Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Tommi Kuorilehto"'
Autor:
Niku Oksala, Marianne Jaroma, Juha-Pekka Pienimäki, Tommi Kuorilehto, Teemu Vänttinen, Antti Lehtomäki, Veli-Pekka Suominen, Prasun Dastidar, Kimmo Mäkinen, Timo Erkinjuntti, Juha-Pekka Salenius
Publikováno v:
Cerebrovascular Diseases Extra, Vol 4, Iss 2, Pp 122-131 (2014)
Background: Cerebral white matter lesions (WMLs) predict long-term survival of conservatively treated acute stroke patients with etiology other than carotid stenosis. In carotid endarterectomy patients, WMLs are associated with severe carotid stenosi
Externí odkaz:
https://doaj.org/article/17f47f6eef2f4340937fd1b380c3b57b
Autor:
Niku Oksala, Velipekka Suominen, Terho Lehtimäki, Niina Khan, Leo-Pekka Lyytikäinen, Tommi Kuorilehto, Antti Lehtomäki, Jahangir Khan, Ilkka Seppälä
Publikováno v:
World journal of surgery. 42(4)
Individuals treated for abdominal aortic aneurysms (AAAs) are high-risk patients in whom better risk prediction could improve survival. Contemporary serum lipid parameters, such as apolipoproteins and lipoprotein subfractions, may improve or compleme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f13eac844c7534115c0610d8ec9542b
https://pubmed.ncbi.nlm.nih.gov/29026969
https://pubmed.ncbi.nlm.nih.gov/29026969
Autor:
Velipekka Suominen, Juha-Pekka Pienimäki, Juha-Pekka Salenius, Timo Erkinjuntti, Niku Oksala, Antti Lehtomäki, Kimmo Mäkinen, Marianne Jaroma, Teemu Vänttinen, Prasun Dastidar, Tommi Kuorilehto
Publikováno v:
Cerebrovascular Diseases Extra, Vol 4, Iss 2, Pp 122-131 (2014)
Cerebrovascular Diseases Extra
Cerebrovascular Diseases Extra
Background: Cerebral white matter lesions (WMLs) predict long-term survival of conservatively treated acute stroke patients with etiology other than carotid stenosis. In carotid endarterectomy patients, WMLs are associated with severe carotid stenosi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1a8458e262196122a22730757751123
http://www.karger.com/Article/FullText/363128
http://www.karger.com/Article/FullText/363128
Autor:
Sirkku Peltonen, Minna Pöyhönen, Juha Peltonen, Tommi Kuorilehto, Pekka Leinonen, Eetu Heervä, Kalervo Väänänen
Publikováno v:
Calcified Tissue International. 92:23-27
The current study is based on our earlier investigation carried out in 1999, where bone mineral density (BMD) of 35 neurofibromatosis type 1 (NF1) patients was measured and osteoporosis was shown to be common in NF1. The findings have been confirmed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::501e87e21abb0377a58818c629917302
https://doi.org/10.1007/s00223-012-9661-y
https://doi.org/10.1007/s00223-012-9661-y
Autor:
Tommi Kuorilehto, Anna Koffert, Hannu T. Aro, Sirkku Peltonen, Elina Jokinen, Juha Peltonen, Eetu Heervä
Publikováno v:
Journal of Bone and Mineral Research. 27(11):2333-2337
Neurofibromatosis 1 (NF1, von Recklinghausen's disease) is an autosomal dominant neurocutaneous-skeletal syndrome in which low bone mineral density (BMD) and osteoporosis are common. Low BMD is, however, not the sole component of fracture risk. In th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e93aeec3c0422d28cd6665b350294d86
https://doi.org/10.1002/jbmr.1685
https://doi.org/10.1002/jbmr.1685
Autor:
Sirkku Peltonen, Maria H. Alanne, Eetu Heervä, Teuvo Hentunen, Juha Peltonen, Tommi Kuorilehto, Kalervo Väänänen
Publikováno v:
Bone. 47:583-590
Neurofibromatosis 1 syndrome (NF1) presents with skeletal involvement suggesting that altered bone dynamics is associated with NF1. Histological analysis of three cases of NF1-related pseudarthrosis revealed numerous osteoclasts in contact with adjac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9472d68ae48330d23ae54ab25288a8c5
https://doi.org/10.1016/j.bone.2010.06.001
https://doi.org/10.1016/j.bone.2010.06.001
Autor:
Juha Peltonen, Ludwine Messiaen, Marja Nissinen, Juha Risteli, Hannu-Ville Leskelä, Pentti Kinnunen, Tommi Kuorilehto, Petri Lehenkari, Jussi Koivunen, Sirkku Peltonen
Publikováno v:
Bone. 44:243-250
Three patients with neurofibromatosis 1 (NF1) were operated for congenital pseudarthrosis (PA) of the tibia. Three non-NF1 patients served as reference. Both NF1 mRNA and protein were detected in the PAs and in rows of osteoblasts and numerous osteoc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9e53580a4df4ac3a82f0dbcb7d0075c
https://doi.org/10.1016/j.bone.2008.10.050
https://doi.org/10.1016/j.bone.2008.10.050
Autor:
Petri Lehenkari, Juha Peltonen, Tommi Kuorilehto, Pentti Kinnunen, Maria Alanne, Hannu-Ville Leskelä, Marja Nissinen
Publikováno v:
Pathology - Research and Practice. 202:687-690
Neurofibromatosis type 1 (NF1) is a common dominantly inherited disease. More than half of NF1 patients suffer from skeletal manifestations, of which congenital pseudarthrosis of tibia (CPT) is one of the most incapacitating lesions. Two NF1 patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c6e0ba3795e29604817bfca6c73be6f
https://doi.org/10.1016/j.prp.2006.03.006
https://doi.org/10.1016/j.prp.2006.03.006
Autor:
Erika Ekholm, K Hietaniemi, Pekka Paavolainen, Risto Penttinen, Ari Hiltunen, Tommi Kuorilehto, Juha Peltonen, Marja Nissinen
Publikováno v:
Journal of Histochemistry & Cytochemistry. 54:363-370
Neurofibromatosis type 1 (NF1) is an inherited disease with an incidence of about 1:3000 worldwide. Approximately half of all patients with NF1 present osseous manifestations, which can vary from mild to severely debilitating changes such as congenit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::361e8d4f6fecf4874f3d229ce8039712
https://doi.org/10.1369/jhc.5a6784.2005
https://doi.org/10.1369/jhc.5a6784.2005
Publikováno v:
Osteoporosis International. 16:928-936
Neurofibromatosis type 1 (NF1) is a dominantly inherited disease. Skeletal ailments such as short stature, kyphoscoliosis, tibial bowing and pseudarthrosis are common osseous manifestations of NF1. Previously, a correlation with scoliosis and decreas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9736995392ff090f6e79efa22b46f036
https://doi.org/10.1007/s00198-004-1801-4
https://doi.org/10.1007/s00198-004-1801-4