BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

227 related articles for article (PubMed ID: 35370956)

  • 21. Bone and Mineral Metabolism Phenotypes in MEN1-Related and Sporadic Primary Hyperparathyroidism, before and after Parathyroidectomy.
    Marini F; Giusti F; Cioppi F; Maraghelli D; Cavalli T; Tonelli F; Brandi ML
    Cells; 2021 Jul; 10(8):. PubMed ID: 34440663
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Coincidence of multiple endocrine neoplasia types 1 and 2: mutations in the RET protooncogene and MEN1 tumor suppressor gene in a family presenting with recurrent primary hyperparathyroidism.
    Frank-Raue K; Rondot S; Hoeppner W; Goretzki P; Raue F; Meng W
    J Clin Endocrinol Metab; 2005 Jul; 90(7):4063-7. PubMed ID: 15870131
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Genetics of parathyroid tumours.
    Thakker RV
    J Intern Med; 2016 Dec; 280(6):574-583. PubMed ID: 27306766
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Parathyroid carcinoma in multiple endocrine neoplasia type 1 (MEN1) syndrome: two case reports of an unrecognised entity.
    Agha A; Carpenter R; Bhattacharya S; Edmonson SJ; Carlsen E; Monson JP
    J Endocrinol Invest; 2007 Feb; 30(2):145-9. PubMed ID: 17392605
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Parathyroid carcinoma in multiple endocrine neoplasm type 1 syndrome: case report and systematic literature review.
    Di Meo G; Sgaramella LI; Ferraro V; Prete FP; Gurrado A; Testini M
    Clin Exp Med; 2018 Nov; 18(4):585-593. PubMed ID: 29922966
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Multiple endocrine neoplasia type 1 (MEN1) gene mutations in a subset of patients with sporadic and familial primary hyperparathyroidism target the coding sequence but spare the promoter region.
    Karges W; Jostarndt K; Maier S; Flemming A; Weitz M; Wissmann A; Feldmann B; Dralle H; Wagner P; Boehm BO
    J Endocrinol; 2000 Jul; 166(1):1-9. PubMed ID: 10856877
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Concurrent primary hyperparathyroidism and humoral hypercalcemia of malignancy in a patient with multiple endocrine neoplasia type 1.
    Milanesi A; Yu R; Geller SA; Burton D; Deftos LJ; Wolin EM
    Pancreas; 2011 May; 40(4):634-7. PubMed ID: 21483254
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Multiple Endocrine Neoplasia Type 1 with Functional Parathyroid Cysts.
    Koyama N; Nagase T; Kure M; Odaka T; Kogure K; Takeda Y; Ishii T; Narisawa K; Fujita T; Fujimori M; Katsura Y
    Intern Med; 2022 Apr; 61(8):1183-1188. PubMed ID: 34645755
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A patient with MEN1-associated hyperparathyroidism, responsive to cinacalcet.
    Falchetti A; Cilotti A; Vaggelli L; Masi L; Amedei A; Cioppi F; Tonelli F; Brandi ML
    Nat Clin Pract Endocrinol Metab; 2008 Jun; 4(6):351-7. PubMed ID: 18414463
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Parathyroid gland-specific deletion of the mouse Men1 gene results in parathyroid neoplasia and hypercalcemic hyperparathyroidism.
    Libutti SK; Crabtree JS; Lorang D; Burns AL; Mazzanti C; Hewitt SM; O'Connor S; Ward JM; Emmert-Buck MR; Remaley A; Miller M; Turner E; Alexander HR; Arnold A; Marx SJ; Collins FS; Spiegel AM
    Cancer Res; 2003 Nov; 63(22):8022-8. PubMed ID: 14633735
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Parathyroid carcinoma in multiple endocrine neoplasia type 1 with a classic germline mutation.
    Shih RY; Fackler S; Maturo S; True MW; Brennan J; Wells D
    Endocr Pract; 2009; 15(6):567-72. PubMed ID: 19491073
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Should routine analysis of the MEN1 gene be performed in all patients with primary hyperparathyroidism under 40 years of age?
    Skandarajah A; Barlier A; Morlet-Barlat N; Sebag F; Enjalbert A; Conte-Devolx B; Henry JF
    World J Surg; 2010 Jun; 34(6):1294-8. PubMed ID: 20058152
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Molecular pathogenesis of primary hyperparathyroidism.
    Cetani F; Pardi E; Borsari S; Marcocci C
    J Endocrinol Invest; 2011 Jul; 34(7 Suppl):35-9. PubMed ID: 21985978
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Multiple Endocrine Neoplasia I (Wermers Syndrome), Forms of Clinical Manifestation, 5 Case Studies].
    Drbalová K; Herdová K; Krejčí P; Nývltová M; Solař S; Vedralová L; Záruba P; Netuka D; Bavor P
    Vnitr Lek; 2016; 62(9 Suppl 3):140-149. PubMed ID: 27734708
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A large functioning parathyroid cyst in a patient with multiple endocrine neoplasia type 1.
    Tamiya H; Miyakawa M; Suzuki H; Takeshita A; Ohashi K; Usui T; Miura D; Takeuchi Y
    Endocr J; 2013; 60(6):709-14. PubMed ID: 23386389
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Prospective study of surgery for primary hyperparathyroidism (HPT) in multiple endocrine neoplasia-type 1 and Zollinger-Ellison syndrome: long-term outcome of a more virulent form of HPT.
    Norton JA; Venzon DJ; Berna MJ; Alexander HR; Fraker DL; Libutti SK; Marx SJ; Gibril F; Jensen RT
    Ann Surg; 2008 Mar; 247(3):501-10. PubMed ID: 18376196
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Frequency of somatic MEN1 gene mutations in monoclonal parathyroid tumours of patients with primary hyperparathyroidism.
    Miedlich S; Krohn K; Lamesch P; Müller A; Paschke R
    Eur J Endocrinol; 2000 Jul; 143(1):47-54. PubMed ID: 10870030
    [TBL] [Abstract][Full Text] [Related]  

  • 38. A newly recognized germline mutation of MEN1 gene identified in a patient with parathyroid adenoma and carcinoma.
    Sato M; Miyauchi A; Namihira H; Bhuiyan MM; Imachi H; Murao K; Takahara J
    Endocrine; 2000 Jun; 12(3):223-6. PubMed ID: 10963041
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Diagnosis by serendipity: Cushing syndrome attributable to cortisol-producing adrenal adenoma as the initial manifestation of multiple endocrine neoplasia type 1 due to a rare splicing site MEN1 gene mutation.
    Alzahrani AS; Al-Khaldi N; Shi Y; Al-Rijjal RA; Zou M; Baitei EY; Amin T
    Endocr Pract; 2008; 14(5):595-602. PubMed ID: 18753104
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Multiple endocrine neoplasia type 1 (MEN1) germline mutations in familial isolated primary hyperparathyroidism.
    Pannett AA; Kennedy AM; Turner JJ; Forbes SA; Cavaco BM; Bassett JH; Cianferotti L; Harding B; Shine B; Flinter F; Maidment CG; Trembath R; Thakker RV
    Clin Endocrinol (Oxf); 2003 May; 58(5):639-46. PubMed ID: 12699448
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.