Proulle V - Search Results

1

Piezo1-xerocytosis red cell metabolome shows impaired glycolysis and increased hemoglobin oxygen affinity.

Kiger L, Oliveira L, Guitton C, Bendélac L, Ghazal K, Proulle V, Galacteros F, Junot C, Fenaille F, Roméo PH, Garçon L, Picard V. Kiger L, et al. Among authors: proulle v. Blood Adv. 2021 Jan 12;5(1):84-88. doi: 10.1182/bloodadvances.2020003028. Blood Adv. 2021. PMID: 33570625 Free PMC article. No abstract available.

2

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. Picard V, et al. Among authors: proulle v. Haematologica. 2019 Aug;104(8):1554-1564. doi: 10.3324/haematol.2018.205328. Epub 2019 Jan 17. Haematologica. 2019. PMID: 30655378 Free PMC article.

3

Rapid Gardos Hereditary Xerocytosis Diagnosis in 8 Families Using Reticulocyte Indices.

Picard V, Guitton C, Mansour-Hendili L, Jondeau B, Bendélac L, Denguir M, Demagny J, Proulle V, Galactéros F, Garçon L. Picard V, et al. Among authors: proulle v. Front Physiol. 2021 Jan 14;11:602109. doi: 10.3389/fphys.2020.602109. eCollection 2020. Front Physiol. 2021. PMID: 33519508 Free PMC article.

4

Red blood cell Gardos channel (KCNN4): the essential determinant of erythrocyte dehydration in hereditary xerocytosis.

Rapetti-Mauss R, Picard V, Guitton C, Ghazal K, Proulle V, Badens C, Soriani O, Garçon L, Guizouarn H. Rapetti-Mauss R, et al. Among authors: proulle v. Haematologica. 2017 Oct;102(10):e415-e418. doi: 10.3324/haematol.2017.171389. Epub 2017 Jun 15. Haematologica. 2017. PMID: 28619848 Free PMC article. No abstract available.

5

A thrombopoietin receptor agonist to rescue an unusual platelet transfusion-induced reaction in a p.V1316M-associated von Willebrand disease type 2B patient.

Casari C, Favier R, Legendre P, Kauskot A, Adam F, Picard V, Lenting PT, Denis CV, Proulle V. Casari C, et al. Among authors: proulle v. Ther Adv Hematol. 2022 Feb 16;13:20406207221076812. doi: 10.1177/20406207221076812. eCollection 2022. Ther Adv Hematol. 2022. PMID: 35186246 Free PMC article.

6

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. Guillet B, et al. Among authors: proulle v. Hum Mutat. 2006 Jul;27(7):676-85. doi: 10.1002/humu.20345. Hum Mutat. 2006. PMID: 16786531

7

Intracerebral hemorrhage associated with a novel antithrombin gene mutation in a neonate.

Baud O, Picard V, Durand P, Duchemin J, Proulle V, Alhenc-Gelas M, Devictor D, Dreyfus M. Baud O, et al. Among authors: proulle v. J Pediatr. 2001 Nov;139(5):741-3. doi: 10.1067/mpd.2001.118191. J Pediatr. 2001. PMID: 11713457

8

A factor VIII-nanobody fusion protein forming an ultrastable complex with VWF: effect on clearance and antibody formation.

Muczynski V, Casari C, Moreau F, Aymé G, Kawecki C, Legendre P, Proulle V, Christophe OD, Denis CV, Lenting PJ. Muczynski V, et al. Among authors: proulle v. Blood. 2018 Sep 13;132(11):1193-1197. doi: 10.1182/blood-2018-01-829523. Epub 2018 Jul 31. Blood. 2018. PMID: 30064978 Free article.

9

A three amino acid deletion in glycoprotein IIIa is responsible for type I Glanzmann's thrombasthenia: importance of residues Ile325Pro326Gly327 for beta3 integrin subunit association.

Morel-Kopp MC, Kaplan C, Proulle V, Jallu V, Melchior C, Peyruchaud O, Aurousseau MH, Kieffer N. Morel-Kopp MC, et al. Among authors: proulle v. Blood. 1997 Jul 15;90(2):669-77. Blood. 1997. PMID: 9226167 Free article.

10

LIM kinase/cofilin dysregulation promotes macrothrombocytopenia in severe von Willebrand disease-type 2B.

Kauskot A, Poirault-Chassac S, Adam F, Muczynski V, Aymé G, Casari C, Bordet JC, Soukaseum C, Rothschild C, Proulle V, Pietrzyk-Nivau A, Berrou E, Christophe OD, Rosa JP, Lenting PJ, Bryckaert M, Denis CV, Baruch D. Kauskot A, et al. Among authors: proulle v. JCI Insight. 2016 Oct 6;1(16):e88643. doi: 10.1172/jci.insight.88643. JCI Insight. 2016. PMID: 27734030 Free PMC article.

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