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2017<\/b><\/span><\/p>\n

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XXXIII National Congress Sociedad Espa\u00f1ola de Trombosis y Hemostasia (SETH) and LIX National Meeting Sociedad Espa\u00f1ola de Hematolog\u00eda y Hemoterapia (SEHH). October 26-28, 2016, Malaga. DIAGN\u00d3STICOS EN ENFERMEDADES HEMATOL\u00d3GICAS HEREDITARIAS MEDIANTE PANELES DE GENES DE NEXT GENERATION SEQUENCING (NGS). Mayka Sanchez-Fernandez, Josep Fita-Torr\u00f3, Beatriz Cadenas-Sevilla, Clara Esteban-Jurado, David Beneitez-Pastor, Jose Luis Dapena, Adoraci\u00f3n Blanco-Alvarez, Victor Marco Betes, Jos\u00e9 Luis Fuster, Mar Berm\u00fadez-Cort\u00e9s, Leonor Arenillas, Sara Montesdeoca, Laia Mart\u00ednez, Carme Pedro, Santiago P\u00e9rez-Montero, In\u00e9s Hern\u00e1ndez-Rodriguez, Cristian Tornador-Antol\u00edn.<\/span><\/span><\/span><\/p>\n<\/li>\n
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The European Iron Club Annual Meeting. 2017. Munster, Germany, 24-26 June 2017.<\/span><\/span><\/span><\/span> Member of the organizing scientific committee and chair woman in session<\/b><\/span><\/span><\/span><\/span>. <\/span><\/span><\/span><\/span>Invited talks:<\/b><\/span><\/span><\/span><\/span> Talk 1: M Sanchez: <\/span><\/span><\/span><\/span>Diagnosis of non-HFE-HH by NGS. Talk 2: M Sanchez. Highlights from BioIron I.<\/span><\/span><\/span><\/span><\/p>\n<\/li>\n
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Annual Meeting of the European Federation of Associations of Patients with Haemochromatosis (EFAPH). <\/span><\/span><\/span>Munster, Germany, 24 June 2017<\/span><\/span><\/span><\/span>. Invited talk: M Sanchez: <\/span><\/span><\/span>BioIron 2017: Any relevant news for HH-Patients?<\/span><\/span>. In addition, attendance as the Spanish representative of the Spanish Association of Hemochromatosis (AEH), present annual Spanish AEH report<\/span><\/span><\/span><\/span><\/span><\/p>\n<\/li>\n
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22nd Annual Congress of the European Hematology Association (EHA) 2017. June 22-25, Madrid, Spain. <\/span><\/span><\/span><\/span>Invited world-wide expert reviewer<\/b><\/span><\/span><\/span><\/span> in the EHA2017 in the topic: Iron Metabolism, deficiency and overload. Poster: MUTATIONS IN YARS2 CAUSE CONGENITAL SIDEROBLASTIC ANEMIA WITHOUT SHOWING EVIDENCES OF MYOPATHY AND LACTIC ACIDOSIS. Beatriz Cadenas, Josep Fita, Sara Montesdeoca, Carme Pedro , Mayka Sanchez<\/span><\/span><\/span><\/span><\/span><\/span><\/p>\n<\/li>\n
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X Congreso Nacional Sociedad Espa\u00f1ola de Hematolog\u00eda y Oncolog\u00eda Pediatricas (SEHOP) 25-27 May 2014, Madrid. <\/span><\/span>Poster<\/b><\/span><\/span>: Anemia ferrop\u00e9nica grave refractaria a ferroterapia oral debido a una forma \u201cIRIDA-like\u201d. Alvaro Diaz, Isabel Badell, Anna Sangorrin, Chiara Victoria Stasi, Mayka Sanchez. <\/span><\/span><\/span><\/span><\/p>\n<\/li>\n
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Seventh Congress of the International BIOIRON Society. BIOIRON 2017. Los Angeles, USA. May 7-11 2017. <\/span><\/span><\/span><\/span>Poster<\/b><\/span><\/span><\/span><\/span>: Inappropriate expression of hepcidin in the liver of Profilin-2 knock out mice.<\/span><\/span><\/span><\/span><\/span><\/span><\/p>\n<\/li>\n
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Biannual General Meeting of Hemochromatosis International (HI). Los Angeles, USA. May 12 2017. <\/span><\/span><\/span><\/span>Invited talk<\/b><\/span><\/span><\/span><\/span>: M Sanchez: Activity Report from the Spanish Hemochromatosis Association.<\/span><\/span><\/span><\/span><\/span><\/span><\/p>\n<\/li>\n
