Updates on the genetics and the clinical impacts on phaeochromocytoma and paraganglioma in the new era-Reference-Cited by-同舟云学术

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Updates on the genetics and the clinical impacts on phaeochromocytoma and paraganglioma in the new era

Published:2016-04 Issue: Volume:100 Page:190-208
ISSN:1040-8428
Container-title:Critical Reviews in Oncology/Hematology
language:en
Short-container-title:Critical Reviews in Oncology/Hematology

Author:

Pillai Suja,Gopalan Vinod,Smith Robert A.,Lam Alfred K.-Y.^ORCID

Publisher

Elsevier BV

Subject

Oncology,Hematology

Reference202 articles.

1. Menin interacts with the AP1 transcription factor JunD and represses JunD-activated transcription;Agarwal;Cell,1999

2. Deletion analysis of the p16 tumour suppressor gene in pheochromocytoma;Aguiar;Clin. Endocrinol. (Oxf).,1996

3. Clinical impacts of mammalian target of rapamycin expression in human colorectal cancers;Alqurashi;Hum. Pathol.,2013

4. Genetic testing in pheochromocytoma or functionalparaganglioma;Amar;J. Clin. Oncol.,2005

5. Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familialparaganglioma;Astuti;Am. J. Hum. Genet.,2001

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1. Genotype and clinical phenotype characteristics of MAX germline mutation–associated pheochromocytoma/paraganglioma syndrome;Frontiers in Endocrinology;2024-08-30

2. Differences between Patients with Sporadic and Familial Pheochromocytoma—Is It Possible to Avoid Genetic Testing in Certain Patients?;Biomedicines;2024-06-18

3. Respuesta a radioterapia conformal en paragangliomas de cabeza y cuello;Gaceta Mexicana de Oncolog�a;2023-11-22

4. The connection between tricarboxylic acid cycle enzyme mutations and pseudohypoxic signaling in pheochromocytoma and paraganglioma;Frontiers in Endocrinology;2023-10-05

5. Case Report: A novel EPAS1 mutation in a case of paraganglioma complicated with polycythemia and atrial septal defect;Frontiers in Endocrinology;2023-07-28

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