Association of a common genetic variant within ANKK1 with six-month cognitive performance after traumatic brain injury.
- Published in:
- Neurogenetics, 2015, v. 16, n. 3, p. 169, doi. 10.1007/s10048-015-0437-1
- By:
- Publication type:
- Article
Works matching IS 13646745 AND DT 2015 AND VI 16 AND IP 3
Results: 12
1
2
Multiple sclerosis risk loci correlate with cervical cord atrophy and may explain the course of disability.
- Published in:
- Neurogenetics, 2015, v. 16, n. 3, p. 161, doi. 10.1007/s10048-015-0438-0
- By:
- Publication type:
- Article
3
Milestones in Friedreich ataxia: more than a century and still learning.
- Published in:
- Neurogenetics, 2015, v. 16, n. 3, p. 151, doi. 10.1007/s10048-015-0439-z
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- Publication type:
- Article
4
MRPS22 mutation causes fatal neonatal lactic acidosis with brain and heart abnormalities.
- Published in:
- Neurogenetics, 2015, v. 16, n. 3, p. 237, doi. 10.1007/s10048-015-0440-6
- By:
- Publication type:
- Article
5
Genetic ablation of ataxin-2 increases several global translation factors in their transcript abundance but decreases translation rate.
- Published in:
- Neurogenetics, 2015, v. 16, n. 3, p. 181, doi. 10.1007/s10048-015-0441-5
- By:
- Publication type:
- Article
6
A start codon CMT1X mutation associated with transient encephalomyelitis causes complete loss of Cx32.
- Published in:
- Neurogenetics, 2015, v. 16, n. 3, p. 193, doi. 10.1007/s10048-015-0442-4
- By:
- Publication type:
- Article
7
Mitochondrial serine protease HTRA2 gene mutation in Asians with coexistent essential tremor and Parkinson disease.
- Published in:
- 2015
- By:
- Publication type:
- Letter
8
Long intervening non-coding RNA 00320 is human brain-specific and highly expressed in the cortical white matter.
- Published in:
- Neurogenetics, 2015, v. 16, n. 3, p. 201, doi. 10.1007/s10048-015-0445-1
- By:
- Publication type:
- Article
9
A defect in the retromer accessory protein, SNX27, manifests by infantile myoclonic epilepsy and neurodegeneration.
- Published in:
- Neurogenetics, 2015, v. 16, n. 3, p. 215, doi. 10.1007/s10048-015-0446-0
- By:
- Publication type:
- Article
10
Erratum to: The L450P mutation in KCND3 brings spinocerebellar ataxia and Brugada syndrome closer together.
- Published in:
- 2015
- By:
- Publication type:
- Erratum
11
The fused in sarcoma protein forms cytoplasmic aggregates in motor neurons derived from integration-free induced pluripotent stem cells generated from a patient with familial amyotrophic lateral sclerosis carrying the FUS-P525L mutation.
- Published in:
- Neurogenetics, 2015, v. 16, n. 3, p. 223, doi. 10.1007/s10048-015-0448-y
- By:
- Publication type:
- Article
12
A novel frameshift mutation in FGF14 causes an autosomal dominant episodic ataxia.
- Published in:
- Neurogenetics, 2015, v. 16, n. 3, p. 233, doi. 10.1007/s10048-014-0436-7
- By:
- Publication type:
- Article