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An outline concerning the potential use of recombinant human thyrotropin for improving radioiodine therapy of multinodular goiter

Endocrine, 2008-04, Vol.33 (2), p.109-117

2008

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The anorectic effect of increasing doses of L-tryptophan in obese patients

Eating and weight disorders, 1997-12, Vol.2 (4), p.211-215

1997

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The p.A2215D Thyroglobulin Gene Mutation Leads to Deficient Synthesis and Secretion of the Mutated Protein and Congenital Hypothyroidism with Wide Phenotype Variation

The journal of clinical endocrinology and metabolism, 2009-08, Vol.94 (8), p.2938-2944

2009

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Metastatic Thyroid Carcinoma Arising from Congenital Goiter due to Mutation in the Thyroperoxidase Gene1

The journal of clinical endocrinology and metabolism, 1998-11, Vol.83 (11), p.4162-4166

1998

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John B. Stanbury (May 15, 1915-July 6, 2015)

Thyroid (New York, N.Y.), 2015-11, Vol.25 (11), p.1177

2015

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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

Thyroid (New York, N.Y.), 2005-02, Vol.15 (2), p.134-139

2005

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Analysis of the PAX8 gene in 32 children with thyroid dysgenesis and functional characterization of a promoter variant

Journal of pediatric endocrinology & metabolism : JPEM, 2016-02, Vol.29 (2), p.193

2016

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Oral ingestion of a hydrolyzed gelatin meal in subjects with normal weight and in obese patients: Postprandial effect on circulating gut peptides, glucose and insulin

Eating and weight disorders, 2008-03, Vol.13 (1), p.48-53

2008

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Levothyroxine Suppressive Therapy is Partially Effective in Treating Patients with Benign, Solid Thyroid Nodules and Multinodular Goiters

Thyroid (New York, N.Y.), 1997-10, Vol.7 (5), p.691-697

1997

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A Novel Mutation (Q40P) in PAX8 Associated with Congenital Hypothyroidism and Thyroid Hypoplasia: Evidence for Phenotypic Variability in Mother and Child

The journal of clinical endocrinology and metabolism, 2001-08, Vol.86 (8), p.3962-3967

2001

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Metastatic thyroid carcinoma arising from congenital goiter due to mutation in the thyroperoxidase gene

The journal of clinical endocrinology and metabolism, 1998-11, Vol.83 (11), p.4162-4166

1998

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Prognostic value of serial serum thyroglobulin determinations after total thyroidectomy for differentiated thyroid cancer

Journal of endocrinological investigation, 2002-02, Vol.25 (2), p.110-115

2002

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Inflammatory proptosis in Rosai-Dorfman disease simulating thyroid-associated ophthalmopathy

Thyroid (New York, N.Y.), 2009-07, Vol.19 (7), p.801

2009

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A Premature Stopcodon in Thyroglobulin Messenger RNA Results in Familial Goiter and Moderate Hypothyroidism

The journal of clinical endocrinology and metabolism, 1999-07, Vol.84 (7), p.2537-2542

1999

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Congenital Goiter with Hypothyroidism Caused by a 5′ Splice Site Mutation in the Thyroglobulin Gene

Thyroid (New York, N.Y.), 2001-07, Vol.11 (7), p.685-690

2001

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A circulating, biologically inactive thyrotropin caused by a mutation in the beta subunit gene

The Journal of clinical investigation, 1996-03, Vol.97 (5), p.1250-1256

1996

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Aggressive Metastatic Follicular Thyroid Carcinoma with Anaplastic Transformation Arising from a Long-Standing Goiter in a Patient with Pendred's Syndrome

Thyroid (New York, N.Y.), 2001-10, Vol.11 (10), p.981-988

2001

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Defective thyroglobulin synthesis and secretion causing goiter and hypothyroidism

Endocrine reviews, 1993-04, Vol.14 (2), p.165-183

1993

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Highlights of the guidelines on the management of hyperthyroidism and other causes of thyrotoxicosis

Thyroid (New York, N.Y.), 2011-06, Vol.21 (6), p.581

2011

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Autosomal recessive deficiency of combined pituitary hormones (except ACTH) in a consanguineous Brazilian kindred

Journal of endocrinological investigation, 1998-06, Vol.21 (6), p.386-391

1998

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Mutations of the thyroglobulin gene and its relevance to thyroid disorders

Current opinion in endocrinology, diabetes, and obesity, 2009-10, Vol.16 (5), p.373-378

2009

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Thyroid in the Third Millennium: Quo Vadis?

