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1
Gastrointestinal side effects of orlistat may be prevented by concomitant prescription of natural fibers (psyllium mucilloid)
Gastrointestinal side effects of orlistat may be prevented by concomitant prescription of natural fibers (psyllium mucilloid)
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Gastrointestinal side effects of orlistat may be prevented by concomitant prescription of natural fibers (psyllium mucilloid)

CAVALIERE, H ; FLORIANO, I ; MEDEIROS-NETO, G

International Journal of Obesity, 2001-07, Vol.25 (7), p.1095-1099 [Periódico revisado por pares]

Basingstoke: Nature Publishing

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2
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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3
Decreased androgen levels in massively obese men may be associated with impaired function of the gonadostat
Decreased androgen levels in massively obese men may be associated with impaired function of the gonadostat
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Decreased androgen levels in massively obese men may be associated with impaired function of the gonadostat

Lima, N ; Cavaliere, H ; Knobel, M ; Halpern, A ; Medeiros-Neto, G

International Journal of Obesity, 2000-11, Vol.24 (11), p.1433-1437 [Periódico revisado por pares]

Basingstoke: Nature Publishing

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4
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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5
Clinical and molecular analysis of three Mexican families with Pendred's syndrome
Clinical and molecular analysis of three Mexican families with Pendred's syndrome
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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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6
Autosomal recessive deficiency of combined pituitary hormones (except ACTH) in a consanguineous Brazilian kindred
Autosomal recessive deficiency of combined pituitary hormones (except ACTH) in a consanguineous Brazilian kindred
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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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7
Administration of a single dose of recombinant human thyrotrophin enhances the efficacy of radioiodine treatment of large compressive multinodular goitres
Administration of a single dose of recombinant human thyrotrophin enhances the efficacy of radioiodine treatment of large compressive multinodular goitres
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Administration of a single dose of recombinant human thyrotrophin enhances the efficacy of radioiodine treatment of large compressive multinodular goitres

Silva, Marcia N. C. ; Rubió, Ileana G. S. ; Romão, Rossana ; Gebrin, Eloisa M. M. S. ; Buchpiguel, Carlos ; Tomimori, Eduardo ; Camargo, Rosalinda ; Cardia, Maria Silvia ; Medeiros-Neto, Geraldo

Clinical endocrinology (Oxford), 2004-03, Vol.60 (3), p.300-308 [Periódico revisado por pares]

Oxford, UK: Blackwell Science Ltd

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8
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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9
Autosomal recessive deficiency of combined pituitary hormones (except ACTH) in a consanguineous Brazilian kindred
Autosomal recessive deficiency of combined pituitary hormones (except ACTH) in a consanguineous Brazilian kindred
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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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10
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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