26 results on '"Fehmi, Janev"'
Search Results
2. Contactin-1 links autoimmune neuropathy and membranous glomerulonephritis
3. Antineurofascin IgG2 ‐associated paediatric autoimmune nodopathy
4. Treatment of CIDP
5. IgG1 pan-neurofascin antibodies define a severe and frequently fatal GBS-like neuropathy which responds to rituximab
6. Leucine‐Rich Glioma‐Inactivated 1 versus Contactin‐Associated Protein‐like 2 Antibody Neuropathic Pain: Clinical and Biological Comparisons
7. IgG1 pan-neurofascin antibodies identify a severe yet treatable neuropathy with a high mortality
8. Serum Contactin-1 in CIDP
9. Nodal and paranodal antibody-associated neuropathies
10. FC 030CONTACTIN-1 IS A NOVEL ANTIGEN IN IDIOPATHIC MEMBRANOUS GLOMERULONEPHRITIS AND IN CIDP- ASSOCIATED GLOMERULONEPHRITIS
11. Antibodies to the Caspr1/contactin-1 complex in chronic inflammatory demyelinating polyradiculoneuropathy
12. IgG1 pan-neurofascin antibodies identify a severe yet treatable neuropathy with a high mortality
13. Epidemiological and cohort study finds no association between COVID-19 and Guillain-Barré syndrome
14. Clinical characteristics, risk factors, and outcomes of POEMS syndrome
15. Immunoadsorption and Plasma Exchange in Seropositive and Seronegative Immune-Mediated Neuropathies
16. Motor neuropathy with conduction block due to pan‐neurofascin antibodies in a patient with chronic lymphocytic leukemia
17. Contactin-1 Antibodies Link Autoimmune Neuropathies to Nephrotic Syndrome
18. Untangling a case of painful neuropathy
19. A rare case of Miller Fisher variant of Guillain-Barré Syndrome (GBS) induced by a checkpoint inhibitor
20. PO224 How effective is simulation-based teaching in cambodia?
21. PO225 Innovation in neurology education in cambodia
22. Nodes, paranodes and neuropathies
23. FEMORAL NEUROPATHY FROM ILIACUS HAEMATOMA AS FIRST PRESENTATION OF HAEMOPHILIA
24. Tumefactive demyelination presenting during bevacizumab treatment
25. Out of hours intravenous fluid therapy: a prompt to guide prescribing
26. Long-term survival of neonatal mitochondrial complex III deficiency associated with a novel BCS1L gene mutation
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