gene Mutation Leads to Deficient Synthesis and Secretion of the Mutated Protein and Congenital Hypothyroidism with Wide Phenotype Variation
12. Association of Low Sodium-Iodide Symporter Messenger Ribonucleic Acid Expression in Malignant Thyroid Nodules with Increased Intracellular Protein Staining
13. Amino acid composition of proteins extracted from endemic goiter glands
14. Studies on functional and morphological aspects in human multinodular simple goiter tissues
15. Prevalence and characteristics of postpartum thyroid dysfunction in São Paulo, Brazil
16. Which Is the Ideal Treatment for Benign Diffuse and Multinodular Non-Toxic Goiters?
17. Monoallelic thyroid peroxidase gene mutation in a patient with congenital hypothyroidism with total iodide organification defect
18. A molecular analysis and long-term follow-up of two siblings with severe congenital hypothyroidism carrying the IVS30+1G>T intronic thyroglobulin mutation
19. A molecular analysis and long-term follow-up of two siblings with severe congenital hypothyroidism carrying the IVS30+1G>T intronic thyroglobulin mutation
20. An outline concerning the potential use of recombinant human thyrotropin for improving radioiodine therapy of multinodular goiter
21. Relevance of iodine intake as a reputed predisposing factor for thyroid cancer
22. SERUM THYROGLOBULIN LEVELS IN PATIENTS WITH GRAVES' DISEASE TREATED WITH METHIMAZOLE: CORRELATION WITH THYROID-STIMULATING AND TSH-BINDING INHIBITING IMMUNOGLOBULINS
23. Impacto médico-social do tratamento medicamentoso da moléstia de Graves-Basedow em Hospital Público Universitário: avaliação retrospectiva e projeção prospectiva de conduta terapêutica
24. Chapter 88 - Iodine Deficiency Disorders
25. Assessment of the Effects of Low-Level Laser Therapy on the Thyroid Vascularization of Patients with Autoimmune Hypothyroidism by Color Doppler Ultrasound
26. Low-level laser in the treatment of patients with hypothyroidism induced by chronic autoimmune thyroiditis: a randomized, placebo-controlled clinical trial
27. Monoallelic thyroid peroxidase gene mutation in a patient with congenital hypothyroidism with total iodide organification defect
28. High Prevalence of Side Effects After Recombinant Human Thyrotropin–Stimulated Radioiodine Treatment with 30 mCi in Patients with Multinodular Goiter and Subclinical/Clinical Hyperthyroidism
29. A molecular analysis and long-term follow-up of two siblings with severe congenital hypothyroidism carrying the IVS30+1G>T intronic thyroglobulin mutation
30. Thyroid and the environment: exposure to excessive nutritional iodine increases the prevalence of thyroid disorders in São Paulo, Brazil
31. Phenotypic Variation Among Four Family Members with Congenital Hypothyroidism Caused by Two Distinct Thyroglobulin Gene Mutations
32. Factitious Thyrotoxicosis Induced by Mesotherapy: A Case Report
33. Relevance of iodine intake as a reputed predisposing factor for thyroid cancer
34. Iodine nutrition: more is better?
35. Human Recombinant TSH Preceding a Therapeutic Dose of Radioiodine for Multinodular Goiters Has No Significant Effect in the Surge of TSH-Receptor and TPO Antibodies
36. Evaluation of a Coated-Tube Assay for Antithyrotropin Receptor Antibodies in Patients with Graves' Disease and Other Thyroid Disorders
37. Moléstias associadas à carência crônica de iodo
38. Thyroperoxidase Gene Mutations in Congenital Goitrous Hypothyroidism with Total and Partial Iodide Organification Defect
39. An Outline of Inherited Disorders of the Thyroid Hormone Generating System
40. Bioequivalência de Preparações Comerciais de L-Tiroxina (100 e 200µg): Avaliação em Pacientes Hipotireóideos Previamente Tireoidectomizados
41. Hipotireoidismo Congênito: Recentes Avanços em Genética Molecular
42. Comparação entre diferentes métodos para avaliar a presença de auto-anticorpos dirigidos ao receptor de TSH em pacientes com moléstia de Graves-Basedow
43. Prevalence and Characteristics of Postpartum Thyroid Dysfunction in São Paulo, Brazil
44. Aspectos ultra-sonográficos e prevalência da tireoidite pós-parto em gestantes sem disfunção tireóidea atendidas em hospital público de São Paulo
45. Genética molecular do hipotireoidismo congênito
46. Elevated Anti-Galactosyl Antibody Titers in Endemic Goiter
47. Doença nodular tireóidea: avaliação clínica e laboratorial
48. Hipotireoidismo e glaucoma: investigação de uma possível associação
49. Prenatal Diagnosis and Treatment of Dyshormonogenetic Fetal Goiter Due to Defective Thyroglobulin Synthesis1
50. Hypothyroidism in a Brazilian Kindred Due to Iodide Trapping Defect Caused by a Homozygous Mutation in the Sodium/Iodide Symporter Gene
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