BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

151 related articles for article (PubMed ID: 2123361)

  • 21. A case of hyperparathyroidism-jaw tumour syndrome found in the treatment of an ossifying fibroma in the maxillary bone.
    Yamashita Y; Akiyama T; Mizusawa N; Yoshimoto K; Goto M
    Int J Oral Maxillofac Surg; 2007 Apr; 36(4):365-9. PubMed ID: 17052894
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Loss of nuclear expression of parafibromin distinguishes parathyroid carcinomas and hyperparathyroidism-jaw tumor (HPT-JT) syndrome-related adenomas from sporadic parathyroid adenomas and hyperplasias.
    Gill AJ; Clarkson A; Gimm O; Keil J; Dralle H; Howell VM; Marsh DJ
    Am J Surg Pathol; 2006 Sep; 30(9):1140-9. PubMed ID: 16931959
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Multiple endocrine neoplasia (MEN)--an overview and case report--patient with sporadic bilateral pheochromocytoma, hyperparathyroidism and marfanoid habitus.
    Fassbender WJ; Krohn-Grimberghe B; Görtz B; Litzlbauer D; Stracke H; Raue F; Kaiser HE
    Anticancer Res; 2000; 20(6C):4877-87. PubMed ID: 11205236
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Large intragenic deletion of CDC73 (exons 4-10) in a three-generation hyperparathyroidism-jaw tumor (HPT-JT) syndrome family.
    Guarnieri V; Seaberg RM; Kelly C; Jean Davidson M; Raphael S; Shuen AY; Baorda F; Palumbo O; Scillitani A; Hendy GN; Cole DEC
    BMC Med Genet; 2017 Aug; 18(1):83. PubMed ID: 28774260
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Molecular diagnosis in an Argentinian family with multiple endocrine neoplasia type-1 (MEN-1)].
    Guadagna M; Migliano M; Herrera J; Rodríguez P; Sciorra J; Alfieri A; Corino M; Costa L; Karothy B; Ortiz J; Tarruella M
    Medicina (B Aires); 1998; 58(5 Pt 1):441-5. PubMed ID: 9922473
    [TBL] [Abstract][Full Text] [Related]  

  • 26. HRPT2 gene alterations in ossifying fibroma of the jaws.
    Pimenta FJ; Gontijo Silveira LF; Tavares GC; Silva AC; Perdigão PF; Castro WH; Gomez MV; Teh BT; De Marco L; Gomez RS
    Oral Oncol; 2006 Aug; 42(7):735-9. PubMed ID: 16458039
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Clinical, genetic, and histopathologic investigation of CDC73-related familial hyperparathyroidism.
    Masi G; Barzon L; Iacobone M; Viel G; Porzionato A; Macchi V; De Caro R; Favia G; Palù G
    Endocr Relat Cancer; 2008 Dec; 15(4):1115-26. PubMed ID: 18755853
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Familial cystic parathyroid adenomatosis.
    Mallette LE; Malini S; Rappaport MP; Kirkland JL
    Ann Intern Med; 1987 Jul; 107(1):54-60. PubMed ID: 3592449
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Familial isolated hyperparathyroidism: a distinct genetic entity with an increased risk of parathyroid cancer.
    Wassif WS; Moniz CF; Friedman E; Wong S; Weber G; Nordenskjöld M; Peters TJ; Larsson C
    J Clin Endocrinol Metab; 1993 Dec; 77(6):1485-9. PubMed ID: 7903311
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome.
    Teh BT; Howell VM; Haven CJ; Kahnoski K; Khoo SK; Petillo D; Chen J; Fleuren GJ; Robinson BG; Delbridge LW; Philips J; Nelson AE; Krause U; Hammje K; Dralle H; Hoang-Vu C; Gimm O; Marsh DJ; Morreau H
    Hum Genet; 2004 Jan; 114(2):224. PubMed ID: 15046109
    [No Abstract]   [Full Text] [Related]  

