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For: Pinxten W, Dierickx K, Nys H. Ethical principles and legal requirements for pediatric research in the EU: an analysis of the European normative and legal framework surrounding pediatric clinical trials. Eur J Pediatr. 2009;168:1225-1234. [PMID: 19142660 DOI: 10.1007/s00431-008-0915-7] [Cited by in Crossref: 16] [Cited by in F6Publishing: 10] [Article Influence: 1.3] [Reference Citation Analysis]
Number Citing Articles
1 Allegaert K. Clinical pharmacological studies in children: From exploratory towards confirmation driven methodology. World J Clin Pediatr. 2012;1:3-7. [PMID: 25254160 DOI: 10.5409/wjcp.v1.i2.3] [Cited by in CrossRef: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.1] [Reference Citation Analysis]
2 De Boeck K, Bulteel V, Tiddens H, Wagner T, Fajac I, Conway S, Dufour F, Smyth AR, Lee T, Sermet I, Kassai B, Elborn S; ECFS-CTN network partners. Guideline on the design and conduct of cystic fibrosis clinical trials: the European Cystic Fibrosis Society-Clinical Trials Network (ECFS-CTN). J Cyst Fibros 2011;10 Suppl 2:S67-74. [PMID: 21658644 DOI: 10.1016/S1569-1993(11)60010-6] [Cited by in Crossref: 18] [Cited by in F6Publishing: 5] [Article Influence: 1.8] [Reference Citation Analysis]
3 Piana C, Kliphuis E, Della Pasqua O. Lack of compliance of European Public Assessment Reports to guidelines for paediatric drug development before the introduction of paediatric investigation plans. Clinical Trials 2013;10:269-79. [DOI: 10.1177/1740774512470220] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 0.5] [Reference Citation Analysis]
4 Janiaud P, Lajoinie A, Cour-Andlauer F, Cornu C, Cochat P, Cucherat M, Gueyffier F, Kassai B. Different treatment benefits were estimated by clinical trials performed in adults compared with those performed in children. J Clin Epidemiol 2015;68:1221-31. [PMID: 26164751 DOI: 10.1016/j.jclinepi.2015.06.021] [Cited by in Crossref: 12] [Cited by in F6Publishing: 8] [Article Influence: 2.0] [Reference Citation Analysis]
5 Hens K, Nys H, Cassiman JJ, Dierickx K. Risks, benefits, solidarity: a framework for the participation of children in genetic biobank research. J Pediatr 2011;158:842-8. [PMID: 21349539 DOI: 10.1016/j.jpeds.2010.12.036] [Cited by in Crossref: 14] [Cited by in F6Publishing: 11] [Article Influence: 1.4] [Reference Citation Analysis]
6 Kuemmerle-Deschner JB, Hansmann S, Wulffraat NM, Vastert SJ, Hens K, Anton J, Avcin T, Martini A, Koné-Paut I, Uziel Y, Ravelli A, Wouters C, Shaw D, Özen S, Eikelberg A, Prakken BJ, Ruperto N, Horneff G, Constantin T, Beresford MW, Sikken M, Foster HE, Haug I, Schuller S, Jägle C, Benseler SM. Recommendations for collaborative paediatric research including biobanking in Europe: a Single Hub and Access point for paediatric Rheumatology in Europe (SHARE) initiative. Ann Rheum Dis 2018;77:319-27. [PMID: 29021237 DOI: 10.1136/annrheumdis-2017-211904] [Cited by in Crossref: 6] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
7 Hens K, Van El CE, Borry P, Cambon-Thomsen A, Cornel MC, Forzano F, Lucassen A, Patch C, Tranebjaerg L, Vermeulen E, Salvaterra E, Tibben A, Dierickx K; PPPC of the European Society of Human Genetics. Developing a policy for paediatric biobanks: principles for good practice. Eur J Hum Genet 2013;21:2-7. [PMID: 22713814 DOI: 10.1038/ejhg.2012.99] [Cited by in Crossref: 42] [Cited by in F6Publishing: 36] [Article Influence: 4.7] [Reference Citation Analysis]
8 Reetz J, Richter G, Borzikowsky C, Glinicke C, Darabaneanu S, Buyx A. Consent to research participation: understanding and motivation among German pupils. BMC Med Ethics 2021;22:93. [PMID: 34271886 DOI: 10.1186/s12910-021-00661-z] [Reference Citation Analysis]
9 Bos W, Tromp K, Tibboel D, Pinxten W. Ethical aspects of clinical research with minors. Eur J Pediatr 2013;172:859-66. [PMID: 23073901 DOI: 10.1007/s00431-012-1856-8] [Cited by in Crossref: 15] [Cited by in F6Publishing: 10] [Article Influence: 1.7] [Reference Citation Analysis]
10 Sheppard DN. The European cystic fibrosis patient registry: The power of sharing data. Journal of Cystic Fibrosis 2010;9:S1-2. [DOI: 10.1016/j.jcf.2010.08.018] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 0.4] [Reference Citation Analysis]