These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

86 related articles for article (PubMed ID: 19201392)

  • 1. Multiple endocrine neoplasia type 2a and germ line C634G RET mutation diagnosed in an 80-year-old patient.
    Sanz C; Vezzosi D; Pigny P; Bennet A; Caron P
    Ann Endocrinol (Paris); 2009 Apr; 70(2):141-4. PubMed ID: 19201392
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Unusual presentation of multiple endocrine neoplasia type 2A in a patient with the C634R mutation of the RET-protooncogene.
    Harzallah F; Barlier A; Feki M; Enjalbert A; Slimane H
    Ann Endocrinol (Paris); 2008 Dec; 69(6):523-5. PubMed ID: 18752792
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A family of multiple endocrine neoplasia type 2A (MEN 2A) with Cys630Tyr RET germline mutation: report of a case.
    Yonekawa H; Sugitani I; Fujimoto Y; Arai M; Yamamoto N
    Endocr J; 2007 Aug; 54(4):531-5. PubMed ID: 17527003
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. When is prophylactic thyroidectomy indicated for patients with the RET codon 609 mutation?
    Calva D; O'Dorisio TM; Sue O'Dorisio M; Lal G; Sugg S; Weigel RJ; Howe JR
    Ann Surg Oncol; 2009 Aug; 16(8):2237-44. PubMed ID: 19472011
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Primary hyperparathyroidism as the first clinical manifestation of multiple endocrine neoplasia type 2A in a 5-year-old child.
    Magalhães PK; Antonini SR; de Paula FJ; de Freitas LC; Maciel LM
    Thyroid; 2011 May; 21(5):547-50. PubMed ID: 21449769
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Uncommon association of germline mutations of RET proto-oncogene and CDKN2A gene.
    Foppiani L; Forzano F; Ceccherini I; Bruno W; Ghiorzo P; Caroli F; Quilici P; Bandelloni R; Arlandini A; Sartini G; Cabria M; Del Monte P
    Eur J Endocrinol; 2008 Mar; 158(3):417-22. PubMed ID: 18299477
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Prophylactic thyroidectomy in children who are carriers of a multiple endocrine neoplasia type 2 mutation: description of 20 cases and recommendations based on the literature].
    de Groot JW; Links TP; Rouwe CW; van der Wal JE; Hofstra RM; Plukker JT
    Ned Tijdschr Geneeskd; 2006 Feb; 150(6):311-8. PubMed ID: 16503023
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Disagreement between findings of 99mTc-MIBI and 99mTc-pertechnetate scintigraphy scans in patients with primary hyperparathyroidism].
    Dolezal J; Horácek J; Ceeová V; Vizd'a J
    Vnitr Lek; 2004 Jan; 50(1):72-5. PubMed ID: 15015233
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 99mTc-MIBI radio-guided minimally invasive parathyroidectomy: experience with patients with normal thyroids and nodular goiters.
    Casara D; Rubello D; Cauzzo C; Pelizzo MR
    Thyroid; 2002 Jan; 12(1):53-61. PubMed ID: 11838731
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Elevated basal serum levels of calcitonin and simultaneous surgery of MEN2A-specific tumors.
    Tang HX; Yang H; Li F; Cao ZL; Huang YT; Qi XP
    Neoplasma; 2021 Sep; 68(5):1098-1106. PubMed ID: 34156257
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [The clinical patterns and RET proto-oncogene in fifteen multiple endocrine neoplasia type 2A pedigrees].
    Zhou YL; Zhu SX; Li JJ; Liu JB; Yin M; Xiao BY; Yu CL; Wang LM; Gu LQ; Cui B; Ning G; Li XY; Zhao YJ
    Zhonghua Nei Ke Za Zhi; 2007 Jun; 46(6):466-70. PubMed ID: 17663821
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Phenotype of the C634Y mutation in the RET proto-oncogene in MEN2A: report of a family].
    Sánchez Sobrino P; Páramo Fernández C; Gil Gil P; Mantiñán Gil B; Pérez Pedrosa A; Palmeiro Carballeira R; García-Mayor RV
    Endocrinol Nutr; 2011 May; 58(5):229-35. PubMed ID: 21530422
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Bilateral Pheochromocytomas in MEN2A Syndrome: A Two-Institution Experience.
    Lang BH; Yu HW; Lo CY; Lee KE; Garcia-Barcelo MM; Woo YC; Lee PC; Wong KP; Tam PK; Lam KS
    World J Surg; 2015 Oct; 39(10):2484-91. PubMed ID: 26071011
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. New mutations in the RET protooncogene-L881V - associated with medullary thyroid carcinoma and -R770Q - in a patient with mixed medullar/follicular thyroid tumour.
    Frank-Raue K; Döhring J; Scheumann G; Rondot S; Lorenz A; Schulze E; Dralle H; Raue F; Leidig-Bruckner G
    Exp Clin Endocrinol Diabetes; 2010 Aug; 118(8):550-3. PubMed ID: 20013610
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Clinical and oncological features of children and young adults with multiple endocrine neoplasia type 2A.
    Puñales MK; da Rocha AP; Meotti C; Gross JL; Maia AL
    Thyroid; 2008 Dec; 18(12):1261-8. PubMed ID: 18991485
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [The role of scintigraphy with dual tracer and potassium perchlorate (99mTcO4 & KClO4/ MIBI) in primary hyperparathyroidism].
    Rubello D; Saladini G; Casara D
    Minerva Endocrinol; 2001 Mar; 26(1):13-21. PubMed ID: 11323563
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Clinical diagnosis and treatment of familial medullary thyroid carcinoma caused by a p.C618Y RET proto-oncogene mutation in a Chinese pedigree].
    Zhao JQ; Guo L; Qi XP; Chen ZG; Wang KJ; Lou JL; Yu XH; Cheng J; Jin HY; Li XL; Ying RB; Zhang XN
    Zhonghua Yi Xue Za Zhi; 2013 Feb; 93(6):440-4. PubMed ID: 23660264
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.