Paquita Nurden

Paquita Nurden

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Paquita Nurden

Publications by authors named "Paquita Nurden"

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A Glanzmann thrombasthenia family associated with a TUBB1-related macrothrombocytopenia.

J Thromb Haemost 2019 Dec 29;17(12):2211-2215. Epub 2019 Sep 29.

Institut de Rhythmologie et de Modélisation Cardiaque, Hôpital Xavier Arnozan, Pessac, France.

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http://dx.doi.org/10.1111/jth.14622DOI Listing
December 2019

Is the mysterious platelet receptor GPV an unsuspected major target for platelet autoantibodies?

Haematologica 2019 06;104(6):1103-1105

Institut Hospitalo-Universitaire LIRYC, Pessac, France.

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http://dx.doi.org/10.3324/haematol.2018.214908DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6545834PMC
June 2019

Autologous fibrin scaffolds: When platelet- and plasma-derived biomolecules meet fibrin.

Biomaterials 2019 02 21;192:440-460. Epub 2018 Nov 21.

Eduardo Anitua Foundation for Biomedical Research, Vitoria, Spain; BTI-Biotechnology Institute ImasD, Vitoria, Spain; University Institute for Regenerative Medicine & Oral Implantology, UIRMI (UPV/EHU-Fundación Eduardo Anitua), Vitoria, Spain. Electronic address:

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http://dx.doi.org/10.1016/j.biomaterials.2018.11.029DOI Listing
February 2019

Management of pregnancy for a patient with the new syndromic macrothrombocytopenia, DIAPH1-related disease.

Platelets 2018 Nov 9;29(7):737-738. Epub 2018 Jul 9.

c Service de Gynécologie-Obstétrique , Hôpital Pellegrin , Bordeaux , France.

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http://dx.doi.org/10.1080/09537104.2018.1492710DOI Listing
November 2018

ADAP deficiency impairs megakaryocyte polarization with ectopic proplatelet release and causes microthrombocytopenia.

Blood 2018 08 27;132(6):635-646. Epub 2018 Jun 27.

Institute of Experimental Biomedicine-Department I, University Hospital, Würzburg, Germany.

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http://dx.doi.org/10.1182/blood-2018-01-829259DOI Listing
August 2018

Mutations of the integrin αIIb/β3 intracytoplasmic salt bridge cause macrothrombocytopenia and enlarged platelet α-granules.

Am J Hematol 2018 02 17;93(2):195-204. Epub 2017 Nov 17.

Institut Hospitalo-Universitaire de Rythmologie et de Modélisation Cardiaque, Plateforme Technologique d'Innovation Biomédicale, Hôpital Xavier Arnozan, Pessac, France.

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http://dx.doi.org/10.1002/ajh.24958DOI Listing
February 2018

High-throughput sequencing for rapid diagnosis of inherited platelet disorders: a case for a European consensus.

Haematologica 2018 01;103(1):6-8

Institut de Rythmologie et de Modélisation Cardiaque, Plateforme Technologique d'Innovation Biomédicale, Hôpital Xavier Arnozan, Pessac, France

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http://dx.doi.org/10.3324/haematol.2017.182295DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5777186PMC
January 2018

Platelet function and microparticle levels in atrial fibrillation: Changes during the acute episode.

Int J Cardiol 2017 Sep;243:216-222

IHU Liryc, Electrophysiology and Heart Modeling Institute, fondation Bordeaux Université, 33600, Pessac, France. Electronic address:

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http://dx.doi.org/10.1016/j.ijcard.2017.03.068DOI Listing
September 2017

Gain-of-Function Mutation in Filamin A Potentiates Platelet Integrin αβ Activation.

Arterioscler Thromb Vasc Biol 2017 06 20;37(6):1087-1097. Epub 2017 Apr 20.

