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Thymic Neuroendocrine Tumors in Multiple Endocrine Neoplasia Type 1: A Comparative Study on 21 Cases Among a Series of 761 MEN1 from the GTE (Groupe des Tumeurs Endocrines)

World journal of surgery, 2009-06, Vol.33 (6), p.1197-1207

2009

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Paraganglioma after Maternal Transmission of a Succinate Dehydrogenase Gene Mutation

The journal of clinical endocrinology and metabolism, 2008-05, Vol.93 (5), p.1609-1615

2008

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Targeted next-generation sequencing detects rare genetic events in pheochromocytoma and paraganglioma

Journal of medical genetics, 2019-08, Vol.56 (8), p.513-520

2019

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Genetic predisposition to neural crest-derived tumors: revisiting the role of KIF1B

Endocrine Connections, 2020-10, Vol.9 (10), p.1042-1050

2020

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Optimization of Next-Generation Sequencing Technologies for von Hippel Lindau (VHL) Mosaic Mutation Detection and Development of Confirmation Methods

The Journal of molecular diagnostics : JMD, 2019-05, Vol.21 (3), p.462-470

2019

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Genetic biomarkers of life-threatening pheochromocytoma-induced cardiomyopathy

Endocrine-related cancer, 2022-05, Vol.29 (5), p.267-272

2022

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MEN1 and the brain: Don’t just look only at the pituitary gland. A case report of anaplastic pleomorphic xanthoastrocytoma in a MEN1 patient, and systematic review

Annales d'endocrinologie, 2023-08, Vol.84 (4), p.424-426

2023

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Local-regional recurrence of sporadic or syndromic abdominal extra-adrenal paraganglioma: Incidence, characteristics, and outcome

Surgery, 2009-12, Vol.146 (6), p.986-992

2009

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Should the GCM2 gene be tested when screening for familial primary hyperparathyroidism?

European journal of endocrinology, 2020-01, Vol.182 (1), p.57-65

2020

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Phakomatoses and Endocrine Gland Tumors: Noteworthy and (Not so) Rare Associations

Frontiers in endocrinology (Lausanne), 2021-05, Vol.12, p.678869-678869

2021

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Long-term results of less than total parathyroidectomy for hyperparathyroidism in multiple endocrine neoplasia type 1

Surgery, 2002-12, Vol.132 (6), p.1119-1125

2002

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The Succinate Dehydrogenase Genetic Testing in a Large Prospective Series of Patients with Paragangliomas

The journal of clinical endocrinology and metabolism, 2009-08, Vol.94 (8), p.2817-2827

2009

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Pheochromocytomas and paragangliomas in pregnancy: About four cases and key messages on management

Gynécologie, obstétrique, fertilité & sénologie, 2021-12, Vol.49 (12), p.881-888

2021

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Prospective Endoscopic Ultrasonographic Evaluation of the Frequency of Nonfunctioning Pancreaticoduodenal Endocrine Tumors in Patients with Multiple Endocrine Neoplasia Type 1

The American journal of gastroenterology, 2006-02, Vol.101 (2), p.266-273

2006

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Hypoparathyroidism and pregnancy

Annales d'endocrinologie, 2016-06, Vol.77 (2), p.172-175

Cardot-Bauters, Catherine

2016

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Evaluation of denaturing high performance liquid chromatography for the mutational analysis of the MEN1 gene

Journal of molecular endocrinology, 2006-04, Vol.36 (2), p.369-376

2006

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A Full Phenotype of Paraganglioma Linked to a Germline SDHB Mosaic Mutation

The journal of clinical endocrinology and metabolism, 2019-08, Vol.104 (8), p.3362-3366

2019

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Serum succinate/fumarate ratio in paraganglioma/pheochromocytoma patients attending an endocrine oncogenetic unit

The journal of clinical endocrinology and metabolism, 2023-03

2023

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Serum Succinate/Fumarate Ratio in Patients With Paraganglioma/Pheochromocytoma Attending an Endocrine Oncogenetic Unit

