88 related articles for article (PubMed ID: 11577645)
1. [Phenotypic expression of a mutation in MEN 2A documented in a family in the western part of Sweden].
Lindskog S; Ahlman H; Illerskog A; Nilsson O; Nilsson B; Tisell LE; Ysander L; Jansson S
Lakartidningen; 2001 Aug; 98(35):3690-1, 3694-5. PubMed ID: 11577645
[TBL] [Abstract][Full Text] [Related]
2. Experience of prophylactic thyroidectomy in multiple endocrine neoplasia type 2A kindreds with RET codon 804 mutations.
Learoyd DL; Gosnell J; Elston MS; Saurine TJ; Richardson AL; Delbridge LW; Aglen JV; Robinson BG
Clin Endocrinol (Oxf); 2005 Dec; 63(6):636-41. PubMed ID: 16343097
[TBL] [Abstract][Full Text] [Related]
3. Multiple endocrine neoplasia 2A due to a unique C609S RET mutation presents with pheochromocytoma and reduced penetrance of medullary thyroid carcinoma.
Kinlaw WB; Scott SM; Maue RA; Memoli VA; Harris RD; Daniels GH; Porter DM; Belloni DR; Spooner ET; Ernesti MM; Noll WW
Clin Endocrinol (Oxf); 2005 Dec; 63(6):676-82. PubMed ID: 16343103
[TBL] [Abstract][Full Text] [Related]
4. RET proto-oncogene testing in infants presenting with Hirschsprung disease identifies 2 new multiple endocrine neoplasia 2A kindreds.
Fialkowski EA; DeBenedetti MK; Moley JF; Bachrach B
J Pediatr Surg; 2008 Jan; 43(1):188-90. PubMed ID: 18206480
[TBL] [Abstract][Full Text] [Related]
5. Familial medullary carcinoma prevention, risk evaluation, and RET in children of families with MEN2.
Moore SW; Appfelstaedt J; Zaahl MG
J Pediatr Surg; 2007 Feb; 42(2):326-32. PubMed ID: 17270543
[TBL] [Abstract][Full Text] [Related]
6. RET mutation status in medullary thyroid cancer(MTC) patients and the significance of genetic screening for mutations in their immediate relatives--a preliminary report.
Menon MM; Simha MR
Indian J Pathol Microbiol; 2005 Apr; 48(2):161-5. PubMed ID: 16758654
[TBL] [Abstract][Full Text] [Related]
7. Age-related neoplastic risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germ line RET Cys634Trp (TGC>TGG) mutation.
Milos IN; Frank-Raue K; Wohllk N; Maia AL; Pusiol E; Patocs A; Robledo M; Biarnes J; Barontini M; Links TP; de Groot JW; Dvorakova S; Peczkowska M; Rybicki LA; Sullivan M; Raue F; Zosin I; Eng C; Neumann HP
Endocr Relat Cancer; 2008 Dec; 15(4):1035-41. PubMed ID: 18794325
[TBL] [Abstract][Full Text] [Related]
8. [Management of multiple endocrine neoplasia syndrome type 2 families in association with rare germline mutations of the RET proto-oncogene].
Fitze G; Saeger HD; Roesner D; Schackert HK
Klin Padiatr; 2004; 216(5):270-6. PubMed ID: 15455293
[TBL] [Abstract][Full Text] [Related]
9. MEN 2A family--prophylactic thyroidectomy for asymptomatic siblings with positive 634 codon mutation.
Agarwal S; Agarwal A; Chand G; Gupta SK; Jain M; Ramakant P
J Assoc Physicians India; 2012 Feb; 60():127-9. PubMed ID: 22715565
[TBL] [Abstract][Full Text] [Related]
10. [Hereditary thyroid cancer can be cured by prophylactic surgery].
