Results 221 to 230 of about 73,068 (324)

Identification of Prognostic Gene Signatures for Survival of Patients With Phaeochromocytoma, Paraganglioma, and Other Tumor Types. [PDF]

Cancer Diagn Progn
Ooko E, Efferth T.
europepmc   +1 more source

Clinical Characterization of the Pheochromocytoma and Paraganglioma Susceptibility Genes SDHA, TMEM127, MAX, and SDHAF2 for Gene-Informed Prevention

JAMA Oncology, 2017
B. Bausch, F. Schiavi, Y. Ni, J. Welander, A. Patócs, J. Ngeow, U. Wellner, Angelica Malinoc, E. Taschin, G. Barbon, Virginia Lanza, P. Söderkvist, Adam Stenman, C. Larsson, Fredrika Svahn, Jinlai Chen, Jessica Marquard, M. Fraenkel, M. Walter, M. Peczkowska, A. Prejbisz, B. Jarzab, K. Hasse-Lazar, S. Petersenn, L. Moeller, A. Meyer, N. Reisch, A. Trupka, C. Brase, M. Galiano, S. Preuss, P. Kwok, N. Lendvai, Gani Berisha, Ö. Makay, C. Boedeker, G. Weryha, K. Rácz, A. Januszewicz, M. Walz, O. Gimm, G. Opocher, C. Eng, H. Neumann   +43 more
semanticscholar   +1 more source

Paraganglioma

Definitions, 2020
Lu Lin, Yining Wang
semanticscholar   +1 more source

Pure tympanic paraganglioma: A characteristic case with imaging correlation. [PDF]

Radiol Case Rep
Romaissaa B, Anas O, Hasna B, Aicha M, Nadia M, Naima EB.   +5 more
europepmc   +1 more source

Estimation of growth rate in patients with head and neck paragangliomas influences the treatment proposal [PDF]

, 2000
Jeroen C. Jansen, René van den Berg, Alex Kuiper, Andel G. L. van der Mey, A. H. Zwinderman, Cees J. Cornelisse   +5 more
openalex   +1 more source

Supraglottic laryngeal paraganglioma: A rare neuroendocrine tumor mimicking benign laryngeal masses and treated with transoral CO₂ laser excision. [PDF]

Radiol Case Rep
Benfadil D, Bouchlarhem S, Sbai AA, Lachkar A.   +3 more
europepmc   +1 more source

Clinical and Genetic Characteristics of Pheochromocytoma and Paraganglioma: A Single-Center Experience Including a Rare VHL Variant. [PDF]

J Clin Med
Korkmaz Yilmaz M, Kandemir Alibakan O, Aydin Gumus A, Gezdirici A, Karatay H, Sari S, Matlim Ozel T, Niyazoglu M, Hatipoglu E.   +8 more
europepmc   +1 more source

Multiple Endocrine Neoplasia Type 5 due to Germline MAX Mutations: A Systematic Review of Tumor Spectrum and Clinical Features. [PDF]

Endocr Pract
Charoenngam N, Thaneerat N, Likasitwatanakul P, Kansuttiviwat C, Mannstadt M.   +4 more
europepmc   +1 more source

Oncogenetic testing for persons with hereditary endocrine cancer syndromes [PDF]

, 2015
Bex, Marie, Bravenboer, Bert, Claes, Kathleen, Lapauw, Bruno, Persu, Alexandre, Poppe, Bruce, Poppe, Kris, Ullman, Urielle, Van Maerken, Tom, Vlayen, Joan, Vroonen, Laurent   +10 more
core   +1 more source

A Conditional Mouse Mutant in the Tumor Suppressor SdhD Gene Unveils a Link between p21(WAF1/Cip1) Induction and Mitochondrial Dysfunction [PDF]

, 2014
Báez Palomo, Alicia, Díaz Castro, Blanca, García Flores, Gloria Paula, López Barneo, José, Millán Uclés, África, Piruat Palomo, José Ignacio, Pérez Simón, José Antonio   +6 more
core   +1 more source