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Your search keyword '"van de Warrenburg, Bart P"' showing total 49 results

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49 results on '"van de Warrenburg, Bart P"'

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1. Genetic risk of Parkinson disease and progression: An analysis of 13 longitudinal cohorts

3. Exome sequencing and network analysis identifies shared mechanisms underlying spinocerebellar ataxia

9. Prediction of the age at onset in spinocerebellar ataxia type 1, 2, 3 and 6

14. Autosomal Recessive Spinocerebellar Ataxia 7 (SCAR7) is Caused by Variants in TPP1, The Gene Involved in Classic Late-Infantile Neuronal Ceroid Lipofuscinosis 2 Disease (CLN2 Disease)

17. Genotype-specific patterns of atrophy progression are more sensitive than clinical decline in SCA1, SCA3 and SCA6

19. Mutations in potassium channel kcnd3 cause spinocerebellar ataxia type 19

26. Presence of ATM Protein and Residual Kinase Activity Correlates with the Phenotype in Ataxia-Telangiectasia: A Genotype–Phenotype Study†

29. Angiogenin Variants in Parkinson Disease and Amyotrophic Lateral Sclerosis

39. Early symptoms in spinocerebellar ataxia type 1, 2, 3, and 6

41. REEP1 mutation spectrum and genotype/phenotype correlation in hereditary spastic paraplegia type 31

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