Loirat C - Search Results

1

Ten candidate ADAMTS13 mutations in six French families with congenital thrombotic thrombocytopenic purpura (Upshaw-Schulman syndrome).

Veyradier A, Lavergne JM, Ribba AS, Obert B, Loirat C, Meyer D, Girma JP. Veyradier A, et al. Among authors: loirat c. J Thromb Haemost. 2004 Mar;2(3):424-9. doi: 10.1111/j.1538-7933.2004.00623.x. J Thromb Haemost. 2004. PMID: 15009458 Free article.

2

Desmopressin, an unexpected link between nocturnal enuresis and inherited thrombotic thrombocytopenic purpura (Upshaw-Schulman syndrome).

Veyradier A, Meyer D, Loirat C. Veyradier A, et al. Among authors: loirat c. J Thromb Haemost. 2006 Mar;4(3):700-1. doi: 10.1111/j.1538-7836.2005.01768.x. J Thromb Haemost. 2006. PMID: 16460464 Free article. No abstract available.

3

Thrombotic thrombocytopenic purpura related to severe ADAMTS13 deficiency in children.

Loirat C, Girma JP, Desconclois C, Coppo P, Veyradier A. Loirat C, et al. Pediatr Nephrol. 2009 Jan;24(1):19-29. doi: 10.1007/s00467-008-0863-5. Epub 2008 Jun 24. Pediatr Nephrol. 2009. PMID: 18574602 Review.

4

Thrombotic thrombocytopenic purpura in children.

Loirat C, Coppo P, Veyradier A. Loirat C, et al. Curr Opin Pediatr. 2013 Apr;25(2):216-24. doi: 10.1097/MOP.0b013e32835e7888. Curr Opin Pediatr. 2013. PMID: 23422353 Review.

5

Thrombotic thrombocytopenic purpura associated with von Willebrand factor-cleaving protease (ADAMTS13) deficiency in children.

Loirat C, Veyradier A, Girma JP, Ribba AS, Meyer D. Loirat C, et al. Semin Thromb Hemost. 2006 Mar;32(2):90-7. doi: 10.1055/s-2006-939764. Semin Thromb Hemost. 2006. PMID: 16575683 Review.

6

[Hereditary hemolytic uremic syndromes and thrombotic thrombocytopenic purpura].

Loirat C, Sellier-Leclerc AL, Frémeaux-Bacchi V, Dragon-Durey A, Girma JP, Veyradier A. Loirat C, et al. Nephrol Ther. 2006 Jan;2 Suppl 2:S149-61. Nephrol Ther. 2006. PMID: 17373216 Review. French.

7

Child-onset and adolescent-onset acquired thrombotic thrombocytopenic purpura with severe ADAMTS13 deficiency: a cohort study of the French national registry for thrombotic microangiopathy.

Joly BS, Stepanian A, Leblanc T, Hajage D, Chambost H, Harambat J, Fouyssac F, Guigonis V, Leverger G, Ulinski T, Kwon T, Loirat C, Coppo P, Veyradier A; French Reference Center for Thrombotic Microangiopathies. Joly BS, et al. Among authors: loirat c. Lancet Haematol. 2016 Nov;3(11):e537-e546. doi: 10.1016/S2352-3026(16)30125-9. Epub 2016 Oct 3. Lancet Haematol. 2016. PMID: 27720178

8

Severe deficiency of the specific von Willebrand factor-cleaving protease (ADAMTS 13) activity in a subgroup of children with atypical hemolytic uremic syndrome.

Veyradier A, Obert B, Haddad E, Cloarec S, Nivet H, Foulard M, Lesure F, Delattre P, Lakhdari M, Meyer D, Girma JP, Loirat C. Veyradier A, et al. Among authors: loirat c. J Pediatr. 2003 Mar;142(3):310-7. doi: 10.1067/mpd.2003.79. J Pediatr. 2003. PMID: 12640381

9

Residual plasmatic activity of ADAMTS13 is correlated with phenotype severity in congenital thrombotic thrombocytopenic purpura.

Lotta LA, Wu HM, Mackie IJ, Noris M, Veyradier A, Scully MA, Remuzzi G, Coppo P, Liesner R, Donadelli R, Loirat C, Gibbs RA, Horne A, Yang S, Garagiola I, Musallam KM, Peyvandi F. Lotta LA, et al. Among authors: loirat c. Blood. 2012 Jul 12;120(2):440-8. doi: 10.1182/blood-2012-01-403113. Epub 2012 Apr 23. Blood. 2012. PMID: 22529288 Free PMC article.

10

Predictive features of severe acquired ADAMTS13 deficiency in idiopathic thrombotic microangiopathies: the French TMA reference center experience.

Coppo P, Schwarzinger M, Buffet M, Wynckel A, Clabault K, Presne C, Poullin P, Malot S, Vanhille P, Azoulay E, Galicier L, Lemiale V, Mira JP, Ridel C, Rondeau E, Pourrat J, Girault S, Bordessoule D, Saheb S, Ramakers M, Hamidou M, Vernant JP, Guidet B, Wolf M, Veyradier A; French Reference Center for Thrombotic Microangiopathies. Coppo P, et al. PLoS One. 2010 Apr 23;5(4):e10208. doi: 10.1371/journal.pone.0010208. PLoS One. 2010. PMID: 20436664 Free PMC article.

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