Vol. 3 No. s1 (2013): Proceedings of the 3rd Pan-European Conference on Haemoglobinopathies and Rare Anaemias | Thalassemia Reports

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2013 Vol.3 No.s1

Published: 2013-03-26

Abstract Book

Breakthroughs in hematology

Ulrich Jäger

e1

https://doi.org/10.4081/thal.2013.s1.e1
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Thalassemia: a dreadful disease turned to a chronic condition

Dimitris Loukopoulos

e2

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

e3

https://doi.org/10.4081/thal.2013.s1.e3
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Genetic/metabolic effect of iron metabolism and rare anemias

Clara Camaschella

e4

https://doi.org/10.4081/thal.2013.s1.e4
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Iron load

Filippo Cassarà, Aurelio Maggio

e5

https://doi.org/10.4081/thal.2013.s1.e5
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Monitoring and treatment iron overload in thalassaemia

John Porter

e6

https://doi.org/10.4081/thal.2013.s1.e6
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Pathophysiology of cardiovascular disease in rare anemias

Athanasios Aessopos, Dimitrios Farmakis

e7

https://doi.org/10.4081/thal.2013.s1.e7
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Thalassaemia major and the heart

J. Malcolm Walker

e8

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

e9

https://doi.org/10.4081/thal.2013.s1.e9
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Hypercoagulability and thrombosis

Maria Domenica Cappellini, Erika Poggiali

e10

https://doi.org/10.4081/thal.2013.s1.e10
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Iron overload in non-transfusion-dependent thalassemia

Khaled M. Musallam

e11

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

e12

https://doi.org/10.4081/thal.2013.s1.e12
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Recent advances in molecular understanding of NTDT: 2012

Vip Viprakasit

e13

https://doi.org/10.4081/thal.2013.s1.e13
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Prevention of the hemoglobinopathies

Dimitris Loukopoulos

e14

https://doi.org/10.4081/thal.2013.s1.e14
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Overview of technical methods of prevention

Marina Kleanthous

e15

https://doi.org/10.4081/thal.2013.s1.e15
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Renal complications in hemoglobinopathies

Miguel R. Abboud

e16

https://doi.org/10.4081/thal.2013.s1.e16
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Liver disease and thalassaemia

George Constantinou

e17

https://doi.org/10.4081/thal.2013.s1.e17
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Diabetes and thalassaemia

Maria Barnard, Ploutarchos Tzoulis

e18

https://doi.org/10.4081/thal.2013.s1.e18
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Gonadal function and fertility issues in Thalassaemia

Nicos Skordis

e19

https://doi.org/10.4081/thal.2013.s1.e19
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Bone disease in haemoglobin disorders

Ersi Voskaridou, Evangelos Terpos

e20

https://doi.org/10.4081/thal.2013.s1.e20
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Pain and its management in thalassaemia

Antonio Piga

e21

https://doi.org/10.4081/thal.2013.s1.e21
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Overview of recommended blood transfusion therapy in thalassaemia major

John Porter

e22

https://doi.org/10.4081/thal.2013.s1.e22
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Blood transfusion: safety, optimisation and new advances

Shubha Allard

e23

https://doi.org/10.4081/thal.2013.s1.e23
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Pathogen inactivation. New progress

Antonio Piga

e24

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

e25

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

e26

https://doi.org/10.4081/thal.2013.s1.e26
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European patients academy on therapeutic innovation

Mathew May

e27

https://doi.org/10.4081/thal.2013.s1.e27
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Thalassemia in Israel: 2012

Pinhas Stark

e28

https://doi.org/10.4081/thal.2013.s1.e28
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Guidelines for adults

Paul Telfer

e29

https://doi.org/10.4081/thal.2013.s1.e29
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Expert services for rare anaemias across Europe

Beatrice Gulbis

e30

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

e31

https://doi.org/10.4081/thal.2013.s1.e31
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Current diagnostic approach and screening methods for hereditary spherocytosis

Paola Bianchi

e32

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

e33

https://doi.org/10.4081/thal.2013.s1.e33
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Micromapping of very rare anemias: the model of CDA

Hermann Heimpel

e34

https://doi.org/10.4081/thal.2013.s1.e34
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Genetic counselling in the beta-thalassaemias

Adonis S. Ioannides

e35

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

e36

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

e37

https://doi.org/10.4081/thal.2013.s1.e37
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The deep project

Evi Missouri-Khetab

e38

https://doi.org/10.4081/thal.2013.s1.e38
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Induction of HBF

Mehran Karimi, Nader Cohan

e39

https://doi.org/10.4081/thal.2013.s1.e39
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Decrease of alpha-chains in beta-thalassemia

M. Papadaki, George Vassilopoulos

e40

https://doi.org/10.4081/thal.2013.s1.e40
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Development of model systems for b-thalassaemia

Jim Vadolas

e41

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

e42

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

e43

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

e44

https://doi.org/10.4081/thal.2013.s1.e44
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