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Items: 22

1.

Is follow-up still mandatory more than 5 years after surgery for colorectal cancer?

Frontali A, Benichou B, Valcea I, Maggiori L, Prost À la Denise J, Panis Y.

Updates Surg. 2019 Sep 12. doi: 10.1007/s13304-019-00678-5. [Epub ahead of print]

PMID:
31515690
2.

Low-dose agalsidase beta treatment in male pediatric patients with Fabry disease: A 5-year randomized controlled trial.

Ramaswami U, Bichet DG, Clarke LA, Dostalova G, Fainboim A, Fellgiebel A, Forcelini CM, An Haack K, Hopkin RJ, Mauer M, Najafian B, Scott CR, Shankar SP, Thurberg BL, Tøndel C, Tylki-Szymanska A, Bénichou B, Wijburg FA.

Mol Genet Metab. 2019 May;127(1):86-94. doi: 10.1016/j.ymgme.2019.03.010. Epub 2019 Apr 3.

3.

Liver Expression of a MiniATP7B Gene Results in Long-Term Restoration of Copper Homeostasis in a Wilson Disease Model in Mice.

Murillo O, Moreno D, Gazquez C, Barberia M, Cenzano I, Navarro I, Uriarte I, Sebastian V, Arruebo M, Ferrer V, Bénichou B, Combal JP, Prieto J, Hernandez-Alcoceba R, Gonzalez Aseguinolaza G.

Hepatology. 2019 Jul;70(1):108-126. doi: 10.1002/hep.30535. Epub 2019 Mar 20.

PMID:
30706949
4.

Laparoscopic conversion of sleeve gastrectomy to Roux-en-Y gastric bypass: indications and preliminary results.

Iannelli A, Debs T, Martini F, Benichou B, Ben Amor I, Gugenheim J.

Surg Obes Relat Dis. 2016 Sep - Oct;12(8):1533-1538. doi: 10.1016/j.soard.2016.04.008. Epub 2016 Apr 12.

PMID:
27425833
5.

Characterization of early disease status in treatment-naive male paediatric patients with Fabry disease enrolled in a randomized clinical trial.

Wijburg FA, Bénichou B, Bichet DG, Clarke LA, Dostalova G, Fainboim A, Fellgiebel A, Forcelini C, An Haack K, Hopkin RJ, Mauer M, Najafian B, Scott CR, Shankar SP, Thurberg BL, Tøndel C, Tylki-Szymańska A, Ramaswami U.

PLoS One. 2015 May 8;10(5):e0124987. doi: 10.1371/journal.pone.0124987. eCollection 2015.

6.

Effective clearance of GL-3 in a human iPSC-derived cardiomyocyte model of Fabry disease.

Itier JM, Ret G, Viale S, Sweet L, Bangari D, Caron A, Le-Gall F, Bénichou B, Leonard J, Deleuze JF, Orsini C.

J Inherit Metab Dis. 2014 Nov;37(6):1013-22. doi: 10.1007/s10545-014-9724-5. Epub 2014 May 22.

PMID:
24850378
7.

Evaluation of a low dose, after a standard therapeutic dose, of agalsidase beta during enzyme replacement therapy in patients with Fabry disease.

Lubanda JC, Anijalg E, Bzdúch V, Thurberg BL, Bénichou B, Tylki-Szymanska A.

Genet Med. 2009 Apr;11(4):256-64. doi: 10.1097/GIM.0b013e3181981d82.

PMID:
19265719
8.

A retrospective analysis of the potential impact of IgG antibodies to agalsidase beta on efficacy during enzyme replacement therapy for Fabry disease.

Bénichou B, Goyal S, Sung C, Norfleet AM, O'Brien F.

Mol Genet Metab. 2009 Jan;96(1):4-12. doi: 10.1016/j.ymgme.2008.10.004. Epub 2008 Nov 20.

PMID:
19022694
9.

Further evidence for genetic heterogeneity within type II autosomal dominant osteopetrosis.

