Pages that link to "Q45929818"
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The following pages link to Pilar Gómez-Garre (Q45929818):
Displaying 39 items.
- A novel protein tyrosine phosphatase gene is mutated in progressive myoclonus epilepsy of the Lafora type (EPM2) (Q22001499) (← links)
- Autosomal dominant nocturnal frontal lobe epilepsy with a mutation in the CHRNB2 gene (Q24295109) (← links)
- Common variation in the LRRK2 gene is a risk factor for Parkinson's disease (Q30531323) (← links)
- Novel Lrrk2-p.S1761R mutation is not a common cause of Parkinson's disease in Spain. (Q30540754) (← links)
- Familial partial epilepsy with variable foci: a new family with suggestion of linkage to chromosome 22q12. (Q33640669) (← links)
- A PTG variant contributes to a milder phenotype in Lafora disease (Q33954771) (← links)
- Lafora disease due to EPM2B mutations: a clinical and genetic study. (Q34405204) (← links)
- GBA Variants Influence Motor and Non-Motor Features of Parkinson's Disease (Q36234536) (← links)
- Lower levels of uric acid and striatal dopamine in non-tremor dominant Parkinson's disease subtype. (Q36328177) (← links)
- Genetic factors influencing frontostriatal dysfunction and the development of dementia in Parkinson's disease (Q36343417) (← links)
- GDNF gene is associated with tourette syndrome in a family study (Q37282946) (← links)
- Low serum uric acid levels in progressive supranuclear palsy. (Q40190481) (← links)
- Low serum uric acid concentration in Parkinson's disease in southern Spain (Q44003807) (← links)
- Genome-wide association study in musician's dystonia: a risk variant at the arylsulfatase G locus? (Q44248875) (← links)
- Analysis of c.801-2A>G mutation in the DNAJC6 gene in Parkinson's disease in southern Spain. (Q45929748) (← links)
- Genetic variability related to serum uric acid concentration and risk of Parkinson's disease. (Q45980386) (← links)
- Genetic linkage of autosomal dominant progressive supranuclear palsy to 1q31.1. (Q46456078) (← links)
- Prevalence and clinical features of LRRK2 mutations in patients with Parkinson's disease in southern Spain (Q47716761) (← links)
- Hepatic disease as the first manifestation of progressive myoclonus epilepsy of Lafora (Q48192052) (← links)
- The effect of BDNF val66met polymorphism on visuomotor adaptation. (Q48391048) (← links)
- MRI volumetry and proton MR spectroscopy of the brain in Lafora disease (Q48560170) (← links)
- BDNF Val66Met polymorphism in primary adult-onset dystonia: a case-control study and meta-analysis (Q48717867) (← links)
- Genetic analysis of CHCHD2 in a southern Spanish population (Q50224204) (← links)
- Lack of validation of variants associated with cervical dystonia risk: a GWAS replication study. (Q50459514) (← links)
- Systematic mutational analysis of FBXO7 in a Parkinson's disease population from southern Spain (Q50484907) (← links)
- Intermediate alleles at the FRAXA and FRAXE loci in Parkinson's disease (Q51818186) (← links)
- Variability of age at onset in siblings with familial Alzheimer disease. (Q53290987) (← links)
- New type of mutations in three spanish families with choroideremia. (Q54539164) (← links)
- TMEM230 in Parkinson's disease in a southern Spanish population. (Q54969961) (← links)
- Lack of sequence variations in THAP1 gene and THAP1-binding sites in TOR1A promoter of DYT1 patients (Q57243893) (← links)
- Founder Effect with Variable Age at Onset in Arab Families with Lafora Disease and EPM2A Mutation (Q58417024) (← links)
- Familial Partial Epilepsy with Variable Foci: Clinical Features and Linkage to Chromosome 22q12 (Q58417098) (← links)
- Mutational spectrum of the EPM2A gene in progressive myoclonus epilepsy of Lafora: high degree of allelic heterogeneity and prevalence of deletions (Q59273673) (← links)
- PSMC1Gene in Parkinson s Disease (Q61883771) (← links)
- Characterization of a 6p21 translocation breakpoint in a family with idiopathic generalized epilepsy (Q61883823) (← links)
- A replication study of GWAS-genetic risk variants associated with Parkinson's disease in a Spanish population (Q92728486) (← links)
- A genetic analysis of a Spanish population with early onset Parkinson's disease (Q98880957) (← links)
- Integrating genetic and clinical data to predict impulse control disorders in Parkinson's disease (Q100534472) (← links)
- Mutational spectrum of GNAL, THAP1 and TOR1A genes in isolated dystonia: study in a population from Spain and systematic literature review (Q101567983) (← links)