UB Paderborn / Katalog / Suche / in CDI

1 – 19 von 19

Sortiert nach

Phenotypic variation among four family members with congenital hypothyroidism caused by two distinct thyroglobulin gene mutations

Thyroid (New York, N.Y.), 2008-07, Vol.18 (7), p.783

2008

Volltextzugriff (PDF)

Congenital hypothyroidism and thyroid cancer

Endocrine-related cancer, 2021-09, Vol.28 (9), p.R217-R230

2021

Volltextzugriff (PDF)

The Prevalence of Thyroid Dysfunction in Elderly Cardiology Patients with Mild Excessive Iodine Intake in the Urban Area of São Paulo

Clinics (São Paulo, Brazil), 2009-02, Vol.64 (2), p.135-142

2009

Volltextzugriff (PDF)

Hypermethylation of a New Distal Sodium/Iodide Symporter (NIS) Enhancer (NDE) Is Associated With Reduced NIS Expression in Thyroid Tumors

The journal of clinical endocrinology and metabolism, 2014-06, Vol.99 (6), p.E944-E952

2014

Volltextzugriff (PDF)

Sesquiterpene Lactones from Calea pinnatifida : Absolute Configuration and Structural Requirements for Antitumor Activity

Molecules (Basel, Switzerland), 2020-06, Vol.25 (13), p.3005

2020

Volltextzugriff (PDF)

Thyroid and the environment: exposure to excessive nutritional iodine increases the prevalence of thyroid disorders in Sao Paulo, Brazil

European journal of endocrinology, 2008-09, Vol.159 (3), p.293

2008

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

HOPX homeobox methylation in differentiated thyroid cancer and its clinical relevance

Endocrine Connections, 2018-12, Vol.7 (12), p.1333-1342

2018

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

Volltextzugriff (PDF)

Iodine-Deficiency Disorders

Endocrinology: Adult and Pediatric, 2016, p.1584-1600.e3

Seventh Edition, 2016

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)

Prolonged follow-up of multinodular goitre patients treated with radioiodine preceded or not by human recombinant TSH

Clinical endocrinology (Oxford), 2006-04, Vol.64 (4), p.474-474

2006

Volltextzugriff (PDF)

Thyroperoxidase Gene Mutations in Congenital Goitrous Hypothyroidism with Total and Partial Iodide Organification Defect

Thyroid (New York, N.Y.), 2003-12, Vol.13 (12), p.1145-1151

2003

Volltextzugriff (PDF)

A novel system of genetic transformation allows multiple integrations of a desired gene in Saccharomyces cerevisiae chromosomes

Journal of microbiological methods, 2006-12, Vol.67 (3), p.437-445

2006

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Administration of a single dose of recombinant human thyrotrophin enhances the efficacy of radioiodine treatment of large compressive multinodular goitres

Clinical endocrinology (Oxford), 2004-03, Vol.60 (3), p.300-308

2004

Volltextzugriff (PDF)

Chapter 91 - Iodine-Deficiency Disorders

Endocrinology, 2016, p.1584-1600.e3

Seventh Edition, 2016

Volltextzugriff (PDF)

A molecular analysis and long-term follow-up of two siblings with severe congenital hypothyroidism carrying the IVS30+1G>T intronic thyroglobulin mutation

Arquivos brasileiros de endocrinologia e metabologia, 2008-11, Vol.52 (8), p.1337-1344

2008

Volltextzugriff (PDF)

1 – 19 von 19

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(16)
Mit Volltextzugriff
(14)

Publikationsform

Artikel
(17)
Buchkapitel
(2)

Sprache

Erscheinungsjahr

n.n

Menü

Weitere Dienste

Einstellungen

Phenotypic variation among four family members with congenital hypothyroidism caused by two distinct thyroglobulin gene mutations

Congenital hypothyroidism and thyroid cancer

The Prevalence of Thyroid Dysfunction in Elderly Cardiology Patients with Mild Excessive Iodine Intake in the Urban Area of São Paulo

Hypermethylation of a New Distal Sodium/Iodide Symporter (NIS) Enhancer (NDE) Is Associated With Reduced NIS Expression in Thyroid Tumors

Sesquiterpene Lactones from Calea pinnatifida : Absolute Configuration and Structural Requirements for Antitumor Activity

Thyroid and the environment: exposure to excessive nutritional iodine increases the prevalence of thyroid disorders in Sao Paulo, Brazil

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

Mutations of the thyroglobulin gene and its relevance to thyroid disorders

HOPX homeobox methylation in differentiated thyroid cancer and its clinical relevance

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

Iodine-Deficiency Disorders

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

Prolonged follow-up of multinodular goitre patients treated with radioiodine preceded or not by human recombinant TSH

Thyroperoxidase Gene Mutations in Congenital Goitrous Hypothyroidism with Total and Partial Iodide Organification Defect

A novel system of genetic transformation allows multiple integrations of a desired gene in Saccharomyces cerevisiae chromosomes

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

Administration of a single dose of recombinant human thyrotrophin enhances the efficacy of radioiodine treatment of large compressive multinodular goitres

Chapter 91 - Iodine-Deficiency Disorders

A molecular analysis and long-term follow-up of two siblings with severe congenital hypothyroidism carrying the IVS30+1G>T intronic thyroglobulin mutation

Suchergebnisse filtern