Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Outi Kovero"'
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.
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
Publikováno v:
Acta Odontologica Scandinavica. 61:149-153
The aim of the present study was to detect possible associations between trunk and cervical asymmetry and facial symmetry. Frontal cephalograms prepared in the natural head position, representing 79 subjects (40 males, 39 females) with mild to modera
Craniofacial features in Cohen syndrome: an anthropometric and cephalometric analysis of 14 patients
Publikováno v:
Clinical Genetics. 62:157-164
Cohen syndrome (Mendelian Inheritance in Man [MIM] no. 216550) is a rare, autosomal-recessive inherited disorder with mental retardation and a typical appearance. The condition is relatively common in Finland where 35 patients have been diagnosed. We
Autor:
Mauno Könönen, Outi Kovero
Publikováno v:
Acta Odontologica Scandinavica. 54:271-274
Signs and symptoms of temporomandibular disorders (TMDs) and the frequency of radiologically observed abnormalities in the condyles of temporomandibular joints (TMJs) of adolescent violin players (VP group) were investigated in a group of 31 music st
Autor:
Mauno Könönen, Outi Kovero
Publikováno v:
Acta Odontologica Scandinavica. 53:81-84
The frequency of temporomandibular disorders (TMDs) and radiologically observed abnormalities in the condyles of the temporomandibular joints (TMJs) of professional violin and viola players was investigated in 26 orchestra violinists/violists (VP gro
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
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.
Autor:
Satu Alaluusua, Donald G. Patterson, Outi Kovero, Jouko Tuomisto, Pirjo-Liisa Lukinmaa, Larry L. Needham, Pier Calderara, Pier Mario Gerthoux, Paolo Mocarelli
Publikováno v:
Environmental Health Perspectives
Children’s developing teeth may be sensitive to environmental dioxins, and in animal studies developing teeth are one of the most sensitive targets of toxicity of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD). Twenty-five years after the dioxin accide
Publikováno v:
Cranio : the journal of craniomandibular practice. 21(4)
The purpose of this population-based cohort was to measure maximal bite force (MBF) in the molar and incisal regions and to examine whether MBF was associated with TMD, gender, occlusion (in terms of overjet, overbite, and total number of occluding c