Thyroid (New York, N.Y.), 2000-03, Vol.10 (3), p.227-227

Medeiros-Neto, Geraldo

2000

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Searching for Iodine Deficiency Disorders in Schoolchildren from Brazil: The Thyromobil Project

Thyroid (New York, N.Y.), 2001-07, Vol.11 (7), p.661-663

2001

Volltextzugriff (PDF)

High prevalence of side effects after recombinant human thyrotropin-stimulated radioiodine treatment with 30 mCi in patients with multinodular goiter and subclinical/clinical hyperthyroidism

Thyroid (New York, N.Y.), 2009-09, Vol.19 (9), p.945

2009

Volltextzugriff (PDF)

Association of Low Sodium-Iodide Symporter Messenger Ribonucleic Acid Expression in Malignant Thyroid Nodules with Increased Intracellular Protein Staining

The journal of clinical endocrinology and metabolism, 2008-10, Vol.93 (10), p.4141-4145

2008

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An outline concerning the potential use of recombinant human thyrotropin for improving radioiodine therapy of multinodular goiter

The anorectic effect of increasing doses of L-tryptophan in obese patients

The p.A2215D Thyroglobulin Gene Mutation Leads to Deficient Synthesis and Secretion of the Mutated Protein and Congenital Hypothyroidism with Wide Phenotype Variation

Metastatic Thyroid Carcinoma Arising from Congenital Goiter due to Mutation in the Thyroperoxidase Gene1

John B. Stanbury (May 15, 1915-July 6, 2015)

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

Analysis of the PAX8 gene in 32 children with thyroid dysgenesis and functional characterization of a promoter variant

Oral ingestion of a hydrolyzed gelatin meal in subjects with normal weight and in obese patients: Postprandial effect on circulating gut peptides, glucose and insulin

Levothyroxine Suppressive Therapy is Partially Effective in Treating Patients with Benign, Solid Thyroid Nodules and Multinodular Goiters

A Novel Mutation (Q40P) in PAX8 Associated with Congenital Hypothyroidism and Thyroid Hypoplasia: Evidence for Phenotypic Variability in Mother and Child

Metastatic thyroid carcinoma arising from congenital goiter due to mutation in the thyroperoxidase gene

Prognostic value of serial serum thyroglobulin determinations after total thyroidectomy for differentiated thyroid cancer

Inflammatory proptosis in Rosai-Dorfman disease simulating thyroid-associated ophthalmopathy

A Premature Stopcodon in Thyroglobulin Messenger RNA Results in Familial Goiter and Moderate Hypothyroidism

Congenital Goiter with Hypothyroidism Caused by a 5′ Splice Site Mutation in the Thyroglobulin Gene

A circulating, biologically inactive thyrotropin caused by a mutation in the beta subunit gene

Aggressive Metastatic Follicular Thyroid Carcinoma with Anaplastic Transformation Arising from a Long-Standing Goiter in a Patient with Pendred's Syndrome

Defective thyroglobulin synthesis and secretion causing goiter and hypothyroidism

Highlights of the guidelines on the management of hyperthyroidism and other causes of thyrotoxicosis

Autosomal recessive deficiency of combined pituitary hormones (except ACTH) in a consanguineous Brazilian kindred

Mutations of the thyroglobulin gene and its relevance to thyroid disorders

Thyroid in the Third Millennium: Quo Vadis?

Searching for Iodine Deficiency Disorders in Schoolchildren from Brazil: The Thyromobil Project

High prevalence of side effects after recombinant human thyrotropin-stimulated radioiodine treatment with 30 mCi in patients with multinodular goiter and subclinical/clinical hyperthyroidism

Association of Low Sodium-Iodide Symporter Messenger Ribonucleic Acid Expression in Malignant Thyroid Nodules with Increased Intracellular Protein Staining

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