From the INSERM UMR_S 1176, Université Paris-Sud, Université Paris-Saclay, Le Kremlin Bicêtre, France (E.B., F.A., M.L., V.P., O.I., J.-P.R., M.B.); INSERM UMR_S 1211, Université de Bordeaux, CHU Bordeaux UNIV EA 4576, Place Aurélie Raba-Léon, France (P.F., I.C., C.G.); CHU Bordeaux, Centre de Référence Anomalies du Développement Embryonnaire, Service de Génétique Médicale, Hôpital Pellegrin, Place Aurélie Raba-Léon, France (P.F., C.G.); Unité d'Hémostase Biologique, Hospices Civils de Lyon, CBE Bron, EA4609 and CIQLE-Lyon Bio Image, Université Lyon, France (J.-C.B.); Institut Hospitalo-Universitaire LIRYC PTIB, Hôpital Xavier Arnozan, av du Haut Lévêque, Pessac, France (P.N.); and Département de Biochimie et Génétique, INSERM UMR_S 1083 - CNRS 6214, CHU Angers, Angers, France (D.B., E.C.).

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http://dx.doi.org/10.1161/ATVBAHA.117.309337DOI Listing
June 2017

An intracytoplasmic β3 Leu718 deletion in a patient with a novel platelet phenotype.

Blood Adv 2017 Mar 10;1(8):494-499. Epub 2017 Mar 10.

Institut Hospitalo-Universitaire de Rhythmologie et de Modélisation Cardiaque, Plateforme Technologique d'Innovation Biomédicale, Hôpital Xavier Arnozan, Pessac, France.

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http://dx.doi.org/10.1182/bloodadvances.2016002808DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5728455PMC
March 2017

A diagnostic approach that may help to discriminate inherited thrombocytopenia from chronic immune thrombocytopenia in adult patients.

Platelets 2016 Sep 30;27(6):555-62. Epub 2016 Mar 30.

b Reference Centre for Platelet Disorders , Bordeaux University Hospital Centre , Pessac , France.

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http://dx.doi.org/10.3109/09537104.2016.1143920DOI Listing
September 2016

Should any genetic defect affecting α-granules in platelets be classified as gray platelet syndrome?

Am J Hematol 2016 07 26;91(7):714-8. Epub 2016 Apr 26.

Institut de Rhythmologie et de Modélisation Cardiaque, Plateforme Technologique d'Innovation Biomédicale, Hôpital Xavier Arnozan, Pessac, France.

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http://dx.doi.org/10.1002/ajh.24359DOI Listing
July 2016

A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders.

Blood 2016 06 15;127(23):2791-803. Epub 2016 Apr 15.

Department of Haematology, University of Cambridge, National Institute for Health Research BioResource-Rare Diseases, Cambridge University Hospitals, and National Health Service Blood and Transplant, Cambridge Biomedical Campus, Cambridge, United Kingdom; Medical Research Council Biostatistics Unit, Cambridge Institute of Public Health, Cambridge Biomedical Campus, Cambridge, United Kingdom;

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http://dx.doi.org/10.1182/blood-2015-12-688267DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5016734PMC
June 2016

A dominant gain-of-function mutation in universal tyrosine kinase SRC causes thrombocytopenia, myelofibrosis, bleeding, and bone pathologies.

Sci Transl Med 2016 Mar 2;8(328):328ra30. Epub 2016 Mar 2.

Department of Haematology, University of Cambridge, Cambridge Biomedical Campus, Cambridge CB2 0PT, UK. National Health Service (NHS) Blood and Transplant, Cambridge Biomedical Campus, Cambridge CB2 0PT, UK. National Institute for Health Research (NIHR) BioResource-Rare Diseases, Cambridge University Hospitals, Cambridge Biomedical Campus, Cambridge CB2 0PT, UK. Human Genetics, Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge CB10 1SA, UK.

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http://dx.doi.org/10.1126/scitranslmed.aad7666DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5903547PMC
March 2016

Single thrombopoietin dose alleviates hematopoietic stem cells intrinsic short- and long-term ionizing radiation damage. In vivo identification of anatomical cell expansion sites.

Radiat Res 2015 Jan 7;183(1):52-63. Epub 2015 Jan 7.

a  CEA, SRHI, Institute of Emerging Diseases and Innovative Therapies (iMETI), 75010 Paris, France.

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http://dx.doi.org/10.1667/RR13742.1DOI Listing
January 2015

Gray platelet syndrome: proinflammatory megakaryocytes and α-granule loss cause myelofibrosis and confer metastasis resistance in mice.

