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Muscle-eye-brain disease: a neuropathological study.
Haltia M, Leivo I, Somer H, Pihko H, Paetau A, Kivelä T, Tarkkanen A, Tomé F, Engvall E, Santavuori P. Haltia M, et al. Among authors: somer h. Ann Neurol. 1997 Feb;41(2):173-80. doi: 10.1002/ana.410410208. Ann Neurol. 1997. PMID: 9029066
Muscle-eye-brain disease (MEB).
Santavuori P, Somer H, Sainio K, Rapola J, Kruus S, Nikitin T, Ketonen L, Leisti J. Santavuori P, et al. Among authors: somer h. Brain Dev. 1989;11(3):147-53. doi: 10.1016/s0387-7604(89)80088-9. Brain Dev. 1989. PMID: 2751061
MRI of the brain in muscle-eye-brain (MEB) disease.
Valanne L, Pihko H, Katevuo K, Karttunen P, Somer H, Santavuori P. Valanne L, et al. Among authors: somer h. Neuroradiology. 1994 Aug;36(6):473-6. doi: 10.1007/BF00593687. Neuroradiology. 1994. PMID: 7991095
Muscle-eye-brain disease and Walker-Warburg syndrome.
Santavuori P, Pihko H, Sainio K, Lappi M, Somer H, Haltia M, Raitta C, Ketonen L, Leisti J. Santavuori P, et al. Among authors: somer h. Am J Med Genet. 1990 Jul;36(3):371-4. doi: 10.1002/ajmg.1320360334. Am J Med Genet. 1990. PMID: 2363444 No abstract available.
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. Neuromuscul Disord. 1991;1(4):267-73. doi: 10.1016/0960-8966(91)90100-7. Neuromuscul Disord. 1991. PMID: 1822805
Gene deletions in X-linked muscular dystrophy.
Lindlöf M, Kiuru A, Kääriäinen H, Kalimo H, Lang H, Pihko H, Rapola J, Somer H, Somer M, Savontaus ML, et al. Lindlöf M, et al. Among authors: somer h, somer m. Am J Hum Genet. 1989 Apr;44(4):496-503. Am J Hum Genet. 1989. PMID: 2929594 Free PMC article.
140 results