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EHA-SWG Scientific Meeting on Anaemias: Diagnosis and Traetmnet in the Omics Era. February 2-4, 2017, Barcelona, Spain. <\/span><\/span><\/span><\/span>Member of the organizing scientific committee <\/b><\/span><\/span><\/span><\/span>and<\/span><\/span><\/span><\/span> <\/b>Invited speaker: <\/b><\/span><\/span><\/span><\/span>Clinical Cases solved by NGS.<\/span><\/span><\/span><\/span><\/span><\/span><\/p>\n<\/li>\n<\/ol>\n
2016<\/b><\/span><\/span><\/span><\/p>\n
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XXXII National Congress Sociedad Espa\u00f1ola de Trombosis y Hemostasia (SETH) and LVIII National Meeting Sociedad Espa\u00f1ola de Hematolog\u00eda y Hemostasia (SEHH). October 20-22, 2016, Santiago de Compostela. <\/span><\/span><\/span><\/span>Poster Comentado<\/b><\/span><\/span><\/span><\/span> PC-323: Una mutaci\u00f3n en el elemento de respuesta al hierro (IRE) del gen <\/span><\/span><\/span><\/span>ALAS2<\/i><\/span><\/span><\/span><\/span> es un modificador de la gravedad cl\u00ednica en Protoporfiria eritropoy\u00e9tica.<\/span><\/span><\/span><\/span><\/span><\/span><\/p>\n<\/li>\n
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The European Society of Human Genetics (ESHG) International congress. 2016. Barcelona, Spain, 21-24 May 2016. <\/span><\/span><\/span>Poster<\/b><\/span><\/span><\/span> Presentation: P13.03C: Aceruloplasminemia: new cases with novel mutations in <\/span><\/span><\/span>CP <\/i><\/span><\/span><\/span>gene. <\/span><\/span><\/span><\/span><\/span><\/p>\n<\/li>\n
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The European Iron Club Annual Meeting. 2016. Innsbruck, Vienna, 7-10 April 2016.<\/span><\/span><\/span><\/span> Member of the organizing scientific committee <\/b><\/span><\/span><\/span><\/span>and<\/span><\/span><\/span><\/span> chairwoman on Iron deficiency and anaemia session<\/b><\/span><\/span><\/span><\/span> on Fidasy 8<\/span><\/span><\/span><\/span>^{th<\/span><\/span><\/span><\/sup><\/span> April 2016. Poster <\/span><\/span><\/span><\/span>Presentations: P84: Aceruloplasminemia: new cases with novel mutations in Ceruloplasmin gene. P75: Is the blood from Haemochromatosis subjects accepted for transfusion?- An European survey among thirteen countries.<\/span><\/span><\/span><\/span><\/span><\/p>\n<\/li>\n<\/ol>\n}
2015<\/b><\/span><\/span><\/span><\/p>\n
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2<\/span><\/span><\/span><\/span>^{nd<\/span><\/span><\/span><\/sup><\/span> international conference on RNA Biology in Cancer and other Diseases -RNAREG-IJC. November 24-26<\/span><\/span><\/span><\/span>^{th<\/span><\/span><\/span><\/sup><\/span> 2015, Barcelona. <\/span><\/span><\/span><\/span>Congress Organizer<\/b><\/span><\/span><\/span><\/span>. Oral presentation: Post-transcriptional regulation by the Iron regulatory proteins and iron<\/span><\/span><\/span><\/span>\u2010<\/span><\/span><\/span><\/span>responsive element system: new players. <\/span><\/span><\/span><\/span>2 Posters<\/b><\/span><\/span><\/span><\/span>: P3# mRNA SPLICING DEFECT AS CAUSE OF CONGENITAL HYPOTRANSFERRINEMIA, P7# PROFILIN-2, A NEW PLAYER IN IRON METABOLISM<\/span><\/span><\/span><\/span><\/span><\/span><\/p>\n<\/li>\n}}
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Conference on Hereditary Hemochromatosis, Reflections on Clinical and Practical Aspects inside the 11<\/span><\/span><\/span><\/span>^{th<\/span><\/span><\/span><\/sup><\/span> General Meeting of EFAPH: 2015. 16-17<\/span><\/span><\/span><\/span>^{th<\/span><\/span><\/span><\/sup><\/span> October 2015, <\/span><\/span><\/span><\/span>St Franziskus Hospital, Cologne. <\/span><\/span><\/span><\/span>Invited speaker:<\/b><\/span><\/span><\/span><\/span> The Catalunya approach in Spain by Dr. Mayka Sanchez (inside the session Blood donation and Hereditary Hemochromatosis). <\/span><\/span><\/span><\/span><\/span><\/span><\/p>\n<\/li>\n}}
