Romanet P - Search Results

1

Genetic testing in prolactinomas: a cohort study.

Boukerrouni A, Cuny T, Anjou T, Raingeard I, Ferrière A, Grunenwald S, Maïza JC, Marquant E, Sahakian N, Fodil-Cherif S, Salle L, Niccoli P, Randrianaivo H, Sonnet E, Chevalier N, Thuillier P, Vezzosi D, Reynaud R, Dufour H, Brue T, Tabarin A, Delemer B, Kerlan V, Castinetti F, Barlier A, Romanet P. Boukerrouni A, et al. Among authors: romanet p. Eur J Endocrinol. 2023 Dec 6;189(6):567-574. doi: 10.1093/ejendo/lvad148. Eur J Endocrinol. 2023. PMID: 37956455

2

Case report of GNAS epigenetic defect revealed by a congenital hypothyroidism.

Romanet P, Osei L, Netchine I, Pertuit M, Enjalbert A, Reynaud R, Barlier A. Romanet P, et al. Pediatrics. 2015 Apr;135(4):e1079-83. doi: 10.1542/peds.2014-2806. Pediatrics. 2015. PMID: 25802348

3

Pathological and Genetic Characterization of Bilateral Adrenomedullary Hyperplasia in a Patient with Germline MAX Mutation.

Romanet P, Guerin C, Pedini P, Essamet W, Castinetti F, Sebag F, Roche P, Cascon A, Tischler AS, Pacak K, Barlier A, Taïeb D. Romanet P, et al. Endocr Pathol. 2017 Dec;28(4):302-307. doi: 10.1007/s12022-016-9460-5. Endocr Pathol. 2017. PMID: 27838885 Free PMC article.

4

Implications of SDHB genetic testing in patients with sporadic pheochromocytoma.

Maignan A, Guerin C, Julliard V, Paladino NC, Kim E, Roche P, Castinetti F, Essamet W, Mancini J, Imperiale A, Clifton-Bligh R, Romanet P, Barlier A, Pacak K, Sebag F, Taïeb D. Maignan A, et al. Among authors: romanet p. Langenbecks Arch Surg. 2017 Aug;402(5):787-798. doi: 10.1007/s00423-017-1564-y. Epub 2017 Feb 22. Langenbecks Arch Surg. 2017. PMID: 28229225 Free PMC article.

5

Looking beyond the thyroid: advances in the understanding of pheochromocytoma and hyperparathyroidism phenotypes in MEN2 and of non-MEN2 familial forms.

Guerin C, Romanet P, Taieb D, Brue T, Lacroix A, Sebag F, Barlier A, Castinetti F. Guerin C, et al. Among authors: romanet p. Endocr Relat Cancer. 2018 Feb;25(2):T15-T28. doi: 10.1530/ERC-17-0266. Epub 2017 Sep 5. Endocr Relat Cancer. 2018. PMID: 28874394 Review.

6

Quantitative ¹⁸F-DOPA PET/CT in pheochromocytoma: the relationship between tumor secretion and its biochemical phenotype.

Amodru V, Guerin C, Delcourt S, Romanet P, Loundou A, Viana B, Brue T, Castinetti F, Sebag F, Pacak K, Taïeb D. Amodru V, et al. Among authors: romanet p. Eur J Nucl Med Mol Imaging. 2018 Feb;45(2):278-282. doi: 10.1007/s00259-017-3833-y. Epub 2017 Sep 16. Eur J Nucl Med Mol Imaging. 2018. PMID: 28918451 Free PMC article.

7

18F-FDOPA PET/CT Imaging of MAX-Related Pheochromocytoma.

Taïeb D, Jha A, Guerin C, Pang Y, Adams KT, Chen CC, Romanet P, Roche P, Essamet W, Ling A, Quezado MM, Castinetti F, Sebag F, Pacak K. Taïeb D, et al. Among authors: romanet p. J Clin Endocrinol Metab. 2018 Apr 1;103(4):1574-1582. doi: 10.1210/jc.2017-02324. J Clin Endocrinol Metab. 2018. PMID: 29534198 Free PMC article.

8

Functioning Mediastinal Paraganglioma Associated with a Germline Mutation of von Hippel-Lindau Gene.

Bahougne T, Romanet P, Mohamed A, Caselles K, Cuny T, Barlier A, Niccoli P. Bahougne T, et al. Among authors: romanet p. J Clin Med. 2018 May 23;7(6):116. doi: 10.3390/jcm7060116. J Clin Med. 2018. PMID: 29789510 Free PMC article.

9

Heterozygous LHX3 mutations may lead to a mild phenotype of combined pituitary hormone deficiency.

Jullien N, Romanet P, Philippon M, Quentien MH, Beck-Peccoz P, Bergada I, Odent S, Reynaud R, Barlier A, Saveanu A, Brue T, Castinetti F. Jullien N, et al. Among authors: romanet p. Eur J Hum Genet. 2019 Feb;27(2):216-225. doi: 10.1038/s41431-018-0264-6. Epub 2018 Sep 27. Eur J Hum Genet. 2019. PMID: 30262920 Free PMC article.

10

UMD-MEN1 Database: An Overview of the 370 MEN1 Variants Present in 1676 Patients From the French Population.

Romanet P, Mohamed A, Giraud S, Odou MF, North MO, Pertuit M, Pasmant E, Coppin L, Guien C, Calender A, Borson-Chazot F, Béroud C, Goudet P, Barlier A. Romanet P, et al. J Clin Endocrinol Metab. 2019 Mar 1;104(3):753-764. doi: 10.1210/jc.2018-01170. J Clin Endocrinol Metab. 2019. PMID: 30339208

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