Zobrazeno 1 - 10
of 704
pro vyhledávání: '"B Falck"'
Autor:
Kevin V. Pixley, Jose B. Falck-Zepeda, Robert L. Paarlberg, Peter W. B. Phillips, Inez H. Slamet-Loedin, Kanwarpal S. Dhugga, Hugo Campos, Neal Gutterson
Publikováno v:
Nature Genetics. 54:364-367
Autor:
Fred Gould, Richard M. Amasino, Dominique Brossard, C. Robin Buell, Richard A. Dixon, Jose B. Falck-Zepeda, Michael A. Gallo, Ken E. Giller, Leland L. Glenna, Timothy Griffin, Daniel Magraw, Carol Mallory-Smith, Kevin V. Pixley, Elizabeth P. Ransom, David M. Stelly, C. Neal Stewart
Publikováno v:
Science (New York, N.Y.). 377(6610)
Current process-based approaches to regulation are no longer fit for purpose
Akademický článek
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Publikováno v:
Journal of Rehabilitation Medicine. 17:101-105
The aim of this study was to assess the cognitive skills and visuo-motor performances of patients with type-2 diabetes. An ADL questionnaire, neurophysiological EEG recordings and a comprehensive battery of neuropsychological tests were administered
Autor:
B Falck, L Puksa, J Paniagua Soto, P Torné-Poyatos, F Reche-Lorite, Satu K. Jääskeläinen, Carmen Martinez-Aparicio
Publikováno v:
European Journal of Neurology. 27:529-535
Background and purpose It is well established that patient-related constitutional features predispose to focal peripheral neuropathies. Some of these risk factors were investigated in common focal neuropathies encountered in patients referred for ele
Publikováno v:
Banks and Bank Systems, Vol 8, Iss 4 (2013)
Externí odkaz:
https://doaj.org/article/b1da64fe3f6c489cb92541a37ec095b9
Akademický článek
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Autor:
R. J. Marttila, H. Kalimo, B. Falck, E. Aarnisalo, Reidar Grénman, A. Anttinen, Eeva Nikoskelainen
Publikováno v:
Acta Neurologica Scandinavica. 73:180-190
A family with hereditary, neuropathologically confirmed olivopontocerebellar atrophy (OPCA) associated with macular degeneration is described. The mode of inheritance was autosomal dominant. The first symptom was insidious, progressive visual loss ca
Autor:
Olli Simell, Satu K. Jääskeläinen, Olli J. Heinonen, K. Heinanen, Kirsti Näntö-Salonen, B. Falck, K. E. Peltola
Publikováno v:
Neurology. 59:735-740
Objective: To evaluate peripheral nervous system involvement in gyrate atrophy of the choroid and retina with hyperornithinemia (GA). Background: GA is an inborn error of amino acid metabolism caused by mutations in the enzyme ornithine aminotransfer
Publikováno v:
Protoplasma. 192:20-27
Pinocytosis induced by Na+ was assayed by phase contrast microscopy in 8–12 days starvedAmoeba proteus. These cultures were inactive with respect to calcium-dependent Na+-induced pinocytosis, but treatment with amino acid methyl and ethyl esters in