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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1992 | 2 |
1994 | 1 |
2001 | 1 |
2024 | 0 |
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Asymptomatic homozygous gene carrier in a family with type I familial amyloid polyneuropathy.
Eur Neurol. 1992;32(6):308-13. doi: 10.1159/000116850.
Eur Neurol. 1992.
PMID: 1490495
Homozygosity for the transthyretin-Met30-gene in seven individuals with familial amyloidosis with polyneuropathy detected by restriction enzyme analysis of amplified genomic DNA sequences.
Holmgren G, Bergström S, Drugge U, Lundgren E, Nording-Sikström C, Sandgren O, Steen L.
Holmgren G, et al.
Clin Genet. 1992 Jan;41(1):39-41. doi: 10.1111/j.1399-0004.1992.tb03627.x.
Clin Genet. 1992.
PMID: 1353008
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A case of familial amyloid polyneuropathy homozygous for the transthyretin Val30Met gene with motor-dominant sensorimotor polyneuropathy and unusual sural nerve pathological findings.
Yoshioka A, Yamaya Y, Saiki S, Hirose G, Shimazaki K, Nakamura M, Ando Y.
Yoshioka A, et al.
Arch Neurol. 2001 Nov;58(11):1914-8. doi: 10.1001/archneur.58.11.1914.
Arch Neurol. 2001.
PMID: 11709003
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[Three siblings homozygous for the transthyretin-Met30 gene in familial amyloidotic polyneuropathy--evaluation of their clinical pictures with reference to those of other 10 cases reported].
Yoshinaga T, Nakazato M, Ikeda S, Ohnishi A.
Yoshinaga T, et al.
Rinsho Shinkeigaku. 1994 Feb;34(2):99-105.
Rinsho Shinkeigaku. 1994.
PMID: 8194279
Review.
Japanese.
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