Giraud S - Search Results

1

Stroke following pulmonary arteriovenous fistula embolization in a patient with HHT.

Felix S, Jeannin S, Goizet C, Thambo JB, Giraud S, Plauchu H, Montaudon M, Sibon I. Felix S, et al. Among authors: giraud s. Neurology. 2008 Dec 9;71(24):2012-4. doi: 10.1212/01.wnl.0000336973.27761.45. Neurology. 2008. PMID: 19064885 No abstract available.

2

Phenotype variability of two FAP families with an identical APC germline mutation at codon 1465: a potential modifier effect?

Martin-Denavit T, Duthel S, Giraud S, Olschwang S, Saurin JC, Plauchu H. Martin-Denavit T, et al. Among authors: giraud s. Clin Genet. 2001 Aug;60(2):125-31. doi: 10.1034/j.1399-0004.2001.600206.x. Clin Genet. 2001. PMID: 11553046

3

[Neurosarcoma associated with neurofibromatosis 1. Apropos of a case and review of the literature].

Ligneau B, Freyer G, Giraud S, Isaac S, Bombaron P, Espinouse D, Plauchu H, Fischer G, Gérard JP, Lenoir G, Trillet-Lenoir V. Ligneau B, et al. Among authors: giraud s. Presse Med. 1997 Mar 29;26(10):458-63. Presse Med. 1997. PMID: 9137367 Review. French.

4

[Ethical recommendations for the genetic screening of hereditary endocrine diseases].

Calender A, Giraud S, Guichard-Rode S. Calender A, et al. Among authors: giraud s. Ann Endocrinol (Paris). 1997;58(4):343-8. Ann Endocrinol (Paris). 1997. PMID: 9436486 French.

5

[Clinicogenetic study of MEN1: recent physiopathological data and clinical applications. Study Group of Multiple Endocrine Neoplasia (GENEM)].

Calender A, Giraud S, Porchet N, Gaudray P, Cadiot G, Mignon M. Calender A, et al. Among authors: giraud s. Ann Endocrinol (Paris). 1998;59(6):444-51. Ann Endocrinol (Paris). 1998. PMID: 10189986 Review. French.

6

Screening of mutations in genes that predispose to hereditary paragangliomas and pheochromocytomas.

Lefebvre S, Borson-Chazot F, Boutry-Kryza N, Wion N, Schillo F, Peix JL, Brunaud L, Finat A, Calender A, Giraud S. Lefebvre S, et al. Among authors: giraud s. Horm Metab Res. 2012 May;44(5):334-8. doi: 10.1055/s-0032-1306308. Epub 2012 Apr 19. Horm Metab Res. 2012. PMID: 22517554

7

Germline mutation profile of the VHL gene in von Hippel-Lindau disease and in sporadic hemangioblastoma.

Olschwang S, Richard S, Boisson C, Giraud S, Laurent-Puig P, Resche F, Thomas G. Olschwang S, et al. Among authors: giraud s. Hum Mutat. 1998;12(6):424-30. doi: 10.1002/(SICI)1098-1004(1998)12:6<424::AID-HUMU9>3.0.CO;2-H. Hum Mutat. 1998. PMID: 9829912

8

Lack of referral for genetic counseling and testing in BRCA1/2 and Lynch syndromes: a nationwide study based on 240,134 consultations and 134,652 genetic tests.

Pujol P, Lyonnet DS, Frebourg T, Blin J, Picot MC, Lasset C, Dugast C, Berthet P, de Paillerets BB, Sobol H, Grandjouan S, Soubrier F, Buecher B, Guimbaud R, Lidereau R, Jonveaux P, Houdayer C, Giraud S, Olschwang S, Nogue E, Galibert V, Bara C, Nowak F, Khayat D, Nogues C. Pujol P, et al. Among authors: giraud s. Breast Cancer Res Treat. 2013 Aug;141(1):135-44. doi: 10.1007/s10549-013-2669-9. Epub 2013 Aug 24. Breast Cancer Res Treat. 2013. PMID: 23974829

9

Unraveling the intrafamilial correlations and heritability of tumor types in MEN1: a Groupe d'étude des Tumeurs Endocrines study.

Thevenon J, Bourredjem A, Faivre L, Cardot-Bauters C, Calender A, Le Bras M, Giraud S, Niccoli P, Odou MF, Borson-Chazot F, Barlier A, Lombard-Bohas C, Clauser E, Tabarin A, Pasmant E, Chabre O, Castermans E, Ruszniewski P, Bertherat J, Delemer B, Christin-Maitre S, Beckers A, Guilhem I, Rohmer V, Goichot B, Caron P, Baudin E, Chanson P, Groussin L, Du Boullay H, Weryha G, Lecomte P, Schillo F, Bihan H, Archambeaud F, Kerlan V, Bourcigaux N, Kuhn JM, Vergès B, Rodier M, Renard M, Sadoul JL, Binquet C, Goudet P. Thevenon J, et al. Among authors: giraud s. Eur J Endocrinol. 2015 Dec;173(6):819-26. doi: 10.1530/EJE-15-0691. Epub 2015 Sep 21. Eur J Endocrinol. 2015. PMID: 26392472

10

[Von Hippel-Lindau disease: a hereditary disease that impacts multiple tissues].

Richard S, Giraud S, Hammel P, Beroud C, Joly D, Olschwang S, Resche F. Richard S, et al. Among authors: giraud s. Presse Med. 1998 Jun 20;27(22):1112-20. Presse Med. 1998. PMID: 9767816 Review. French. No abstract available.

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