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Pamela Correa

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Articles 7
Citations 111
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Recent Articles
1.
Carling T, Du Y, Fang W, Correa P, Huang S
Surgery . 2003 Dec; 134(6):932-9. PMID: 14668725
Background: Loss of heterozygosity (LOH) at chromosome 1p is a common abnormality in both parathyroid tumors and pheochromocytomas. The recently characterized tumor suppressor gene RIZ1, located at 1p36, has emerged...
2.
Correa P, Segersten U, Hellman P, Akerstrom G, Westin G
J Clin Endocrinol Metab . 2002 Dec; 87(12):5826-9. PMID: 12466393
Vitamin D analogues are in clinical use for prevention and treatment of secondary hyperparathyroidism (HPT) in chronic renal failure. Despite recent advances there is a need for vitamin D derivatives...
3.
Correa P, Akerstrom G, Westin G
Eur J Endocrinol . 2002 Nov; 147(5):671-5. PMID: 12444900
Objective: Primary hyperparathyroidism (pHPT) is characterized by excessive production of parathyroid hormone (PTH) due to parathyroid adenomas while uremic secondary HPT (sHPT) is caused by parathyroid hyperplasia in response to...
4.
Correa P, Akerstrom G, Westin G
Clin Endocrinol (Oxf) . 2002 Oct; 57(4):501-5. PMID: 12354132
Objective: Glial cells missing (Gcm) was first identified as a binary switch between neuronal and glial determination in Drosophila. Two homologues of Drosophila Gcm have been identified in mice and...
5.
Correa P, Lundgren E, Rastad J, Akerstrom G, Westin G, Carling T
Surgery . 2002 Sep; 132(3):450-5. PMID: 12324758
Background: Sporadic primary hyperparathyroidism (pHPT) occurs separately and in several hereditary disorders including multiple endocrine neoplasia type 1. Irradiation to the neck, female gender, and age are well-identified risk factors...
6.
Segersten U, Correa P, Hewison M, Hellman P, Dralle H, Carling T, et al.
J Clin Endocrinol Metab . 2002 Jun; 87(6):2967-72. PMID: 12050281
Active vitamin D, 1,25-dihydroxyvitamin D(3) [1,25(OH)(2)D(3)], plays a pivotal role in calcium homeostasis and bone metabolism. Circulating levels of 1,25(OH)(2)D(3) are thought to be dependent mainly on the activity of...
7.
Correa P, Juhlin C, Rastad J, Akerstrom G, Westin G, Carling T
Clin Endocrinol (Oxf) . 2002 Feb; 56(1):113-7. PMID: 11849254
Objective: Parathyroid adenomas frequently harbour deletions of genomic DNA at chromosome regions 1p, 6q and 11q. In this study we related clinical characteristics in 56 patients with primary hyperparathyroidism (pHPT)...