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Thyroid : Official Journal of the American Thyroid Association
|
December 14, 1999
Thyrotropin receptor mutations in hyperfunctioning thyroid adenomas from Brazil
C R Nogueira, P Kopp, O K Arseven, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 1, 1991
Genetic linkage studies of thyroid peroxidase (TPO) gene in families with TPO deficiency
A Mangklabruks, A E Billerbeck, B Wajchenberg, et al.
Thyroid : Official Journal of the American Thyroid Association
|
May 20, 1998
Evidence for the segregation of three different mutated alleles of the thyroglobulin gene in a Brazilian family with congenital goiter and hypothyroidism
H M Targovnik, G D Frechtel, F M Mendive, et al.
Journal of Endocrinological Investigation
|
December 1, 1989
Qualitative and quantitative defects of thyroglobulin resulting in congenital goiter. Absence of gross gene deletion of coding sequences in the TG gene structure
G Medeiros-Neto, H Targovnik, M Knobel, et al.
Endocrinology
|
June 1, 1996
Immunosuppression of thyroiditis
V C Guimaraes, J Quintans, M E Fisfalen, et al.
Clinical Endocrinology
|
September 1, 1999
A novel mutation in the TPO gene in goitrous hypothyroid patients with iodide organification defect
C L Santos, H Bikker, K G Rego, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 1, 1995
A 138-nucleotide deletion in the thyroglobulin ribonucleic acid messenger in a congenital goiter with defective thyroglobulin synthesis
H M Targovnik, J Vono, A E Billerbeck, et al.
The Journal of Clinical Investigation
|
December 15, 1996
Congenital hypothyroid goiter with deficient thyroglobulin. Identification of an endoplasmic reticulum storage disease with induction of molecular chaperones
G Medeiros-Neto, P S Kim, S E Yoo, et al.
The Journal of Clinical Endocrinology and Metabolism
|
January 27, 1999
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
P Kopp, O K Arseven, L Sabacan, et al.
Thyroid : Official Journal of the American Thyroid Association
|
June 12, 1999
Elevated anti-galactosyl antibody titers in endemic goiter
M Knobel, E S Umezawa, M S Cardia, et al.
Page
of 8
Search research articles
Search
Showing results (61-70 of 78) with videos related to
Sort By:
Page
of 8
Thyroid : Official Journal of the American Thyroid Association
|
December 14, 1999
Thyrotropin receptor mutations in hyperfunctioning thyroid adenomas from Brazil
C R Nogueira, P Kopp, O K Arseven, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 1, 1991
Genetic linkage studies of thyroid peroxidase (TPO) gene in families with TPO deficiency
A Mangklabruks, A E Billerbeck, B Wajchenberg, et al.
Thyroid : Official Journal of the American Thyroid Association
|
May 20, 1998
Evidence for the segregation of three different mutated alleles of the thyroglobulin gene in a Brazilian family with congenital goiter and hypothyroidism
H M Targovnik, G D Frechtel, F M Mendive, et al.
Journal of Endocrinological Investigation
|
December 1, 1989
Qualitative and quantitative defects of thyroglobulin resulting in congenital goiter. Absence of gross gene deletion of coding sequences in the TG gene structure
G Medeiros-Neto, H Targovnik, M Knobel, et al.
Endocrinology
|
June 1, 1996
Immunosuppression of thyroiditis
V C Guimaraes, J Quintans, M E Fisfalen, et al.
Clinical Endocrinology
|
September 1, 1999
A novel mutation in the TPO gene in goitrous hypothyroid patients with iodide organification defect
C L Santos, H Bikker, K G Rego, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 1, 1995
A 138-nucleotide deletion in the thyroglobulin ribonucleic acid messenger in a congenital goiter with defective thyroglobulin synthesis
H M Targovnik, J Vono, A E Billerbeck, et al.
The Journal of Clinical Investigation
|
December 15, 1996
Congenital hypothyroid goiter with deficient thyroglobulin. Identification of an endoplasmic reticulum storage disease with induction of molecular chaperones
G Medeiros-Neto, P S Kim, S E Yoo, et al.
The Journal of Clinical Endocrinology and Metabolism
|
January 27, 1999
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
P Kopp, O K Arseven, L Sabacan, et al.
Thyroid : Official Journal of the American Thyroid Association
|
June 12, 1999
Elevated anti-galactosyl antibody titers in endemic goiter
M Knobel, E S Umezawa, M S Cardia, et al.
Page
of 8