Zobrazeno 1 - 10
of 66
pro vyhledávání: '"L, Luostarinen"'
Autor:
Cheng Qian, Seppo Juvela, L. Kupila, Michaela K. Bode, Juha Huhtakangas, M. Savolainen, Turgut Tatlisumak, Sami Tetri, H. Numminen, J. Ollikainen, L. Luostarinen
Backround: Venous thromboembolism (VTE) after primary intracerebral hemorrhage (ICH) worsens patient prognosis. Administering low-molecular weight heparins (LMWH) to prevent VTE early (24 h) may increase the risk of hematoma enlargement, whereas admi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1badfbfa08fcee64439b6ea2a80d29c6
http://hdl.handle.net/10138/330705
http://hdl.handle.net/10138/330705
Introduction Sex hormones have been implicated in the etiology of a number of diseases. To better understand disease etiology and the mechanisms of disease-risk factor associations, this analysis aimed to investigate the associations of anthropometri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::5fc426150615fc11d92707af33b37ad9
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3056612
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3056612
Autor:
M, Arvio, L, Luostarinen
Publikováno v:
Clinical genetics. 90(5)
In 1988, we assessed the adaptive skills of 45 adults with Down syndrome (DS) (21 women and 24 men, age 20-58) with the Portage scale. Since then, we have followed them and also screened for signs of clinical dementia with the Present Psychiatric Sta
Autor:
Johanna Uusimaa, Anna H. Hakonen, Ilse Paetau, Tuula Lönnqvist, Leena Valanne, Helena Pihko, Anders Paetau, Pirjo Isohanni, Anu Suomalainen, Elina Liukkonen, Tiina Wallden, L. Luostarinen, Tarja Linnankivi, Liliya Euro
Publikováno v:
Neurology. 76:811-815
Objective: Mitochondrial DNA polymerase γ (POLG1) mutations in children often manifest as Alpers syndrome, whereas in adults, a common manifestation is mitochondrial recessive ataxia syndrome (MIRAS) with severe epilepsy. Because some patients with
Akademický článek
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Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 74:490-494
Objectives: A body of evidence shows that coeliac disease is associated with protean manifestations outside the intestine, and neurological disorders are well recognised. However, it remains obscure whether there are signs of clinical or subclinical
Autor:
M. Mäki, T. Pirttilä, L. Luostarinen, T. Erila, Pekka Collin, Markku Peräaho, Prasun Dastidar
Publikováno v:
European Neurology. 46:187-191
Patients with epilepsy and posterior cerebral calcifications have an increased risk of coeliac disease (CD). The occurrence of this syndrome and the overall risk of CD and epilepsy remain still poorly understood. This study presents the prevalence of
Publikováno v:
European Neurology. 42:132-135
It is well known that coeliac disease may be associated with various neurological manifestations. We have had a high index of suspicion of coeliac disease during recent years in our neurological clinic. As a result 10 (7%) out of 144 of our new coeli
Autor:
Sabine Fitzek, Péter Klivényi, C. Pierrot Deseilligny, Philip Bartels, Ji Yeon Ryu, Jose F. Tellez-Zenteno, H. Diehl, Silvia Angeli, C. Laske, M. Danis, Yoshiyuki Kuroiwa, M.M. Thiebaut, J. Tofighi, Seunghoon Lee, Hanns Christian Hopf, M. Mäki, Yuji Johmura, Margit Török, Ken Johkura, Krisztina Bencsik, P. Dastidar, Hidehiro Mizusawa, H. Traupe, P. Oschmann, Eisuke Ozawa, T. Erilä, Carlo Tosi, Maurizio Ferrari, Takehiko Nishiyama, Sang-Ahm Lee, José María Remes-Troche, Juan Garduño-Espinoza, Allison Chan, R. Bauer, N. Chatzimanolis, P. Collin, Gary N. McAbee, Kazuo Nagashima, Claudio Städler, Bruno Estañol, Tamás Járdánházy, Soon Keum Lee, B.S. Kühne, F. Bricaire, Enos Bernasconi, Ullrich Meier, T. Bregenzer, Hitoshi Yamada, T. Pirttilä, Dong-Wha Kang, Manho Kim, Guillermo García-Ramos, M. Kaps, Takayuki Momoo, E. Roze, László Vécsei, Marina Grandis, Teruaki Oka, Paola Carrera, Joong-Koo Kang, J. Kraus, Carlo Gandolfo, Satoshi Orimo, E. Caumes, M. Peräaho, Claudio Gobbi, Nobuyuki Sodeyama, Clemens Fitzek, Judit Füvesi, D. Mazevet, Cecilia Rajda, Claude Merenda, Kon Chu, Andrea Assini, Massimo Del Sette, Donatella Biancolini, L. Luostarinen
Publikováno v:
European Neurology. 46:233-235
Akademický článek
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