Molecular Genetic Advances in Neurological Disease: Special Review Issue.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. R1, p. R1, doi. 10.1093/hmg/ddq193
- By:
- Publication type:
- Article
Works matching IS 09646906 AND DT 2010 AND VI 19 AND IP R1
Results: 19
1
2
Parkinson's disease: insights from pathways.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. R1, p. R21, doi. 10.1093/hmg/ddq167
- By:
- Publication type:
- Article
3
Subscription Page.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. R1, p. NP, doi. 10.1093/hmg/ddq195
- Publication type:
- Article
4
Inclusion body myopathy, Paget's disease of the bone and fronto-temporal dementia: a disorder of autophagy.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. R1, p. R38
- By:
- Publication type:
- Article
5
Current status on Alzheimer disease molecular genetics: from past, to present, to future.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. R1, p. R4, doi. 10.1093/hmg/ddq142
- By:
- Publication type:
- Article
6
Editorial Board.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. R1, p. NP, doi. 10.1093/hmg/ddq194
- Publication type:
- Article
7
Genetics of neurodegenerative diseases: insights from high-throughput resequencing.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. R1, p. R65, doi. 10.1093/hmg/ddq162
- By:
- Publication type:
- Article
8
Molecular mechanisms of neurodegeneration in Alzheimer's disease.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. R1, p. R12, doi. 10.1093/hmg/ddq160
- By:
- Publication type:
- Article
9
Understanding the molecular mechanisms of Friedreich's ataxia to develop therapeutic approaches.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. R1, p. R103, doi. 10.1093/hmg/ddq165
- By:
- Publication type:
- Article
10
Partners in crime: bidirectional transcription in unstable microsatellite disease.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. R1, p. R77, doi. 10.1093/hmg/ddq132
- By:
- Publication type:
- Article
11
TDP-43 and FUS/TLS: emerging roles in RNA processing and neurodegeneration.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. R1, p. R46, doi. 10.1093/hmg/ddq137
- By:
- Publication type:
- Article
12
Pluripotent stem cells in neurodegenerative and neurodevelopmental diseases.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. R1, p. R71, doi. 10.1093/hmg/ddq159
- By:
- Publication type:
- Article
13
A pivotal role for PINK1 and autophagy in mitochondrial quality control: implications for Parkinson disease.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. R1, p. R28, doi. 10.1093/hmg/ddq143
- By:
- Publication type:
- Article
14
Advances in understanding the molecular basis of FXTAS.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. R1, p. R83, doi. 10.1093/hmg/ddq166
- By:
- Publication type:
- Article
15
Huntington's disease: progress toward effective disease-modifying treatments and a cure.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. R1, p. R98, doi. 10.1093/hmg/ddq148
- By:
- Publication type:
- Article
16
Molecular therapy in myotonic dystrophy: focus on RNA gain-of-function.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. R1, p. R90, doi. 10.1093/hmg/ddq161
- By:
- Publication type:
- Article
17
Contents Page.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. R1, p. NP, doi. 10.1093/hmg/ddq191
- Publication type:
- Article
18
Cover Page.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. R1, p. NP, doi. 10.1093/hmg/ddq192
- Publication type:
- Article
19
Spinal muscular atrophy: mechanisms and therapeutic strategies.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. R1, p. R111, doi. 10.1093/hmg/ddq147
- By:
- Publication type:
- Article