769 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. Drug screening identifies tazarotene and bexarotene as therapeutic agents in multiple sulfatase deficiency
6. Deep breathing couples CSF and venous flow dynamics
7. Autorenverzeichnis
8. Pädiatrische MS
9. Atlas‐based assessment of hypomyelination: Quantitative MRI in Pelizaeus‐Merzbacher disease.
10. Long term follow-up in GAMT deficiency – Correlation of therapy regimen, biochemical and in vivo brain proton MR spectroscopy data
11. Corrigendum: Wild-type microglia do not reverse pathology in mouse models of Rett syndrome.
12. Wild-type microglia do not reverse pathology in mouse models of Rett syndrome.
13. Interferon-driven brain phenotype in a mouse model of RNaseT2 deficient leukoencephalopathy
14. Multiple Sklerose im Kindes- und Jugendalter
15. Pretreatment Neurofilament Light Chain Serum Levels, Early Disease Severity, and Treatment Response in Pediatric Multiple Sclerosis
16. Arzneimittel für neuartige Therapien: Kurzfassung der Stellungnahme der Deutschen Gesellschaft für Kinder- und Jugendmedizin e. V. (DGKJ)
17. Bi‐allelic VPS16 variants limit HOPS/CORVET levels and cause a mucopolysaccharidosis‐like disease
18. Ketogenic diet ameliorates axonal defects and promotes myelination in Pelizaeus–Merzbacher disease
19. Genetics of intellectual disability in consanguineous families
20. Upward movement of cerebrospinal fluid in obstructive hydrocephalus—revision of an old concept
21. Peroxisomale Krankheiten
22. Multiple Sklerose und andere entzündliche demyelinisierende Erkrankungen des zentralen Nervensystems
23. Neurodegenerative Erkrankungen der weißen Hirnsubstanz
24. Adressen
25. Tumefactive inflammatory lesions in juvenile metachromatic leukodystrophy
26. Folate receptor α deficiency – Myelin‐sensitive MRI as a reliable biomarker to monitor the efficacy and long‐term outcome of a new therapeutic approach.
27. Serum neurofilament light chain is a useful biomarker in pediatric multiple sclerosis
28. „Vanishing white matter disease“ im Erwachsenenalter
29. Molecularly defined diffuse leptomeningeal glioneuronal tumor (DLGNT) comprises two subgroups with distinct clinical and genetic features
30. Evaluation of Novel Enhancer Compounds in Gentamicin-Mediated Readthrough of Nonsense Mutations in Rett Syndrome
31. Neurodegenerative Erkrankungen der weißen Hirnsubstanz
32. Multiple Sklerose und andere entzündliche demyelinisierende Erkrankungen des zentralen Nervensystems bei Kindern und Jugendlichen
33. Peroxisomale Krankheiten
34. Neurologic phenotypes associated with COL4A1/2 mutations: Expanding the spectrum of disease
35. Spinal CSF flow in response to forced thoracic and abdominal respiration
36. Multiple Sulfatase Deficiency from an Ophthalmologist’s Perspective—Case Report and Literature Review
37. Association of Overweight and Obesity With Bell Palsy in Children
38. Pädiatrische multiple Sklerose
39. Autorenverzeichnis
40. Correction to: Ketogenic diet ameliorates axonal defects and promotes myelination in Pelizaeus–Merzbacher disease
41. A new CUL4B variant associated with a mild phenotype and an exceptional pattern of leukoencephalopathy
42. Mutations inTAF8cause a neurodegenerative disorder
43. TTC5 syndrome: Clinical and molecular spectrum of a severe and recognizable condition
44. Cln5 represents a new type of cysteine-basedS-depalmitoylase linked to neurodegeneration
45. sj-docx-1-tan-10.1177_17562864211070449 – Supplemental material for Improving pediatric multiple sclerosis interventional phase III study design: a meta-analysis
46. sj-docx-2-tan-10.1177_17562864211070449 – Supplemental material for Improving pediatric multiple sclerosis interventional phase III study design: a meta-analysis
47. Ärztliche Aus-, Weiter- und Fortbildung – für eine lebenslange Wissenschaftskompetenz in der Medizin
48. Leukoencephalopathy and early death associated with an Ashkenazi-Jewish founder mutation in the Hikeshi gene
49. Improving pediatric multiple sclerosis interventional phase III study design: a meta-analysis
50. Severe neonatal multiple sulfatase deficiency presenting with hydrops fetalis in a preterm birth patient
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