Blood 2014 Dec 25;124(24):3624-35. Epub 2014 Sep 25.

Department of Haematology, University of Cambridge, and National Health Service Blood and Transplant, Cambridge Biomedical Campus, Cambridge, United Kingdom;

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http://dx.doi.org/10.1182/blood-2014-04-566760DOI Listing
December 2014

Megakaryocyte-specific Profilin1-deficiency alters microtubule stability and causes a Wiskott-Aldrich syndrome-like platelet defect.

Nat Commun 2014 Sep 4;5:4746. Epub 2014 Sep 4.

1] Department of Experimental Biomedicine, University Hospital, University of Würzburg, Würzburg 97080, Germany [2] Rudolf Virchow Centre, University of Würzburg, Würzburg 97080, Germany.

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http://dx.doi.org/10.1038/ncomms5746DOI Listing
September 2014

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

Haematologica 2014 Aug 24;99(8):1387-94. Epub 2014 Apr 24.

Department of Medicine and Haematology, University Hospital of Verona, Verona, Italy.

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http://dx.doi.org/10.3324/haematol.2014.105924DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4116839PMC
August 2014

The Nbeal2(-/-) mouse as a model for the gray platelet syndrome.

Rare Dis 2013 26;1:e26561. Epub 2013 Sep 26.

University of Würzburg; Department of Experimental Biomedicine; University Hospital and Rudolf Virchow Center; DFG Research Center for Experimental Biomedicine; Würzburg, Germany ; Department of Neurology; University of Würzburg; Würzburg, Germany.

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http://dx.doi.org/10.4161/rdis.26561DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3915564PMC
July 2014

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

Mol Genet Genomic Med 2014 Jul 7;2(4):297-312. Epub 2014 Feb 7.

Service d'Hématologie Biologique and National Reference Center on Inherited Platelet Disorders, Hôpital Robert-Debré 48 Boulevard Sérurier, 75019, Paris, France.

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http://doi.wiley.com/10.1002/mgg3.68
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http://dx.doi.org/10.1002/mgg3.68DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4113270PMC
July 2014

Platelet-targeted gene therapy with human factor VIII establishes haemostasis in dogs with haemophilia A.

Nat Commun 2013 ;4:2773

1] Department of Pediatrics, Medical College of Wisconsin, Milwaukee, Wisconsin 53226, USA [2] Children's Research Institute, Children's Hospital of Wisconsin, Milwaukee, Wisconsin 53226, USA [3] MACC Fund Research Center, Milwaukee, Wisconsin 53226, USA.

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http://dx.doi.org/10.1038/ncomms3773DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3868233PMC
June 2014

Congenital platelet disorders and understanding of platelet function.

Br J Haematol 2014 Apr 29;165(2):165-78. Epub 2013 Nov 29.

L'Institut de Rhythmologie et Modélisation Cardiaque (LIRYC), Plateforme Technologique et d'Innovation Biomédicale, Hôpital Xavier Arnozan, Pessac, France.

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http://dx.doi.org/10.1111/bjh.12662DOI Listing
April 2014

Crucial role for endoplasmic reticulum stress during megakaryocyte maturation.

Arterioscler Thromb Vasc Biol 2013 Dec 10;33(12):2750-8. Epub 2013 Oct 10.

From the Inserm U770, Université Paris-Sud, Le Kremlin-Bicêtre, France (J.J.L., C.C., L.A., E.P., S.D., J.E., R.B.); INSERM UMR1009, Institut Gustave Roussy, Université Paris-Sud, Villejuif, France (A.P., K.L., N.D.); and Centre de Référence des Pathologies Plaquettaires, Plateforme Technologique d'Innovation Biomédicale, Hôpital Xavier Arnozan, Pessac, France (P.N.).

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https://www.ahajournals.org/doi/10.1161/ATVBAHA.113.302184
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http://dx.doi.org/10.1161/ATVBAHA.113.302184DOI Listing
December 2013

[Glycoproteins, inherited diseases of platelets, and the role of platelets in wound healing].

