Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Marina, Kolkka"'
Autor:
Marina Kolkka, Satu K. Jääskeläinen, Heli Forssell, Arja Virtanen, Antti Puhakka, Ullamari Pesonen
Publikováno v:
European Journal of Pain. 23:1153-1161
BACKGROUND AND AIMS Neuropathic mechanisms are involved in burning mouth syndrome (BMS), and variation of the dopamine D2 receptor (DRD2) gene contributes to experimental pain perception. We investigated whether neurophysiologic findings differ in BM
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a633e549dfe24d0c3a150e1d7cd05ba7
https://doi.org/10.1002/ejp.1382
https://doi.org/10.1002/ejp.1382
Autor:
Satu K. Jääskeläinen, Heli Forssell, Antti Puhakka, Arja Virtanen, Ullamari Pesonen, Marina Kolkka-Palomaa
Publikováno v:
Clinical Neurophysiology. 128:e295-e296
Background and aims Neuropathic mechanisms are involved in burning mouth syndrome (BMS), and variation of dopamine D2 receptor (DRD2) gene may contribute to pain perception. We investigated whether the neurophysiologic findings differ in BMS patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9b4356fe79305ef2797e9286e62eb0b6
https://doi.org/10.1016/j.clinph.2017.07.371
https://doi.org/10.1016/j.clinph.2017.07.371
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:
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