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Results:
1-7
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Results: 7
Authors:
Kaariainen, H
Wallgren-Pettersson, C
Clarke, A
Pihko, H
Taskinen, H
Rintala, R
Citation: H. Kaariainen et al., Hirschsprung disease, mental retardation and dysmorphic facial features infive unrelated children, CLIN DYSMOR, 10(3), 2001, pp. 157-163
Authors:
Cormand, B
Pihko, H
Bayes, M
Valanne, L
Santavuori, P
Talim, B
Gershoni-Baruch, R
Ahmad, A
van Bokhoven, H
Brunner, HG
Voit, T
Topaloglu, H
Dobyns, WB
Lehesjoki, AE
Citation: B. Cormand et al., Clinical and genetic distinction between Walker-Warburg syndrome and muscle-eye-brain disease, NEUROLOGY, 56(8), 2001, pp. 1059-1069
Authors:
Talim, B
Ferreiro, A
Cormand, B
Vignier, N
Oto, A
Gogus, S
Cila, A
Lehesjoki, AE
Pihko, H
Guicheney, P
Topaloglu, H
Citation: B. Talim et al., Merosin-deficient congenital muscular dystrophy with mental retardation and cerebellar cysts unlinked to the LAMA2, FCMD and MEB loci, NEUROMUSC D, 10(8), 2000, pp. 548-552
Authors:
Auranen, M
Rapola, J
Pihko, H
Haltia, M
Leivo, I
Soinila, S
Virtanen, I
Kalimo, H
Anderson, LVB
Santavuori, P
Somer, H
Citation: M. Auranen et al., Muscle membrane-skeleton protein changes and histopathological characterization of muscle-eye-brain disease, NEUROMUSC D, 10(1), 2000, pp. 16-23
Authors:
Tyni, T
Pihko, H
Citation: T. Tyni et H. Pihko, Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency, ACT PAEDIAT, 88(3), 1999, pp. 237-245
Authors:
Corman, B
Avela, K
Pihko, H
Santavuori, P
Talim, B
Topaloglu, H
de la Chapelle, A
Lehesjoki, AE
Citation: B. Corman et al., Assignment of the muscle-eye-brain disease gene to 1p32-p34 by linkage analysis and homozygosity mapping, AM J HU GEN, 64(1), 1999, pp. 126-135
Authors:
Lonnqvist, T
Paetau, A
Nikali, K
von Boguslawski, K
Pihko, H
Citation: T. Lonnqvist et al., Infantile onset spinocerebellar ataxia with sensory neuropathy (IOSCA): neuropathological features, J NEUR SCI, 161(1), 1998, pp. 57-65
Risultati:
1-7
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