Search

Your search keyword '"craniobulbar"' showing total 36 results

Search Constraints

Start Over You searched for: "craniobulbar" Remove constraint "craniobulbar" Search Limiters Full Text Remove constraint Search Limiters: Full Text
36 results on '"craniobulbar"'

Search Results

1. Differential changes in human pharyngoesophageal motor excitability induced by swallowing, pharyngeal stimulation, and anesthesia.

2. Congenital Myasthenia Syndrome Due to a Novel DPAGT1 Gene Mutation – An Error of Glycosylation Masquerading as a Congenital Myopathy.

3. Tumefactive Demyelination--A Rare Presentation of Anti-MOG Syndrome.

5. Novel TFG mutation causes autosomal-dominant spastic paraplegia and defects in autophagy.

6. Spastic Paraparesis in Donnai--Barrow Syndrome: A Rare Case Report from India.

7. Spastic ataxia with sensory neuropathy sans cerebral leukodystrophy in probable adult polyglucosan body disease.

8. Abstracts.

9. Muscle MRI-Based Atrophy Pattern Recognition: Notable Findings in a Case of Pathologically Proven Lipid Storage Myopathy.

10. Correlative study between C-reactive protein, clinical severity, and nerve conduction studies in Guillain-Barrè syndrome.

11. Painless legs and moving toes in chronic inflammatory demyelinating polyradiculoneuropathy.

12. Prolonged Limb and Respiratory Muscle Weakness Associated with Japanese Encephalitis Virus Infection: A Case Report

13. Correlative study between C-reactive protein, clinical severity, and nerve conduction studies in Guillain-Barrè syndrome

14. Severe statin-induced autoimmune myopathy successfully treated with intravenous immunoglobulin.

15. Clinical features of congenital myasthenic syndrome due to mutations in DPAGT1

16. Exploring the effects of synchronous pharyngeal electrical stimulation with swallowing carbonated water on cortical excitability in the human pharyngeal motor system

17. Levodopa-induced Dyskinesia: Clinical Features, Pathophysiology, and Medical Management.

18. Research of antibodies to the acetylcholine receptors in patients with myasthenia gravis

19. Association of Sjögren’s syndrome with myotonic dystrophy type 1.

20. Poster Abstracts.

21. Rapidly progressive foot drop: an uncommon and underappreciated cause of Chiari I malformation and holocord syrinx.

25. Isolated deep peroneal nerve palsy: Role of magnetic resonance imaging in localization.

27. Clinical features in a large Iranian family with a limb-girdle congenital myasthenic syndrome due to a mutation in DPAGT1

28. Clinical features of the myasthenic syndrome arising from mutations in GMPPB

29. The Neuromuscular Junction and Wide Heterogeneity of Congenital Myasthenic Syndromes.

30. MuSK-Ab positive myasthenia: Not always grave

32. Miller-Fisher syndrome and Hodgkin's disease

34. Hereditary spastic paraplegia due to LYST gene mutation: A novel causative gene

35. Spastic paraplegia type 8: A first report from India

Catalog

Books, media, physical & digital resources