Wallin G; Bondesson AG; Farnebo LO; Hallengren B; Hamberger B; Jansson S; Nilsson O; Nordenskjöld M; Smeds S; Svensson KA; Wihlborg O; Zedenius J
Lakartidningen; 2001 Jun; 98(25):3024-8. PubMed ID: 11462876
[TBL] [Abstract][Full Text] [Related]
11. [C634R mutation of the protooncongene RET and molecular diagnosis in multiple endocrine neoplasia type 2 in a large Moroccan family].
Benazzouz B; Hafidi A; Benkhira S; Chraibi A; Kadiri A; Hilal L
Bull Cancer; 2008 Apr; 95(4):457-63. PubMed ID: 18495576
[TBL] [Abstract][Full Text] [Related]
12. Pheochromocytoma and medullary thyroid carcinoma in a pregnant multiple endocrine neoplasia-2A patient.
Sarathi V; Bandgar TR; Menon PS; Shah NS
Gynecol Endocrinol; 2011 Aug; 27(8):533-5. PubMed ID: 20672905
[TBL] [Abstract][Full Text] [Related]
13. Molecular diagnosis of multiple endocrine neoplasia Type 2.
Bugalho MJ; Domingues R; Sobrinho L
Expert Rev Mol Diagn; 2003 Nov; 3(6):769-79. PubMed ID: 14628904
[TBL] [Abstract][Full Text] [Related]
14. [MEN 2A syndrome: report of a family].
Krassowski J; Gabryelewicz MB; Jeske W; Zgliczyński S
Pol Merkur Lekarski; 2000 Jul; 8(49):481-2. PubMed ID: 11070721
[TBL] [Abstract][Full Text] [Related]
15. Surgical management of MEN-1 and -2: state of the art.
Akerström G; Stålberg P
Surg Clin North Am; 2009 Oct; 89(5):1047-68. PubMed ID: 19836484
[TBL] [Abstract][Full Text] [Related]
16. Multiple endocrine neoplasias type 2A and thyroid medullary carcinoma: an interdisciplinary challenge.
Haecker FM; Oertli D; Gissler S; Zumsteg U; Avoledo P; von Schweinitz D
Pediatr Surg Int; 2003 Apr; 19(1-2):62-4. PubMed ID: 12721726
[TBL] [Abstract][Full Text] [Related]
17. [Analysis of mutations in the RET proto-oncogene in patients with medullary thyroid tumor].
Amosenko FA; Brzhezovskiĭ VZh; Liubchenko LN; Shabanov MA; Kozlova VM; Vanushko VE; Kazubskaia TP; Gar'kavtseva RF; Kalinin VN
Genetika; 2003 Jun; 39(6):847-54. PubMed ID: 12884527
[TBL] [Abstract][Full Text] [Related]
18. [Diagnosis and treatment of syndrome of multiple endocrine neoplasia type 2].
Kuznetsov NS; Bel'tsevich DG; Poliakova EIu; Vasil'ev EV; Nemtsova MV
Khirurgiia (Mosk); 2002; (2):4-9. PubMed ID: 12418313
[TBL] [Abstract][Full Text] [Related]
19. RET proto-oncogene mutations are restricted to codons 634 and 918 in mainland Chinese families with MEN2A and MEN2B.
Zhou Y; Zhao Y; Cui B; Gu L; Zhu S; Li J; Liu J; Yin M; Zhao T; Yin Z; Yu C; Chen C; Wang L; Xiao B; Hong J; Zhang Y; Tang Z; Wang S; Li X; Ning G
Clin Endocrinol (Oxf); 2007 Oct; 67(4):570-6. PubMed ID: 17573899
[TBL] [Abstract][Full Text] [Related]
20. Phenotypic expression of a family with multiple endocrine neoplasia type 2A due to a RET mutation at codon 618.
Lindskog S; Nilsson O; Jansson S; Nilsson B; Illerskog AC; Ysander L; Ahlman H; Tisell LE
Br J Surg; 2004 Jun; 91(6):713-8. PubMed ID: 15164440
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
