Works matching IS 13646745 AND DT 2008 AND VI 9 AND IP 1
Results: 10
Identification and characterization of a new alpha-synuclein isoform and its role in Lewy body diseases.
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- Neurogenetics, 2008, v. 9, n. 1, p. 15, doi. 10.1007/s10048-007-0106-0
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- Article
Myotonic dystrophy type 2 in Japan: ancestral origin distinct from Caucasian families.
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- Neurogenetics, 2008, v. 9, n. 1, p. 61, doi. 10.1007/s10048-007-0110-4
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- Article
Different spectra of genomic deletions within the CCM genes between Italian and American CCM patient cohorts.
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- Neurogenetics, 2008, v. 9, n. 1, p. 25, doi. 10.1007/s10048-007-0109-x
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- Article
Towards a pathway definition of Parkinson’s disease: a complex disorder with links to cancer, diabetes and inflammation.
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- Neurogenetics, 2008, v. 9, n. 1, p. 1, doi. 10.1007/s10048-007-0116-y
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- Article
A neonatal encephalopathy with seizures in standard poodle dogs with a missense mutation in the canine ortholog of ATF2.
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- Neurogenetics, 2008, v. 9, n. 1, p. 41, doi. 10.1007/s10048-007-0112-2
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- Article
Identification of new ANG gene mutations in a large cohort of Italian patients with amyotrophic lateral sclerosis.
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- Neurogenetics, 2008, v. 9, n. 1, p. 33, doi. 10.1007/s10048-007-0111-3
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- Article
Age-at-onset linkage analysis in Caribbean Hispanics with familial late-onset Alzheimer’s disease.
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- Neurogenetics, 2008, v. 9, n. 1, p. 51, doi. 10.1007/s10048-007-0103-3
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- Article
Familial cases presenting very early onset autosomal dominant Alzheimer’s disease with I143T in presenilin-1 gene: implication for genotype–phenotype correlation.
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- 2008
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- Letter
Refinement of the 2p11.1-q12.2 locus responsible for cortical tremor associated with epilepsy and exclusion of candidate genes.
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- 2008
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- Publication type:
- Letter
Genetic susceptibility to Parkinson’s disease among South and North Indians: I. Role of polymorphisms in dopamine receptor and transporter genes and association of DRD4 120-bp duplication marker.
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- 2008
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