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Refinado por: Nome da Publicação: The Journal Of Clinical Endocrinology And Metabolism remover idioma: Inglês remover
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Metastatic thyroid carcinoma arising from congenital goiter due to mutation in the thyroperoxidase gene
Metastatic thyroid carcinoma arising from congenital goiter due to mutation in the thyroperoxidase gene
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Metastatic thyroid carcinoma arising from congenital goiter due to mutation in the thyroperoxidase gene

MEDEIROS-NETO, G ; GIL-DA-COSTA, M. J ; SANTOS, C. L. S ; MEDINA, A. M ; COSTA E SILVA, J ; TSOU, R. M ; SOBRINHO-SIMOES, M

The journal of clinical endocrinology and metabolism, 1998-11, Vol.83 (11), p.4162-4166 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

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2
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
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
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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

KOPP, P ; ARSEVEN, O. K ; SABACAN, L ; KOTLAR, T ; DUPUIS, J ; CAVALIERE, H ; SANTOS, C. L. S ; JAMESON, J. L ; MEDEIROS-NETO, G

The journal of clinical endocrinology and metabolism, 1999, Vol.84 (1), p.336-341 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

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3
Prenatal diagnosis and treatment of dyshormonogenetic fetal goiter due to defective thyroglobulin synthesis
Prenatal diagnosis and treatment of dyshormonogenetic fetal goiter due to defective thyroglobulin synthesis
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Prenatal diagnosis and treatment of dyshormonogenetic fetal goiter due to defective thyroglobulin synthesis

MEDEIROS-NETO, G ; BUNDUKI, V ; TOMIMORI, E ; GOMES, S ; KNOBEL, M ; MARTIN, R. T ; ZUGAIB, M

The journal of clinical endocrinology and metabolism, 1997-12, Vol.82 (12), p.4239-4242 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

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4
A novel mutation (Q40p) in PAX8 associated with congenital hypothyroidism and thyroid hypoplasia : Evidence for phenotypic variability in mother and child
A novel mutation (Q40p) in PAX8 associated with congenital hypothyroidism and thyroid hypoplasia : Evidence for phenotypic variability in mother and child
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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

CONGDON, Tamara ; NGUYEN, Lynda Q ; NOGUEIRA, Celia R ; HABIBY, Reema L ; MEDEIROS-NETO, Geraldo ; KOPP, Peter

The journal of clinical endocrinology and metabolism, 2001-08, Vol.86 (8), p.3962-3967 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

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5
Two Distinct Compound Heterozygous Constellations (R277X/IVS34–1G>C and R277X/R1511X) in the Thyroglobulin (TG) Gene in Affected Individuals of a Brazilian Kindred with Congenital Goiter and Defective TG Synthesis
Two Distinct Compound Heterozygous Constellations (R277X/IVS34–1G>C and R277X/R1511X) in the Thyroglobulin (TG) Gene in Affected Individuals of a Brazilian Kindred with Congenital Goiter and Defective TG Synthesis
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Two Distinct Compound Heterozygous Constellations (R277X/IVS34–1G>C and R277X/R1511X) in the Thyroglobulin (TG) Gene in Affected Individuals of a Brazilian Kindred with Congenital Goiter and Defective TG Synthesis

Gutnisky, Viviana J ; Moya, Christian M ; Rivolta, Carina M ; Domené, Sabina ; Varela, Viviana ; Toniolo, Jussara V ; Medeiros-Neto, Geraldo ; Targovnik, Héctor M

The journal of clinical endocrinology and metabolism, 2004-02, Vol.89 (2), p.646-657 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

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6
Pathogenesis of myxedematous endemic cretinism
Pathogenesis of myxedematous endemic cretinism
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Pathogenesis of myxedematous endemic cretinism

Boyages, S C ; Medeiros-Neto, G

The journal of clinical endocrinology and metabolism, 1996-04, Vol.81 (4), p.1671-1674 [Periódico revisado por pares]

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7
A Premature Stopcodon in Thyroglobulin Messenger RNA Results in Familial Goiter and Moderate Hypothyroidism
A Premature Stopcodon in Thyroglobulin Messenger RNA Results in Familial Goiter and Moderate Hypothyroidism
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A Premature Stopcodon in Thyroglobulin Messenger RNA Results in Familial Goiter and Moderate Hypothyroidism

van de Graaf, Simone A. R ; Ris-Stalpers, Carrie ; Veenboer, Geertruda J. M ; Cammenga, Marianne ; Santos, Cécilia ; Targovnik, Héctor M ; de Vijlder, Jan J. M ; Medeiros-Neto, Geraldo

The journal of clinical endocrinology and metabolism, 1999-07, Vol.84 (7), p.2537-2542 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

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8
Pathogenesis of myxedematous endemic cretinism
Pathogenesis of myxedematous endemic cretinism
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Pathogenesis of myxedematous endemic cretinism

Boyages, S C ; Medeiros-Neto, G

The journal of clinical endocrinology and metabolism, 1996-04, Vol.81 (4), p.1671-1674 [Periódico revisado por pares]

United States

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9
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 1
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 1
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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 1

Kopp, P. ; Arseven, O. Karamanoglu ; Sabacan, L. ; Kotlar, T. ; Dupuis, J. ; Cavaliere, H. ; Santos, C. L. S. ; Jameson, J. L. ; Medeiros-Neto, G.

The journal of clinical endocrinology and metabolism, 1999-01, Vol.84 (1), p.336-341 [Periódico revisado por pares]

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10
Phenocopies for Deafness and Goiter Development in a Large Inbred Brazilian Kindred with Pendred’s Syndrome Associated with a Novel Mutation in the PDS Gene1
Phenocopies for Deafness and Goiter Development in a Large Inbred Brazilian Kindred with Pendred’s Syndrome Associated with a Novel Mutation in the PDS Gene1
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Phenocopies for Deafness and Goiter Development in a Large Inbred Brazilian Kindred with Pendred’s Syndrome Associated with a Novel Mutation in the PDS Gene1

Kopp, P ; Arseven, O. Karamanoglu ; Sabacan, L ; Kotlar, T ; Dupuis, J ; Cavaliere, H ; Santos, C. L. S ; Jameson, J. L ; Medeiros-Neto, G

The journal of clinical endocrinology and metabolism, 1999-01, Vol.84 (1), p.336-341 [Periódico revisado por pares]

Endocrine Society

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