Zobrazeno 1 - 10
of 123
pro vyhledávání: '"AULA, Pertti"'
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 1984 Feb . 81(4), 1169-1173.
Externí odkaz:
https://www.jstor.org/stable/23269
The purpose of the research is to explore cultural diversity in design consciousness in light of the Popperian world-view. An additional aim of the study is to describe issues pertaining to cross-language design research. The paper focuses on the fol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::976337c42d1f84624b0e9bab258a23a6
Autor:
Mykkänen, Juha, Toivonen, Minna, Kleemola, Maaria, Savontaus, Marja-Liisa, Simell, Olli, Aula, Pertti, Huoponen, Kirsi
Publikováno v:
In Biochemical and Biophysical Research Communications 2003 301(4):855-861
Publikováno v:
In Molecular Genetics and Metabolism September-October 2002 77(1-2):99-107
Autor:
Toivonen, Minna, Mykkänen, Juha, Aula, Pertti, Simell, Olli, Savontaus, Marja-Liisa, Huoponen, Kirsi
Publikováno v:
In Biochemical and Biophysical Research Communications 15 March 2002 291(5):1173-1179
Autor:
Varho, Tarja T. ∗, *, Alajoki, Liisa E. ∗, Posti, Kristiina M. ∗, Korhonen, Tapio T., Renlund, Martin G. ∗∗, Nyman, Samuel R.G., Sillanpää, Matti L., Aula, Pertti P. ∗
Publikováno v:
In Pediatric Neurology 2002 26(4):267-273
Autor:
Aula, Nina, Salomäki, Pirjo, Timonen, Ritva, Verheijen, Frans, Mancini, Grazia, Månsson, Jan-Eric, Aula, Pertti, Peltonen, Leena
Publikováno v:
In The American Journal of Human Genetics 2000 67(4):832-840
Autor:
Aula, Pertti, Von Koskull, Harriet, Teramo, Kari, Karjalainen, Olavi, Virtanen, Ismo, Lehto, Veli-Pekka, Dahl, Doris
Publikováno v:
The British Medical Journal, 1980 Nov . 281(6253), 1456-1457.
Externí odkaz:
https://www.jstor.org/stable/25442272
Autor:
Jalanko, Hannu, Aula, Pertti
Publikováno v:
British Medical Journal (Clinical Research Edition), 1982 May . 284(6329), 1593-1594.
Externí odkaz:
https://www.jstor.org/stable/29506613
Autor:
Silander, Kaisa, Meretoja, Päivi, Nelis, Eva, Timmerman, Vincent, Van Broeckhoven, Christine, Aula, Pertti, Savontaus, Marja-Liisa
Publikováno v:
Human mutation
Dejerine-Sottas syndrome (DSS), or hereditary motor and sensory neuropathy (HMSN) type III, is a severe hypertrophic demyelinating neuropathy with infantile onset. The clinical symptoms are similar to those found in Charcot-Marie-Tooth disease type 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2097::830aab8064c21f5b548a7b2b46fe8f97
https://hdl.handle.net/10067/996840151162165141
https://hdl.handle.net/10067/996840151162165141