Cardot-Bauters C - Search Results

1

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

Cardot-Bauters C, Vantyghem MC, Do Cao C, Desailloud R, Joubert M, Coppin L, Odou MF, Pigny P. Cardot-Bauters C, et al. Ann Endocrinol (Paris). 2024 Jul;85(4):276-283. doi: 10.1016/j.ando.2024.05.024. Epub 2024 May 28. Ann Endocrinol (Paris). 2024. PMID: 38815921 Free article.

2

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

Bancel LP, Masso V, Dessein AF, Aubert S, Leteurtre E, Coppin L, Odou MF, Cao CD, Cardot-Bauters C, Pigny P. Bancel LP, et al. Among authors: cardot bauters c. J Clin Endocrinol Metab. 2023 Aug 18;108(9):2343-2352. doi: 10.1210/clinem/dgad109. J Clin Endocrinol Metab. 2023. PMID: 36848172

3

[Genetic diagnosis of phaeochromocytomas and paragangliomas].

Cardot-Bauters C, Ainaouï M, Coppin L, Pigny P. Cardot-Bauters C, et al. Presse Med. 2014 Apr;43(4 Pt 1):460-7. doi: 10.1016/j.lpm.2013.07.032. Epub 2014 Mar 4. Presse Med. 2014. PMID: 24612707 Review. French.

4

p.Ala541Thr variant of MEN1 gene: a non deleterious polymorphism or a pathogenic mutation?

Nozières C, Zhang CX, Buffet A, Dupasquier S, Vargas-Poussou R, Guillaud-Bataille M, Cordier-Bussat M, Ruszniewski P, Christin-Maitre S, Murat A, Groussin L, Vezzosi D, Cardot-Bauters C, Hervieu V, Joly MO, Giraud S, Odou MF, Gimenez-Roqueplo AP, Goudet P, Borson-Chazot F, Calender A; Groupe français des tumeurs endocrines (GTE). Nozières C, et al. Ann Endocrinol (Paris). 2014 Jul;75(3):133-40. doi: 10.1016/j.ando.2014.05.003. Epub 2014 Jul 2. Ann Endocrinol (Paris). 2014. PMID: 24997771

5

Genetic biomarkers of life-threatening pheochromocytoma-induced cardiomyopathy.

Amar J, Brunel J, Cardot Bauters C, Jacques V, Delmas C, Odou MF, Savagner F. Amar J, et al. Among authors: cardot bauters c. Endocr Relat Cancer. 2022 Apr 22;29(5):267-272. doi: 10.1530/ERC-21-0373. Endocr Relat Cancer. 2022. PMID: 35258481

6

Should genetic testing be performed in each patient with sporadic pheochromocytoma at presentation?

Pigny P, Cardot-Bauters C, Do Cao C, Vantyghem MC, Carnaille B, Pattou F, Caron P, Wemeau JL, Porchet N. Pigny P, et al. Eur J Endocrinol. 2009 Feb;160(2):227-31. doi: 10.1530/EJE-08-0574. Epub 2008 Nov 24. Eur J Endocrinol. 2009. PMID: 19029228

7

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

Van Slycke S, Caiazzo R, Pigny P, Cardot-Bauters C, Arnalsteen L, D'Herbomez M, Leteurtre E, Rouaix-Emery N, Ernst O, Huglo D, Vantyghem MC, Wemeau JL, Carnaille B, Pattou F. Van Slycke S, et al. Surgery. 2009 Dec;146(6):986-92. doi: 10.1016/j.surg.2009.10.055. Surgery. 2009. PMID: 19958924

8

VHL mosaicism can be detected by clinical next-generation sequencing and is not restricted to patients with a mild phenotype.

Coppin L, Grutzmacher C, Crépin M, Destailleur E, Giraud S, Cardot-Bauters C, Porchet N, Pigny P. Coppin L, et al. Eur J Hum Genet. 2014 Sep;22(9):1149-52. doi: 10.1038/ejhg.2013.279. Epub 2013 Dec 4. Eur J Hum Genet. 2014. PMID: 24301059 Free PMC article.

9

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

Cardot-Bauters C, Carnaille B, Aubert S, Crépin M, Boury S, Burnichon N, Pigny P. Cardot-Bauters C, et al. J Clin Endocrinol Metab. 2019 Aug 1;104(8):3362-3366. doi: 10.1210/jc.2019-00175. J Clin Endocrinol Metab. 2019. PMID: 31046099

10

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

Coppin L, Dufosse M, Romanet P, Giraud S, North MO, Cardot Bauters C, Borson-Chazot F, Duchesne L, Métallo M, Lovecchio T, Barlier A, Odou MF. Coppin L, et al. Eur J Endocrinol. 2020 Jan;182(1):57-65. doi: 10.1530/EJE-19-0641. Eur J Endocrinol. 2020. PMID: 31671402

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