Nogueira CR - Search Results

1

Histopathological Characterization and Whole Exome Sequencing of Ectopic Thyroid: Fetal Architecture in a Functional Ectopic Gland from Adult Patient.

Camargo RY, Kanamura CT, Friguglietti CU, Nogueira CR, Iorcansky S, Tincani AJ, Bezerra AK, Brust E, Koyama FC, Camargo AA, Rego FOR, Galante PAF, Medeiros-Neto G, Rubio IGS. Camargo RY, et al. Among authors: nogueira cr. Int J Endocrinol. 2018 Feb 8;2018:4682876. doi: 10.1155/2018/4682876. eCollection 2018. Int J Endocrinol. 2018. PMID: 29593791 Free PMC article.

2

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

Nogueira CR, Leite CC, Chedid EP, Liberman B, Pimentel-Filho FR, Kopp P, Medeiros-Neto GA. Nogueira CR, et al. J Endocrinol Invest. 1997 Nov;20(10):629-33. doi: 10.1007/BF03346922. J Endocrinol Invest. 1997. PMID: 9438923

3

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

Nogueira CR, Leite CC, Chedid EP, Liberman B, Pimentel-Filho FR, Kopp P, Medeiros-Neto GA. Nogueira CR, et al. J Endocrinol Invest. 1998 Jun;21(6):386-91. doi: 10.1007/BF03350775. J Endocrinol Invest. 1998. PMID: 9699131

4

Combined pituitary hormone deficiency in an inbred Brazilian kindred associated with a mutation in the PROP-1 gene.

Nogueira CR, Sabacan L, Jameson JL, Medeiros-Neto G, Kopp P. Nogueira CR, et al. Mol Genet Metab. 1999 May;67(1):58-61. doi: 10.1006/mgme.1999.2841. Mol Genet Metab. 1999. PMID: 10329025

5

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

Nogueira CR, Nguyen LQ, Coelho-Neto JR, Arseven OK, Jameson JL, Kopp P, Medeiros-Neto GA. Nogueira CR, et al. Thyroid. 1999 Jun;9(6):523-9. doi: 10.1089/thy.1999.9.523. Thyroid. 1999. PMID: 10411113 Clinical Trial.

6

Thyrotropin receptor mutations in hyperfunctioning thyroid adenomas from Brazil.

Nogueira CR, Kopp P, Arseven OK, Santos CL, Jameson JL, Medeiros-Neto G. Nogueira CR, et al. Thyroid. 1999 Nov;9(11):1063-8. doi: 10.1089/thy.1999.9.1063. Thyroid. 1999. PMID: 10595453

7

A novel mutation (Q40P) in PAX8 associated with congenital hypothyroidism and thyroid hypoplasia: evidence for phenotypic variability in mother and child.

Congdon T, Nguyen LQ, Nogueira CR, Habiby RL, Medeiros-Neto G, Kopp P. Congdon T, et al. Among authors: nogueira cr. J Clin Endocrinol Metab. 2001 Aug;86(8):3962-7. doi: 10.1210/jcem.86.8.7765. J Clin Endocrinol Metab. 2001. PMID: 11502839

8

Analysis of the PAX8 gene in 32 children with thyroid dysgenesis and functional characterization of a promoter variant.

Perone D, Medeiros-Neto G, Nogueira CR, Chagas AJ, Alves Dias VM, Viana MF, Kopp P. Perone D, et al. Among authors: nogueira cr. J Pediatr Endocrinol Metab. 2016 Feb;29(2):193-201. doi: 10.1515/jpem-2015-0199. J Pediatr Endocrinol Metab. 2016. PMID: 26495924

9

Editorial: New insights in thyroid and Covid-19.

Sgarbi JA, Nogueira CR, Brenta G, Campinho MA. Sgarbi JA, et al. Among authors: nogueira cr. Front Endocrinol (Lausanne). 2022 Dec 23;13:1112695. doi: 10.3389/fendo.2022.1112695. eCollection 2022. Front Endocrinol (Lausanne). 2022. PMID: 36619533 Free PMC article. No abstract available.

10

Editorial: The thyroid and Covid-19, volume II.

Brenta G, Campinho MA, Nogueira CR, Sgarbi J. Brenta G, et al. Among authors: nogueira cr. Front Endocrinol (Lausanne). 2023 Nov 27;14:1331452. doi: 10.3389/fendo.2023.1331452. eCollection 2023. Front Endocrinol (Lausanne). 2023. PMID: 38089608 Free PMC article. No abstract available.

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