Bull Acad Natl Med 2013 Feb;197(2):349-58; discussion 358-9

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February 2013

Deep Vein Thrombosis, Raynaud's Phenomenon, and Prinzmetal Angina in a Patient with Glanzmann Thrombasthenia.

Case Rep Hematol 2012 31;2012:156290. Epub 2012 Dec 31.

Plateforme Technologique et d'Innovation Biomédicale, Hôpital Xavier Arnozan, 33600 Pessac, France.

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http://dx.doi.org/10.1155/2012/156290DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3549378PMC
January 2013

Clinical utility gene card for: Glanzmann thrombasthenia.

Eur J Hum Genet 2012 Oct 11;20(10). Epub 2012 Jul 11.

Centre de Référence des Pathologies Plaquettaires, Plateforme Technologique d'Innovation Biomédicale, Hôpital Xavier Arnozan, Pessac, France.

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http://dx.doi.org/10.1038/ejhg.2012.151DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3449071PMC
October 2012

Understanding the genetic basis of Glanzmann thrombasthenia: implications for treatment.

Expert Rev Hematol 2012 Oct;5(5):487-503

Plateforme Technologique et d'Innovation Biomédicale, Hôpital Xavier Arnozan, Pessac, France.

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http://dx.doi.org/10.1586/ehm.12.46DOI Listing
October 2012

Are bone defects in rare patients with Glanzmann's thrombasthenia associated with ITGB3 or ITGA2B mutations?

Platelets 2011 11;22(7):547-51. Epub 2011 May 11.

Centre de Référence des Pathologies Plaquettaires, Plateforme Technologique et d'Innovation Biomédicale, Hôpital Xavier Arnozan, Pessac, France.

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http://dx.doi.org/10.3109/09537104.2011.573600DOI Listing
January 2012

Glanzmann thrombasthenia: a review of ITGA2B and ITGB3 defects with emphasis on variants, phenotypic variability, and mouse models.

Blood 2011 Dec 13;118(23):5996-6005. Epub 2011 Sep 13.

Centre de Référence des Pathologies Plaquettaires, Plateforme Technologique et d'Innovation Biomédicale, Hôpital Xavier Arnozan, Pessac, France.

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http://www.bloodjournal.org/cgi/doi/10.1182/blood-2011-07-36
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http://dx.doi.org/10.1182/blood-2011-07-365635DOI Listing
December 2011

Founder effect and estimation of the age of the French Gypsy mutation associated with Glanzmann thrombasthenia in Manouche families.

Eur J Hum Genet 2011 Sep 13;19(9):981-7. Epub 2011 Apr 13.

Centre de Référence des Pathologies Plaquettaires, Plateforme Technologique d'Innovation Biomédicale, Hôpital Xavier Arnozan, Pessac, France.

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http://dx.doi.org/10.1038/ejhg.2011.61DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3179361PMC
September 2011

Megakaryocytes possess a functional intrinsic apoptosis pathway that must be restrained to survive and produce platelets.

J Exp Med 2011 Sep 12;208(10):2017-31. Epub 2011 Sep 12.

Molecular Medicine Division, Cancer and Hematology Division, The Walter and Eliza Hall Institute of Medical Research, Parkville 3052, Australia; Department of Medical Biology, The University of Melbourne, Parkville 3010, Australia.

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http://www.jem.org/lookup/doi/10.1084/jem.20110750
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http://dx.doi.org/10.1084/jem.20110750DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3182050PMC
September 2011

Glanzmann thrombasthenia-like syndromes associated with Macrothrombocytopenias and mutations in the genes encoding the αIIbβ3 integrin.

Semin Thromb Hemost 2011 Sep 18;37(6):698-706. Epub 2011 Nov 18.

Centre de Référence des Pathologies Plaquettaires, Plateforme Technologique et d'Innovation Biomédicale, Hôpital Xavier Arnozan, Pessac, France.

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http://dx.doi.org/10.1055/s-0031-1291380DOI Listing
September 2011

Antagonism of P2Y₁₂ reduces physiological thromboxane levels.

Platelets 2010 ;21(8):604-9

Department of Physiology, Temple University School of Medicine, Philadelphia, PA 19140, USA.

