Kopp PA - Search Results

1

Denosumab for management of parathyroid carcinoma-mediated hypercalcemia.

Vellanki P, Lange K, Elaraj D, Kopp PA, El Muayed M. Vellanki P, et al. Among authors: kopp pa. J Clin Endocrinol Metab. 2014 Feb;99(2):387-90. doi: 10.1210/jc.2013-3031. Epub 2013 Oct 31. J Clin Endocrinol Metab. 2014. PMID: 24178790 Free PMC article.

2

Acute diabetes insipidus mediated by vasopressinase after placental abruption.

Wallia A, Bizhanova A, Huang W, Goldsmith SL, Gossett DR, Kopp P. Wallia A, et al. J Clin Endocrinol Metab. 2013 Mar;98(3):881-6. doi: 10.1210/jc.2012-3548. Epub 2013 Feb 7. J Clin Endocrinol Metab. 2013. PMID: 23393172

3

Mutations in the Pendred Syndrome (PDS/SLC26A) gene: an increasingly complex phenotypic spectrum from goiter to thyroid hypoplasia.

Kopp P. Kopp P. J Clin Endocrinol Metab. 2014 Jan;99(1):67-9. doi: 10.1210/jc.2013-4319. J Clin Endocrinol Metab. 2014. PMID: 24384016 No abstract available.

4

Release and Decay Kinetics of Copeptin vs AVP in Response to Osmotic Alterations in Healthy Volunteers.

Fenske WK, Schnyder I, Koch G, Walti C, Pfister M, Kopp P, Fassnacht M, Strauss K, Christ-Crain M. Fenske WK, et al. J Clin Endocrinol Metab. 2018 Feb 1;103(2):505-513. doi: 10.1210/jc.2017-01891. J Clin Endocrinol Metab. 2018. PMID: 29267966 Clinical Trial.

5

Denosumab for the Treatment of Hypercalcemia in a Patient With Parathyroid Carcinoma: A Case Report.

Roukain A, Alwan H, Bongiovanni M, Sykiotis GP, Kopp PA. Roukain A, et al. Among authors: kopp pa. Front Endocrinol (Lausanne). 2022 Jan 31;12:794988. doi: 10.3389/fendo.2021.794988. eCollection 2021. Front Endocrinol (Lausanne). 2022. PMID: 35173680 Free PMC article. Review.

6

The thyrotropin (TSH) receptor transmembrane domain mutation (Pro556-Leu) in the hypothyroid hyt/hyt mouse results in plasma membrane targeting but defective TSH binding.

Gu WX, Du GG, Kopp P, Rentoumis A, Albanese C, Kohn LD, Madison LD, Jameson JL. Gu WX, et al. Endocrinology. 1995 Jul;136(7):3146-53. doi: 10.1210/endo.136.7.7789342. Endocrinology. 1995. PMID: 7789342

7

Sexually dimorphic transcriptional responses to gonadotropin-releasing hormone require chronic in vivo exposure to estradiol.

Colin IM, Bauer-Dantoin AC, Sundaresan S, Kopp P, Jameson JL. Colin IM, et al. Endocrinology. 1996 Jun;137(6):2300-7. doi: 10.1210/endo.137.6.8641179. Endocrinology. 1996. PMID: 8641179

8

The thyroid hormone receptor variant alpha2 is a weak antagonist because it is deficient in interactions with nuclear receptor corepressors.

Tagami T, Kopp P, Johnson W, Arseven OK, Jameson JL. Tagami T, et al. Endocrinology. 1998 May;139(5):2535-44. doi: 10.1210/endo.139.5.6011. Endocrinology. 1998. PMID: 9564869

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.

Kopp P, Arseven OK, Sabacan L, Kotlar T, Dupuis J, Cavaliere H, Santos CL, Jameson JL, Medeiros-Neto G. Kopp P, et al. J Clin Endocrinol Metab. 1999 Jan;84(1):336-41. doi: 10.1210/jcem.84.1.5398. J Clin Endocrinol Metab. 1999. PMID: 9920104

10

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. J Clin Endocrinol Metab. 2001 Aug;86(8):3962-7. doi: 10.1210/jcem.86.8.7765. J Clin Endocrinol Metab. 2001. PMID: 11502839

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