169 related articles for article (PubMed ID: 34446941)
21. Hereditary Medullary Thyroid Cancer Genotype-Phenotype Correlation.
Frank-Raue K; Raue F
Recent Results Cancer Res; 2015; 204():139-56. PubMed ID: 26494387
[TBL] [Abstract][Full Text] [Related]
22. Orolabial signs are important clues for diagnosis of the rare endocrine syndrome MEN 2B. Presentation of two unrelated cases.
Sallai A; Hosszú E; Gergics P; Rácz K; Fekete G
Eur J Pediatr; 2008 Apr; 167(4):441-6. PubMed ID: 17576593
[TBL] [Abstract][Full Text] [Related]
23. Multiple endocrine neoplasia-IIb with RET gene mutation p.M918T: A case report.
Jin P; Hu W; Yang Y; Long X; Mo Z
Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2020 Oct; 45(10):1261-1265. PubMed ID: 33268590
[TBL] [Abstract][Full Text] [Related]
24. Multiple endocrine neoplasia 2B syndrome due to codon 918 mutation: clinical manifestation and course in early and late onset disease.
Brauckhoff M; Gimm O; Weiss CL; Ukkat J; Sekulla C; Brauckhoff K; Thanh PN; Dralle H
World J Surg; 2004 Dec; 28(12):1305-11. PubMed ID: 15517484
[TBL] [Abstract][Full Text] [Related]
25. Increased in vivo phosphorylation of ret tyrosine 1062 is a potential pathogenetic mechanism of multiple endocrine neoplasia type 2B.
Salvatore D; Melillo RM; Monaco C; Visconti R; Fenzi G; Vecchio G; Fusco A; Santoro M
Cancer Res; 2001 Feb; 61(4):1426-31. PubMed ID: 11245446
[TBL] [Abstract][Full Text] [Related]
26. SOS1 frameshift mutations cause pure mucosal neuroma syndrome, a clinical phenotype distinct from multiple endocrine neoplasia type 2B.
Owens M; Kivuva E; Quinn A; Brennan P; Caswell R; Lango Allen H; Vaidya B; Ellard S
Clin Endocrinol (Oxf); 2016 May; 84(5):715-9. PubMed ID: 26708403
[TBL] [Abstract][Full Text] [Related]
27. Multiple Endocrine Neoplasia Type 2B Presents Early in Childhood but Often Is Undiagnosed for Years.
Makri A; Akshintala S; Derse-Anthony C; Widemann B; Stratakis CA; Glod J; Lodish M
J Pediatr; 2018 Dec; 203():447-449. PubMed ID: 30314660
[TBL] [Abstract][Full Text] [Related]
28. Hereditary medullary thyroid carcinoma syndromes: experience from western India.
Diwaker C; Sarathi V; Jaiswal SK; Shah R; Deshmukh A; Thomas AE; Prakash G; Malhotra G; Patil V; Lila A; Shah N; Bandgar T
Fam Cancer; 2021 Jul; 20(3):241-251. PubMed ID: 33392850
[TBL] [Abstract][Full Text] [Related]
29. Multiple endocrine neoplasia 2B: delayed presentation, rapid diagnosis.
Balachandran K; Kamalanathan S; Gopalakrishnan S; Murugananadham K
BMJ Case Rep; 2013 May; 2013():. PubMed ID: 23645647
[TBL] [Abstract][Full Text] [Related]
30. Vandetanib in children and adolescents with multiple endocrine neoplasia type 2B associated medullary thyroid carcinoma.
Fox E; Widemann BC; Chuk MK; Marcus L; Aikin A; Whitcomb PO; Merino MJ; Lodish M; Dombi E; Steinberg SM; Wells SA; Balis FM
Clin Cancer Res; 2013 Aug; 19(15):4239-48. PubMed ID: 23766359
[TBL] [Abstract][Full Text] [Related]
31. Presence of the 918 mutation in the RET proto-oncogene in a Mexican patient with multiple endocrine neoplasia type 2B.
Hidalgo A; Medrano ME; Rodrìguez S; Franco C; Martinez I; Benítez L; Salcedo M
J Exp Clin Cancer Res; 1998 Jun; 17(2):149-52. PubMed ID: 9700574
[TBL] [Abstract][Full Text] [Related]
32. Genotype-phenotype relationship in multiple endocrine neoplasia type 2. Implications for clinical management.
Raue F; Frank-Raue K
Hormones (Athens); 2009; 8(1):23-8. PubMed ID: 19269918
[TBL] [Abstract][Full Text] [Related]
33. Late diagnosis of metastatic pheochromocytoma in multiple endocrine neoplasia 2B with rapid clinical decline.
Jester G; Hassanein H; El-Far A
BMJ Case Rep; 2021 Feb; 14(2):. PubMed ID: 33541961
[TBL] [Abstract][Full Text] [Related]
34. A Girl with Delayed Puberty and Bumpy Lips.
Andrade S; Sirchia F; Faleschini E; Barbi E
J Pediatr; 2018 Dec; 203():454-454.e1. PubMed ID: 30025668
[No Abstract] [Full Text] [Related]
35. [Multiple endocrine neoplasia type 2B].
Pijnenburg-Kleizen KJ; van Santen HM; Koolen DA; Claahsen-van der Grinten HL
Ned Tijdschr Geneeskd; 2015; 159():A7719. PubMed ID: 25944066
[TBL] [Abstract][Full Text] [Related]
36. Laryngeal Ganglioneuromatosis in a Child With Multiple Endocrine Neoplasia Type 2B (MEN2B): Case Report and Review of Literature.
Chornenkyy Y; Than J; Ghadersohi S; Melin-Aldana H; Chou P
Cureus; 2024 Mar; 16(3):e55406. PubMed ID: 38562350
[TBL] [Abstract][Full Text] [Related]
37. Characterization of gene expression induced by RET with MEN2A or MEN2B mutation.
Watanabe T; Ichihara M; Hashimoto M; Shimono K; Shimoyama Y; Nagasaka T; Murakumo Y; Murakami H; Sugiura H; Iwata H; Ishiguro N; Takahashi M
Am J Pathol; 2002 Jul; 161(1):249-56. PubMed ID: 12107109
[TBL] [Abstract][Full Text] [Related]
38. Medullary thyroid carcinoma in children.
Viola D; Romei C; Elisei R
Endocr Dev; 2014; 26():202-13. PubMed ID: 25231454
[TBL] [Abstract][Full Text] [Related]
39. Transcriptome analysis in mouse tumors induced by Ret-MEN2/FMTC mutations reveals subtype-specific role in survival and interference with immune surveillance.
Engelmann D; Koczan D; Ricken P; Rimpler U; Pahnke J; Li Z; Pützer BM
Endocr Relat Cancer; 2009 Mar; 16(1):211-24. PubMed ID: 18984779
[TBL] [Abstract][Full Text] [Related]
40. RET activation by germline MEN2A and MEN2B mutations.
Borrello MG; Smith DP; Pasini B; Bongarzone I; Greco A; Lorenzo MJ; Arighi E; Miranda C; Eng C; Alberti L
Oncogene; 1995 Dec; 11(11):2419-27. PubMed ID: 8570194
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]