Nr.
Eintrag
1
Rosenecker, J. :Aktuelle Entwicklung der Gentherapie bei paediatrischen Erkrankungen. Molekulare Praezisionsmedizin als kausale Therapie bei angeborenen und erworbenen Erkrankungen. In: Monatsschrift Kinderheilkunde, 2020, Vol. 168 (1), 28-38
2
Rubeis, Giovanni ; Steger, Florian :Saving whom? The ethical challenges of harvesting tissue from savior siblings. In: European Journal of Haematology, 2019, Vol. 103 (5), 478-48
3
Rußwurm, Katja :Erste Ergebnisse lassen hoffen: Gentherapie CRISPR/Cas9 erfolgreich : Am Universitätsklinikum Regensburg (UKR) wurde die erste Beta-Thalassämie-Patientin mit dem CRISPR/Cas9-Verfahren behandelt. Eine weitere Studie läuft im Bereich der Sichelzellerkrankungen. Nun wurde in einer ersten Zwischenbilanz ein positives Resümee gezogen. In: Informationsdienst Wissenschaft, 2019 (2019-11-20)
4
Hadjiafxenti, Charitini ; Neitzke, Gerald :Genetisches Screening, Thalassämie und Ethik : eine Interviewstudie mit Betroffenen auf Zypern 2017
5
Caocci, Giovanni et al.: Ethical issues of unrelated hematopoietic stem cell transplantation in adult thalassemia patients. In: BMC medical ethics, 2011, 12, 4
6
Devettere, Raymond J. :Medical genetics In: Practical Decision Making in Health Care Ethics: Cases and Concepts. 3rd edition. Washington, DC: Georgetown University Press, 2010: 420-457
7
Kontoghiorghes, George J :The 18th ICOC Proceedings in Athens, Greece: New breakthrough in thalassemia leading to the complete treatment of iron overload and to hundreds of patients achieving and maintaining normal body iron stores. Ethical questions on chelation therapy. In: Hemoglobin, 2010, Vol. 34 (3), 199-203
8
Sui, Suli ; Sleeboom-Faulkner, Margaret :Choosing offspring: prenatal genetic testing for thalassaemia and the production of a 'saviour sibling' in China. In: Culture, health & sexuality, 2010, Vol. 12 (2), 167-75
9
Ballantyne, Angela et al.: Prenatal diagnosis and abortion for congenital abnormalities: is it ethical to provide one without the other? In: American Journal of Bioethics, 2009, Vol. 9 (8), 48-56
10
Cowan, Ruth Schwartz :Moving up the slippery slope: mandated genetic screening on Cyprus. In: American Journal of Medical Genetics. Part C, Seminars in Medical Genetics 2009 February 15; 151C(1): 95-103
11
Giordano, P.C. :Starting neonatal screening for haemoglobinopathies in The Netherlands. In: Journal of Clinical Pathology, 2009, Vol. 62 (1), 18-21
12
Arif, Muhammad Osman et al.: Attitudes and perceptions about prenatal diagnosis and induced abortion among adults of Pakistani population. In: Prenatal Diagnosis, 2008, Vol. 28 (12), 1149-1155
13
Atkin, Karl et al.: Decision-making and ante-natal screening for sickle cell and thalassaemia disorders In: Current Sociology, 2008, Vol. 56 (1), 77-98
14
Biral, E. et al.: Multiple BM harvests in pediatric donors for thalassemic siblings: safety, efficacy and ethical issues. In: Bone Marrow Transplantation, 2008, Vol. 42 (6), 379-384
15
Kalokairinou, E.M. :The experience of beta-thalassaemia and its prevention in Cyprus In: Medicine and Law: The World Association for Medical Law, 2008, Vol. 27 (4), 825-842
16
Karimi, Mehran et al.: Termination of pregnancy due to Thalassemia major, Hemophilia, and Down's syndrome: the views of Iranian physicians. In: BMC Medical Ethics, 2008, 9, 19 4 p. [Online]. Accessed: http://www.biomedcentral.com/1472-6939/9/19 [2008 February 23]
17
Larijani, Bagher ; Zahedi, Farzaneh :Islamic principles and decision making in bioethics [letter] In: Nature Genetics, 2008, Vol. 40 (2), 123
18
Li, Dongzhi ; Liao, Can :Incidental discovery of nonpaternity during prenatal testing of genetic disease. In: Fetal Diagnosis and Therapy, 2008, Vol. 24 (1), 39-41
19
Locock, Louise ; Kai, Joe :Parents' experiences of universal screening for haemoglobin disorders: implications for practice in a new genetics era. In: British Journal of General Practice, 2008, Vol. 58 (548), 161-168
20
Van den Heuvel, Ananda et al.: Informed choice to undergo prenatal screening for thalassemia: a description of written information given to pregnant women in Europe and beyond In: Prenatal Diagnosis, 2008, Vol. 28 (8), 727-734