about
Diffusion-weighted brain imaging study of patients with clinical diagnosis of corticobasal degeneration, progressive supranuclear palsy and Parkinson's diseaseImaging brain functional and metabolic changes in restless legs syndrome.Brain magnetic resonance metabolic and microstructural changes in adult-onset autosomal dominant leukodystrophy.Diffusion-weighted imaging study of patients with essential tremor.Pitfalls and advantages of different strategies for the absolute quantification of N-acetyl aspartate, creatine and choline in white and grey matter by 1H-MRS.Abnormal medial thalamic metabolism in patients with idiopathic restless legs syndrome.Secondary post-geniculate involvement in Leber's hereditary optic neuropathyEnergy metabolism in migraine.Magnetic resonance diagnostic markers in clinically sporadic prion disease: a combined brain magnetic resonance imaging and spectroscopy study.Combined brain voxel-based morphometry and diffusion tensor imaging study in idiopathic restless legs syndrome patients.A combined a-EEG and MR spectroscopy study in term newborns with hypoxic-ischemic encephalopathy.Diffusivity of cerebellar hemispheres enables discrimination of cerebellar or parkinsonian multiple system atrophy from progressive supranuclear palsy-Richardson syndrome and Parkinson disease.Low brain iron content in idiopathic restless legs syndrome patients detected by phase imaging.Effects of exercise-induced intracellular acidosis on the phosphocreatine recovery kinetics: a 31P MRS study in three muscle groups in humans.Distribution of neurochemical abnormalities in patients with narcolepsy with cataplexy: An in vivo brain proton MR spectroscopy study.Cytosolic pH buffering during exercise and recovery in skeletal muscle of patients with McArdle's disease.Bayesian analysis of in vivo dynamic 13C-edited 1H images.Randomized, placebo-controlled, double-blind pilot trial of ramipril in McArdle's disease.Cerebral Mitochondrial Microangiopathy Leads to Leukoencephalopathy in Mitochondrial Neurogastrointestinal Encephalopathy.Polysomnographic and neurometabolic features may mark preclinical autosomal dominant cerebellar ataxia, deafness, and narcolepsy due to a mutation in the DNA (cytosine-5-)-methyltransferase gene, DNMT1.The contribution of cerebellar proton magnetic resonance spectroscopy in the differential diagnosis among parkinsonian syndromes.Diffusion Tensor Imaging Mapping of Brain White Matter Pathology in Mitochondrial Optic Neuropathies.Study of hypothalamic metabolism in cluster headache by proton MR spectroscopy.Defective mitochondrial adenosine triphosphate production in skeletal muscle from patients with dominant optic atrophy due to OPA1 mutations.Prostate cancer: sextant localization with MR imaging, MR spectroscopy, and 11C-choline PET/CT.The role of pH on the thermodynamics and kinetics of muscle biochemistry: an in vivo study by (31)P-MRS in patients with myo-phosphorylase deficiency.Double-resonance J-edited (1)H-NMR detection of 6-(13)C-D-2-deoxyglucose uptake in glioma cells.Prognostic value of brain proton MR spectroscopy and diffusion tensor imaging in newborns with hypoxic-ischemic encephalopathy treated by brain coolingBrain diffusion-weighted imaging in Friedreich's ataxiaAccuracy of MRI/MRSI-based transrectal ultrasound biopsy in peripheral and transition zones of the prostate gland in patients with prior negative biopsy
P50
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P50
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hulumtuese
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հետազոտող
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Claudia Testa
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Claudia Testa
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Claudia Testa
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Claudia Testa
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Claudia Testa
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Claudia Testa
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Claudia Testa
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Claudia Testa
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CLAUDIA TESTA
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Claudia Testa
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Claudia Testa
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Claudia Testa
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Claudia Testa
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P106
P21
P31
P496
0000-0002-8591-9803