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1
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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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
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Artigo
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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
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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Artigo
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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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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 Gene1
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Artigo
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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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5
Thyrotropin Receptor Mutations in Hyperfunctioning Thyroid Adenomas from Brazil
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Artigo
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Thyrotropin Receptor Mutations in Hyperfunctioning Thyroid Adenomas from Brazil

Nogueira, C R ; Kopp, P ; Arseven, O K ; Santos, C L ; Jameson, J L ; Medeiros-Neto, G

Thyroid (New York, N.Y.), 1999-11, Vol.9 (11), p.163-1068 [Periódico revisado por pares]

United States

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6
Cloning of the cat TSH receptor and evidence against an autoimmune etiology of feline hyperthyroidism
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Artigo
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Cloning of the cat TSH receptor and evidence against an autoimmune etiology of feline hyperthyroidism

Nguyen, Lynda Q ; Arseven, Onur Karamanoglu ; Gerber, Hans ; Stein, Barbara S ; Jameson, J Larry ; Kopp, Peter

Endocrinology (Philadelphia), 2002-02, Vol.143 (2), p.395-402 [Periódico revisado por pares]

United States

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