Bénichou OD, Bénichou B, Copin H, De Vernejoul MC, Van Hul W.

J Bone Miner Res. 2000 Oct;15(10):1900-4.

10.

Clinical characteristics of a familial inherited myxomatous valvular dystrophy mapped to Xq28.

Trochu JN, Kyndt F, Schott JJ, Gueffet JP, Probst V, Bénichou B, Le Marec H.

J Am Coll Cardiol. 2000 Jun;35(7):1890-7.

11.

Osteopetrosis as a model for studying bone resorption.

Bénichou OD, Bénichou B, de Vernejoul MC.

Rev Rhum Engl Ed. 1998 Dec;65(12):778-87. Review. No abstract available.

PMID:
9923047
12.

Rapid diagnostic test for detection of Cys282Tyr mutation in hereditary hemochromatosis.

Andre MT, Jacquemont S, Renault S, Airaud F, Herbert O, Moisan JP, Benichou B, Raguenes O.

Dig Dis Sci. 1998 Jun;43(6):1339-40. No abstract available.

PMID:
9635628
13.

Mapping of X-linked myxomatous valvular dystrophy to chromosome Xq28.

Kyndt F, Schott JJ, Trochu JN, Baranger F, Herbert O, Scott V, Fressinaud E, David A, Moisan JP, Bouhour JB, Le Marec H, Bénichou B.

Am J Hum Genet. 1998 Mar;62(3):627-32.

14.

Possible misdiagnosis of factor VIII gene inversion in a case of severe hemophilia A.

Bénichou B, Herbert O, Huet S, André MT, Bézieau S, Le Roux MG, Fiks-Siguad M, Moisan JP.

Blood. 1996 Apr 15;87(8):3525-6. No abstract available.

PMID:
8605378
15.

Study on possible increase in twinning rate at a small village in south Brazil.

Matte U, Le Roux MG, Bénichou B, Moisan JP, Giugliani R.

Acta Genet Med Gemellol (Roma). 1996;45(4):431-7.

PMID:
9181177
16.

Identification and characterization of a spinal muscular atrophy-determining gene.

Lefebvre S, Bürglen L, Reboullet S, Clermont O, Burlet P, Viollet L, Benichou B, Cruaud C, Millasseau P, Zeviani M, et al.

Cell. 1995 Jan 13;80(1):155-65.

17.

Large deletion of the peroxisomal acyl-CoA oxidase gene in pseudoneonatal adrenoleukodystrophy.

Fournier B, Saudubray JM, Benichou B, Lyonnet S, Munnich A, Clevers H, Poll-The BT.

J Clin Invest. 1994 Aug;94(2):526-31.

18.

De novo and inherited deletions of the 5q13 region in spinal muscular atrophies.

Melki J, Lefebvre S, Burglen L, Burlet P, Clermont O, Millasseau P, Reboullet S, Bénichou B, Zeviani M, Le Paslier D, et al.

Science. 1994 Jun 3;264(5164):1474-7.

PMID:
7910982
19.

[Physical study of big fragments and search strategy of genes. Application to locus of infant spinal muscular atrophies].

Melki J, Lefebvre S, Burglen L, Burlet P, Clermont O, Millasseau P, Reboulet S, Benichou B, Zeviani M, Le Paslier D, et al.

C R Seances Soc Biol Fil. 1994;188(5-6):495-8. Review. French.

PMID:
7780792
20.

[Emergency actions].

Benichou B.

Rev Odontostomatol (Paris). 1991 Sep-Oct;20(5):421-9. French.

PMID:
1811309
21.

Mutations in the D strand of the human CD4 V1 domain affect CD4 interactions with the human immunodeficiency virus envelope glycoprotein gp120 and HLA class II antigens similarly.

Piatier-Tonneau D, Gastinel LN, Moussy G, Bénichou B, Amblard F, Vaigot P, Auffray C.

Proc Natl Acad Sci U S A. 1991 Aug 1;88(15):6858-62.

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