Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Krista Rantakari"'
Autor:
Simo Särkkä, Jaakko Hollmén, Petri Rahkonen, Markus Leskinen, Päivi Nevalainen, Olli-Pekka Rinta-Koski, Aulikki Lano, Leena Lauronen, Sture Andersson, Krista Rantakari, Marjo Metsäranta
Publikováno v:
Pediatric Research
Background Extremely low gestational age newborns (ELGANs) are at risk of neurodevelopmental impairments that may originate in early NICU care. We hypothesized that early oxygen saturations (SpO2), arterial pO2 levels, and supplemental oxygen (FiO2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e72dd8045409fb966d762de6a0059eb2
https://aaltodoc.aalto.fi/handle/123456789/111360
https://aaltodoc.aalto.fi/handle/123456789/111360
Publikováno v:
Acta Paediatrica. 108:443-451
AIM We investigated the characteristics and effects of sleep stage, supplemental oxygen and caffeine on periodic breathing (PB) and apnoea of prematurity (AOP) in preterm infants. METHODS This 2013-2015 study recruited 21 preterm infants on neonatal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::adbd2245dc9268b16c260317e05a12bb
https://doi.org/10.1111/apa.14541
https://doi.org/10.1111/apa.14541
Autor:
Markus Leskinen, Simo Särkkä, Jaakko Hollmén, Olli-Pekka Rinta-Koski, Sture Andersson, Krista Rantakari
Publikováno v:
2017 IEEE Life Sciences Conference (LSC).
Bronchopulmonary dysplasia (BPD), necrotizing enterocolitis (NEC), and retinopathy of prematurity (ROP) are severe complications affecting Very Low Birth Weight (VLBW) infants. Our findings show that data gathered in the intensive care unit during th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f949626bc17ca56a11ddf1fd4109699
https://doi.org/10.1109/lsc.2017.8268174
https://doi.org/10.1109/lsc.2017.8268174
Autor:
Marja Ojaniemi, Teemu Kuulasmaa, Jukka Kero, Krista Rantakari, Jaakko Ignatius, Juha-Pekka Pursiheimo, Jorma Toppari, Christoffer Löf, Henriette Undeutsch, Jarmo Jääskeläinen, Markku Laakso, Konrad Patyra, Heike Biebermann, Tuulia Pajunen, Gunnar Kleinau, Taina Mustila, Heiko Krude, Jagadish Vangipurapu, Andreina Kero, Päivi J. Miettinen, Turkka Kirjavainen, Peter Kühnen, Holger Jaeschke
Publikováno v:
Thyroid
Background: Congenital hypothyroidism (CH) is defined as the lack of thyroid hormones at birth. Mutations in at least 15 different genes have been associated with this disease. While up to 20% of CH cases are hereditary, the majority of cases are spo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::178eb13c0d0bc3c4ff9ae436f667f551
https://pubmed.ncbi.nlm.nih.gov/27373559
https://pubmed.ncbi.nlm.nih.gov/27373559