21 results on '"Munain, Adolfo López de"'
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2. Additional file 1 of Frizzled related protein deficiency impairs muscle strength, gait and calpain 3 levels
3. Additional file 4: Figure S4. of Parkinson disease-associated mutations in LRRK2 cause centrosomal defects via Rab8a phosphorylation
4. Additional file 1: Figure S1. of Parkinson disease-associated mutations in LRRK2 cause centrosomal defects via Rab8a phosphorylation
5. Additional file 5: Figure S5. of Parkinson disease-associated mutations in LRRK2 cause centrosomal defects via Rab8a phosphorylation
6. Additional file 2: Figure S2. of Parkinson disease-associated mutations in LRRK2 cause centrosomal defects via Rab8a phosphorylation
7. A Nonsynonymous Mutation in PLCG2 Reduces the Risk of Alzheimer's Disease, Dementia with Lewy-Bodies and Frontotemporal Dementia, and Increases the Likelihood of Longevity
8. Additional file 2: of Mutations in LRRK2 impair NF-κB pathway in iPSC-derived neurons
9. Additional file 3: of Mutations in LRRK2 impair NF-κB pathway in iPSC-derived neurons
10. Additional file 4: of Mutations in LRRK2 impair NF-κB pathway in iPSC-derived neurons
11. Additional file 1: Table S1. of Mutations in LRRK2 impair NF-κB pathway in iPSC-derived neurons
12. Additional file 5: of Mutations in LRRK2 impair NF-κB pathway in iPSC-derived neurons
13. Nonsense mutations in alpha-II spectrin in three families with juvenile onset hereditary motor neuropathy.
14. Novel valosin containing protein mutation in a Swiss family with hereditary inclusion body myopathy and dementia
15. Neurodegenerative Disease Phenotypes in Carriers of MAPT p.A152T, A Risk Factor for Frontotemporal Dementia Spectrum Disorders and Alzheimer Disease
16. Erratum to ‘Clinical outcome in 19 French and Spanish patients with valosin-containing protein myopathy associated with Paget’s disease of bone and frontotemporal dementia’ [Neuromuscular Disorders 19 (2009) 316–323]
17. Additional file 7: Figure S7. of Parkinson disease-associated mutations in LRRK2 cause centrosomal defects via Rab8a phosphorylation
18. Additional file 6: Figure S6. of Parkinson disease-associated mutations in LRRK2 cause centrosomal defects via Rab8a phosphorylation
19. Additional file 6: Figure S6. of Parkinson disease-associated mutations in LRRK2 cause centrosomal defects via Rab8a phosphorylation
20. Additional file 7: Figure S7. of Parkinson disease-associated mutations in LRRK2 cause centrosomal defects via Rab8a phosphorylation
21. Kynurenic Acid Levels are Increased in the CSF of Alzheimer's Disease Patients.
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