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263 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: haltia m. Neuromuscul Disord. 1991;1(4):267-73. doi: 10.1016/0960-8966(91)90100-7. Neuromuscul Disord. 1991. PMID: 1822805
Gelsolin-related spinal and cerebral amyloid angiopathy.
Kiuru S, Salonen O, Haltia M. Kiuru S, et al. Among authors: haltia m. Ann Neurol. 1999 Mar;45(3):305-11. doi: 10.1002/1531-8249(199903)45:3<305::aid-ana5>3.0.co;2-e. Ann Neurol. 1999. PMID: 10072044
Multiple schwannomas: schwannomatosis or neurofibromatosis type 2?
Seppälä MT, Sainio MA, Haltia MJ, Kinnunen JJ, Setälä KH, Jääskeläinen JE. Seppälä MT, et al. Among authors: haltia mj. J Neurosurg. 1998 Jul;89(1):36-41. doi: 10.3171/jns.1998.89.1.0036. J Neurosurg. 1998. PMID: 9647170
Autosomal dominant progressive external ophthalmoplegia with multiple deletions of mtDNA: clinical, biochemical, and molecular genetic features of the 10q-linked disease.
Suomalainen A, Majander A, Wallin M, Setälä K, Kontula K, Leinonen H, Salmi T, Paetau A, Haltia M, Valanne L, Lonnqvist J, Peltonen L, Somer H. Suomalainen A, et al. Among authors: haltia m. Neurology. 1997 May;48(5):1244-53. doi: 10.1212/wnl.48.5.1244. Neurology. 1997. PMID: 9153451
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. Ann Neurol. 1997 Feb;41(2):173-80. doi: 10.1002/ana.410410208. Ann Neurol. 1997. PMID: 9029066
An autosomal locus predisposing to deletions of mitochondrial DNA.
Suomalainen A, Kaukonen J, Amati P, Timonen R, Haltia M, Weissenbach J, Zeviani M, Somer H, Peltonen L. Suomalainen A, et al. Among authors: haltia m. Nat Genet. 1995 Feb;9(2):146-51. doi: 10.1038/ng0295-146. Nat Genet. 1995. PMID: 7719341
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