untitled
<OAI-PMH schemaLocation=http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd>
<responseDate>2018-01-15T18:33:00Z</responseDate>
<request identifier=oai:HAL:inserm-01081709v1 verb=GetRecord metadataPrefix=oai_dc>http://api.archives-ouvertes.fr/oai/hal/</request>
<GetRecord>
<record>
<header>
<identifier>oai:HAL:inserm-01081709v1</identifier>
<datestamp>2017-12-21</datestamp>
<setSpec>type:ART</setSpec>
<setSpec>subject:sdv</setSpec>
<setSpec>collection:INSERM</setSpec>
<setSpec>collection:UNIV-REUNION</setSpec>
<setSpec>collection:UNIV-AG</setSpec>
<setSpec>collection:UNIV-PARIS7</setSpec>
<setSpec>collection:SANTE_PUB_INSERM</setSpec>
<setSpec>collection:APHP</setSpec>
<setSpec>collection:USPC</setSpec>
</header>
<metadata><dc>
<publisher>HAL CCSD</publisher>
<title lang=en>Impaired blood rheology plays a role inthe chronic disorders associated with sickle cell- hemoglobin C disease</title>
<title lang=en>Impaired blood rheology plays a role inthe chronic disorders associated with sickle cell- hemoglobin C disease : Blood viscosity in hemoglobin SC disease</title>
<creator>Lemonne, Nathalie</creator>
<creator>Lamarre, Yann</creator>
<creator>Romana, Marc</creator>
<creator>Hardy-Dessources, Marie-Dominique</creator>
<creator>Lionnet, François</creator>
<creator>Waltz, Xavier</creator>
<creator>Tarer, Vanessa</creator>
<creator>Mougenel, Danielle</creator>
<creator>Tressières, Benoît</creator>
<creator>Lalanne-Mistrih, Marie-Laure</creator>
<creator>Etienne-Julan, Maryse</creator>
<creator>Connes, Philippe</creator>
<creator>Connes, Philippe</creator>
<contributor>Unité Transversale de la Drépanocytose ; Hôpital Ricou - CHU de Pointe-à-Pitre/Abymes</contributor>
<contributor>Protéines de la membrane érythrocytaire et homologues non-érythroides ; Université des Antilles et de la Guyane (UAG) - Institut National de la Transfusion Sanguine [Paris] (INTS) - Université Paris Diderot - Paris 7 (UPD7) - Université de la Réunion (UR) - Institut National de la Santé et de la Recherche Médicale (INSERM)</contributor>
<contributor>Laboratory of Excellence GR-Ex "The red cell: from genesis to death" ; PRES Sorbonne Paris Cité</contributor>
<contributor>Centre de référence des syndromes drépanocytaires majeurs ; Assistance publique - Hôpitaux de Paris (AP-HP) - Hôpital Henri Mondor</contributor>
<contributor>Adaptations au Climat Tropical, Exercice et Santé (ACTES) ; Université des Antilles et de la Guyane (UAG)</contributor>
<contributor>Centre de référence maladies rares pour la drépanocytose aux Antilles-Guyane ; Centre Hospitalier et Universitaire de Pointe-à-Pitre</contributor>
<contributor>Centre d'investigation clinique Antilles-Guyane ; Institut National de la Santé et de la Recherche Médicale (INSERM) - CH Cayenne</contributor>
<contributor>Institut Universitaire de France (IUF) ; Ministère de l'Éducation nationale, de l’Enseignement supérieur et de la Recherche (M.E.N.E.S.R.)</contributor>
<contributor>the regional council of Guadeloupe ; the association “Ensemble contre la drépanocytose” and the regional council of Guadeloupe</contributor>
<description>International audience</description>
<source>ISSN: 0390-6078</source>
<source>EISSN: 1592-8721</source>
<source>Haematologica</source>
<publisher>Ferrata Storti Foundation</publisher>
<identifier>inserm-01081709</identifier>
<identifier>http://www.hal.inserm.fr/inserm-01081709</identifier>
<identifier>http://www.hal.inserm.fr/inserm-01081709/document</identifier>
<identifier>http://www.hal.inserm.fr/inserm-01081709/file/2014%2C%20Lemonne%20-%20Impaired%20blood%20rheology%20plays%20a%20role%20in%20the%20chronic%20disorders%20associated%20with%20sickle%20cell-hemoglobin%20C%20disease.pdf</identifier>
<source>http://www.hal.inserm.fr/inserm-01081709</source>
<source>Haematologica, Ferrata Storti Foundation, 2014, pp.74-75</source>
<identifier>PUBMED : 24633868</identifier>
<relation>info:eu-repo/semantics/altIdentifier/pmid/24633868</relation>
<language>en</language>
<subject lang=en>Sickle cell disease</subject>
<subject lang=en>sickle cell-hemoglobin C disease</subject>
<subject lang=en>blood viscosity</subject>
<subject lang=en>otologic disorders</subject>
<subject lang=en>retinopathy</subject>
<subject>[SDV.SPEE] Life Sciences [q-bio]/Santé publique et épidémiologie</subject>
<type>info:eu-repo/semantics/article</type>
<type>Journal articles</type>
<description lang=en>Lionnet et al. recently reported a high prevalence of retinopathy (RET) and otologic disorders (OTD) in patients with sickle cell-hemoglobin C disease (SC), while a significant number of patients had renal diseases (mainly glomerulopathy; GLO) and osteonecrosis (OST). The pathophysiological processes of these complications in SC are not well defined, although blood hyperviscosity has been suspected, but never tested to the best of our knowledge, as responsible for several chronic complications in SC disease1,2. The aim of this study was to analyze the associations between hematological and hemorheological parameters and chronic complications in adult SC patients.</description>
<date>2014-03-14</date>
</dc>
</metadata>
</record>
</GetRecord>
</OAI-PMH>