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http://dx.doi.org/10.3109/09537104.2010.511684DOI Listing
February 2011

Abnormal VWF modifies megakaryocytopoiesis: studies of platelets and megakaryocyte cultures from patients with von Willebrand disease type 2B.

Blood 2010 Apr 29;115(13):2649-56. Epub 2010 Jan 29.

Centre de Référence des Pathologies Plaquettaires, Plateforme Technologique et d'Innovation Biomédicale, Hôpital Xavier Arnozan, Pessac, France.

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http://dx.doi.org/10.1182/blood-2009-07-231886DOI Listing
April 2010

Thrombocytopenia after abciximab use results from different mechanisms.

Thromb Haemost 2010 Mar 13;103(3):651-61. Epub 2010 Jan 13.

Centre de Référence des Pathologies Plaquettaires, Plateforme Technologique et d'Innovation Biomédicale, Hôpital Xavier Arnozan, Pessac, France.

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http://dx.doi.org/10.1160/TH09-08-0603DOI Listing
March 2010

Dual requirement for the ETS transcription factors Fli-1 and Erg in hematopoietic stem cells and the megakaryocyte lineage.

Proc Natl Acad Sci U S A 2009 Aug 31;106(33):13814-9. Epub 2009 Jul 31.

Divisions of Molecular Medicine and Cancer and Haematology, The Walter and Eliza Hall Institute of Medical Research, 1G Royal Parade, Parkville 3052, Australia.

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http://www.pnas.org/cgi/doi/10.1073/pnas.0906556106
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http://dx.doi.org/10.1073/pnas.0906556106DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2728977PMC
August 2009

New-generation drugs that stimulate platelet production in chronic immune thrombocytopenic purpura.

Lancet 2009 May 25;373(9674):1562-9. Epub 2009 Mar 25.

French National Reference Centre for Platelet Disorders, Hôpital Xavier Arnozan, Pessac, France.

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http://dx.doi.org/10.1016/S0140-6736(09)60255-5DOI Listing
May 2009

The VWD2B saga continues to Montreal.

Authors:
Paquita Nurden

Blood 2009 Apr;113(14):3134-5

French National Reference Center.

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http://dx.doi.org/10.1182/blood-2009-01-197608DOI Listing
April 2009

Genetic testing in the diagnostic evaluation of inherited platelet disorders.

Semin Thromb Hemost 2009 Mar 30;35(2):204-12. Epub 2009 Apr 30.

Centre de Référence des Pathologies Plaquettaires, Plateforme Technologique et d'Innovation Biomédicale, Hôpital Xavier Arnozan, Pessac, France.

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http://dx.doi.org/10.1055/s-0029-1220328DOI Listing
March 2009

Phenotypic heterogeneity in the Gray platelet syndrome extends to the expression of TREM family member, TLT-1.

Thromb Haemost 2008 Jul;100(1):45-51

Centre de Référence des Pathologies Plaquettaires, Plateforme Technologique et d'Innovation Biomédicale, Hôpital Xavier Arnozan, 33600 Pessac, France.

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http://www.thieme-connect.de/DOI/DOI?10.1160/TH08-02-0067
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http://dx.doi.org/10.1160/TH08-02-0067DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2694056PMC
July 2008

Platelets and wound healing.

Front Biosci 2008 May 1;13:3532-48. Epub 2008 May 1.

Centre de Reference des Pathologies Plaquettaires, Plateforme Technologique et d'Innovation Biomedicale, Hopital Xavier Arnozan, Pessac, France.

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May 2008

Increasing the platelet count in chronic ITP.

Lancet 2008 Feb;371(9610):362-4

Centre de Référence des Pathologies Plaquettaires, Hôpital Xavier Arnosan, 33600 Pessac, France.

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http://dx.doi.org/10.1016/S0140-6736(08)60178-6DOI Listing
February 2008

Congenital disorders associated with platelet dysfunctions.

Thromb Haemost 2008 Feb;99(2):253-63

CRPP/PTIB, Hôpital Xavier Arnozan, Pessac, France.

