Laurence Bendelac
Overview
Explore the profile of Laurence Bendelac including associated specialties, affiliations and a list of published articles.
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Articles
4
Citations
64
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Recent Articles
1.
Kiger L, Oliveira L, Guitton C, Bendelac L, Ghazal K, Proulle V, et al.
Blood Adv
. 2021 Feb;
5(1):84-88.
PMID: 33570625
No abstract available.
2.
Picard V, Guitton C, Mansour-Hendili L, Jondeau B, Bendelac L, Denguir M, et al.
Front Physiol
. 2021 Feb;
11:602109.
PMID: 33519508
Gardos channelopathy (Gardos-HX) or type 2 stomatocytosis/xerocytosis is a hereditary hemolytic anemia due to mutations in the gene. It is rarer than inherited type 1 xerocytosis due to mutations (Piezo1-HX)...
3.
Picard V, Guitton C, Thuret I, Rose C, Bendelac L, Ghazal K, et al.
Haematologica
. 2019 Jan;
104(8):1554-1564.
PMID: 30655378
We describe the clinical, hematologic and genetic characteristics of a retrospective series of 126 subjects from 64 families with hereditary xerocytosis. Twelve patients from six families carried a mutation, five...
4.
Guillet B, Lambert T, dOiron R, Proulle V, Plantier J, Rafowicz A, et al.
Hum Mutat
. 2006 Jun;
27(7):676-85.
PMID: 16786531
Hemophilia A (HA) is an X-linked hereditary bleeding disorder defined by a qualitative and/or quantitative factor VIII (FVIII) deficiency. The molecular diagnosis of HA is challenging because of the high...