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Germán Moris

International Sleep Products Association

10

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457

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Parkinsonism and spastic paraplegia type 7: Expanding the spectrum of mitochondrial Parkinsonism

2019 Movement Disorders
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HTT gene intermediate alleles in neurodegeneration: evidence for association with Alzheimer's disease

2019 Neurobiology of Aging
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SPG7 mutational screening in spastic paraplegia patients supports a dominant effect for some mutations and a pathogenic role for p.A510V

2013 Clinical Genetics
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Profile of microRNAs in the plasma of Parkinson's disease patients and healthy controls

2013 Journal of Neurology
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Analysis of the Micro-RNA-133 and PITX3 Genes in Parkinson's Disease

2010 American Journal of Medical Genetics
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FGF20 rs12720208 SNP and microRNA-433 variation: No association with Parkinson's disease in Spanish patients

2010 Neuroscience Letters
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LRRK2 mutations are a common cause of Parkinson's disease in Spain

2006 European Journal of Neurology
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Association between an α2 Macroglobulin DNA Polymorphism and Late-Onset Alzheimer's Disease

1999 Biochemical and Biophysical Research Communications
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Citations (41)