Search Results - "Ebeling, T. M. L."

Multiple endocrine neoplasia type 1 in Northern Finland; clinical features and genotype–phenotype correlation by Vierimaa, O, Ebeling, T M L, Kytölä, S, Bloigu, R, Eloranta, E, Salmi, J, Korpi-Hyövälti, E, Niskanen, L, Orvola, A, Elovaara, E, Gynther, A, Sane, T, Välimäki, M, Ignatius, J, Leisti, J, Salmela, P I

“…Objective: The existence of genotype–phenotype correlation in multiple endocrine neoplasia type 1 (MEN1) is controversial. Two founder mutations of the MEN1…”
Get full text

Mutation analysis of MEN1, HRPT2, CASR, CDKN1B, and AIP genes in primary hyperparathyroidism patients with features of genetic predisposition by Vierimaa, O., Villablanca, A., Alimov, A., Georgitsi, M., Raitila, A., Vahteristo, P., Larsson, C., Ruokonen, A., Eloranta, E., Ebeling, T. M. L., Ignatius, J., Aaltonen, L. A., Leisti, J., Salmela, P. I.

“…Objective : Primary hyperparathyroidism (PHPT), a common endocrine condition, is usually caused by sporadically occurring parathyroid adenoma. A subset of…”
Get full text

Mutation analysis of MEN1, HRPT2, CASR, CDKN1B, and AIP genes in primary hyperparathyroidism patients with features of genetic predisposition by Vierimaa, O, Villablanca, A, Alimov, A, Georgitsi, M, Raitila, A, Vahteristo, P, Larsson, C, Ruokonen, A, Eloranta, E, Ebeling, T M L, Ignatius, J, Aaltonen, L A, Leisti, J, Salmela, P I

“…OBJECTIVEPrimary hyperparathyroidism (PHPT), a common endocrine condition, is usually caused by sporadically occurring parathyroid adenoma. A subset of…”
Get full text