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1
Clinical and molecular analysis of three Mexican families with Pendred's syndrome
Clinical and molecular analysis of three Mexican families with Pendred's syndrome
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

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

O. Gonzalez Trevino O Arseven Karamanoglu; C. J Ceballos; V. I Vives; R. C Ramirez; V. V Gomez; G Medeiros-Neto; P Kopp

European Journal of Endocrinology Reino Unido v. 144, n. 6, p. 585-593, 2001

Reino Unido 2001

Item não circula. Consulte sua biblioteca.(Acessar)

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
Material Type:
Artigo 		Adicionar ao Meu Espaço

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. Karamanoglu Arseven; L Sabacan; T Kotlar; J Dupuis; H Cavalieri; C. L. S Santos; J. L Jameson; Geraldo Antônio Medeiros Neto

Journal of Clinical Endocrinology & Metabolism Bethesda v. 84, n. 1, p. 336-341, 1999

Bethesda 1999

Item não circula. Consulte sua biblioteca.(Acessar)

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
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
Material Type:
Artigo 		Adicionar ao Meu Espaço

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. Karamanoglu Arseven; L Sabacan; T Kotlar; J Dupuis; H Cavalieri; C. L. S Santos; J. L Jameson; Geraldo Antônio Medeiros Neto

Journal of Clinical Endocrinology & Metabolism Bethesda v. 84, n. 1, p. 336-341, 1999

Bethesda 1999

Item não circula. Consulte sua biblioteca.(Acessar)

4
Structural analysis of the thyrotropin receptor in four patients with congenital hypothyroidism due to thyroid hypoplasia
Structural analysis of the thyrotropin receptor in four patients with congenital hypothyroidism due to thyroid hypoplasia
Material Type:
Artigo 		Adicionar ao Meu Espaço

Structural analysis of the thyrotropin receptor in four patients with congenital hypothyroidism due to thyroid hypoplasia

Célia R. Nogueira Lynda Q Nguyen; José R Coelho-Neto; Onur Karamanoglu Arseven; Larry Jameson; Peter Kopp; Geraldo Antônio Medeiros Neto

Thyroid v. 9, n. 6, p. 523-529, 1999

1999

Localização: FM - Fac. Medicina    (BCSEP 99031 )(Acessar)

5
Thyrotropin receptor mutations in hyperfunctioning thyroid adenomas from Brazil
Thyrotropin receptor mutations in hyperfunctioning thyroid adenomas from Brazil
Material Type:
Artigo 		Adicionar ao Meu Espaço

Thyrotropin receptor mutations in hyperfunctioning thyroid adenomas from Brazil

Célia R. Nogueira Peter Kopp; Onur Karamanoglu Arseven; Cecilia L. S Santos; J. Larry Jameson; Geraldo Antônio Medeiros Neto

Thyroid v. 9, n. 11, p. 1063-1068, 1999

1999

Localização: FM - Fac. Medicina    (BCSEP 200013 )(Acessar)

6
Structural analysis of the thyrotropin receptor in four patients with congenital hypothyroidism due to thyroid hypoplasia
Structural analysis of the thyrotropin receptor in four patients with congenital hypothyroidism due to thyroid hypoplasia
Material Type:
Artigo 		Adicionar ao Meu Espaço

Structural analysis of the thyrotropin receptor in four patients with congenital hypothyroidism due to thyroid hypoplasia

Célia R. Nogueira Lynda Q Nguyen; José R Coelho-Neto; Onur Karamanoglu Arseven; Larry Jameson; Peter Kopp; Geraldo Antônio Medeiros Neto

Thyroid v. 9, n. 6, p. 523-529, 1999

1999

Localização: FM - Fac. Medicina    (BCSEP 99031 )(Acessar)

7
Thyrotropin receptor mutations in hyperfunctioning thyroid adenomas from Brazil
Thyrotropin receptor mutations in hyperfunctioning thyroid adenomas from Brazil
Material Type:
Artigo 		Adicionar ao Meu Espaço

Thyrotropin receptor mutations in hyperfunctioning thyroid adenomas from Brazil

Célia R. Nogueira Peter Kopp; Onur Karamanoglu Arseven; Cecilia L. S Santos; J. Larry Jameson; Geraldo Antônio Medeiros Neto

Thyroid v. 9, n. 11, p. 1063-1068, 1999

1999

Localização: FM - Fac. Medicina    (BCSEP 200013 )(Acessar)

8
Clinical and molecular analysis of three Mexican families with Pendred's syndrome
Clinical and molecular analysis of three Mexican families with Pendred's syndrome
Material Type:
Artigo 		Adicionar ao Meu Espaço

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

Texto completo disponível

Citações Citado por
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
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
Material Type:
Artigo 		Adicionar ao Meu Espaço

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

Texto completo disponível

Citações Citado por
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
Material Type:
Artigo 		Adicionar ao Meu Espaço

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

Texto completo disponível

Citações Citado por

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Deste Autor:

  1. Kopp, P
  2. Medeiros-Neto, G
  3. Arseven, O
  4. Santos, C
  5. Jameson, J

Neste Assunto:

  1. Life Sciences & Biomedicine
  2. Endocrinologia
  3. Science & Technology
  4. Endocrinology & Metabolism
  5. Humans

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

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