202 results on '"Salameh, Johnny"'
Search Results
2. Kennedy’s disease: an under-recognized motor neuron disorder
3. Nonmotor Symptoms in Amyotrophic Lateral Sclerosis and Their Correlation With Disease Progression
4. Efficacy of apraclonidine eye drops in treating ptosis secondary to myasthenia gravis: A pilot clinical trial
5. Partial loss of TDP-43 function causes phenotypes of amyotrophic lateral sclerosis
6. ALS‐linked protein disulfide isomerase variants cause motor dysfunction
7. Efficacy of Apraclonidine in Treating Ptosis Secondary to Myasthenia Gravis (P6-13.001)
8. Low-level overexpression of wild type TDP-43 causes late-onset, progressive neurodegeneration and paralysis in mice
9. Adeno-associated virus–delivered artificial microRNA extends survival and delays paralysis in an amyotrophic lateral sclerosis mouse model
10. Safety and Efficacy of Subcutaneous Immunoglobulin in the Treatment of Neuromuscular Disorders
11. A phase III trial of tirasemtiv as a potential treatment for amyotrophic lateral sclerosis
12. Amyotrophic Lateral Sclerosis: Review
13. Necrotizing Myopathies: An Update
14. An open label pilot study of the safety and tolerability of perampanel in amyotrophic lateral sclerosis
15. Low-level overexpression of wild type TDP-43 causes late-onset, progressive neurodegeneration and paralysis in mice
16. Peripheral Neuropathy After Hair Dye Exposure: A Case Report
17. Phosphoglycerate mutase deficiency with tubular aggregates in a patient from panama
18. Role of Activity-Dependent Conduction Block in the Diagnosis of Primary Demyelinating Polyneuropathy
19. Traumatic Brain Injury: Oxidative Stress and Novel Anti-Oxidants Such as Mitoquinone and Edaravone
20. Characteristics of amyotrophic lateral sclerosis in Lebanon-a chart review
21. Absent sural responses in tethered cord syndrome
22. ADDED SAMPLING IMPROVES REPRODUCIBILITY OF MULTIPOINT MOTOR UNIT ESTIMATES
23. PATIENT WITH AMYLOIDOMA OF THE ULNAR NERVE AND SALIVARY GLANDS
24. SOD1 (A4V)-MEDIATED ALS PRESENTING WITH LOWER MOTOR NEURON FACIAL DIPLEGIA AND UNILATERAL VOCAL CORD PARALYSIS
25. Novel SPG3A and SPG4 Mutations in Two Patients With Silver Syndrome
26. Selection design phase II trial of high dosages of tamoxifen and creatine in amyotrophic lateral sclerosis
27. Guillain–Barre Syndrome
28. Common Entrapment Neuropathies
29. Adult onset Sandhoff disease: a rare mimicker of amyotrophic lateral sclerosis
30. An Acute Cervical Radiculopathy After Electric Injury
31. Selection design phase II trial of high dosages of tamoxifen and creatine in amyotrophic lateral sclerosis.
32. Medical research productivity in the Arab countries: 2007-2016 bibliometric analysis
33. Codeine-Induced Sensory Neuropathy, Autonomic Dysfunction, and Myopathy
34. Loss of Sarm1 does not suppress motor neuron degeneration in the SOD1G93A mouse model of amyotrophic lateral sclerosis
35. Pyridoxine-induced sensory ataxic ganglionopathy: a case report and literature review
36. An open label study of a novel immunosuppression intervention for the treatment of amyotrophic lateral sclerosis
37. Recurrent Cushing’s Syndrome Manifesting as Pseudotumor Cerebri with Isolated Cranial Nerve Six Palsy.
38. Post-Partum Reversible Cerebral Vasoconstriction Syndrome Associated with Coronary Vasospasm
39. Interesting Presentation of Acute Intravenous Methotrexate Leukoencephalopathy
40. AAV delivered artificial microRNA extends survival and delays paralysis in an Amyotrophic Lateral Sclerosis mouse model
41. Human C9ORF72 Hexanucleotide Expansion Reproduces RNA Foci and Dipeptide Repeat Proteins but Not Neurodegeneration in BAC Transgenic Mice
42. Monitoring peripheral nerve degeneration in ALS by label-free stimulated Raman scattering imaging
43. Impaired neurodevelopment by the low complexity domain of CPEB4 reveals a convergent pathway with neurodegeneration
44. Adult onset Sandhoff disease: a rare mimicker of amyotrophic lateral sclerosis.
45. A dystonia-like movement disorder with brain and spinal neuronal defects is caused by mutation of the mouse laminin β1 subunit, Lamb1
46. Author response: A dystonia-like movement disorder with brain and spinal neuronal defects is caused by mutation of the mouse laminin β1 subunit, Lamb1
47. Human C9ORF72 Hexanucleotide Expansion Reproduces RNA Foci and Dipeptide Repeat Proteins but Not Neurodegeneration in BAC Transgenic Mice
48. Pearls & Oy-sters: An isolated cranial nerve 6 palsy as a presentation of polycythemia vera
49. 341. Therapeutic Approach for SOD1-ALS Using AAV9 Delivered Artificial microRNAs
50. A Unique Presentation of a Novel Mutation in the SETX Gene (S17.007)
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.