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Results: 5

Authors: Nokelainen, P Heiskala, H Raininko, R Autti, T Wirtavuori, K Hakkinen, AM Flint, J
Citation: P. Nokelainen et al., Two brothers with macrocephaly, progressive cerebral atrophy and abnormal white matter, severe mental retardation, and Lennox-Gastaut spectrum type epilepsy: An inherited encephalopathy of childhood?, AM J MED G, 103(3), 2001, pp. 198-206

Authors: Lindblom, N Heiskala, H Hatonen, T Mustanoja, S Alfthan, H Alila-Johansson, A Laakso, ML
Citation: N. Lindblom et al., No evidence for extraocular light induced phase shifting of human melatonin, cortisol and thyrotropin rhythms, NEUROREPORT, 11(4), 2000, pp. 713-717

Authors: Nokelainen, P Heiskala, H Lehesjoki, AE Kaski, M
Citation: P. Nokelainen et al., A patient with 2 different repeat expansion mutations, ARCH NEUROL, 57(8), 2000, pp. 1199-1203

Authors: Hatonen, T Kirveskari, E Heiskala, H Sainio, K Laakso, ML Santavuori, P
Citation: T. Hatonen et al., Melatonin ineffective in neuronal ceroid lipofuscinosis patients with fragmented or normal motor activity rhythms recorded by wrist actigraphy, MOL GEN MET, 66(4), 1999, pp. 401-406

Authors: Autti, T Muttilainen, M Raininko, R Heiskala, H Puranen, J Hakkinen, AM Tienari, P Santavuori, P Suominen, P Somer, M
Citation: T. Autti et al., Extensive cerebral white matter abnormality without clinical symptoms: A new hereditary condition?, ANN NEUROL, 45(6), 1999, pp. 801-805
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