446 related articles for article (PubMed ID: 9506756)
21. Pituitary macroadenoma in a 5-year-old: an early expression of multiple endocrine neoplasia type 1.
Stratakis CA; Schussheim DH; Freedman SM; Keil MF; Pack SD; Agarwal SK; Skarulis MC; Weil RJ; Lubensky IA; Zhuang Z; Oldfield EH; Marx SJ
J Clin Endocrinol Metab; 2000 Dec; 85(12):4776-80. PubMed ID: 11134142
[TBL] [Abstract][Full Text] [Related]
22. A novel mutation of the MEN1 gene in a Japanese kindred with familial isolated primary hyperparathyroidism.
Honda M; Tsukada T; Tanaka H; Maruyama K; Yamaguchi K; Obara T; Yamaji T; Ishibashi M
Eur J Endocrinol; 2000 Feb; 142(2):138-43. PubMed ID: 10664521
[TBL] [Abstract][Full Text] [Related]
23. The parathyroid/pituitary variant of multiple endocrine neoplasia type 1 usually has causes other than p27Kip1 mutations.
Ozawa A; Agarwal SK; Mateo CM; Burns AL; Rice TS; Kennedy PA; Quigley CM; Simonds WF; Weinstein LS; Chandrasekharappa SC; Collins FS; Spiegel AM; Marx SJ
J Clin Endocrinol Metab; 2007 May; 92(5):1948-51. PubMed ID: 17299066
[TBL] [Abstract][Full Text] [Related]
24. Alterations of the MEN1 gene in sporadic parathyroid tumors.
Farnebo F; Teh BT; Kytölä S; Svensson A; Phelan C; Sandelin K; Thompson NW; Höög A; Weber G; Farnebo LO; Larsson C
J Clin Endocrinol Metab; 1998 Aug; 83(8):2627-30. PubMed ID: 9709922
[TBL] [Abstract][Full Text] [Related]
25. Loss of heterozygosity of the MEN1 gene in a large series of TSH-secreting pituitary adenomas.
Asteria C; Anagni M; Persani L; Beck-Peccoz P
J Endocrinol Invest; 2001 Nov; 24(10):796-801. PubMed ID: 11765049
[TBL] [Abstract][Full Text] [Related]
26. The MEN-1 gene is rarely down-regulated in pituitary adenomas.
Asa SL; Somers K; Ezzat S
J Clin Endocrinol Metab; 1998 Sep; 83(9):3210-2. PubMed ID: 9745428
[TBL] [Abstract][Full Text] [Related]
27. MEN1 gene mutations in Hungarian patients with multiple endocrine neoplasia type 1.
Balogh K; Hunyady L; Patocs A; Gergics P; Valkusz Z; Toth M; Racz K
Clin Endocrinol (Oxf); 2007 Nov; 67(5):727-34. PubMed ID: 17953629
[TBL] [Abstract][Full Text] [Related]
28. Familial isolated hyperparathyroidism caused by single adenoma: a distinct entity different from multiple endocrine neoplasia.
Watanabe T; Tsukamoto F; Shimizu T; Sugimoto T; Taguchi T; Nishisho I; Nakazawa H; Shiba E; Shishiba Y; Takai S
Endocr J; 1998 Oct; 45(5):637-46. PubMed ID: 10395244
[TBL] [Abstract][Full Text] [Related]
29. Involvement of the MEN1 gene locus in familial isolated hyperparathyroidism.
Villablanca A; Wassif WS; Smith T; Höög A; Vierimaa O; Kassem M; Dwight T; Forsberg L; Du Q; Learoyd D; Jones K; Stranks S; Juhlin C; Teh BT; Carling T; Robinson B; Larsson C
Eur J Endocrinol; 2002 Sep; 147(3):313-22. PubMed ID: 12213668
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. Germline mutations of the MEN1 gene in familial multiple endocrine neoplasia type 1 and related states.
