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3. Prevention in neurology

7. Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis

8. Neurogenetics: single gene disorders

12. Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis

16. Genome-wide Analyses Identify KIF5A as a Novel ALS Gene

17. Genome-wide Analyses Identify KIF5A as a Novel ALS Gene

23. Consensus Paper: Pathological Mechanisms Underlying Neurodegeneration in Spinocerebellar Ataxias.

24. Consensus Paper: Pathological Mechanisms Underlying Neurodegeneration in Spinocerebellar Ataxias

26. The prevalence and wide clinical spectrum of the spinocerebellar ataxia type 2 trinucleotide repeat in patients with autosomal dominant cerebellar ataxia

28. A conserved eEF2 coding variant in SCA26 leads to loss of translational fidelity and increased susceptibility to proteostatic insult

31. Clinical Characteristics of Spinocerebellar Ataxias 1, 2, 3 and 6 (S12.002)

33. Screening for mutations in synaptotagmin XI in Parkinson's disease.

45. Spinocerebellar ataxia type 6

46. 1-29-12 Clinical, genetic and molecular studies in spinocerebellar ataxia type 2

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