Dementia with Lewy bodies: no association of polymorphisms in the human synphilin gene.
- Published in:
- 2004
- By:
- Publication type:
- Letter
Works matching IS 13646745 AND DT 2004 AND VI 5 AND IP 4
Results: 9
1
2
Early onset autosomal dominant spastic paraplegia caused by novel mutations inSPG3A.
- Published in:
- Neurogenetics, 2004, v. 5, n. 4, p. 239, doi. 10.1007/s10048-004-0191-2
- By:
- Publication type:
- Article
3
Fine mapping of 16q-linked autosomal dominant cerebellar ataxia type III in Japanese families.
- Published in:
- Neurogenetics, 2004, v. 5, n. 4, p. 215, doi. 10.1007/s10048-004-0194-z
- By:
- Publication type:
- Article
4
Alternative splicing in the N-terminus of Alzheimer’s presenilin 1.
- Published in:
- Neurogenetics, 2004, v. 5, n. 4, p. 223, doi. 10.1007/s10048-004-0195-y
- By:
- Publication type:
- Article
5
Convulsive disorder and genetic polymorphism. Association of idiopathic generalized epilepsy with haptoglobin polymorphism.
- Published in:
- Neurogenetics, 2004, v. 5, n. 4, p. 245, doi. 10.1007/s10048-004-0192-1
- By:
- Publication type:
- Article
6
Comprehensive association analysis ofAPOEregulatory region polymorphisms in Alzheimer disease.
- Published in:
- Neurogenetics, 2004, v. 5, n. 4, p. 201, doi. 10.1007/s10048-004-0189-9
- By:
- Publication type:
- Article
7
Apolipoprotein E is associated with age at onset of amyotrophic lateral sclerosis.
- Published in:
- Neurogenetics, 2004, v. 5, n. 4, p. 209, doi. 10.1007/s10048-004-0193-0
- By:
- Publication type:
- Article
8
A novel three extra-repeat insertion in the prion protein gene(PRNP)in a patient with Creutzfeldt-Jakob disease.
- Published in:
- 2004
- By:
- Publication type:
- Letter
9
Mutation in the gene encoding lysosomal acid phosphatase (Acp2) causes cerebellum and skin malformation in mouse.
- Published in:
- Neurogenetics, 2004, v. 5, n. 4, p. 229, doi. 10.1007/s10048-004-0197-9
- By:
- Publication type:
- Article