A novel heat shock protein alpha 8 ( Hspa8) molecular network mediating responses to stress- and ethanol-related behaviors.
- Published in:
- Neurogenetics, 2016, v. 17, n. 2, p. 91, doi. 10.1007/s10048-015-0470-0
- By:
- Publication type:
- Article
Works matching IS 13646745 AND DT 2016 AND VI 17 AND IP 2
Results: 8
1
2
A heritable form of SMARCE1-related meningiomas with important implications for follow-up and family screening.
- Published in:
- Neurogenetics, 2016, v. 17, n. 2, p. 83, doi. 10.1007/s10048-015-0472-y
- By:
- Publication type:
- Article
3
Spinocerebellar ataxia type 3/Machado-Joseph disease starting before adolescence.
- Published in:
- Neurogenetics, 2016, v. 17, n. 2, p. 107, doi. 10.1007/s10048-016-0473-5
- By:
- Publication type:
- Article
4
Multiple sclerosis in families: risk factors beyond known genetic polymorphisms.
- Published in:
- Neurogenetics, 2016, v. 17, n. 2, p. 131, doi. 10.1007/s10048-016-0474-4
- By:
- Publication type:
- Article
5
Erratum to: Clinical and molecular study in a long-surviving patient with MLASA syndrome due to novel PUS1 mutations.
- Published in:
- 2016
- By:
- Publication type:
- Erratum
6
Mutations in GALC cause late-onset Krabbe disease with predominant cerebellar ataxia.
- Published in:
- Neurogenetics, 2016, v. 17, n. 2, p. 137, doi. 10.1007/s10048-016-0476-2
- By:
- Publication type:
- Article
7
Recessive mutations of TMC1 associated with moderate to severe hearing loss.
- Published in:
- Neurogenetics, 2016, v. 17, n. 2, p. 115, doi. 10.1007/s10048-016-0477-1
- By:
- Publication type:
- Article
8
Slc20a2 is critical for maintaining a physiologic inorganic phosphate level in cerebrospinal fluid.
- Published in:
- Neurogenetics, 2016, v. 17, n. 2, p. 125, doi. 10.1007/s10048-015-0469-6
- By:
- Publication type:
- Article