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104. Diagnostic features of initial demyelinating events associated with serum MOG-IgG

108. Neurological Complications and Neural Autoantibody Profiles Associated with Immune Checkpoint Inhibitors (4215)

115. LGI1 antibody encephalitis: acute treatment comparisons and outcome.

116. Plasma vitronectin is reduced in patients with myasthenia gravis: Diagnostic and pathophysiological potential

117. Neuro-Ophthalmic Complications in Patients Treated With CTLA-4 and PD-1/PD-L1 Checkpoint Blockade.

119. Humoral immunity response to HERV-K/W differentiates between amyotrophic lateral sclerosis and other neurological diseases

120. Plasma vitronectin is reduced in patients with myasthenia gravis: Diagnostic and pathophysiological potential

122. A Population-Based Study of Idiopathic Transverse Myelitis with Aquaporin-4-IgG and Myelin-Oligodendrocyte-Glycoprotein-IgG Assessment (S11.007)

123. Myelin Oligodendrocyte Glycoprotein Autoantibody Myelitis; Clinical characteristics, MRI clues and discriminators from other demyelinating myelitis etiologies (S21.005)

125. Neurofilament light chain serum levels reflect disease severity in MOG-Ab associated disorders

126. Clinical, Radiologic, and Prognostic Features of Myelitis Associated With Myelin Oligodendrocyte Glycoprotein Autoantibody

128. Inflammatory activity following motor progression due to critical CNS demyelinating lesions.

129. Onset of progressive motor impairment in patients with critical central nervous system demyelinating lesions.

130. Critical spinal cord lesions associate with secondary progressive motor impairment in long-standing MS: A population-based case-control study.

131. Brainstem and cerebellar involvement in MOG-IgG-associated disorder versus aquaporin-4-IgG and MS.

132. Frequency and characteristics of MRI-negative myelitis associated with MOG autoantibodies.

133. Glial fibrillary acidic protein IgG related myelitis: characterisation and comparison with aquaporin-4-IgG myelitis

135. Mycobacterium avium subspecies paratuberculosis and myelin basic protein specific epitopes are highly recognized by sera from patients with Neuromyelitis optica spectrum disorder

136. Glial Fibrillary Acid Protein Immunoglobulin G (GFAP-IgG) Related Myelitis: Characterization and Comparison with Aquaporin-4-IgG Myelitis (S13.006)

137. Antibody response against HERV-W env surface peptides differentiates multiple sclerosis and neuromyelitis optica spectrum disorder

140. Serum and CSF neurofilament light chain levels in antibody-mediated encephalitis.

144. Late presentation of NMOSD as rapidly progressive leukoencephalopathy with atypical clinical and radiological findings.

145. Exploratory screening for Fabry’s disease in young adults with cerebrovascular disorders in northern Sardinia

148. Glial fibrillary acidic protein IgG related myelitis: characterisation and comparison with aquaporin-4-IgG myelitis.

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