36 results on '"Avignone, Sabrina"'
Search Results
2. Osmotic demyelination syndrome and leukoencephalopathy in FGF23-related hypophosphatemia: a case report
3. Normal Development
4. Electroclinical phenotype in Rubinstein–Taybi syndrome
5. Altered prefrontal cortex activity during working memory task in Bipolar Disorder: A functional Magnetic Resonance Imaging study in euthymic bipolar I and II patients
6. A Translational Approach to Spinal Neurofibromatosis: Clinical and Molecular Insights from a Wide Italian Cohort
7. High resolution post-mortem MRI of non-fixed in situ foetal brain in the second trimester of gestation: Normal foetal brain development
8. Balò’s concentric sclerosis: still to be considered as a variant of multiple sclerosis?
9. Neurodevelopmental outcome at 36 months in very low birth weight premature infants with MR diffuse excessive high signal intensity (DEHSI) of cerebral white matter
10. Takayasu's artheritis presenting as a large sellar mass with neurological and hypopituitarism manifestations
11. A Translational Approach to Spinal Neurofibromatosis: Clinical and Molecular Insights from a Wide Italian Cohort.
12. Intracranial haemorrhage: an incidental finding at magnetic resonance imaging in a cohort of late preterm and term infants
13. Suspected fetal brain metallic embolic microfragment detected by MR imaging
14. Efficacy of B-Cell Targeted Therapy With Rituximab in Patients With Active Moderate to Severe Gravesʼ Orbitopathy: A Randomized Controlled Study
15. Histone Deacetylase Inhibitors Ameliorate Morphological Defects and Hypoexcitability of iPSC-Neurons from Rubinstein-Taybi Patients
16. Diagnosi e terapia degli adenomi ipofisari non funzionanti
17. Pediatric Metronidazole-Induced Encephalopathy: A Case Report and Review of the Literature
18. Olfactory Malformations in Mendelian Disorders of the Epigenetic Machinery
19. Risk of Optic Pathway Glioma in Neurofibromatosis Type 1: No Evidence of Genotype–Phenotype Correlations in a Large Independent Cohort
20. Hypogonadotropic hypogonadism and pituitary hypoplasia as recurrent features in Ulnar-Mammary syndrome
21. Pediatric Metronidazole-Induced Encephalopathy: A Case Report and Review of the Literature.
22. Rubinstein-Taybi syndrome: New neuroradiological and neuropsychiatric insights from a multidisciplinary approach
23. New Insights into Kleefstra Syndrome: Report of Two Novel Cases with Previously Unreported Features and Literature Review
24. The ‘full-blown’ MRI of sudden hearing loss: 3D FLAIR in a patient with bilateral metastases in the internal auditory canals
25. Occlusione del sifone carotideo in paziente con lesione granulomatosa dell’ipofisi
26. Aneurisma intrasellare in paziente con quadro clinico suggestivo per apoplessia ipofisaria
27. Fetal development of the corpus callosum: Insights from a 3T DTI and tractography study in a patient with segmental callosal agenesis
28. High resolution post-mortem MRI of non-fixed in situ foetal brain in the second trimester of gestation: Normal foetal brain development.
29. 48, XXXY/49, XXXXY mosaic: new neuroradiological features in an ultra-rare syndrome
30. Effect of a very low dose of rituximab on active moderate-severe Graves' orbitopathy: an interim report
31. Suspected fetal brain metallic embolic microfragment detected by MR imaging
32. Intracranial haemorrhage: an incidental finding at magnetic resonance imaging in a cohort of late preterm and term infants
33. A Quantitative Method for Assessing the Degree of Axial Proptosis in Relation to Orbital Tissue Involvement in Graves' Orbitopathy
34. The ‘full-blown’ MRI of sudden hearing loss: 3D FLAIR in a patient with bilateral metastases in the internal auditory canals.
35. Efficacy of rituximab treatment for thyroid-associated ophthalmopathy as a result of intraorbital B-cell depletion in one patient unresponsive to steroid immunosuppression
36. A Translational Approach to Spinal Neurofibromatosis: Clinical and Molecular Insights from a Wide Italian Cohort
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