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106 results
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Benign muscular dystrophy with autosomal dominant inheritance.
Somer H, Laulumaa V, Paljärvi L, Partanen J, Lamminen A, Pihko H, Sariola H, Haltia M. Somer H, et al. Among authors: paljarvi l. Neuromuscul Disord. 1991;1(4):267-73. doi: 10.1016/0960-8966(91)90100-7. Neuromuscul Disord. 1991. PMID: 1822805
Taurine in normal and diseased human skeletal muscle.
Airaksinen EM, Paljärvi L, Partanen J, Collan Y, Laakso R, Pentikäinen T. Airaksinen EM, et al. Among authors: paljarvi l. Acta Neurol Scand. 1990 Jan;81(1):1-7. doi: 10.1111/j.1600-0404.1990.tb00923.x. Acta Neurol Scand. 1990. PMID: 2330810
Minicore myopathy with dominant inheritance.
Paljärvi L, Kalimo H, Lang H, Savontaus ML, Sonninen V. Paljärvi L, et al. J Neurol Sci. 1987 Jan;77(1):11-22. doi: 10.1016/0022-510x(87)90202-4. J Neurol Sci. 1987. PMID: 3806134
Late onset foot-drop muscular dystrophy with rimmed vacuoles.
Partanen J, Laulumaa V, Paljärvi L, Partanen K, Naukkarinen A. Partanen J, et al. Among authors: paljarvi l. J Neurol Sci. 1994 Sep;125(2):158-67. doi: 10.1016/0022-510x(94)90029-9. J Neurol Sci. 1994. PMID: 7807161
The KID-syndrome in Finland. A report of four cases.
Tuppurainen K, Fräki J, Karjalainen S, Paljärvi L, Suhonen R, Ryynänen M. Tuppurainen K, et al. Among authors: paljarvi l. Acta Ophthalmol (Copenh). 1988 Dec;66(6):692-8. doi: 10.1111/j.1755-3768.1988.tb04063.x. Acta Ophthalmol (Copenh). 1988. PMID: 3232512
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