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2. Fine-tuning of canted magnetization in stepped Fe films through thickness variation, Au capping, and quantum confinement

3. Fine-tuning of canted magnetization in stepped Fe films through thickness variation, Au capping, and quantum confinement

4. The emerging spectrum of neurodevelopmental comorbidities in early-onset Spinal Muscular Atrophy

5. Temperature Dependence of Magnetic Excitations: Terahertz Magnons above the Curie Temperature

6. Three dimensional boundary displacement due to stable ideal kink modes excited by external n=2 magnetic perturbations

7. Asymmetric Spin-wave Dispersion on Fe(110): Direct Evidence of Dzyaloshinskii--Moriya Interaction

8. The role of electron confinement in Pd films for the oscillatory magnetic anisotropy in an adjacent Co layer

10. Ferromagnetism of Pd(001) substrate induced by Antiferromagnetic CoO

12. Canted stripe phase evolution due to a spin reorientation transition in Fe films grown on Ag(001) vicinal surface

13. P196 Age at loss of ambulation in patients with DMD from the STRIDE registry and the CINRG natural history study: a matched cohort analysis

14. P198 Updated demographics and safety data from patients with nonsense mutation Duchenne muscular dystrophy receiving ataluren in the STRIDE registry

15. P230 Safety update: Risdiplam clinical trial program for spinal muscular atrophy (SMA)

16. P197 Pulmonary function in patients with Duchenne muscular dystrophy from the STRIDE registry and CINRG natural history study: a matched cohort analysis

17. The Multiple Sclerosis Inventory of Cognition for Adolescents (MUSICADO): A brief screening instrument to assess cognitive dysfunction, fatigue and loss of health-related quality of life in pediatric-onset multiple sclerosis

19. Huge magneto-crystalline anisotropy of x-ray linear dichroism observed on Co/FeMn bilayers

20. Three-dimensional magnetic flux-closure patterns in mesoscopic Fe islands

22. Effect of hydrogen on the atomic structure of Pd(001)

23. Angular-dependence of magnetization switching for a multi-domain dot: experiment and simulation

27. Safety, tolerability and pharmacokinetics of eteplirsen in young boys aged 6–48 months with Duchenne muscular dystrophy amenable to exon 51 skipping

28. Correction to: Risdiplam in Patients Previously Treated with Other Therapies for Spinal Muscular Atrophy: An Interim Analysis from the JEWELFISH Study (Neurology and Therapy, (2023), 12, 2, (543-557), 10.1007/s40120-023-00444-1)

29. Characterization of pulmonary function in 10–18 year old patients with Duchenne muscular dystrophy

30. Real-World Data on the Efficacy of Gene Replacement Therapy for Spinal Muscular Atrophy (SMA).

31. Ocular Myasthenia: It's Worth a Second Look.

33. Idebenone reduces respiratory complications in patients with Duchenne muscular dystrophy

37. P.113 Safety update: Risdiplam clinical trial development program

38. P.110 JEWELFISH: 24-month safety and pharmacodynamic data in non-treatment-naïve patients with spinal muscular atrophy (SMA)

39. P.103 Onasemnogene abeparvovec (OA) treatment outcomes by patient weight at infusion: Initial findings from the RESTORE registry

40. VP.20 Cathepsin D as biomarker in CSF of nusinersen-treated patients with spinal muscular atrophy

41. P.35 Genetic newborn screening and digital technologies to accelerate rare disease diagnosis: The EU-IMI screen4Care project

42. P.122 Comparative safety and efficacy of different corticosteroid regimens in boys with Duchenne muscular dystrophy: results of a randomized controlled trial

43. VP.51 Impact of nusinersen on caregiver experience and health-related quality of life (HRQoL) when initiated in the presymptomatic stage of SMA in NURTURE

44. P.23 Pulmonary function in patients with Duchenne muscular dystrophy from the STRIDE Registry and CINRG Natural History Study: a matched cohort analysis

45. P.22 Age at loss of ambulation in patients with DMD from the STRIDE registry and the CINRG natural history study: A matched cohort analysis

46. P.19 Updated demographics and safety data from patients with nonsense mutation Duchenne muscular dystrophy receiving ataluren in the STRIDE Registry

48. P.114 SUNFISH parts 1 and 2: 3-year efficacy and safety of risdiplam in types 2 and 3 spinal muscular atrophy (SMA)

49. P.104 Treatments and outcomes for patients with spinal muscular atrophy (SMA) type 2: Findings from RESTORE registry

50. P.105 Safety and effectiveness of onasemnogene abeparvovec (OA) alone or with other disease-modifying therapies (DMTs): Findings from RESTORE

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