UB Paderborn / Katalog / Suche / in CDI

Iodine-Induced Hyperthyroidism: Occurrence and Epidemiology

Thyroid (New York, N.Y.), 1998-01, Vol.8 (1), p.83-100

1998

Volltextzugriff (PDF)

Remote Sensing from Ground to Space Platforms Associated with Terrain Attributes as a Hybrid Strategy on the Development of a Pedological Map

Remote sensing (Basel, Switzerland), 2016-10, Vol.8 (10), p.826-826

2016

Volltextzugriff (PDF)

Gastrointestinal side effects of orlistat may be prevented by concomitant prescription of natural fibers (psyllium mucilloid)

International Journal of Obesity, 2001-07, Vol.25 (7), p.1095-1099

2001

Volltextzugriff (PDF)

Methylation levels of sodium–iodide symporter (NIS) promoter in benign and malignant thyroid tumors with reduced NIS expression

Endocrine, 2013-02, Vol.43 (1), p.225-229

2013

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Decreased androgen levels in massively obese men may be associated with impaired function of the gonadostat

International Journal of Obesity, 2000-11, Vol.24 (11), p.1433-1437

2000

Volltextzugriff (PDF)

Excessive Iodine Intake and Ultrasonographic Thyroid Abnormalities in Schoolchildren

Journal of Pediatric Endocrinology and Metabolism, 2009, Vol.22 (4), p.327-334

2009

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Phenocopies for deafness and goiter development in a large inbred Brazilian kindred with Pendred's syndrome associated with a novel mutation in the PDS gene

The journal of clinical endocrinology and metabolism, 1999, Vol.84 (1), p.336-341

1999

Volltextzugriff (PDF)

An Outline of Inherited Disorders of the Thyroid Hormone Generating System

Thyroid (New York, N.Y.), 2003-08, Vol.13 (8), p.771-801

2003

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Peripheral blood levels of thyroglobulin mRNA and serum thyroglobulin concentrations after radioiodine ablation of multinodular goiter with or without pre-treatment with recombinant human thyrotropin

Journal of endocrinological investigation, 2007-07, Vol.30 (7), p.535-540

2007

Volltextzugriff (PDF)

Clinical and molecular analysis of three Mexican families with Pendred's syndrome

European journal of endocrinology, 2001-06, Vol.144 (6), p.585

2001

Volltextzugriff (PDF)

Thyroid in the Third Millennium: Quo Vadis?

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

Medeiros-Neto, Geraldo

2000

Volltextzugriff (PDF)

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)

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

Volltextzugriff (PDF)

Prevalence of Incidental Thyroid Disease in a Relatively Low Iodine Intake Area

Thyroid (New York, N.Y.), 1995-08, Vol.5 (4), p.273-276

1995

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)

Prenatal diagnosis and treatment of dyshormonogenetic fetal goiter due to defective thyroglobulin synthesis

The journal of clinical endocrinology and metabolism, 1997-12, Vol.82 (12), p.4239-4242

1997

Volltextzugriff (PDF)

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

Journal of endocrinological investigation, 1997-11, Vol.20 (10), p.629-633

1997

Volltextzugriff (PDF)

Naturally Occurring Mutations in the Thyroglobulin Gene

Thyroid (New York, N.Y.), 2005-09, Vol.15 (9), p.121-1033

2005

Volltextzugriff (PDF)

Evaluation of a Coated-Tube Assay for Antithyrotropin Receptor Antibodies in Patients with Graves' Disease and Other Thyroid Disorders

Thyroid (New York, N.Y.), 2004-04, Vol.14 (4), p.295-300

2004

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Towards the eradication of iodine-deficiency disorders in Brazil through a salt iodination programme

Bulletin of the World Health Organization, 1988, Vol.66 (5), p.637-642

MEDEIROS-NETO, G. A

1988

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)

Menü

Weitere Dienste

Einstellungen

Iodine-Induced Hyperthyroidism: Occurrence and Epidemiology

Remote Sensing from Ground to Space Platforms Associated with Terrain Attributes as a Hybrid Strategy on the Development of a Pedological Map

Gastrointestinal side effects of orlistat may be prevented by concomitant prescription of natural fibers (psyllium mucilloid)

Methylation levels of sodium–iodide symporter (NIS) promoter in benign and malignant thyroid tumors with reduced NIS expression

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

Decreased androgen levels in massively obese men may be associated with impaired function of the gonadostat

Excessive Iodine Intake and Ultrasonographic Thyroid Abnormalities in Schoolchildren

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

Phenocopies for deafness and goiter development in a large inbred Brazilian kindred with Pendred's syndrome associated with a novel mutation in the PDS gene

An Outline of Inherited Disorders of the Thyroid Hormone Generating System

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

Peripheral blood levels of thyroglobulin mRNA and serum thyroglobulin concentrations after radioiodine ablation of multinodular goiter with or without pre-treatment with recombinant human thyrotropin

Clinical and molecular analysis of three Mexican families with Pendred's syndrome

Thyroid in the Third Millennium: Quo Vadis?

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

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

Prevalence of Incidental Thyroid Disease in a Relatively Low Iodine Intake Area

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

Prenatal diagnosis and treatment of dyshormonogenetic fetal goiter due to defective thyroglobulin synthesis

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

Naturally Occurring Mutations in the Thyroglobulin Gene

Evaluation of a Coated-Tube Assay for Antithyrotropin Receptor Antibodies in Patients with Graves' Disease and Other Thyroid Disorders

A novel mutation (Q40p) in PAX8 associated with congenital hypothyroidism and thyroid hypoplasia : Evidence for phenotypic variability in mother and child

Towards the eradication of iodine-deficiency disorders in Brazil through a salt iodination programme

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

Suchergebnisse filtern