A-p Roqueplo-Gimenez
Paris, 75015, France
Last Updated: 09/26/2026
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Found 9 publications
Phaeochromocytoma and paraganglioma
Journal: La Revue de medecine interne
Published: February 24, 2019
Reassessing the clinical spectrum associated with hereditary leiomyomatosis and renal cell carcinoma syndrome in French FH mutation carriers.
Journal: Clinical genetics
Published: January 24, 2017
Rethinking pheochromocytomas and paragangliomas from a genomic perspective.
Journal: Oncogene
Published: January 20, 2015
Screening in asymptomatic SDHx mutation carriers: added value of ¹⁸F-FDG PET/CT at initial diagnosis and 1-year follow-up.
Journal: European journal of nuclear medicine and molecular imaging
Published: December 04, 2014
Malignant head/neck paragangliomas. Comparative study.
Journal: European annals of otorhinolaryngology, head and neck diseases
Published: March 19, 2013
Presymptomatic genetic testing in minors at risk of paraganglioma and pheochromocytoma: our experience of oncogenetic multidisciplinary consultation.
Journal: Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme
Published: April 21, 2012
A decade (2001-2010) of genetic testing for pheochromocytoma and paraganglioma.
Journal: Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme
Published: April 21, 2012
Long-term postoperative follow-up in patients with apparently benign pheochromocytoma and paraganglioma.
Journal: Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme
Published: February 22, 2012
The genetics of paragangliomas.
Journal: European annals of otorhinolaryngology, head and neck diseases
Published: January 03, 2012
Showing 1-9 of 9
Last Updated: 09/26/2026