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New application of intelligent agents in sporadic amyotrophic lateral sclerosis identifies unexpected specific genetic background.
- Published in:
- BMC Bioinformatics, 2008, v. 9, p. 1, doi. 10.1186/1471-2105-9-254
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- Publication type:
- Article
Familial cerebral cavernous malformation: report of a further Italian family.
- Published in:
- Neurological Sciences, 2009, v. 30, n. 2, p. 143, doi. 10.1007/s10072-009-0020-3
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- Publication type:
- Article
Capillary electrophoresis of polymerase chain reaction-amplified products in polymer networks: The case of Kennedy's disease.
- Published in:
- Electrophoresis, 1994, v. 15, n. 1, p. 644, doi. 10.1002/elps.1150150190
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- Publication type:
- Article
A new mutation (TTR Ala-47) in the transthyretin gene associated with hereditary amyloidosis.
- Published in:
- Human Mutation, 1994, v. 4, n. 1, p. 61, doi. 10.1002/humu.1380040110
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- Publication type:
- Article
SOD1 mutations in amyotrophic lateral sclerosis.
- Published in:
- Journal of Neurology, 2005, v. 252, n. 7, p. 782, doi. 10.1007/s00415-005-0742-y
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- Publication type:
- Article
Assay Using Succinyldithiocholine as Substrate: The Method of Choice for the Measurement of Cholinesterase Catalytic Activity in Serum to Diagnose Succinyldicholine Sensitivity.
- Published in:
- Clinical Chemistry & Laboratory Medicine, 2003, v. 41, n. 3, p. 317, doi. 10.1515/CCLM.2003.051
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- Publication type:
- Article
Homozygosity and heterozygosity for the transthyretin Leu64 mutation: clinical, biochemical and molecular findings.
- Published in:
- Clinical Genetics, 1996, v. 49, n. 1, p. 10, doi. 10.1111/j.1399-0004.1996.tb04317.x
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- Publication type:
- Article
An Italian kindred with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).
- Published in:
- 1995
- By:
- Publication type:
- journal article