84 related articles for article (PubMed ID: 12166655)
1. A rapid and easy method for multiple endocrine neoplasia type 1 mutation detection using conformation-sensitive gel electrophoresis.
Arancha C; Ruíz-Llorente S; Cascón A; Osorio A; Martínez-Delgado B; Benítez J; Robledo M
J Hum Genet; 2002; 47(4):190-5. PubMed ID: 12166655
[TBL] [Abstract][Full Text] [Related]
2. Genetic screening methods for the detection of mutations responsible for multiple endocrine neoplasia type 1.
Balogh K; Patócs A; Majnik J; Rácz K; Hunyady L
Mol Genet Metab; 2004; 83(1-2):74-81. PubMed ID: 15464422
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Novel germline mutations of the MEN1 gene in Japanese patients with multiple endocrine neoplasia type 1.
Hamaguchi K; Nguyen DC; Yanase T; Ikuyama S; Goto K; Takayanagi R; Nawata H; Kusuda Y; Fukagawa K; Sakata T
J Hum Genet; 1999; 44(1):43-7. PubMed ID: 9929977
[TBL] [Abstract][Full Text] [Related]
5. Novel mutations in the MEN1 gene in subjects with multiple endocrine neoplasia-1.
Jap TS; Chiu CY; Won JG; Wu YC; Chen HS
Clin Endocrinol (Oxf); 2005 Mar; 62(3):336-42. PubMed ID: 15730416
[TBL] [Abstract][Full Text] [Related]
6. Efficient mutation detection in MEN1 gene using a combination of single-strand conformation polymorphism (MDGA) and heteroduplex analysis.
Crépin M; Escande F; Pigny P; Buisine MP; Calender A; Porchet N; Odou MF;
Electrophoresis; 2003 Jan; 24(1-2):26-33. PubMed ID: 12652570
[TBL] [Abstract][Full Text] [Related]
7. [Clinical symptoms, diagnosis and treatment of multiple endocrine neoplasia type 1. Results of genetic screening in Hungarian patients].
Balogh K; Hunyady L; Patócs A; Valkusz Z; Bertalan R; Gergics P; Majnik J; Toke J; Tóth M; Szucs N; Gláz E; Futo L; Horányi J; Rácz K; Tulassay Z
Orv Hetil; 2005 Oct; 146(43):2191-7. PubMed ID: 16323565
[TBL] [Abstract][Full Text] [Related]
8. Characteristics of the Danish families with multiple endocrine neoplasia type 1.
Jäger AC; Friis-Hansen L; Hansen TV; Eskildsen PC; Sølling K; Knigge U; Hansen CP; Andersen PH; Brixen K; Feldt-Rasmussen U; Kroustrup JP; Mollerup CL; Rehfeld JF; Blichert-Toft M; Nielsen FC
Mol Cell Endocrinol; 2006 Apr; 249(1-2):123-32. PubMed ID: 16563611
[TBL] [Abstract][Full Text] [Related]
9. Analysis of gross deletions in the MEN1 gene in patients with multiple endocrine neoplasia type 1.
Owens M; Ellard S; Vaidya B
Clin Endocrinol (Oxf); 2008 Mar; 68(3):350-4. PubMed ID: 17854391
[TBL] [Abstract][Full Text] [Related]
10. MEN1 mutation analysis in Chinese patients with multiple endocrine neoplasia type 1.
Jiang XH; Lu JL; Cui B; Zhao YJ; Wang WQ; Liu JM; Fang WQ; Cao YN; Ge Y; Zhang CX; Casse H; Li XY; Ning G
Endocr Relat Cancer; 2007 Dec; 14(4):1073-9. PubMed ID: 18045958
[TBL] [Abstract][Full Text] [Related]
11. Detection of an MEN1 gene mutation depends on clinical features and supports current referral criteria for diagnostic molecular genetic testing.
Ellard S; Hattersley AT; Brewer CM; Vaidya B
Clin Endocrinol (Oxf); 2005 Feb; 62(2):169-75. PubMed ID: 15670192
[TBL] [Abstract][Full Text] [Related]
12. Alport syndrome. Molecular genetic aspects.
Hertz JM
Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. A whole MEN1 gene deletion flanked by Alu repeats in a family with multiple endocrine neoplasia type 1.
Fukuuchi A; Nagamura Y; Yaguchi H; Ohkura N; Obara T; Tsukada T
Jpn J Clin Oncol; 2006 Nov; 36(11):739-44. PubMed ID: 17000701
[TBL] [Abstract][Full Text] [Related]
15. Identification of factor VIII gene mutations in 101 patients with haemophilia A: mutation analysis by inversion screening and multiplex PCR and CSGE and molecular modelling of 10 novel missense substitutions.
Jayandharan G; Shaji RV; Baidya S; Nair SC; Chandy M; Srivastava A
Haemophilia; 2005 Sep; 11(5):481-91. PubMed ID: 16128892
[TBL] [Abstract][Full Text] [Related]
16. Pituitary tumors and hyperplasia in multiple endocrine neoplasia type 1 syndrome (MEN1): a case-control study in a series of 77 patients versus 2509 non-MEN1 patients.
Trouillas J; Labat-Moleur F; Sturm N; Kujas M; Heymann MF; Figarella-Branger D; Patey M; Mazucca M; Decullier E; Vergès B; Chabre O; Calender A;
Am J Surg Pathol; 2008 Apr; 32(4):534-43. PubMed ID: 18300794
[TBL] [Abstract][Full Text] [Related]
17. Novel 14 base-pair deletion of the MEN1 gene in a patient with recurrent primary hyperparathyroidism.
Katai M; Sakurai A; Uchino S; Minemura K; Hashizume K; Fukushima Y
Jpn J Clin Oncol; 2006 Jun; 36(6):395-7. PubMed ID: 16714299
[TBL] [Abstract][Full Text] [Related]
18. A novel mutation E179K of the MEN1 gene predisposes for multiple endocrine neoplasia-type 1 (MEN1).
Weinhaeusel A; Vierhapper H; Schlegl R; Wagner T; Muhr D; Scheuba C; Niederle B; Haas OA
Hum Mutat; 2000 Dec; 16(6):533. PubMed ID: 11102994
[No Abstract] [Full Text] [Related]
19. Microadenomatosis of the endocrine pancreas in patients with and without the multiple endocrine neoplasia type 1 syndrome.
Anlauf M; Schlenger R; Perren A; Bauersfeld J; Koch CA; Dralle H; Raffel A; Knoefel WT; Weihe E; Ruszniewski P; Couvelard A; Komminoth P; Heitz PU; Klöppel G
Am J Surg Pathol; 2006 May; 30(5):560-74. PubMed ID: 16699310
[TBL] [Abstract][Full Text] [Related]
20. Thymic carcinoid in multiple endocrine neoplasia 1: genotype-phenotype correlation and prevention.
Lim LC; Tan MH; Eng C; Teh BT; Rajasoorya RC
J Intern Med; 2006 Apr; 259(4):428-32. PubMed ID: 16594911
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
