Zobrazeno 1 - 10
of 48
pro vyhledávání: '"Sylvia Bellucci"'
Autor:
Jacques Caen, Sylvia Bellucci
Publikováno v:
Bulletin de l'Académie Nationale de Médecine. 197:343-347
RESUME Grâce a l’etude des thrombopathies constitutionnelles, des progres notables ont ete obtenus dans la comprehension de la physiologie plaquettaire permettant le developpement d’agents antiplaquettaires utilises a grande echelle au cours des
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::efc5187d8518fe7ee5f02be61fe0c97f
https://doi.org/10.1016/s0001-4079(19)31589-4
https://doi.org/10.1016/s0001-4079(19)31589-4
Publikováno v:
Europe PubMed Central
A population of haematopoietic cells co-expressing glycoprotein IIIa (GPIIIa), which has been shown to be present in the megakaryocyte-platelet lineage, and glycophorin A, which has been shown to be specific for the erythroid lineage, has been identi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::89c6d23e6fcb7f4e4d2127067ce348ce
https://doi.org/10.1111/j.1600-0609.1992.tb01804.x
https://doi.org/10.1111/j.1600-0609.1992.tb01804.x
Autor:
Sylvia Bellucci
Publikováno v:
Bulletin de l'Académie Nationale de Médecine. 191:519-533
Vascular manifestations are the main clinical complication of essential thrombocythemia (ET). They include arterial thrombosis (30-40% of patients), venous thrombosis (5%), and ischemia due to microcirculatory disorders. Their incidence is highest at
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::05e77b433ab1fc21949f1e99844a81eb
https://doi.org/10.1016/s0001-4079(19)33042-0
https://doi.org/10.1016/s0001-4079(19)33042-0
Autor:
Sylvia Bellucci
Publikováno v:
EMC - Hématologie. 1:1-9
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::755848428fc20ead5ff8713cfea9ae32
https://doi.org/10.1016/s1155-1984(02)00039-0
https://doi.org/10.1016/s1155-1984(02)00039-0
Autor:
Guy Simoneau, Claire Bal dit Sollier, Ludovic Drouet, Jean-Philippe Brouland, Sylvia Bellucci, Patrick Andre, Jacques P. Caen, Patricia Hainaud
Publikováno v:
British Journal of Haematology. 119:998-1004
To explore the possible role of a residual or variant alphaIIbbeta3 integrin (alphaIIbbeta3) in thrombogenesis, we used a new ex vivo perfusion chamber model to examine blood from patients with different subtypes of Glanzmann's thrombasthenia (GT). N
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::784d4aeab0c6cfc806eae526e8fd837f
https://doi.org/10.1046/j.1365-2141.2002.03966.x
https://doi.org/10.1046/j.1365-2141.2002.03966.x
Autor:
Sylvia Bellucci, Gérard Sebahoun
Publikováno v:
Hématologie. 15:019-021
Auteur(s) : Sylvia Bellucci1, Gerard Sebahoun2 1Laboratoire d’hematologie, Hopital Lariboisiere, Paris 2Laboratoire d’hematologie, Hopital Nord, Marseille Criteres conventionnels Il est habituel actuellement de considerer l’existence d’une in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0acdd9dc4b6da7d598669da108a660d9
https://doi.org/10.1684/hma.2009.0315
https://doi.org/10.1684/hma.2009.0315
Publikováno v:
British Journal of Haematology. 104:886-892
Anagrelide (imidazoquinazolin derivative) is a new compound proposed for the treatment of myeloproliferative disorders. In this study, Anagrelide was given to patients with essential thrombocythaemia (ET) in a compassionate-use protocol. The aim of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e1eaaf7dddc878e5c87457442043da04
https://doi.org/10.1046/j.1365-2141.1999.01234.x
https://doi.org/10.1046/j.1365-2141.1999.01234.x
Publikováno v:
Thrombosis Research. 136:839-840
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7852c5c3ee74ffa4bd06d760fdb587cd
https://doi.org/10.1016/j.thromres.2015.07.026
https://doi.org/10.1016/j.thromres.2015.07.026
Autor:
Sylvia Bellucci
Publikováno v:
Baillière's Clinical Haematology. 10:149-162
Inherited thrombocytopenias may be divided into two groups. In the first group, there is no marked thrombocytopathy. Although numerous in the bone marrow, megakaryocytes often are abnormal cytologically. A dysmegakaryocytopoiesis with defective plate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b8cddc69c9fb2bb5dc3eac308bea5914
https://doi.org/10.1016/s0950-3536(97)80055-8
https://doi.org/10.1016/s0950-3536(97)80055-8
Publikováno v:
British journal of haematology. 160(1)
Delta storage pool deficiency (δ-SPD) is a rare heterogeneous group of platelet disorders characterized by a reduction in the number or content of dense granules. δ-SPD causes a mild to moderate bleeding diathesis characterized mainly by mucocutane
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4a364721a806bfa35b2efb5b11167f8
https://pubmed.ncbi.nlm.nih.gov/23025459
https://pubmed.ncbi.nlm.nih.gov/23025459