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496 results on '"Moller, R."'

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1. Sympathetic cooling schemes for separately trapped ions coupled via image currents

2. mGlu3 metabotropic glutamate receptors as a target for the treatment of absence epilepsy: Preclinical and human genetics data

3. Estimating the effects of Bose-Einstein correlations on the W mass measurement at LEP2

4. Determination of the mass of the W boson

5. QCD Event Generators

7. Sympathetic cooling schemes for separately trapped ions coupled via image currents

8. Sympathetic cooling schemes for separately trapped ions coupled via image currents

9. Association of ultra-rare coding variants with genetic generalized epilepsy: A case–control whole exome sequencing study

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

14. Gene family information facilitates variant interpretation and identification of disease-associated genes in neurodevelopmental disorders

15. Antiepileptic Drug Teratogenicity and De Novo Genetic Variation Load

16. Mowat-Wilson syndrome:growth charts

18. De novo variants in neurodevelopmental disorders with epilepsy

19. Android subcutaneous adipose tissue topography in lean and obese women suffering from PCOS: comparison with type 2 diabetic women

22. Diagnostic implications of genetic copy number variation in epilepsy plus

23. A genome-wide association study of sodium levels and drug metabolism in an epilepsy cohort treated with carbamazepine and oxcarbazepine

24. Clinical and genetic spectrum of SCN2A-associated episodic ataxia

25. Heat transfer between two metallic surfaces at small distances

27. KCNB1 MUTATIONS ARE CAUSING A NEURODEVELOPMENTAL DISORDER INCLUDING EPILEPSY AND AUTISM

28. DGNB building certification companion: Sustainability Tool for Assessment, Planning, Learning, and Engaging (STAPLE)

34. Determination of the mass of the W boson

35. Genetic and neurodevelopmental spectrum of SYNGAP1-associated intellectual disability and epilepsy

36. CLINICAL HETEROGENEITY AND ITS POTENTIAL THERAPEUTIC IMPLICATIONS IN CHILDREN WITH SCN2A-RELATED DISORDERS

38. Recessive mutations in SLC13A5 result in a loss of citrate transport and cause neonatal epilepsy, developmental delay and teeth hypoplasia

39. A semantic approach to polystores

42. Mutations in STX1B, encoding a presynaptic protein, cause fever-associated epilepsy syndromes

45. DE NOVO LOSS- OR GAIN-OF-FUNCTION MUTATIONS IN KCNA2 CAUSE EPILEPTIC ENCEPHALOPATHY

46. TARGETED NEXT GENERATION SEQUENCING AS A DIAGNOSTIC TOOL IN 163 PATIENTS WITH EPILEPTIC ENCEPHALOPATHIES

47. Scalable End-User Access to Big Data

48. A study of the production of two direct photons inpp collisions at the CERN ISR

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