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1
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
Clinical and molecular analysis of three Mexican families with Pendred's syndrome
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Artigo
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Clinical and molecular analysis of three Mexican families with Pendred's syndrome

GONZALEZ TREVINO, O ; KARAMANOGLU ARSEVEN, O ; CEBALLOS, C. J ; VIVES, V. I ; RAMIREZ, R. C ; GOMEZ, V. V ; MEDEIROS-NETO, G ; KOPP, P

European journal of endocrinology, 2001-06, Vol.144 (6), p.585-593 [Periódico revisado por pares]

Colchester: Portland Press

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3
Autosomal recessive deficiency of combined pituitary hormones (except ACTH) in a consanguineous Brazilian kindred
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Artigo
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Autosomal recessive deficiency of combined pituitary hormones (except ACTH) in a consanguineous Brazilian kindred

NOGUEIRA, C. R ; LEITE, C. C ; CHEDID, E. P. T ; LIBERMAN, B ; PIMENTEL-FILHO, F. R ; KOPP, P ; MEDEIROS-NETO, G. A

Journal of endocrinological investigation, 1998-06, Vol.21 (6), p.386-391 [Periódico revisado por pares]

Milano: Kurtis

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4
Prenatal diagnosis and treatment of dyshormonogenetic fetal goiter due to defective thyroglobulin synthesis
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Artigo
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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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5
Autosomal recessive deficiency of combined pituitary hormones (except ACTH) in a consanguineous Brazilian kindred
Material Type:
Artigo
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Autosomal recessive deficiency of combined pituitary hormones (except ACTH) in a consanguineous Brazilian kindred

NOGUEIRA, C. R ; LEITE, C. C ; CHEDID, E. P. T ; LIBERMAN, B ; PIMENTEL-FILHO, F. R ; KOPP, P ; MEDEIROS-NETO, G. A

Journal of endocrinological investigation, 1997-11, Vol.20 (10), p.629-633 [Periódico revisado por pares]

Milano: Kurtis

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6
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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Artigo
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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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7
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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8
Structural Analysis of the Thyrotropin Receptor in Four Patients with Congenital Hypothyroidism Due to Thyroid Hypoplasia
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Structural Analysis of the Thyrotropin Receptor in Four Patients with Congenital Hypothyroidism Due to Thyroid Hypoplasia

Nogueira, C R ; Nguyen, L Q ; Coelho-Neto, J R ; Arseven, O K ; Jameson, J L ; Kopp, P ; Medeiros-Neto, G A

Thyroid (New York, N.Y.), 1999-06, Vol.9 (6), p.523-529 [Periódico revisado por pares]

United States

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9
Hypothyroidism in a Brazilian Kindred Due to Iodide Trapping Defect Caused by a Homozygous Mutation in the Sodium/Iodide Symporter Gene
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Hypothyroidism in a Brazilian Kindred Due to Iodide Trapping Defect Caused by a Homozygous Mutation in the Sodium/Iodide Symporter Gene

Pohlenz, Joachim ; Medeiros-Neto, Geraldo ; Gross, Jorge L. ; Silveiro, Sandra P. ; Knobel, Meyer ; Refetoff, Samuel

Biochemical and biophysical research communications, 1997-11, Vol.240 (2), p.488-491 [Periódico revisado por pares]

United States: Elsevier Inc

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10
Aggressive Metastatic Follicular Thyroid Carcinoma with Anaplastic Transformation Arising from a Long-Standing Goiter in a Patient with Pendred's Syndrome
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Artigo
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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

Camargo, Rosalinda ; Limbert, Eduardo ; Gillam, Mary ; Henriques, Maria Manuela ; Fernandes, Carlos ; Catarino, Ana Luisa ; Soares, Jorge ; Alves, Venancio A.F. ; Kopp, Peter ; Medeiros-Neto, Geraldo

Thyroid (New York, N.Y.), 2001-10, Vol.11 (10), p.981-988 [Periódico revisado por pares]

United States: Mary Ann Liebert, Inc

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