Agarwal SK; Kester MB; Debelenko LV; Heppner C; Emmert-Buck MR; Skarulis MC; Doppman JL; Kim YS; Lubensky IA; Zhuang Z; Green JS; Guru SC; Manickam P; Olufemi SE; Liotta LA; Chandrasekharappa SC; Collins FS; Spiegel AM; Burns AL; Marx SJ
Hum Mol Genet; 1997 Jul; 6(7):1169-75. PubMed ID: 9215689
[TBL] [Abstract][Full Text] [Related]
32. Clinical features of multiple endocrine neoplasia type 1 (MEN1) phenocopy without germline MEN1 gene mutations: analysis of 20 Japanese sporadic cases with MEN1.
Hai N; Aoki N; Shimatsu A; Mori T; Kosugi S
Clin Endocrinol (Oxf); 2000 Apr; 52(4):509-18. PubMed ID: 10762295
[TBL] [Abstract][Full Text] [Related]
33. Germline mutations of the MEN1 gene in Korean families with multiple endocrine neoplasia type 1 (MEN1) or MEN1-related disorders.
Park JH; Kim IJ; Kang HC; Lee SH; Shin Y; Kim KH; Lim SB; Kang SB; Lee K; Kim SY; Lee MS; Lee MK; Park JH; Moon SD; Park JG
Clin Genet; 2003 Jul; 64(1):48-53. PubMed ID: 12791038
[TBL] [Abstract][Full Text] [Related]
34. Prevalence of multiple endocrine neoplasia type 1 in young patients with apparently sporadic primary hyperparathyroidism or pancreaticoduodenal endocrine tumours.
Langer P; Wild A; Hall A; Celik I; Rothmund M; Bartsch DK
Br J Surg; 2003 Dec; 90(12):1599-603. PubMed ID: 14648742
[TBL] [Abstract][Full Text] [Related]
35. An unusual kindred of the multiple endocrine neoplasia type 1 (MEN1) in Japanese.
Abe T; Yoshimoto K; Taniyama M; Hanakawa K; Izumiyama H; Itakura M; Matsumoto K
J Clin Endocrinol Metab; 2000 Mar; 85(3):1327-30. PubMed ID: 10720085
[No Abstract] [Full Text] [Related]
36. Germ-line mutation analysis in patients with multiple endocrine neoplasia type 1 and related disorders.
Giraud S; Zhang CX; Serova-Sinilnikova O; Wautot V; Salandre J; Buisson N; Waterlot C; Bauters C; Porchet N; Aubert JP; Emy P; Cadiot G; Delemer B; Chabre O; Niccoli P; Leprat F; Duron F; Emperauger B; Cougard P; Goudet P; Sarfati E; Riou JP; Guichard S; Rodier M; Meyrier A; Caron P; Vantyghem MC; Assayag M; Peix JL; Pugeat M; Rohmer V; Vallotton M; Lenoir G; Gaudray P; Proye C; Conte-Devolx B; Chanson P; Shugart YY; Goldgar D; Murat A; Calender A
Am J Hum Genet; 1998 Aug; 63(2):455-67. PubMed ID: 9683585
[TBL] [Abstract][Full Text] [Related]
37. Somatic mutations in MEN type 1 tumors, consistent with the Knudson "two-hit" hypothesis.
Pannett AA; Thakker RV
J Clin Endocrinol Metab; 2001 Sep; 86(9):4371-4. PubMed ID: 11549677
[TBL] [Abstract][Full Text] [Related]
38. Molecular characterization of the men1 tumor suppressor gene in sporadic pituitary tumors.
Prezant TR; Levine J; Melmed S
J Clin Endocrinol Metab; 1998 Apr; 83(4):1388-91. PubMed ID: 9543172
[TBL] [Abstract][Full Text] [Related]
39. Loss of heterozygosity in 11q13-14 regions in gastric neuroendocrine tumors not associated with multiple endocrine neoplasia type 1 syndrome.
D'Adda T; Keller G; Bordi C; Höfler H
Lab Invest; 1999 Jun; 79(6):671-7. PubMed ID: 10378509
[TBL] [Abstract][Full Text] [Related]
40. Genotyping of adrenocortical tumors: very frequent deletions of the MEN1 locus in 11q13 and of a 1-centimorgan region in 2p16.
Kjellman M; Roshani L; Teh BT; Kallioniemi OP; Höög A; Gray S; Farnebo LO; Holst M; Bäckdahl M; Larsson C
J Clin Endocrinol Metab; 1999 Feb; 84(2):730-5. PubMed ID: 10022445
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