  • 31. Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome.
    Teh BT; Howell VM; Haven CJ; Kahnoski K; Khoo SK; Petillo D; Chen J; Fleuren GJ; Robinson BG; Delbridge LW; Philips J; Nelson AE; Krause U; Hammje K; Dralle H; Hoang-Vu C; Gimm O; Marsh DJ; Morreau H
    Hum Genet; 2004 Jan; 114(2):223. PubMed ID: 15046107
    [No Abstract]   [Full Text] [Related]  

  • 32. Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome.
    Teh BT; Howell VM; Haven CJ; Kahnoski K; Khoo SK; Petillo D; Chen J; Fleuren GJ; Robinson BG; Delbridge LW; Philips J; Nelson AE; Krause U; Hammje K; Dralle H; Hoang-Vu C; Gimm O; Marsh DJ; Morreau H
    Hum Genet; 2004 Jan; 114(2):223. PubMed ID: 15046105
    [No Abstract]   [Full Text] [Related]  

  • 33. Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome.
    Teh BT; Howell VM; Haven CJ; Kahnoski K; Khoo SK; Petillo D; Chen J; Fleuren GJ; Robinson BG; Delbridge LW; Philips J; Nelson AE; Krause U; Hammje K; Dralle H; Hoang-Vu C; Gimm O; Marsh DJ; Morreau H
    Hum Genet; 2004 Jan; 114(2):223. PubMed ID: 15046102
    [No Abstract]   [Full Text] [Related]  

  • 34. Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome.
    Teh BT; Howell VM; Haven CJ; Kahnoski K; Khoo SK; Petillo D; Chen J; Fleuren GJ; Robinson BG; Delbridge LW; Philips J; Nelson AE; Krause U; Hammje K; Dralle H; Hoang-Vu C; Gimm O; Marsh DJ; Morreau H
    Hum Genet; 2004 Jan; 114(2):222. PubMed ID: 15046098
    [No Abstract]   [Full Text] [Related]  

  • 35. Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome.
    Teh BT; Howell VM; Haven CJ; Kahnoski K; Khoo SK; Petillo D; Chen J; Fleuren GJ; Robinson BG; Delbridge LW; Philips J; Nelson AE; Krause U; Hammje K; Dralle H; Hoang-Vu C; Gimm O; Marsh DJ; Morreau H
    Hum Genet; 2004 Jan; 114(2):222. PubMed ID: 15046094
    [No Abstract]   [Full Text] [Related]  

  • 36. Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome.
    Teh BT; Howell VM; Haven CJ; Kahnoski K; Khoo SK; Petillo D; Chen J; Fleuren GJ; Robinson BG; Delbridge LW; Philips J; Nelson AE; Krause U; Hammje K; Dralle H; Hoang-Vu C; Gimm O; Marsh DJ; Morreau H
    Hum Genet; 2004 Jan; 114(2):221. PubMed ID: 15046050
    [No Abstract]   [Full Text] [Related]  

  • 37. CDC73 intragenic deletion in familial primary hyperparathyroidism associated with parathyroid carcinoma.
    Korpi-Hyövälti E; Cranston T; Ryhänen E; Arola J; Aittomäki K; Sane T; Thakker RV; Schalin-Jäntti C
    J Clin Endocrinol Metab; 2014 Sep; 99(9):3044-8. PubMed ID: 24823466
    [TBL] [Abstract][Full Text] [Related]  

  • 38. HRPT2, a tumor suppressor gene for hyperparathyroidism-jaw tumor syndrome.
    Wang PF; Tan MH; Zhang C; Morreau H; Teh BT
    Horm Metab Res; 2005 Jun; 37(6):380-3. PubMed ID: 16001331
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Somatic mutations of the multiple endocrine neoplasia type 1 (MEN1) gene in patients with sporadic, nonfamilial primary hyperparathyroidism.
    Sato K; Yamazaki K; Zhu H; Kanbe M; Iihara M; Wada Y; Tanaka R; Okamoto T; Ito Y; Obara T
    Surgery; 2000 Mar; 127(3):337-41. PubMed ID: 10715991
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Hyperparathyroidism-jaw tumour syndrome.
    Chen JD; Morrison C; Zhang C; Kahnoski K; Carpten JD; Teh BT
    J Intern Med; 2003 Jun; 253(6):634-42. PubMed ID: 12755959
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.