Vol 3, No 1s (2013): Proceedings of the 3rd Pan-European Conference on Haemoglobinopathies and Rare Anaemias

Published: 2013-03-26

Abstract Book

Breakthroughs in hematology

Ulrich Jäger
DOI https://doi.org/10.4081/thal.2013.s1.e1

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Thalassemia: a dreadful disease turned to a chronic condition

Dimitris Loukopoulos
DOI https://doi.org/10.4081/thal.2013.s1.e2

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The molecular and cellular basis of iron toxicity in Iron Overload (IO) disorders. Diagnostic and therapeutic approaches

Zvi Ioav Cabantchik, Yan Sung Sohn, William Breuer, Breno Pannia Espósito
DOI https://doi.org/10.4081/thal.2013.s1.e3

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Genetic/metabolic effect of iron metabolism and rare anemias

Clara Camaschella
DOI https://doi.org/10.4081/thal.2013.s1.e4

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Iron load

Filippo Cassarà, Aurelio Maggio
DOI https://doi.org/10.4081/thal.2013.s1.e5

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Monitoring and treatment iron overload in thalassaemia

John Porter
DOI https://doi.org/10.4081/thal.2013.s1.e6

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Pathophysiology of cardiovascular disease in rare anemias

Athanasios Aessopos, Dimitrios Farmakis
DOI https://doi.org/10.4081/thal.2013.s1.e7

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Thalassaemia major and the heart

J. Malcolm Walker
DOI https://doi.org/10.4081/thal.2013.s1.e8

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Epidemiology of non-transfusion dependent thalassaemias: an emerging global concern

Androulla Eleftheriou
DOI https://doi.org/10.4081/thal.2013.s1.e9

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Hypercoagulability and thrombosis

Maria Domenica Cappellini, Erika Poggiali
DOI https://doi.org/10.4081/thal.2013.s1.e10

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Iron overload in non-transfusion-dependent thalassemia

Khaled M. Musallam
DOI https://doi.org/10.4081/thal.2013.s1.e11

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Approaches to management of beta-thalassemia intermedia

Joseph E. Maakaron, Ali T. Taher
DOI https://doi.org/10.4081/thal.2013.s1.e12

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Recent advances in molecular understanding of NTDT: 2012

Vip Viprakasit
DOI https://doi.org/10.4081/thal.2013.s1.e13

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Prevention of the hemoglobinopathies

Dimitris Loukopoulos
DOI https://doi.org/10.4081/thal.2013.s1.e14

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Overview of technical methods of prevention

Marina Kleanthous
DOI https://doi.org/10.4081/thal.2013.s1.e15

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Renal complications in hemoglobinopathies

Miguel R. Abboud
DOI https://doi.org/10.4081/thal.2013.s1.e16

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Liver disease and thalassaemia

George Constantinou
DOI https://doi.org/10.4081/thal.2013.s1.e17

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Diabetes and thalassaemia

Maria Barnard, Ploutarchos Tzoulis
DOI https://doi.org/10.4081/thal.2013.s1.e18

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Gonadal function and fertility issues in Thalassaemia

Nicos Skordis
DOI https://doi.org/10.4081/thal.2013.s1.e19

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Bone disease in haemoglobin disorders

Ersi Voskaridou, Evangelos Terpos
DOI https://doi.org/10.4081/thal.2013.s1.e20

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Pain and its management in thalassaemia

Antonio Piga
DOI https://doi.org/10.4081/thal.2013.s1.e21

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Overview of recommended blood transfusion therapy in thalassaemia major

John Porter
DOI https://doi.org/10.4081/thal.2013.s1.e22

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Blood transfusion: safety, optimisation and new advances

Shubha Allard
DOI https://doi.org/10.4081/thal.2013.s1.e23

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Pathogen inactivation. New progress

Antonio Piga
DOI https://doi.org/10.4081/thal.2013.s1.e24

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Treatment of hepatitis C in patients with thalassaemia. Where are we now?

Geoffrey Dusheiko
DOI https://doi.org/10.4081/thal.2013.s1.e25

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The role of the molecular biology laboratory in the management of chronic hepatitis B and C

Peter Karayiannis
DOI https://doi.org/10.4081/thal.2013.s1.e26

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European patients academy on therapeutic innovation

Mathew May
DOI https://doi.org/10.4081/thal.2013.s1.e27

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Thalassemia in Israel: 2012

Pinhas Stark
DOI https://doi.org/10.4081/thal.2013.s1.e28

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Guidelines for adults

Paul Telfer
DOI https://doi.org/10.4081/thal.2013.s1.e29

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Expert services for rare anaemias across Europe

Beatrice Gulbis
DOI https://doi.org/10.4081/thal.2013.s1.e30

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Laboratory diagnosis of the rare anaemias: external quality assessment benefits patient care

Barbara De La Salle, Andrea Mosca, Renata Paleari, Vasileios Rapanakis, Keith Hyde
DOI https://doi.org/10.4081/thal.2013.s1.e31

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Current diagnostic approach and screening methods for hereditary spherocytosis

Paola Bianchi
DOI https://doi.org/10.4081/thal.2013.s1.e32

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Diagnosis and epidemiology of red blood cell enzyme disorders

Richard Van Wijk
DOI https://doi.org/10.4081/thal.2013.s1.e33

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Micromapping of very rare anemias: the model of CDA

Hermann Heimpel
DOI https://doi.org/10.4081/thal.2013.s1.e34

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Genetic counselling in the beta-thalassaemias

Adonis S. Ioannides
DOI https://doi.org/10.4081/thal.2013.s1.e35

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Torwards a more patient-centred healthcare system and effective services

Philip Michael Chircop
DOI https://doi.org/10.4081/thal.2013.s1.e36

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A patient centred approach to care planning for patients with chronic genetic diseases

Alastair Kent
DOI https://doi.org/10.4081/thal.2013.s1.e37

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The deep project

Evi Missouri-Khetab
DOI https://doi.org/10.4081/thal.2013.s1.e38

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Induction of HBF

Mehran Karimi, Nader Cohan
DOI https://doi.org/10.4081/thal.2013.s1.e39

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Decrease of alpha-chains in beta-thalassemia

M. Papadaki, George Vassilopoulos
DOI https://doi.org/10.4081/thal.2013.s1.e40

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Development of model systems for b-thalassaemia

Jim Vadolas
DOI https://doi.org/10.4081/thal.2013.s1.e41

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Bone marrow transplantation for thalassemia: a global perspective

Mohamed Hamed Hussein, Mohamed El Missiry, Sadaf Khalid, Naila Yaqub, Sarah Khan Gilani, Itrat Fatima, Tatheer Zara, Priya Marwah, Rajpreet Soni, Frederic Bernard, Annunziata Manna, Cornelio Uderzo, Lawrence Faulkner
DOI https://doi.org/10.4081/thal.2013.s1.e42

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Five year outcome of lentiviral gene therapy for human beta-thalassemia, lessons and prospects

Philippe Leboulch
DOI https://doi.org/10.4081/thal.2013.s1.e43

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ENERCA - European Network for Rae and Congenital Anaemias 2002-2012. 10 years of life

Joan Lluis Vives-Corrons
DOI https://doi.org/10.4081/thal.2013.s1.e44

Pages e44

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