Béroud C - Search Results

1

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. Among authors: beroud c. J Clin Endocrinol Metab. 2019 Mar 1;104(3):753-764. doi: 10.1210/jc.2018-01170. J Clin Endocrinol Metab. 2019. PMID: 30339208

2

Central nervous system hemangioblastomas, endolymphatic sac tumors, and von Hippel-Lindau disease.

Richard S, David P, Marsot-Dupuch K, Giraud S, Béroud C, Resche F. Richard S, et al. Among authors: beroud c. Neurosurg Rev. 2000 Mar;23(1):1-22; discussion 23-4. doi: 10.1007/s101430050024. Neurosurg Rev. 2000. PMID: 10809480 Review.

3

Germline mutation profile of MEN1 in multiple endocrine neoplasia type 1: search for correlation between phenotype and the functional domains of the MEN1 protein.

Wautot V, Vercherat C, Lespinasse J, Chambe B, Lenoir GM, Zhang CX, Porchet N, Cordier M, Béroud C, Calender A. Wautot V, et al. Among authors: beroud c. Hum Mutat. 2002 Jul;20(1):35-47. doi: 10.1002/humu.10092. Hum Mutat. 2002. PMID: 12112656

4

Retinal hemangioblastoma in von Hippel-Lindau disease: a clinical and molecular study.

Dollfus H, Massin P, Taupin P, Nemeth C, Amara S, Giraud S, Béroud C, Dureau P, Gaudric A, Landais P, Richard S. Dollfus H, et al. Among authors: beroud c. Invest Ophthalmol Vis Sci. 2002 Sep;43(9):3067-74. Invest Ophthalmol Vis Sci. 2002. PMID: 12202531

5

Genotype-phenotype correlation in von Hippel-Lindau families with renal lesions.

Gallou C, Chauveau D, Richard S, Joly D, Giraud S, Olschwang S, Martin N, Saquet C, Chrétien Y, Méjean A, Correas JM, Benoît G, Colombeau P, Grünfeld JP, Junien C, Béroud C. Gallou C, et al. Among authors: beroud c. Hum Mutat. 2004 Sep;24(3):215-24. doi: 10.1002/humu.20082. Hum Mutat. 2004. PMID: 15300849

6

The UMD TP53 database and website: update and revisions.

Hamroun D, Kato S, Ishioka C, Claustres M, Béroud C, Soussi T. Hamroun D, et al. Among authors: beroud c. Hum Mutat. 2006 Jan;27(1):14-20. doi: 10.1002/humu.20269. Hum Mutat. 2006. PMID: 16278824

7

A new locus-specific database (LSDB) for mutations in the TGFBR2 gene: UMD-TGFBR2.

Frederic MY, Hamroun D, Faivre L, Boileau C, Jondeau G, Claustres M, Béroud C, Collod-Béroud G. Frederic MY, et al. Among authors: beroud c. Hum Mutat. 2008 Jan;29(1):33-8. doi: 10.1002/humu.20602. Hum Mutat. 2008. PMID: 17935258 Free article.

8

UMD-CFTR: a database dedicated to CF and CFTR-related disorders.

Bareil C, Thèze C, Béroud C, Hamroun D, Guittard C, René C, Paulet D, Georges Md, Claustres M. Bareil C, et al. Among authors: beroud c. Hum Mutat. 2010 Sep;31(9):1011-9. doi: 10.1002/humu.21316. Hum Mutat. 2010. PMID: 20607857

9

DYT6 dystonia: review of the literature and creation of the UMD Locus-Specific Database (LSDB) for mutations in the THAP1 gene.

Blanchard A, Ea V, Roubertie A, Martin M, Coquart C, Claustres M, Béroud C, Collod-Béroud G. Blanchard A, et al. Among authors: beroud c. Hum Mutat. 2011 Nov;32(11):1213-24. doi: 10.1002/humu.21564. Epub 2011 Sep 15. Hum Mutat. 2011. PMID: 21793105 Free article. Review.

10

UMD-DYSF, a novel locus specific database for the compilation and interactive analysis of mutations in the dysferlin gene.

Blandin G, Beroud C, Labelle V, Nguyen K, Wein N, Hamroun D, Williams B, Monnier N, Rufibach LE, Urtizberea JA, Cau P, Bartoli M, Lévy N, Krahn M. Blandin G, et al. Among authors: beroud c. Hum Mutat. 2012 Mar;33(3):E2317-31. doi: 10.1002/humu.22015. Epub 2011 Dec 29. Hum Mutat. 2012. PMID: 22213072

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