Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Tuija Löppönen"'
Autor:
Liisa Lehtonen, Outi Tammela, Tuija Löppönen, Vineta Fellman, Anu Haavisto, Liisa Klenberg, Viena Tommiska, Aulikki Lano, Kaija Mikkola, Annika Koivisto, Marit Korkman, Päivi Olsén
Publikováno v:
BMJ Paediatrics Open, Vol 6, Iss 1 (2022)
Externí odkaz:
https://doaj.org/article/483350c6eddf4a65aea3e71a666f02ed
Autor:
Viena Tommiska, Aulikki Lano, Päivi Kleemola, Liisa Klenberg, Liisa Lehtonen, Tuija Löppönen, Päivi Olsen, Outi Tammela, Vineta Fellman, for the Finnish ELBW Cohort Study Group (FinELBW)
Publikováno v:
Health Science Reports, Vol 3, Iss 3, Pp n/a-n/a (2020)
Abstract Background and aims Children with extremely low‐birth weight (ELBW) have a high risk for cognitive, motor, and attention impairments and learning disabilities. Longitudinal follow‐up studies to a later age are needed in order to increase
Externí odkaz:
https://doaj.org/article/866021db95b946bcbb08a2277b55fdbf
Autor:
Liisa Kröger, Tuija Löppönen, Leena Ala‐Kokko, Heikki Kröger, Hanna‐Mari Jauhonen, Kaisa Lehti, Jarmo Jääskeläinen
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 7, Iss 8, Pp n/a-n/a (2019)
Abstract Background MONA, which stands for a spectrum of Multicentric Osteolysis, subcutaneous Nodulosis, and Athropathia, is an ultra rare autosomal recessive disorder caused by mutations in the matrix metallopeptidase 2 (MMP2) gene. To date only 44
Externí odkaz:
https://doaj.org/article/752194ac4f204239acc65aa174e54cec
Autor:
Tuija Löppönen, Tuula Lönnqvist, Marja-Leena Lamidi, Tuomas Selander, Antti Saari, Leo Dunkel, Marjo Karvonen, Ulla Sankilampi
Publikováno v:
Acta Paediatrica. 110:881-888
Aim The aim was to compare the performances of the World Health Organization (WHO) and population-based (PB) references in the screening for hydrocephalus in infants aged less than two years. Methods We collected 341 longitudinal head circumference (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::45531e5808a78915fcdd89676f7b7919
https://doi.org/10.1111/apa.15533
https://doi.org/10.1111/apa.15533
Autor:
Outi Tammela, Liisa Lehtonen, Viena Tommiska, Vineta Fellman, Tuija Löppönen, Päivi Kleemola, Päivi Olsén, Liisa Klenberg, Aulikki Lano
Publikováno v:
Health Science Reports
Health Science Reports, Vol 3, Iss 3, Pp n/a-n/a (2020)
Health Science Reports, Vol 3, Iss 3, Pp n/a-n/a (2020)
Background and aims: Children with extremely low-birth weight (ELBW) have a high risk for cognitive, motor, and attention impairments and learning disabilities. Longitudinal follow-up studies to a later age are needed in order to increase understandi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ad2d9d9d428828d02e71ac79cae9da9
https://pubmed.ncbi.nlm.nih.gov/32832703
https://pubmed.ncbi.nlm.nih.gov/32832703
Autor:
Päivi Lindholm, Tuija Löppönen, Johanna Uusimaa, Elina Mäki-Torkko, Mirja Luotonen, J. Leisti, Marja-Leena Väisänen, Mirja Väyrynen, Minna Allinen, Heikki Löppönen
Publikováno v:
The Laryngoscope. 113:1758-1763
Objective: The aims of the present study were to evaluate the role of the gap junction protein β-2 gene (GJB2), encoding connexin 26 (Cx26), in children with moderate to profound prelingual nonsyndromic sensorineural hearing impairment (HI) and to i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c276d32d0ce04186fba5fb95c283009
https://doi.org/10.1097/00005537-200310000-00018
https://doi.org/10.1097/00005537-200310000-00018
Publikováno v:
International Journal of Pediatric Otorhinolaryngology. 73:1353-1357
Objective The purpose of this study was to determine the prevalence and etiology of congenital or early acquired bilateral sensorineural hearing impairment (SNHI) in children born from 1988 to 2002 in the district of Kuopio University Hospital, Finla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1ad59203d3d46fe2cd2c055f1d17d9d
https://doi.org/10.1016/j.ijporl.2009.06.009
https://doi.org/10.1016/j.ijporl.2009.06.009
Autor:
Ulpu Seppänen, Tuija Lundán, Tuija Löppönen, Jarmo Körkkö, Jaakko Ignatius, Helena Kääriäinen
Publikováno v:
Arthritis Care & Research. 51:925-932
Objective To define the clinical, radiologic, and molecular genetic characteristics of a family with early progressive osteoarthritis mimicking childhood rheumatoid arthritis, Scheuermann-like changes of the spine, tall stature, short 3 and 4 metatar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aac9d030c3012f6cbe57ecf5e85735f1
https://doi.org/10.1002/art.20817
https://doi.org/10.1002/art.20817
Publikováno v:
The Cleft Palate-Craniofacial Journal. 41:651-654
ObjectiveThe aim of this study was to examine the relationship between dental maturation and somatic development and to discover their possible deviations in children with shunt-treated hydrocephalus.DesignRadiographs (orthopantomogram and hand-wrist
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::573eba2514b4410ae4af52982bd6a0b2
https://doi.org/10.1597/03-018.1
https://doi.org/10.1597/03-018.1
Autor:
J Pyhtinen, Willy Serlo, Juhani Laitinen, Mikael Knip, Tuija Löppönen, A.-L. Saukkonen, Eija Pääkkö
Publikováno v:
Archives of Disease in Childhood. 70:530-5
OBJECTIVE--To study the role of magnetic resonance imaging (MRI) in evaluating children with shunted hydrocephalus. METHODS--Sixty one asymptomatic children with shunted hydrocephalus or cystic cerebrospinal fluid collections were studied by cranial
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::564608280910498bd7b6ecd6b6975bff
https://doi.org/10.1136/adc.70.6.530
https://doi.org/10.1136/adc.70.6.530