Search
| Leader | 00000nz a2200037n 45 0 | ||
|---|---|---|---|
| 001 | WKP|Q84828922 (VIAF cluster) (Authority/Source Record) | ||
| 003 | WKP | ||
| 005 | 20241221010859.0 | ||
| 008 | 241221nneanz||abbn n and d | ||
| 035 | ‡a (WKP)Q84828922 | ||
| 024 | ‡a 0000-0002-4317-0662 ‡2 orcid | ||
| 035 | ‡a (OCoLC)Q84828922 | ||
| 100 | 0 | ‡a Ismael Huertas-Fernández ‡c researcher ‡9 en | |
| 400 | 0 | ‡a Ismael Huertas-Fernández ‡c wetenschapper ‡9 nl | |
| 670 | ‡a Author's Analysis of c.801-2A>G mutation in the DNAJC6 gene in Parkinson's disease in southern Spain. | ||
| 670 | ‡a Author's BDNF Val66Met polymorphism in primary adult-onset dystonia: a case-control study and meta-analysis | ||
| 670 | ‡a Author's Clinical features and 123I-FP-CIT SPECT imaging in vascular parkinsonism and Parkinson's disease. | ||
| 670 | ‡a Author's GDNF gene is associated with tourette syndrome in a family study | ||
| 670 | ‡a Author's Lack of validation of variants associated with cervical dystonia risk: a GWAS replication study. | ||
| 670 | ‡a Author's Systematic mutational analysis of FBXO7 in a Parkinson's disease population from southern Spain | ||
| 909 | ‡a (orcid) 0000000243170662 ‡9 1 | ||
| 919 | ‡a analysisof1008012agmutationinthednajc6geneinparkinsonsdiseaseinsouthernspain ‡A Analysis of c.801-2A>G mutation in the DNAJC6 gene in Parkinson's disease in southern Spain. ‡9 1 | ||
| 919 | ‡a bdnfval66metpolymorphisminprimaryadultonsetdystoniaacasecontrolstudyandmetaanalysis ‡A BDNF Val66Met polymorphism in primary adult-onset dystonia: a case-control study and meta-analysis ‡9 1 | ||
| 919 | ‡a clinicalfeaturesand123ifpcitspectimaginginvascularparkinsonismandparkinsonsdisease ‡A Clinical features and 123I-FP-CIT SPECT imaging in vascular parkinsonism and Parkinson's disease. ‡9 1 | ||
| 919 | ‡a gdnfgeneisassociatedwithtourettesyndromeinafamilystudy ‡A GDNF gene is associated with tourette syndrome in a family study ‡9 1 | ||
| 919 | ‡a lackofvalidationofvariantsassociatedwithcervicaldystoniariskagwasreplicationstudy ‡A Lack of validation of variants associated with cervical dystonia risk: a GWAS replication study. ‡9 1 | ||
| 919 | ‡a systematicmutationalanalysisoffbxo7inaparkinsonsdiseasepopulationfromsouthernspain ‡A Systematic mutational analysis of FBXO7 in a Parkinson's disease population from southern Spain ‡9 1 | ||
| 996 | ‡2 ISNI|0000000043940941 | ||
| 996 | ‡2 ICCU|CUBV063229 | ||
| 996 | ‡2 ISNI|000000011784788X | ||
| 996 | ‡2 BNE|XX924731 | ||
| 996 | ‡2 DNB|142673323 | ||
| 996 | ‡2 SUDOC|190142383 | ||
| 996 | ‡2 BNC|981058605479306706 | ||
| 996 | ‡2 DNB|1056358548 | ||
| 996 | ‡2 RERO|A018119631 | ||
| 996 | ‡2 ISNI|0000000072453771 | ||
| 996 | ‡2 BNE|XX1011905 | ||
| 996 | ‡2 BNC|981058518497306706 | ||
| 996 | ‡2 ISNI|0000000000374855 | ||
| 996 | ‡2 BNE|XX1060866 | ||
| 996 | ‡2 BNE|XX894490 | ||
| 996 | ‡2 CAOONL|ncf10725729 | ||
| 996 | ‡2 BIBSYS|12065989 | ||
| 996 | ‡2 LC|no 00066787 | ||
| 996 | ‡2 BNF|12236322 | ||
| 996 | ‡2 LC|n 2024052933 | ||
| 996 | ‡2 RERO|A003238427 | ||
| 996 | ‡2 NTA|115198741 | ||
| 996 | ‡2 BNE|XX5569997 | ||
| 996 | ‡2 BIBSYS|1081384 | ||
| 996 | ‡2 ISNI|0000000060149924 | ||
| 996 | ‡2 BNC|981058514300506706 | ||
| 996 | ‡2 BNF|14477390 | ||
| 996 | ‡2 SUDOC|031076084 | ||
| 997 | ‡a 0 0 lived 0 0 ‡9 1 |
