Picard V - Search Results

1

Galaxy Is a Suitable Bioinformatics Platform for the Molecular Diagnosis of Human Genetic Disorders Using High-Throughput Sequencing Data Analysis: Five Years of Experience in a Clinical Laboratory.

Chappell K, Francou B, Habib C, Huby T, Leoni M, Cottin A, Nadal F, Adnet E, Paoli E, Oliveira C, Verstuyft C, Davit-Spraul A, Gaignard P, Lebigot E, Duclos-Vallee JC, Young J, Kamenicky P, Adams D, Echaniz-Laguna A, Gonzales E, Bouvattier C, Linglart A, Picard V, Bergoin E, Jacquemin E, Guiochon-Mantel A, Proust A, Bouligand J. Chappell K, et al. Among authors: picard v. Clin Chem. 2022 Feb 1;68(2):313-321. doi: 10.1093/clinchem/hvab220. Clin Chem. 2022. PMID: 34871369

2

PIEZO1-gene gain-of-function mutations with lower limb lymphedema onset in an adult: Clinical, scintigraphic, and noncontrast magnetic resonance lymphography findings.

Vignes S, Kaltenbach S, Garçon L, Arrivé L, Asnafi V, Guitton C, Bouligand J, Delarue A, Picard V. Vignes S, et al. Among authors: picard v. Am J Med Genet A. 2022 Jan;188(1):243-248. doi: 10.1002/ajmg.a.62476. Epub 2021 Sep 3. Am J Med Genet A. 2022. PMID: 34477311

3

Homozygous Southeast Asian ovalocytosis is a severe dyserythropoietic anemia associated with distal renal tubular acidosis.

Picard V, Proust A, Eveillard M, Flatt JF, Couec ML, Caillaux G, Fénéant-Thibault M, Finkelstein A, Raphaël M, Delaunay J, Bruce LJ, Pissard S, Thomas C. Picard V, et al. Blood. 2014 Mar 20;123(12):1963-5. doi: 10.1182/blood-2014-01-548149. Blood. 2014. PMID: 24652967 Free article. No abstract available.

4

Exome sequencing for diagnosis of congenital hemolytic anemia.

Mansour-Hendili L, Aissat A, Badaoui B, Sakka M, Gameiro C, Ortonne V, Wagner-Ballon O, Pissard S, Picard V, Ghazal K, Bahuau M, Guitton C, Mansour Z, Duplan M, Petit A, Costedoat-Chalumeau N, Michel M, Bartolucci P, Moutereau S, Funalot B, Galactéros F. Mansour-Hendili L, et al. Among authors: picard v. Orphanet J Rare Dis. 2020 Jul 8;15(1):180. doi: 10.1186/s13023-020-01425-5. Orphanet J Rare Dis. 2020. PMID: 32641076 Free PMC article.

5

Topology of the stable serpin-protease complexes revealed by an autoantibody that fails to react with the monomeric conformers of antithrombin.

Picard V, Marque PE, Paolucci F, Aiach M, Le Bonniec BF. Picard V, et al. J Biol Chem. 1999 Feb 19;274(8):4586-93. doi: 10.1074/jbc.274.8.4586. J Biol Chem. 1999. PMID: 9988693 Free article.

6

Recurrent mutation in the PIEZO1 gene in two families of hereditary xerocytosis with fetal hydrops.

Beneteau C, Thierry G, Blesson S, Le Vaillant C, Picard V, Béné MC, Eveillard M, Le Caignec C. Beneteau C, et al. Among authors: picard v. Clin Genet. 2014 Mar;85(3):293-5. doi: 10.1111/cge.12147. Epub 2013 Apr 14. Clin Genet. 2014. PMID: 23581886 No abstract available.

7

Infantile pyknocytosis, a rare cause of hemolytic anemia in newborns: report of two cases in twin girls and literature overview.

El Nabouch M, Rakotoharinandrasana I, Ndayikeza A, Picard V, Kayemba-Kay's S. El Nabouch M, et al. Among authors: picard v. Clin Case Rep. 2015 Jul;3(7):535-8. doi: 10.1002/ccr3.288. Epub 2015 May 8. Clin Case Rep. 2015. PMID: 26273436 Free PMC article.

8

A Gardos channelopathy associated with nonimmune hydrops and fetal loss.

Ghesh L, Besnard T, Joubert M, Picard V, Le Vaillant C, Beneteau C. Ghesh L, et al. Among authors: picard v. Clin Genet. 2022 Dec;102(6):543-547. doi: 10.1111/cge.14217. Epub 2022 Sep 13. Clin Genet. 2022. PMID: 36031591

9

Primary red cell hydration disorders: Pathogenesis and diagnosis.

Caulier A, Rapetti-Mauss R, Guizouarn H, Picard V, Garçon L, Badens C. Caulier A, et al. Among authors: picard v. Int J Lab Hematol. 2018 May;40 Suppl 1:68-73. doi: 10.1111/ijlh.12820. Int J Lab Hematol. 2018. PMID: 29741259 Review.

10

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. Front Physiol. 2021 Jan 14;11:602109. doi: 10.3389/fphys.2020.602109. eCollection 2020. Front Physiol. 2021. PMID: 33519508 Free PMC article.

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