Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Kaija Kuurila"'
Publikováno v:
Pediatric Anesthesia. 16:548-553
Summary Background: Pain following tonsillectomy is often intense. Nonsteroidal anti-inflammatory drugs and opioids are effective, but both can cause adverse effects. Tramadol may be a viable alternative for post-tonsillectomy pain. This study was de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a468200da0c26200f1fb7d65d024ac7
https://doi.org/10.1111/j.1460-9592.2005.01819.x
https://doi.org/10.1111/j.1460-9592.2005.01819.x
Autor:
Marina Kolkka, Outi Kovero, Kaija Kuurila, Ilkka Kaitila, Seppo Pynnönen, Janna Waltimo-Sirén
Publikováno v:
American Journal of Medical Genetics Part A. :142-150
Osteogenesis imperfecta (OI) is a heterogeneous group of connective tissue diseases that mainly manifest as bone fragility and skeletal deformity. In most families it segregates as a dominant trait and results from mutations in type I collagen genes.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9b9e34ac5a626a6aaba74f8cef4cc4d0
https://doi.org/10.1002/ajmg.a.30523
https://doi.org/10.1002/ajmg.a.30523
Autor:
Leena Ala-Kokko, Reidar Grénman, Kaija Kuurila, Seppo Pynnönen, Jarmo Körkkö, James C. Hyland, Heini Hartikka, Ilkka Kaitila
Publikováno v:
Human Mutation. 24:147-154
Osteogenesis imperfecta (OI) is caused by mutations in COL1A1 and COL1A2 that code for the alpha1 and alpha2 chains of type I collagen. Phenotypes correlate with the mutation types in that COL1A1 null mutations lead to OI type I, and structural mutat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::00694795865d0d5555cb04c6a34101ad
https://doi.org/10.1002/humu.20071
https://doi.org/10.1002/humu.20071
Autor:
Reidar Grénman, Ilkka Kaitila, S. Karjalainen, E. Kentala, Seppo Pynnönen, Outi Kovero, Kaija Kuurila, J. Waltimo
Publikováno v:
American Journal of Medical Genetics Part A. :350-358
Progressive hearing loss is a major symptom in osteogenesis imperfecta (OI), a genetic brittle bone disease. Vertigo is frequently associated with otosclerosis in which the hearing loss clinically resembles that in OI. Vertigo is also common in basil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f664d4599a98dc09fdb0d1698eec2b5e
https://doi.org/10.1002/ajmg.a.20088
https://doi.org/10.1002/ajmg.a.20088
Publikováno v:
European Journal of Pediatrics. 159:515-519
Osteogenesis imperfecta (OI) is a genetic disorder of connective tissue. Progressive hearing loss is one of the principal symptoms of OI, affecting about 50% of adult patients. Hearing loss may also occur in childhood and results in additional disabi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a8080cc5e4ef382eeaefab6cd68f3cc
https://doi.org/10.1007/s004310051322
https://doi.org/10.1007/s004310051322
Autor:
Christine D Kuslich, James D. San Antonio, Joan C. Marini, Raymond Dalgleish, Peter J. Roughley, James Troendle, Wayne A. Cabral, Sarah A. Milgrom, Diana Chen, Paul Coucke, Peter H. Byers, Aileen M. Barnes, Deborah Krakow, Kathleen Yang, Daniel H. Cohn, Darwin J. Prockop, Heini Hartikka, Jarmo Körkkö, James C. Hyland, Monica Mottes, Sofie Symoens, Francis H. Glorieux, Antonella Forlino, Alan M. Lund, Kaija Kuurila-Svahn, Anne De Paepe, Ulrike Schwarze
Osteogenesis imperfecta (OI) is a generalized disorder of connective tissue characterized by fragile bones and easy susceptibility to fracture. Most cases of OI are caused by mutations in type I collagen. We have identified and assembled structural m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::293c8613a984ed63dc7f45d49e357267
http://hdl.handle.net/11562/232426
http://hdl.handle.net/11562/232426
Publikováno v:
Journal of neurosurgery. 105(3)
Object Osteogenesis imperfecta (OI), which usually results from mutations in type I collagen genes, causes bone fragility and deformities. The head is often abnormally shaped, and changes in skull base anatomy in the form of basilar impression and ba
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10099fc59d42726fef1a0ff603f6d5ce
https://pubmed.ncbi.nlm.nih.gov/16961126
https://pubmed.ncbi.nlm.nih.gov/16961126
Autor:
Janna, Waltimo-Sirén, Marina, Kolkka, Seppo, Pynnönen, Kaija, Kuurila, Ilkka, Kaitila, Outi, Kovero
Publikováno v:
American journal of medical genetics. Part A. (2)
Osteogenesis imperfecta (OI) is a heterogeneous group of connective tissue diseases that mainly manifest as bone fragility and skeletal deformity. In most families it segregates as a dominant trait and results from mutations in type I collagen genes.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8e36492fb77912d537b6c6fa5e11004d
https://pubmed.ncbi.nlm.nih.gov/15666304
https://pubmed.ncbi.nlm.nih.gov/15666304
Autor:
Reidar Grénman, Kaija Kuurila
Publikováno v:
Clinical otolaryngology and allied sciences. 29(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d25305f2c053e62a700a9331ae41392
https://pubmed.ncbi.nlm.nih.gov/12755755
https://pubmed.ncbi.nlm.nih.gov/12755755
Publikováno v:
The Annals of otology, rhinology, and laryngology. 113(3 Pt 1)
We present the surgical findings and audiometric results of ear surgery performed between 1961 and 2002 on 33 Finnish patients (43 operations) with osteogenesis imperfecta (OI). The mean age at the time of the first operation was 30.1 years. The typi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed2a8316173a3fceee68eab155e0bdda
https://pubmed.ncbi.nlm.nih.gov/15053199
https://pubmed.ncbi.nlm.nih.gov/15053199