Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 16

1.

Novel ACTN1 variants in cases of thrombocytopenia.

Vincenot A, Saultier P, Kunishima S, Poggi M, Hurtaud-Roux MF, Roussel A; ACTN1 study co-investigators, Schlegel N, Alessi MC.

Hum Mutat. 2019 Jun 25. doi: 10.1002/humu.23840. [Epub ahead of print]

PMID:
31237726
2.

ANKRD26 normocytic thrombocytopenia: a family report.

Vincenot A, Hurtaud-Roux MF, René O, Binard S, Fenneteau O, Schlegel N.

Ann Biol Clin (Paris). 2016 Jun 1;74(3):317-22. doi: 10.1684/abc.2016.1142.

3.

Mutation spectrum and genotype-phenotype correlations in a large French cohort of MYH9-Related Disorders.

Saposnik B, Binard S, Fenneteau O, Nurden A, Nurden P, Hurtaud-Roux MF, Schlegel N; French MYH9 networka.

Mol Genet Genomic Med. 2014 Jul;2(4):297-312. doi: 10.1002/mgg3.68. Epub 2014 Feb 7.

4.

Spectrum of the mutations in Bernard-Soulier syndrome.

Savoia A, Kunishima S, De Rocco D, Zieger B, Rand ML, Pujol-Moix N, Caliskan U, Tokgoz H, Pecci A, Noris P, Srivastava A, Ward C, Morel-Kopp MC, Alessi MC, Bellucci S, Beurrier P, de Maistre E, Favier R, Hézard N, Hurtaud-Roux MF, Latger-Cannard V, Lavenu-Bombled C, Proulle V, Meunier S, Négrier C, Nurden A, Randrianaivo H, Fabris F, Platokouki H, Rosenberg N, HadjKacem B, Heller PG, Karimi M, Balduini CL, Pastore A, Lanza F.

Hum Mutat. 2014 Sep;35(9):1033-45. doi: 10.1002/humu.22607. Epub 2014 Jul 15. Review.

PMID:
24934643
5.

Analysis of 339 pregnancies in 181 women with 13 different forms of inherited thrombocytopenia.

Noris P, Schlegel N, Klersy C, Heller PG, Civaschi E, Pujol-Moix N, Fabris F, Favier R, Gresele P, Latger-Cannard V, Cuker A, Nurden P, Greinacher A, Cattaneo M, De Candia E, Pecci A, Hurtaud-Roux MF, Glembotsky AC, Muñiz-Diaz E, Randi ML, Trillot N, Bury L, Lecompte T, Marconi C, Savoia A, Balduini CL, Bayart S, Bauters A, Benabdallah-Guedira S, Boehlen F, Borg JY, Bottega R, Bussel J, De Rocco D, de Maistre E, Faleschini M, Falcinelli E, Ferrari S, Ferster A, Fierro T, Fleury D, Fontana P, James C, Lanza F, Le Cam Duchez V, Loffredo G, Magini P, Martin-Coignard D, Menard F, Mercier S, Mezzasoma A, Minuz P, Nichele I, Notarangelo LD, Pippucci T, Podda GM, Pouymayou C, Rigouzzo A, Royer B, Sie P, Siguret V, Trichet C, Tucci A, Saposnik B, Veneri D; European Hematology Association – Scientific Working Group on Thrombocytopenias and Platelet Function Disorders.

Haematologica. 2014 Aug;99(8):1387-94. doi: 10.3324/haematol.2014.105924. Epub 2014 Apr 24.

6.

[Usefulness of gray platelets observation in ARC syndrome].

Benet B, Lainey E, Fenneteau O, Baudouin V, Hurtaud-Roux MF.

Ann Biol Clin (Paris). 2010 Jul-Aug;68(4):485-9. doi: 10.1684/abc.2010.0453. French.

7.

[Neonatal renal venous thrombosis in 2008].

Dauger S, Michot C, Garnier A, Hurtaud-Roux MF.

Arch Pediatr. 2009 Feb;16(2):132-41. doi: 10.1016/j.arcped.2008.11.014. Epub 2009 Jan 15. Review. French.

PMID:
19150233
8.

Acute renal cortical necrosis due to acquired antiprotein S antibodies.

Larakeb AS, Evrard S, Louillet F, Kwon T, Djaffar H, Llanas B, Deschênes G, Hurtaud-Roux MF, Baudouin V.

Pediatr Nephrol. 2009 Jan;24(1):207-9. doi: 10.1007/s00467-008-0967-y. Epub 2008 Sep 6.

PMID:
18777044
9.

The decrease of fibrinogen is an early predictor of the severity of postpartum hemorrhage.

Charbit B, Mandelbrot L, Samain E, Baron G, Haddaoui B, Keita H, Sibony O, Mahieu-Caputo D, Hurtaud-Roux MF, Huisse MG, Denninger MH, de Prost D; PPH Study Group.

J Thromb Haemost. 2007 Feb;5(2):266-73. Epub 2006 Nov 6.

10.

[Normal and abnormal cytological aspects of peripheral blood cells in neonates and young children].

Fenneteau O, Hurtaud-Roux MF, Schlegel N.

Ann Biol Clin (Paris). 2006 Jan-Feb;64(1):17-36. Review. French.

11.

Biochemical markers of neonatal sepsis: value of procalcitonin in the emergency setting.

Guibourdenche J, Bedu A, Petzold L, Marchand M, Mariani-Kurdjian P, Hurtaud-Roux MF, Aujard Y, Porquet D.

Ann Clin Biochem. 2002 Mar;39(Pt 2):130-5.

PMID:
11928760
12.

Effect of individual plasma lipoprotein(a) variations in vivo on its competition with plasminogen for fibrin and cell binding: An in vitro study using plasma from children with idiopathic nephrotic syndrome.

Soulat T, Loyau S, Baudouin V, Maisonneuve L, Hurtaud-Roux MF, Schlegel N, Loirat C, Anglés-Cano E.

Arterioscler Thromb Vasc Biol. 2000 Feb;20(2):575-84.

PMID:
10669658
13.

Recombinant tissue-type plasminogen activator therapy of thrombosis in 16 neonates.

Farnoux C, Camard O, Pinquier D, Hurtaud-Roux MF, Sebag G, Schlegel N, Beaufils F.

J Pediatr. 1998 Jul;133(1):137-40.

PMID:
9672527
14.

[Breast-feeding is possible in case of maternal treatment with enoxaparin].

Guillonneau M, de Crepy A, Aufrant C, Hurtaud-Roux MF, Jacqz-Aigrain E.

Arch Pediatr. 1996 May;3(5):513-4. French. No abstract available.

PMID:
8763733
15.

The molecular genetic basis of Glanzmann's thrombasthenia in a gypsy population in France: identification of a new mutation on the alpha IIb gene.

Schlegel N, Gayet O, Morel-Kopp MC, Wyler B, Hurtaud-Roux MF, Kaplan C, Mc Gregor J.

Blood. 1995 Aug 1;86(3):977-82.

PMID:
7620188
16.

[Characteristics of the fibrinolytic system in the newborn].

Schlegel N, Hurtaud-Roux MF, Beaufils F.

Ann Pediatr (Paris). 1993 Feb;40(2):70-4. Review. French.

PMID:
8457135

Supplemental Content

Loading ...
Support Center