Search

Your search keyword '"Wolfram S"' showing total 1,441 results

Search Constraints

Start Over You searched for: Author "Wolfram S" Remove constraint Author: "Wolfram S" Publication Year Range Last 50 years Remove constraint Publication Year Range: Last 50 years
1,441 results on '"Wolfram S"'

Search Results

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. Rasmussen’s encephalitis: structural, functional, and clinical correlates of contralesional epileptiform activity

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

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

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

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

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

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

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

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

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

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

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

24. De Novo Variants in RAB11B Cause Various Degrees of Global Developmental Delay and Intellectual Disability in Children

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

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

33. Mitochondrial mutation spectrum in Chordates: damage versus replication signatures, causes, and dynamics

34. Guide to the Pharmacology of Mitochondrial Potassium Channels

35. Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study

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

37. Homozygous mutation in TXNRD1 is associated with genetic generalized epilepsy

38. Selenium Ameliorated Oxidized Fish Oil-Induced Lipotoxicity via the Inhibition of Mitochondrial Oxidative Stress, Remodeling of Usp4-Mediated Deubiquitination, and Stabilization of Pparα.

40. The Fate of Oxidative Strand Breaks in Mitochondrial DNA

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

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

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

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

50. Mitochondrial Retinopathy

Catalog

Books, media, physical & digital resources