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2. Secondary structure of the human mitochondrial genome affects formation of deletions

3. Testing for pharmacogenomic predictors of ppRNFL thinning in individuals exposed to vigabatrin

4. Assessing the role of rare genetic variants in drug‐resistant, non‐lesional focal epilepsy

5. The Fate of Oxidative Strand Breaks in Mitochondrial DNA

6. Loss of the Immunomodulatory Transcription Factor BATF2 in Humans Is Associated with a Neurological Phenotype

7. Genomic and clinical predictors of lacosamide response in refractory epilepsies

8. Genotypes and phenotypes of patients with Lafora disease living in Germany

9. Comparative effectiveness of antiepileptic drugs in juvenile myoclonic epilepsy

10. Role of Common Genetic Variants for Drug-Resistance to Specific Anti-Seizure Medications

11. Heart failure after pressure overload in autosomal-dominant desminopathies: Lessons from heterozygous DES-p.R349P knock-in mice.

12. Linear mitochondrial DNA is rapidly degraded by components of the replication machinery

13. Exonic microdeletions of the gephyrin gene impair GABAergic synaptic inhibition in patients with idiopathic generalized epilepsy

14. Evaluation of Presumably Disease Causing SCN1A Variants in a Cohort of Common Epilepsy Syndromes.

15. Mitochondrial dysfunction, peroxidation damage and changes in glutathione metabolism in PARK6

16. Burden analysis of rare microdeletions suggests a strong impact of neurodevelopmental genes in genetic generalised epilepsies.

17. Binding of copper is a mechanism of homocysteine toxicity leading to COX deficiency and apoptosis in primary neurons, PC12 and SHSY-5Y cells

18. Loss of UCP2 attenuates mitochondrial dysfunction without altering ROS production and uncoupling activity.

19. Parkinson phenotype in aged PINK1-deficient mice is accompanied by progressive mitochondrial dysfunction in absence of neurodegeneration.

20. Secondary structure of the human mitochondrial genome affects formation of deletions

21. Shared genetic basis between genetic generalized epilepsy and background electroencephalographic oscillations

22. Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals

24. Identification of galectin-3 as a novel potential prognostic/predictive biomarker and therapeutic target for cerebral cavernous malformation disease

26. Parkinson phenotype in aged PINK1-deficient mice is accompanied by progressive mitochondrial dysfunction in absence of neurodegeneration.

28. The Fate of Oxidative Strand Breaks in Mitochondrial DNA

29. Whole-Exome sequencing identifies GYS2 biallelic variants in individuals with suspected epilepsy

33. Testing for pharmacogenomic predictors of ppRNFL thinning in individuals exposed to vigabatrin.

34. Transcatheter bicuspid venous valve prostheses: fluid mechanical performance testing of artificial nonwoven leaflets

35. Quantification of breast biopsy clip marker artifact on routine breast MRI sequences: a phantom study

38. Mitochondrial Retinopathy

39. Additional file 1 of Secondary structure of the human mitochondrial genome affects formation of deletions

40. Additional file 2 of Secondary structure of the human mitochondrial genome affects formation of deletions

41. Additional file 4 of Secondary structure of the human mitochondrial genome affects formation of deletions

42. Additional file 3 of Secondary structure of the human mitochondrial genome affects formation of deletions

43. A mitochondria-specific mutational signature of aging: increased rate of A > G substitutions on the heavy strand

46. Defective lipid signalling caused by mutations in PIK3C2B underlies focal epilepsy

47. A mitochondria-specific mutational signature of aging: increased rate of A > G substitutions on the heavy strand

48. Defective lipid signalling caused by mutations inPIK3C2Bunderlies focal epilepsy

49. Dopamine neurons encode trial-by-trial subjective reward value in an auction-like task

50. Young people’s trust in institutions, civic knowledge and their dispositions toward civic engagement

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