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Annals of the New York Academy of Sciences|November 15, 2006
Transcription association of VHL and SDH mutations link hypoxia and oxidoreductase signals in pheochromocytomasPatricia L M Dahia, Cancer Cell|February 16, 2017
Pheochromocytomas and Paragangliomas, Genetically Diverse and Minimalist, All at Once!Patricia L M DahiaFrontiers of Hormone Research|May 9, 2013
Novel hereditary forms of pheochromocytomas and paragangliomasPatricia L M DahiaNature Reviews. Cancer|January 21, 2014
Pheochromocytoma and paraganglioma pathogenesis: learning from genetic heterogeneityPatricia L M DahiaCurrent Opinion in Oncology|December 17, 2005
Evolving concepts in pheochromocytoma and paragangliomaPatricia L M DahiaBest Practice & Research. Clinical Endocrinology & Metabolism|September 14, 2010
VHL diseaseMarta Barontini, Patricia L M DahiaEndocrinology|March 31, 2011
Minireview: the busy road to pheochromocytomas and paragangliomas has a new member, TMEM127Shoulei Jiang, Patricia L M DahiaCurrent Opinion in Endocrinology, Diabetes, and Obesity|April 15, 2015
Next-generation sequencing for the diagnosis of hereditary pheochromocytoma and paraganglioma syndromesRodrigo A Toledo, Patricia L M DahiaEndocrine-Related Cancer|February 7, 2023
Update on the genetics of paragangliomasAnne-Paule Gimenez-Roqueplo, Mercedes Robledo, Patricia L M DahiaEndocrine|January 3, 2006
A RET mutation with decreased penetrance in the family of a patient with a "sporadic" pheochromocytomaSeth M Arum, Patricia L M Dahia, Katherine Schneider, et al.Pageof 6