The journal of clinical endocrinology and metabolism, 2023-08, Vol.108 (9), p.2343-2352

2023

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Serum fatty acid profiling in patients with SDHx mutations: New advances on cellular metabolism in SDH deficiency

Biochimie, 2022-10, Vol.201, p.196-203

2022

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Genetic predisposition to pheochromocytoma and paraganglioma: 21 years of experience in the field

Annales d'endocrinologie, 2024-07, Vol.85 (4), p.276-283

2024

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Frequency and Incidence of Carney Complex Manifestations: A Prospective Multicenter Study With a Three-Year Follow-Up

The journal of clinical endocrinology and metabolism, 2020-03, Vol.105 (3), p.e436-e446

2020

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Thymic Neuroendocrine Tumors in Multiple Endocrine Neoplasia Type 1: A Comparative Study on 21 Cases Among a Series of 761 MEN1 from the GTE (Groupe des Tumeurs Endocrines)

Paraganglioma after Maternal Transmission of a Succinate Dehydrogenase Gene Mutation

Targeted next-generation sequencing detects rare genetic events in pheochromocytoma and paraganglioma

Genetic predisposition to neural crest-derived tumors: revisiting the role of KIF1B

Optimization of Next-Generation Sequencing Technologies for von Hippel Lindau (VHL) Mosaic Mutation Detection and Development of Confirmation Methods

Genetic biomarkers of life-threatening pheochromocytoma-induced cardiomyopathy

MEN1 and the brain: Don’t just look only at the pituitary gland. A case report of anaplastic pleomorphic xanthoastrocytoma in a MEN1 patient, and systematic review

Local-regional recurrence of sporadic or syndromic abdominal extra-adrenal paraganglioma: Incidence, characteristics, and outcome

Should the GCM2 gene be tested when screening for familial primary hyperparathyroidism?

Phakomatoses and Endocrine Gland Tumors: Noteworthy and (Not so) Rare Associations

Long-term results of less than total parathyroidectomy for hyperparathyroidism in multiple endocrine neoplasia type 1

The Succinate Dehydrogenase Genetic Testing in a Large Prospective Series of Patients with Paragangliomas

Pheochromocytomas and paragangliomas in pregnancy: About four cases and key messages on management

Prospective Endoscopic Ultrasonographic Evaluation of the Frequency of Nonfunctioning Pancreaticoduodenal Endocrine Tumors in Patients with Multiple Endocrine Neoplasia Type 1

Hypoparathyroidism and pregnancy

Long-term Follow-up of MEN1 Patients Who Do Not Have Initial Surgery for Small ≤2 cm Nonfunctioning Pancreatic Neuroendocrine Tumors, an AFCE and GTE Study

Long-term Follow-up of MEN1 Patients Who Do Not Have Initial Surgery for Small ≤2 cm Nonfunctioning Pancreatic Neuroendocrine Tumors, an AFCE and GTE Study: Association Francophone de Chirurgie Endocrinienne & Groupe d’Etude des Tumeurs Endocrines

Evaluation of denaturing high performance liquid chromatography for the mutational analysis of the MEN1 gene

Metastatic Potential and Survival of Duodenal and Pancreatic Tumors in Multiple Endocrine Neoplasia Type 1: A GTE and AFCE Cohort Study (Groupe d'étude des Tumeurs Endocrines and Association Francophone de Chirurgie Endocrinienne)

A Full Phenotype of Paraganglioma Linked to a Germline SDHB Mosaic Mutation

Serum succinate/fumarate ratio in paraganglioma/pheochromocytoma patients attending an endocrine oncogenetic unit

Serum Succinate/Fumarate Ratio in Patients With Paraganglioma/Pheochromocytoma Attending an Endocrine Oncogenetic Unit

Serum fatty acid profiling in patients with SDHx mutations: New advances on cellular metabolism in SDH deficiency

Genetic predisposition to pheochromocytoma and paraganglioma: 21 years of experience in the field

Frequency and Incidence of Carney Complex Manifestations: A Prospective Multicenter Study With a Three-Year Follow-Up

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