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http://dx.doi.org/10.1160/TH07-09-0568DOI Listing
February 2008

Inherited thrombocytopenias.

Haematologica 2007 Sep;92(9):1158-64

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http://dx.doi.org/10.3324/haematol.11256DOI Listing
September 2007

A second report of platelet-type von Willebrand disease with a Gly233Ser mutation in the GPIBA gene.

Thromb Haemost 2007 Feb;97(2):319-21

Centre de Référence des Pathologies Plaquettaires/Institur Fédératif de Recherche 4, Plate-forme d'Innovation Biomédicale, Hôpotal Xavier Arnozan, Pessac, France. E-mail:

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February 2007

The gray platelet syndrome: clinical spectrum of the disease.

Blood Rev 2007 Jan 25;21(1):21-36. Epub 2006 Jan 25.

IFRN 4/CRPP, Laboratoire d'Hématologie, Hôpital Cardiologique, 33604 Pessac, France.

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http://linkinghub.elsevier.com/retrieve/pii/S0268960X0500071
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http://dx.doi.org/10.1016/j.blre.2005.12.003DOI Listing
January 2007

Impaired megakaryocytopoiesis in type 2B von Willebrand disease with severe thrombocytopenia.

Blood 2006 Oct 23;108(8):2587-95. Epub 2006 May 23.

Centre de Référence des Pathologies Plaquettaires and Institut Fédératif de Recherche No. 4, Laboratoire d'Hématologie, Hôpital Cardiologique, 33604 Pessac, France.

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http://dx.doi.org/10.1182/blood-2006-03-009449DOI Listing
October 2006

New insights into and novel applications for platelet-rich fibrin therapies.

Trends Biotechnol 2006 May 15;24(5):227-34. Epub 2006 Mar 15.

Biotechnology Institute I MAS D, c/ San Antonio 15, 01005 Vitoria, Spain.

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http://dx.doi.org/10.1016/j.tibtech.2006.02.010DOI Listing
May 2006

Inherited disorders of platelets: an update.

Curr Opin Hematol 2006 May;13(3):157-62

Centre de Référence des Pathologies Plaquettaires, Institut Fédératif de Recherche n 4, CHU Bordeaux, Pessac, France.

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http://dx.doi.org/10.1097/01.moh.0000219661.80785.e3DOI Listing
May 2006

Intracellular interaction of von Willebrand factor and factor VIII depends on cellular context: lessons from platelet-expressed factor VIII.

Blood 2005 Jun 24;105(12):4674-6. Epub 2005 Feb 24.

Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.

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http://www.bloodjournal.org/cgi/doi/10.1182/blood-2004-12-47
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http://dx.doi.org/10.1182/blood-2004-12-4701DOI Listing
June 2005

Genetic deletion of mouse platelet glycoprotein Ibbeta produces a Bernard-Soulier phenotype with increased alpha-granule size.

Blood 2004 Oct 22;104(8):2339-44. Epub 2004 Jun 22.

University of Arkansas for Medical Sciences, 4301 W Markham St, Little Rock, AR 72205, USA.

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http://dx.doi.org/10.1182/blood-2004-03-1127DOI Listing
October 2004

Delayed immunologic thrombocytopenia induced by abciximab.

Thromb Haemost 2004 Oct;92(4):820-8

IFR4/FR21, Laboratoire d'Hématologie, Hôpital Cardiologique, 33604 Pessac, France.

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http://dx.doi.org/10.1160/TH04-04-0237DOI Listing
October 2004

The novel human platelet septin SEPT8 is an interaction partner of SEPT4.

Thromb Haemost 2004 May;91(5):959-66

Department of Pediatrics and Adolescent Medicine, University Hospital Freiburg, Mathildenstr. 1, D-79106 Freiburg, Germany.

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http://dx.doi.org/10.1160/TH03-09-0578DOI Listing
May 2004

GPIIb/IIIa antagonists and other anti-integrins.

Semin Vasc Med 2003 May;3(2):123-30

Laboratoire d'Hematologie, UMR 5533 CNRS, Hôpital Cardiologique, Pessac, France.

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http://dx.doi.org/10.1055/s-2003-40670DOI Listing
May 2003