Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Wiebke Sieben"'
Autor:
David Henry Seidel, Martina Markes, Ulrich Grouven, Claudia-Martina Messow, Wiebke Sieben, Marco Knelangen, Rieke Oelkers-Ax, Sebastian Grümer, Heike Kölsch, Mandy Kromp, Markus von Pluto Prondzinski
Publikováno v:
BMC Psychiatry, Vol 24, Iss 1, Pp 1-15 (2024)
Abstract Background Systemic therapy (ST) is a psychotherapeutic intervention in complex human systems (both psychological and interpersonal). Cognitive behavioural therapy (CBT) is an established treatment for children and adolescents with mental di
Externí odkaz:
https://doaj.org/article/f322957a915f47e8ada59934379f28c1
Autor:
Siw Waffenschmidt, Wiebke Sieben, Thomas Jakubeit, Marco Knelangen, Inga Overesch, Stefanie Bühn, Dawid Pieper, Nicole Skoetz, Elke Hausner
Publikováno v:
Systematic Reviews, Vol 12, Iss 1, Pp 1-11 (2023)
Abstract Background Systematic literature screening is a key component in systematic reviews. However, this approach is resource intensive as generally two persons independently of each other (double screening) screen a vast number of search results.
Externí odkaz:
https://doaj.org/article/3d3234191bf84c9b98503bb13f70e429
Autor:
Britta Runkel, Birgit Klüppelholz, Anne Rummer, Wiebke Sieben, Ulrike Lampert, Claudia Bollig, Martina Markes, Ulrike Paschen, Konstanze Angelescu
Publikováno v:
Systematic Reviews, Vol 9, Iss 1, Pp 1-9 (2020)
Abstract Background Sickle cell disease (SCD) is an inherited autosomal recessive disorder caused by the replacement of normal haemoglobin (HbA) by mutant Hb (sickle Hb, HbS). The sickle-shaped red blood cells lead to haemolysis and vaso-occlusion. E
Externí odkaz:
https://doaj.org/article/170136ca73514e71bbd8fc1d7d642063
Publikováno v:
BMC Pregnancy and Childbirth, Vol 20, Iss 1, Pp 1-10 (2020)
Abstract Background All non-sensitized Rhesus D (RhD)-negative pregnant women in Germany receive antenatal anti-D prophylaxis without knowledge of fetal RhD status. Non-invasive prenatal testing (NIPT) of cell-free fetal DNA in maternal plasma could
Externí odkaz:
https://doaj.org/article/ade17ae94a164aaa877bc33777430dd8
Publikováno v:
BMC Medical Research Methodology, Vol 19, Iss 1, Pp 1-9 (2019)
Abstract Background Stringent requirements exist regarding the transparency of the study selection process and the reliability of results. A 2-step selection process is generally recommended; this is conducted by 2 reviewers independently of each oth
Externí odkaz:
https://doaj.org/article/567ba97f039f4e4d9c3ad7691033edaf
Autor:
Siw Waffenschmidt, Elke Hausner, Wiebke Sieben, Thomas Jaschinski, Marco Knelangen, Inga Overesch
Publikováno v:
Systematic Reviews, Vol 7, Iss 1, Pp 1-7 (2018)
Abstract Background Systematic information retrieval generally requires a two-step selection process for studies, which is conducted by two persons independently of one another (double-screening approach). To increase efficiency, two methods seem pro
Externí odkaz:
https://doaj.org/article/98bc6d1afbfd43c6b70e0ab9b018ce16
Publikováno v:
BMC Pregnancy and Childbirth, Vol 20, Iss 1, Pp 1-10 (2020)
BMC Pregnancy and Childbirth
BMC Pregnancy and Childbirth
Background All non-sensitized Rhesus D (RhD)-negative pregnant women in Germany receive antenatal anti-D prophylaxis without knowledge of fetal RhD status. Non-invasive prenatal testing (NIPT) of cell-free fetal DNA in maternal plasma could avoid unn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3869b8bb36f431fe0b4f63fcb0a98b4f
https://doaj.org/article/ade17ae94a164aaa877bc33777430dd8
https://doaj.org/article/ade17ae94a164aaa877bc33777430dd8
Publikováno v:
Medizinische Genetik. 31:275-282
Zusammenfassung Hintergrund Molekulargenetische Tests (NIPT) auf Trisomie sind längst Teil der nicht invasiven Pränataldiagnostik (NIPD). In Deutschland wird derzeit geprüft, ob und für wen diese Tests von den gesetzlichen Krankenkassen künftig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5a2f7b6311da25cf24a185d86a012ec0
https://doi.org/10.1007/s11825-019-00251-w
https://doi.org/10.1007/s11825-019-00251-w
Autor:
Ulrike Paschen, Birgit Klüppelholz, Anne Rummer, Wiebke Sieben, Ulrike Lampert, Konstanze Angelescu, Claudia Bollig, Martina Markes, Britta Runkel
Publikováno v:
Systematic Reviews, Vol 9, Iss 1, Pp 1-9 (2020)
Systematic Reviews
Systematic Reviews
BackgroundSickle cell disease (SCD) is an inherited autosomal recessive disorder caused by the replacement of normal haemoglobin (HbA) by mutant Hb (sickle Hb, HbS). The sickle-shaped red blood cells lead to haemolysis and vaso-occlusion. Especially
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bfd9ffb873a7cb490446826de4a2b175
https://doi.org/10.1186/s13643-020-01504-5
https://doi.org/10.1186/s13643-020-01504-5
Publikováno v:
BMC Medical Research Methodology
BMC Medical Research Methodology, Vol 19, Iss 1, Pp 1-9 (2019)
BMC Medical Research Methodology, Vol 19, Iss 1, Pp 1-9 (2019)
Background Stringent requirements exist regarding the transparency of the study selection process and the reliability of results. A 2-step selection process is generally recommended; this is conducted by 2 reviewers independently of each other (conve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c9644c76295d2abf2c91b1283161a6c0
https://pubmed.ncbi.nlm.nih.gov/31253092
https://pubmed.ncbi.nlm.nih.gov/31253092