Search

Your search keyword '"Reinthaler, Eva M."' showing total 33 results

Search Constraints

Start Over You searched for: Author "Reinthaler, Eva M." Remove constraint Author: "Reinthaler, Eva M."
33 results on '"Reinthaler, Eva M."'

Search Results

1. Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy

2. TPP2 mutation associated with sterile brain inflammation mimicking MS

3. 16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy

4. Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals

5. Rare variants in γ-aminobutyric acid type A receptor genes in rolandic epilepsy and related syndromes

6. Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals

8. DEPDC5 mutations in genetic focal epilepsies of childhood

9. Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A

10. Exome sequencing in multiple sclerosis families identifies 12 candidate genes and nominates biological pathways for the genesis of disease

11. Exome sequencing in multiple sclerosis families identifies 12 candidate genes and nominates biological pathways for the genesis of disease

12. Rare gene deletions in genetic generalized and Rolandic epilepsies

13. Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies

14. Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic Epilepsy

15. Rare gene deletions in genetic generalized and Rolandic epilepsies

16. 16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy

17. Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A

18. Investigation of GRIN2A in common epilepsy phenotypes

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

20. Burden Analysis of Rare Microdeletions Suggests a Strong Impact of Neurodevelopmental Genes in Genetic Generalised Epilepsies

21. Investigation of GRIN2A in common epilepsy phenotypes

22. Burden Analysis of Rare Microdeletions Suggests a Strong Impact of Neurodevelopmental Genes in Genetic Generalised Epilepsies

23. DEPDC5mutations in genetic focal epilepsies of childhood

24. RBFOX1 and RBFOX3 Mutations in Rolandic Epilepsy

25. Correction: RBFOX1 and RBFOX3 Mutations in Rolandic Epilepsy

26. RBFOX1 and RBFOX3 Mutations in Rolandic Epilepsy

27. Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes

28. RBFOX1 and RBFOX3 Mutations in Rolandic Epilepsy.

29. Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A

30. 16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy

31. Rare gene deletions in genetic generalized and Rolandic epilepsies.

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

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

Catalog

Books, media, physical & digital resources