BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

Terms: = Thyroid cancer AND NF1, NFNS, 4763, ENSG00000196712, P21359 AND Diagnosis
15 results:

  • 1. [Pheochromocytoma associated with primary hyperparathyroidism and type 1 neurofibromatosis].
    Ryabchenko EV; Dremlyuga NV; Mezhinskaya EM; Polyansky EA
    Khirurgiia (Mosk); 2023; (7):120-127. PubMed ID: 37379415
    [TBL] [Abstract] [Full Text] [Related]  

  • 2. MULTIPLE NEUROENDOCRINE NEOPLASIA IN A PATIENT WITH TYPE I NEUROFIBROMATOSIS (nf1): REPORT OF A NEW MUTATION (nf1, EXONS 2-30 DELETION) AND LITERATURE REVIEW.
    Kanno DT; Mattos RLM; Campos FG; Siqueira RM; Carvalho RB; Real Martinez CA
    Arq Bras Cir Dig; 2023; 35():e1702. PubMed ID: 36629684
    [TBL] [Abstract] [Full Text] [Related]  

  • 3. Pancreatic Gastrinoma, Gastrointestinal Stromal Tumor (GIST), Pheochromocytoma, and Hürthle Cell Neoplasm in a Patient with Neurofibromatosis Type 1: A Case Report and Literature Review.
    Arif AA; Kim PTW; Melck A; Churg A; Schwartz Z; Stuart HC
    Am J Case Rep; 2021 Jan; 22():e927761. PubMed ID: 33452231
    [TBL] [Abstract] [Full Text] [Related]  

  • 4. diagnosis of neurofibromatosis type 1 after rupture of aneurysm and consequent fatal hemothorax.
    Miyamoto K; Nakamura M; Suzuki K; Katsuki S; Kaki Y; Inoue G; Ohno T; Sasaki J; Dohi K; Hayashi M
    Am J Emerg Med; 2020 Jul; 38(7):1543.e3-1543.e5. PubMed ID: 32305158
    [TBL] [Abstract] [Full Text] [Related]  

  • 5. Screening guidelines and recommendations for patients at high risk of developing endocrine cancers.
    Geurts JL; Strong EA; Wang TS; Evans DB; Clarke CN
    J Surg Oncol; 2020 May; 121(6):975-983. PubMed ID: 32090344
    [TBL] [Abstract] [Full Text] [Related]  

  • 6. Acromegaly caused by a somatotroph adenoma in patient with neurofibromatosis type 1.
    Hozumi K; Fukuoka H; Odake Y; Takeuchi T; Uehara T; Sato T; Inoshita N; Yoshida K; Matsumoto R; Bando H; Hirota Y; Iguchi G; Taniguchi M; Otsuki N; Nishigori C; Kosaki K; Hasegawa T; Ogawa W; Takahashi Y
    Endocr J; 2019 Oct; 66(10):853-857. PubMed ID: 31189769
    [TBL] [Abstract] [Full Text] [Related]  

  • 7. Diagnostic performance of CT in detection of metastatic cervical lymph nodes in patients with thyroid cancer: a systematic review and meta-analysis.
    Cho SJ; Suh CH; Baek JH; Chung SR; Choi YJ; Lee JH
    Eur Radiol; 2019 Sep; 29(9):4635-4647. PubMed ID: 30806803
    [TBL] [Abstract] [Full Text] [Related]  

  • 8. Comprehensive Genetic Analysis of Follicular thyroid Carcinoma Predicts Prognosis Independent of Histology.
    Nicolson NG; Murtha TD; Dong W; Paulsson JO; Choi J; Barbieri AL; Brown TC; Kunstman JW; Larsson C; Prasad ML; Korah R; Lifton RP; Juhlin CC; Carling T
    J Clin Endocrinol Metab; 2018 Jul; 103(7):2640-2650. PubMed ID: 29726952
    [TBL] [Abstract] [Full Text] [Related]  

  • 9. Next-generation panel sequencing identifies
    Gieldon L; Masjkur JR; Richter S; Därr R; Lahera M; Aust D; Zeugner S; Rump A; Hackmann K; Tzschach A; Januszewicz A; Prejbisz A; Eisenhofer G; Schrock E; Robledo M; Klink B
    Eur J Endocrinol; 2018 Feb; 178(2):K1-K9. PubMed ID: 29158289
    [TBL] [Abstract] [Full Text] [Related]  

  • 10. Surgical approaches in hereditary endocrine tumors.
    Iacobone M; Citton M; Viel G; Schiavone D; Torresan F
    Updates Surg; 2017 Jun; 69(2):181-191. PubMed ID: 28455835
    [TBL] [Abstract] [Full Text] [Related]  

  • 11. Mutational burdens and evolutionary ages of thyroid follicular adenoma are comparable to those of follicular carcinoma.
    Jung SH; Kim MS; Jung CK; Park HC; Kim SY; Liu J; Bae JS; Lee SH; Kim TM; Lee SH; Chung YJ
    Oncotarget; 2016 Oct; 7(43):69638-69648. PubMed ID: 27626165
    [TBL] [Abstract] [Full Text] [Related]  

  • 12. A novel RET gene mutation in a patient with apparently sporadic pheochromocytoma.
    Scollo C; Russo M; De Gregorio L; Terranova R; Mangione E; Castoro C; Squatrito S; Pellegriti G
    Endocr J; 2016; 63(1):87-91. PubMed ID: 26497911
    [TBL] [Abstract] [Full Text] [Related]  

  • 13. Testing new susceptibility genes in the cohort of apparently sporadic phaeochromocytoma/paraganglioma patients with clinical characteristics of hereditary syndromes.
    Pęczkowska M; Kowalska A; Sygut J; Waligórski D; Malinoc A; Janaszek-Sitkowska H; Prejbisz A; Januszewicz A; Neumann HP
    Clin Endocrinol (Oxf); 2013 Dec; 79(6):817-23. PubMed ID: 23551045
    [TBL] [Abstract] [Full Text] [Related]  

  • 14. [Genetics of pheochromocytoma].
    Bausch B; Malinoc A; Maruschke L; Offergeld C; Gläsker S; Rischke HC; Brauckhoff M; Boedeker CC; Neumann HP
    Chirurg; 2012 Jun; 83(6):511-8. PubMed ID: 22481546
    [TBL] [Abstract] [Full Text] [Related]  

  • 15. A newly detected mutation of the RET protooncogene in exon 8 as a cause of multiple endocrine neoplasia type 2A.
    Bethanis S; Koutsodontis G; Palouka T; Avgoustis C; Yannoukakos D; Bei T; Papadopoulos S; Linos D; Tsagarakis S
    Hormones (Athens); 2007; 6(2):152-6. PubMed ID: 17704047
    [TBL] [Abstract] [Full Text] [Related]  


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