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Results: 1-6 |
Results: 6

Authors: Auranen, M Vanhala, R Vosman, M Levander, M Varilo, T Hietala, M Riikonen, R Peltonen, L Jarvela, I
Citation: M. Auranen et al., MECP2 gene analysis in classical Rett syndrome and in patients with Rett-like features, NEUROLOGY, 56(5), 2001, pp. 611-617

Authors: Kiuru, M Launonen, V Hietala, M Aittomaki, K Vierimaa, O Salovaara, R Arola, J Pukkala, E Sistonen, P Herva, R Aaltonen, LA
Citation: M. Kiuru et al., Familial cutaneous leiomyomatosis is a two-hit condition associated with renal cell cancer of characteristic histopathology, AM J PATH, 159(3), 2001, pp. 825-829

Authors: Juvonen, V Hietala, M Paivarinta, M Rantamaki, M Hakamies, L Kaakkola, S Vierimaa, O Penttinen, M Savontaus, ML
Citation: V. Juvonen et al., Clinical and genetic findings in Finnish ataxia patients with the spinocerebellar ataxia 8 repeat expansion, ANN NEUROL, 48(3), 2000, pp. 354-361

Authors: Jarvinen, O Hietala, M Aalto, AM Arvio, M Uutela, A Aula, P Kaariainen, H
Citation: O. Jarvinen et al., A retrospective study of long-term psychosocial consequences and satisfaction after carrier testing in childhood in an autosomal recessive disease: aspartylglucosaminuria, CLIN GENET, 58(6), 2000, pp. 447-454

Authors: Autti, T Rapola, J Santavuori, P Raininko, R Renlund, M Liukkonen, E Lauronen, L Wirtavuori, K Hietala, M Saarinen-Pihkala, U
Citation: T. Autti et al., Bone marrow transplantation in aspartylglucosaminuria - Histopathological and MRI study, NEUROPEDIAT, 30(6), 1999, pp. 283-288

Authors: Valkonen, S Hietala, M Savontaus, ML Aula, P
Citation: S. Valkonen et al., Origin of Finnish mutations causing aspartylglucosaminuria, HEREDITAS, 131(3), 1999, pp. 191-195
Risultati: 1-6 |