Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Kaisa Elomaa"'
Autor:
Ralitsa Raycheva, Kostadin Kostadinov, Elena Mitova, Georgi Iskrov, Georgi Stefanov, Merja Vakevainen, Kaisa Elomaa, Yuen-Sum Man, Edith Gross, Jana Zschüntzsch, Richard Röttger, Rumen Stefanov
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-18 (2024)
Abstract Background Patient registries and databases are essential tools for advancing clinical research in the area of rare diseases, as well as for enhancing patient care and healthcare planning. The primary aim of this study is a landscape analysi
Externí odkaz:
https://doaj.org/article/9f9c2028614d49d3b07149f48c552102
Autor:
Valentin Liévin, Jonas Meinertz Hansen, Allan Lund, Deborah Elstein, Mads Emil Matthiesen, Kaisa Elomaa, Kaja Zarakowska, Iris Himmelhan, Jaco Botha, Hanne Borgeskov, Ole Winther
Publikováno v:
PLOS Digital Health, Vol 2, Iss 6, p e0000269 (2023)
Early diagnosis is crucial for well-being and life quality of the rare disease patient. Access to the most complete knowledge about diseases through intelligent user interfaces can play an important role in supporting the physician reaching the corre
Externí odkaz:
https://doaj.org/article/e6f35cb165ba41948900b30991a134c8
Autor:
Minja Pehrsson, Hanna Heikkinen, Ulla Wartiovaara-Kautto, Sampo Mäntylahti, Pia Bäckström, Mariann I. Lassenius, Kristiina Uusi-Rauva, Olli Carpén, Kaisa Elomaa
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 33, Iss , Pp 100911- (2022)
Background: Autosomal recessive Gaucher disease (GD) is likely underdiagnosed in many countries. Because the number of diagnosed GD patients in Finland is relatively low, and the true prevalence is currently not known, it was hypothesized that undiag
Externí odkaz:
https://doaj.org/article/b89df55e164e428891087e026837972c
Autor:
Markku J. Savolainen, Antti Karlsson, Samppa Rohkimainen, Iiro Toppila, Mariann I. Lassenius, Carlos Vaca Falconi, Kristiina Uusi-Rauva, Kaisa Elomaa
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 27, Iss , Pp 100725- (2021)
Background: Gaucher disease (GD) is a rare inherited multiorgan disorder, yet a diagnosis can be significantly delayed due to a broad spectrum of symptoms and lack of disease awareness. Recently, the prototype of a GD point-scoring system (PSS) was e
Externí odkaz:
https://doaj.org/article/38f284b8027447c3a34e8bc0e1e81f11
Autor:
Valentin MSc Eng Liévin, Jonas Meinertz Hansen, Allan Lund, Deborah Elstein, Mads Emil Matthiesen, Kaisa Elomaa, Kaja Zarakowska, Iris Himmelhan, Jaco Botha, Hanne Borgeskov, Ole Winther
Publikováno v:
SSRN Electronic Journal.
Autor:
Michelle Luo, Pravin Kamble, Heather M. Berlin, Peter Szolovits, Irene Y. Chen, Kaisa Elomaa, Song Wang, David Sontag
Publikováno v:
American Journal of Gastroenterology. 116:S353-S353
Autor:
Carlos Vaca Falconi, Mariann I. Lassenius, Markku J. Savolainen, Antti Karlsson, Samppa Rohkimainen, Iiro Toppila, Kaisa Elomaa
Publikováno v:
Molecular Genetics and Metabolism. 129:S143-S144
Publikováno v:
Molecular Genetics and Metabolism. 126:S129
Publikováno v:
Contraception. 63:13-18
Using steady-state conditions the authors aimed to test if administration of oral activated charcoal affects the bioavailability of norethisterone acetate (NET Ac) and gestodene (GEST) by inhibiting their enterohepatic recirculation. 13 volunteers re
Publikováno v:
Human Reproduction. 16:76-81
Ovulatory potential was studied during the use of two oral contraceptive pill preparations, after repeated mid-cycle administration of activated charcoal. Eleven women used monophasic pills containing gestodene, 75 microgram, plus ethinyl oestradiol,