779 results on '"Gärtner, Jutta"'
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2. CSF and venous blood flow from childhood to adulthood studied by real-time phase-contrast MRI
3. Multiple Sklerose im Kindes- und Jugendalter
4. Efficacy and safety of ofatumumab in recently diagnosed, treatment-naive patients with multiple sclerosis: Results from ASCLEPIOS I and II
5. Long term follow-up in GAMT deficiency – Correlation of therapy regimen, biochemical and in vivo brain proton MR spectroscopy data
6. Deep breathing couples CSF and venous flow dynamics
7. Autorenverzeichnis
8. Pädiatrische MS
9. Peroxisomale Krankheiten
10. Multiple Sklerose und andere entzündliche demyelinisierende Erkrankungen des zentralen Nervensystems
11. Neurodegenerative Erkrankungen der weißen Hirnsubstanz
12. Multiple Sklerose im Kindes- und Jugendalter
13. Pretreatment Neurofilament Light Chain Serum Levels, Early Disease Severity, and Treatment Response in Pediatric Multiple Sclerosis
14. Breathing drives CSF : Impact on spaceflight disease and hydrocephalus
15. Folate receptor α deficiency – Myelin‐sensitive MRI as a reliable biomarker to monitor the efficacy and long‐term outcome of a new therapeutic approach.
16. Interferon-driven brain phenotype in a mouse model of RNaseT2 deficient leukoencephalopathy
17. Corrigendum: Wild-type microglia do not reverse pathology in mouse models of Rett syndrome.
18. Wild-type microglia do not reverse pathology in mouse models of Rett syndrome.
19. Arzneimittel für neuartige Therapien: Kurzfassung der Stellungnahme der Deutschen Gesellschaft für Kinder- und Jugendmedizin e. V. (DGKJ)
20. Evaluation of Novel Enhancer Compounds in Gentamicin-Mediated Readthrough of Nonsense Mutations in Rett Syndrome
21. Peroxisomale Krankheiten
22. Multiple Sklerose und andere entzündliche demyelinisierende Erkrankungen des zentralen Nervensystems
23. Neurodegenerative Erkrankungen der weißen Hirnsubstanz
24. Adressen
25. „Vanishing white matter disease“ im Erwachsenenalter
26. Ketogenic diet ameliorates axonal defects and promotes myelination in Pelizaeus–Merzbacher disease
27. Genetics of intellectual disability in consanguineous families
28. Upward movement of cerebrospinal fluid in obstructive hydrocephalus—revision of an old concept
29. Molecularly defined diffuse leptomeningeal glioneuronal tumor (DLGNT) comprises two subgroups with distinct clinical and genetic features
30. Tumefactive inflammatory lesions in juvenile metachromatic leukodystrophy
31. Multiple Sulfatase Deficiency from an Ophthalmologist’s Perspective—Case Report and Literature Review
32. Drug screening identifies tazarotene and bexarotene as therapeutic agents in multiple sulfatase deficiency
33. Association of Overweight and Obesity With Bell Palsy in Children
34. Neurodegenerative Erkrankungen der weißen Hirnsubstanz
35. Multiple Sklerose und andere entzündliche demyelinisierende Erkrankungen des zentralen Nervensystems bei Kindern und Jugendlichen
36. Peroxisomale Krankheiten
37. Serum neurofilament light chain is a useful biomarker in pediatric multiple sclerosis
38. Neurologic phenotypes associated with COL4A1/2 mutations: Expanding the spectrum of disease
39. Stoffwechselkrankheiten mit Dysmorphien
40. Multiple Sklerose (MS) und MS ähnliche Erkrankungen
41. Neurometabolische Erkrankungen
42. Correction to: Ketogenic diet ameliorates axonal defects and promotes myelination in Pelizaeus–Merzbacher disease
43. Pädiatrische multiple Sklerose
44. Autorenverzeichnis
45. Spinal CSF flow in response to forced thoracic and abdominal respiration
46. Lymphoblastoid Cell Lines for Diagnosis of Peroxisome Biogenesis Disorders
47. Mutations inTAF8cause a neurodegenerative disorder
48. TTC5 syndrome: Clinical and molecular spectrum of a severe and recognizable condition
49. Disturbances of Breathing in Rett Syndrome: Results from Patients and Animal Models
50. A new CUL4B variant associated with a mild phenotype and an exceptional pattern of leukoencephalopathy
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