BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

146 related articles for article (PubMed ID: 24882518)

  • 21. Contrast MRI in multiple endocrine neoplasia type 1 (MEN) associated with renal cell carcinoma.
    Mallek R; Mostbeck G; Walter RM; Herold CH; Imhof H; Tscholakoff D
    Eur J Radiol; 1990; 10(2):105-8. PubMed ID: 1970958
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Neuroendocrine Tumors in the Stomach, Duodenum, and Pancreas Accompanied by Novel MEN1 Gene Mutation.
    Yang MA; Lee WK; Shin HS; Park SH; Kim BS; Kim JW; Cho JW; Yun SH
    Korean J Gastroenterol; 2017 Mar; 69(3):181-186. PubMed ID: 28329921
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Loss of wild-type MEN1 gene expression in multiple endocrine neoplasia type 1-associated parathyroid adenoma.
    Ludwig L; Schleithoff L; Kessler H; Wagner PK; Boehm BO; Karges W
    Endocr J; 1999 Aug; 46(4):539-44. PubMed ID: 10580746
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A puzzling case of phospho-soda-induced hypocalcemia in a patient with multiple endocrine neoplasia type 1-associated primary hyperparathyroidism.
    Ozveren A; Akinci B; Makay O; Sarsik B; Simsir IY; Berdeli A; Akyildiz M
    Intern Med; 2012; 51(22):3145-9. PubMed ID: 23154721
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Clinical and genetic features of patients with multiple endocrine tumors who have neither family history nor MEN1 germline mutations.
    Sakurai A; Katai M; Yumita W; Minemura K; Hashizume K
    Endocrine; 2004 Feb; 23(1):45-9. PubMed ID: 15034196
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Adrenal tumors in MEN1 syndrome and the role of menin in adrenal tumorigenesis.
    Patocs A; Balogh K; Racz K
    Adv Exp Med Biol; 2009; 668():97-103. PubMed ID: 20175457
    [No Abstract]   [Full Text] [Related]  

  • 27. [Hereditary variants of primary hyperparathyroidism--MEN1, MEN2, HPT-JT, FHH, FIHPT].
    Frank-Raue K; Leidig-Bruckner G; Lorenz A; Rondot S; Haag C; Schulze E; Büchler M; Raue F
    Dtsch Med Wochenschr; 2011 Sep; 136(38):1889-94. PubMed ID: 21915802
    [TBL] [Abstract][Full Text] [Related]  

  • 28. MEN1 disease occurring before 21 years old: a 160-patient cohort study from the Groupe d'étude des Tumeurs Endocrines.
    Goudet P; Dalac A; Le Bras M; Cardot-Bauters C; Niccoli P; Lévy-Bohbot N; du Boullay H; Bertagna X; Ruszniewski P; Borson-Chazot F; Vergès B; Sadoul JL; Ménégaux F; Tabarin A; Kühn JM; d'Anella P; Chabre O; Christin-Maitre S; Cadiot G; Binquet C; Delemer B
    J Clin Endocrinol Metab; 2015 Apr; 100(4):1568-77. PubMed ID: 25594862
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Multiple endocrine neoplasia type 1 in Brazil: MEN1 founding mutation, clinical features, and bone mineral density profile.
    Lourenço DM; Toledo RA; Mackowiak II; Coutinho FL; Cavalcanti MG; Correia-Deur JE; Montenegro F; Siqueira SA; Margarido LC; Machado MC; Toledo SP
    Eur J Endocrinol; 2008 Sep; 159(3):259-74. PubMed ID: 18524795
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Clinical aspects of multiple endocrine neoplasia type 1.
    Al-Salameh A; Cadiot G; Calender A; Goudet P; Chanson P
    Nat Rev Endocrinol; 2021 Apr; 17(4):207-224. PubMed ID: 33564173
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. Multiple endocrine neoplasia type 1 gene expression is normal in sporadic adrenocortical tumors.
    Zwermann O; Beuschlein F; Mora P; Weber G; Allolio B; Reincke M
    Eur J Endocrinol; 2000 Jun; 142(6):689-95. PubMed ID: 10822234
    [TBL] [Abstract][Full Text] [Related]  

  • 33. MEN1 gene analysis in sporadic adrenocortical neoplasms.
    Heppner C; Reincke M; Agarwal SK; Mora P; Allolio B; Burns AL; Spiegel AM; Marx SJ
    J Clin Endocrinol Metab; 1999 Jan; 84(1):216-9. PubMed ID: 9920087
    [TBL] [Abstract][Full Text] [Related]  

  • 34. MEN1 gene alterations do not correlate with the phenotype of sporadic primary hyperparathyroidism.
    Cetani F; Pardi E; Vignali E; Borsari S; Picone A; Cianferotti L; Ambrogini E; Miccoli P; Pinchera A; Marcocci C
    J Endocrinol Invest; 2002 Jun; 25(6):508-12. PubMed ID: 12109621
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Combined characterization of a pituitary adenoma and a subcutaneous lipoma in a MEN1 patient with a whole gene deletion.
    Rusconi D; Valtorta E; Rodeschini O; Giardino D; Lorenzo I; Predieri B; Losa M; Larizza L; Finelli P
    Cancer Genet; 2011 Jun; 204(6):309-15. PubMed ID: 21763627
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Loss of heterozygosity in sporadic parathyroid tumours: involvement of chromosome 1 and the MEN1 gene locus in 11q13.
    Dwight T; Twigg S; Delbridge L; Wong FK; Farnebo F; Richardson AL; Nelson A; Zedenius J; Philips J; Larsson C; Teh BT; Robinson B
    Clin Endocrinol (Oxf); 2000 Jul; 53(1):85-92. PubMed ID: 10931084
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A case of multiple endocrine neoplasia type 1 combined with papillary thyroid carcinoma.
    Kim HJ; Park JS; Kim CS; Kang ES; Cha BS; Lim SK; Kim KR; Lee HC; Ahn CW
    Yonsei Med J; 2008 Jun; 49(3):503-6. PubMed ID: 18581603
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Incidental occurrence of metastatic medullary thyroid carcinoma in a patient with multiple endocrine neoplasia type 1 carrying germline MEN1 and somatic RET mutations.
    Cetani F; Pardi E; Berardi V; Romei C; Marcocci C; Elisei R
    J Surg Oncol; 2017 Dec; 116(8):1197-1199. PubMed ID: 28968916
    [No Abstract]   [Full Text] [Related]  

  • 39. Acromegaly in a multiple endocrine neoplasia type 1 (MEN1) family with low penetrance of the disease.
    Dreijerink KM; van Beek AP; Lentjes EG; Post JG; van der Luijt RB; Canninga-van Dijk MR; Lips CJ
    Eur J Endocrinol; 2005 Dec; 153(6):741-6. PubMed ID: 16322378
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Expression and functional analysis of menin in a multiple endocrine neoplasia type 1 (MEN1) patient with somatic loss of heterozygosity in chromosome 11q13 and unidentified germline mutation of the MEN1 gene.
    Naito J; Kaji H; Sowa H; Kitazawa R; Kitazawa S; Tsukada T; Hendy GN; Sugimoto T; Chihara K
    Endocrine; 2006 Jun; 29(3):485-90. PubMed ID: 16943588
    [TBL] [Abstract][Full Text] [Related]  

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