135 related articles for article (PubMed ID: 7955451)
1. Familial isolated primary hyperparathyroidism.
Kassem M; Zhang X; Brask S; Eriksen EF; Mosekilde L; Kruse TA
Clin Endocrinol (Oxf); 1994 Oct; 41(4):415-20. PubMed ID: 7955451
[TBL] [Abstract][Full Text] [Related]
2. Genetic studies of a family with hereditary hyperparathyroidism-jaw tumour syndrome.
Wassif WS; Farnebo F; Teh BT; Moniz CF; Li FY; Harrison JD; Peters TJ; Larsson C; Harris P
Clin Endocrinol (Oxf); 1999 Feb; 50(2):191-6. PubMed ID: 10396361
[TBL] [Abstract][Full Text] [Related]
3. Genetic analysis of the MEN1 gene and HPRT2 locus in two Italian kindreds with familial isolated hyperparathyroidism.
Cetani F; Pardi E; Giovannetti A; Vignali E; Borsari S; Golia F; Cianferotti L; Viacava P; Miccoli P; Gasperi M; Pinchera A; Marcocci C
Clin Endocrinol (Oxf); 2002 Apr; 56(4):457-64. PubMed ID: 11966738
[TBL] [Abstract][Full Text] [Related]
4. Familial isolated primary hyperparathyroidism--a multiple endocrine neoplasia type 1 variant?
Miedlich S; Lohmann T; Schneyer U; Lamesch P; Paschke R
Eur J Endocrinol; 2001 Aug; 145(2):155-60. PubMed ID: 11454510
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Mutation analysis of the MEN1 gene in multiple endocrine neoplasia type 1, familial acromegaly and familial isolated hyperparathyroidism.
Teh BT; Kytölä S; Farnebo F; Bergman L; Wong FK; Weber G; Hayward N; Larsson C; Skogseid B; Beckers A; Phelan C; Edwards M; Epstein M; Alford F; Hurley D; Grimmond S; Silins G; Walters M; Stewart C; Cardinal J; Khodaei S; Parente F; Tranebjaerg L; Jorde R; Salmela P
J Clin Endocrinol Metab; 1998 Aug; 83(8):2621-6. PubMed ID: 9709921
[TBL] [Abstract][Full Text] [Related]
7. Familial isolated hyperparathyroidism as a variant of multiple endocrine neoplasia type 1 in a large Danish pedigree.
Kassem M; Kruse TA; Wong FK; Larsson C; Teh BT
J Clin Endocrinol Metab; 2000 Jan; 85(1):165-7. PubMed ID: 10634381
[TBL] [Abstract][Full Text] [Related]
8. Isolated familial somatotropinomas: establishment of linkage to chromosome 11q13.1-11q13.3 and evidence for a potential second locus at chromosome 2p16-12.
Gadelha MR; Une KN; Rohde K; Vaisman M; Kineman RD; Frohman LA
J Clin Endocrinol Metab; 2000 Feb; 85(2):707-14. PubMed ID: 10690880
[TBL] [Abstract][Full Text] [Related]
9. A genotypic and histopathological study of a large Dutch kindred with hyperparathyroidism-jaw tumor syndrome.
Haven CJ; Wong FK; van Dam EW; van der Juijt R; van Asperen C; Jansen J; Rosenberg C; de Wit M; Roijers J; Hoppener J; Lips CJ; Larsson C; Teh BT; Morreau H
J Clin Endocrinol Metab; 2000 Apr; 85(4):1449-54. PubMed ID: 10770180
[TBL] [Abstract][Full Text] [Related]
10. Familial isolated hyperparathyroidism maps to the hyperparathyroidism-jaw tumor locus in 1q21-q32 in a subset of families.
Teh BT; Farnebo F; Twigg S; Höög A; Kytölä S; Korpi-Hyövälti E; Wong FK; Nordenström J; Grimelius L; Sandelin K; Robinson B; Farnebo LO; Larsson C
J Clin Endocrinol Metab; 1998 Jun; 83(6):2114-20. PubMed ID: 9626148
[TBL] [Abstract][Full Text] [Related]
11. Parathyroid MEN1 gene mutations in relation to clinical characteristics of nonfamilial primary hyperparathyroidism.
Carling T; Correa P; Hessman O; Hedberg J; Skogseid B; Lindberg D; Rastad J; Westin G; Akerström G
J Clin Endocrinol Metab; 1998 Aug; 83(8):2960-3. PubMed ID: 9709976
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. A kindred with a variant of multiple endocrine neoplasia type 1 demonstrating frequent expression of pituitary tumors but not linked to the multiple endocrine neoplasia type 1 locus at chromosome region 11q13.
Stock JL; Warth MR; Teh BT; Coderre JA; Overdorf JH; Baumann G; Hintz RL; Hartman ML; Seizinger BR; Larsson C; Aronin N
J Clin Endocrinol Metab; 1997 Feb; 82(2):486-92. PubMed ID: 9024241
[TBL] [Abstract][Full Text] [Related]
14. Mapping eight new polymorphisms in 11q13 in the vicinity of multiple endocrine neoplasia type 1: identification of a new distal recombinant.
Smith CM; Wells SA; Gerhard DS
Hum Genet; 1995 Oct; 96(4):377-87. PubMed ID: 7557957
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. Genetic mapping of the multiple endocrine neoplasia type 1 locus at 11q13.
Teh BT; Cardinal J; Shepherd J; Hayward NK; Weber G; Cameron D; Larsson C
J Intern Med; 1995 Sep; 238(3):249-53. PubMed ID: 7673855
[TBL] [Abstract][Full Text] [Related]
18. Genetic screening for MEN1 mutations in families presenting with familial primary hyperparathyroidism.
Perrier ND; Villablanca A; Larsson C; Wong M; Ituarte P; Teh BT; Clark OH
World J Surg; 2002 Aug; 26(8):907-13. PubMed ID: 12016470
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Linkage analysis of 7 polymorphic markers at chromosome 11p11.2-11q13 in 27 multiple endocrine neoplasia type 1 families.
Thakker RV; Wooding C; Pang JT; Farren B; Harding B; Anderson DC; Besser GM; Bouloux P; Brenton DP; Buchanan KD
Ann Hum Genet; 1993 Jan; 57(1):17-25. PubMed ID: 8101435
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]