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Items: 6

1.

Clinical and biological features in PIEZO1-hereditary xerocytosis and Gardos channelopathy: a retrospective series of 126 patients.

Picard V, Guitton C, Thuret I, Rose C, Bendelac L, Ghazal K, Aguilar-Martinez P, Badens C, Barro C, Bénéteau C, Berger C, Cathébras P, Deconinck E, Delaunay J, Durand JM, Firah N, Galactéros F, Godeau B, Jaïs X, de Jaureguiberry JP, Le Stradic C, Lifermann F, Maffre R, Morin G, Perrin J, Proulle V, Ruivard M, Toutain F, Lahary A, Garçon L.

Haematologica. 2019 Aug;104(8):1554-1564. doi: 10.3324/haematol.2018.205328. Epub 2019 Jan 17.

2.

Insights into retinoic acid deficiency and the induction of craniofacial malformations and microcephaly in fetal alcohol spectrum disorder.

Petrelli B, Bendelac L, Hicks GG, Fainsod A.

Genesis. 2019 Jan;57(1):e23278. doi: 10.1002/dvg.23278. Epub 2019 Jan 21. Review.

PMID:
30614633
3.

Acetaldehyde inhibits retinoic acid biosynthesis to mediate alcohol teratogenicity.

Shabtai Y, Bendelac L, Jubran H, Hirschberg J, Fainsod A.

Sci Rep. 2018 Jan 10;8(1):347. doi: 10.1038/s41598-017-18719-7.

4.

[Mild hemophilia A fortuitously discovered during Henoch-Schönlein purpura].

Joly B, d'Oiron R, Desconclois C, Bendelac L, Rafowicz A, Meyzer C, Labrune P, Veyradier A.

Arch Pediatr. 2015 Nov;22(11):1167-70. doi: 10.1016/j.arcped.2015.07.014. Epub 2015 Sep 26. French.

PMID:
26412326
5.

Detection of 95 novel mutations in coagulation factor VIII gene F8 responsible for hemophilia A: results from a single institution.

Guillet B, Lambert T, d'Oiron R, Proulle V, Plantier JL, Rafowicz A, Peynet J, Costa JM, Bendelac L, Laurian Y, Lavergne JM.

Hum Mutat. 2006 Jul;27(7):676-85.

PMID:
16786531
6.

Comparison of anti-human and anti-porcine factor VIII inhibitor levels in 63 patients with severe haemophilia A. A French Multicentric Study.

Fiks-Sigaud M, Bendelac L, Parquet A, Verroust F, Torchet MF, Berthier AM, Fressinaud E, Guerois C, Aillaud MF, Boneu B, et al.

Vox Sang. 1993;64(4):210-4.

PMID:
8517049

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