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XXXI National Congress Sociedad Espa\u00f1ola de Trombosis y Hemostasia (SETH) and LVII National Meeting Sociedad Espa\u00f1ola de Hematolog\u00eda y Hemostasia (SEHH). October 22-24, 2015, Valencia. <\/span><\/span><\/span><\/span>Comunicaci\u00f3n oral:<\/b><\/span><\/span><\/span><\/span> CO-037 <\/span><\/span><\/span><\/span>Profilina-2, una nueva prote\u00edna en el metabolismo del hierro. Poster Comentado PC-55: Sobrecarga f\u00e9rrica en paciente joven.<\/span><\/span><\/span><\/span><\/span><\/span><\/p>\n<\/li>\n
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Sixth Congress of the International BIOIRON Society. BIOIRON 2015. Hanghzou<\/span><\/span><\/span><\/span>, China September 6-10 2015. <\/span><\/span><\/span>Poster #10<\/b><\/span><\/span><\/span>: Atransferrinemia : an ultra-rare iron-loading anaemia. Report of 6 cases from 4 families. <\/span><\/span><\/span>Poster #22<\/b><\/span><\/span><\/span>: Porfilin-2, a new player in iron metabolism. <\/span><\/span><\/span>Selected oral communication: #39<\/b><\/span><\/span><\/span> A mutation in the Iron-reponsive element of ALAS2 is a modifier of clinical severity in Erythropoietic Protoporphyria. <\/span><\/span><\/span>Poster #63<\/b><\/span><\/span><\/span>: Genotype-phenotype studies in 70 IRIDA patients.<\/span><\/span><\/span><\/span><\/span><\/p>\n<\/li>\n
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EHA-SWG Scientific Meeting: Red Cell and Iron Disorders, and Myelodysplastic Syndrome (MDS). Lisbon, Portugal, 6-8 March 2015. Selected as <\/span><\/span><\/span>poster<\/b><\/span><\/span><\/span>: <\/span><\/span><\/span>Atransferrinemia, an ultra-rare iron-loading anaemia. Report of 6 cases from 4 families.<\/span><\/span><\/span><\/span><\/span><\/span><\/p>\n<\/li>\n<\/ol>\n","protected":false},"excerpt":{"rendered":"
2017 XXXIII National Congress Sociedad Espa\u00f1ola de Trombosis y Hemostasia (SETH) and LIX National Meeting Sociedad Espa\u00f1ola de Hematolog\u00eda y Hemoterapia (SEHH). October 26-28, 2016, Malaga. DIAGN\u00d3STICOS EN ENFERMEDADES HEMATOL\u00d3GICAS HEREDITARIAS MEDIANTE PANELES DE GENES DE NEXT GENERATION SEQUENCING (NGS). Mayka Sanchez-Fernandez, Josep Fita-Torr\u00f3, Beatriz Cadenas-Sevilla, Clara Esteban-Jurado, David Beneitez-Pastor, Jose Luis Dapena, Adoraci\u00f3n Blanco-Alvarez,…<\/p>\n","protected":false},"author":5,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_oct_exclude_from_cache":false,"om_disable_all_campaigns":false,"_monsterinsights_skip_tracking":false,"_monsterinsights_sitenote_active":false,"_monsterinsights_sitenote_note":"","_monsterinsights_sitenote_category":0,"_uf_show_specific_survey":0,"_uf_disable_surveys":false,"footnotes":""},"class_list":["post-597","page","type-page","status-publish","hentry","description-off"],"jetpack_sharing_enabled":true,"_links":{"self":[{"href":"https:\/\/bloodgenetics.com\/wp-json\/wp\/v2\/pages\/597","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/bloodgenetics.com\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/bloodgenetics.com\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/bloodgenetics.com\/wp-json\/wp\/v2\/users\/5"}],"replies":[{"embeddable":true,"href":"https:\/\/bloodgenetics.com\/wp-json\/wp\/v2\/comments?post=597"}],"version-history":[{"count":3,"href":"https:\/\/bloodgenetics.com\/wp-json\/wp\/v2\/pages\/597\/revisions"}],"predecessor-version":[{"id":2454,"href":"https:\/\/bloodgenetics.com\/wp-json\/wp\/v2\/pages\/597\/revisions\/2454"}],"wp:attachment":[{"href":"https:\/\/bloodgenetics.com\/wp-json\/wp\/v2\/media?parent=597"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}