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2. Digenic inheritance involving a muscle-specific protein kinase and the giant titin protein causes a skeletal muscle myopathy

5. Efficacy and safety of gene therapy with onasemnogene abeparvovec in children with spinal muscular atrophy in the D-A-CH-region: a population-based observational study

11. Long-term efficacy and safety of nusinersen in adults with 5q spinal muscular atrophy: a prospective European multinational observational study

14. The clinical and molecular landscape of congenital myasthenic syndromes in Austria: a nationwide study

23. Epilepsy and Alterations of the Blood–Brain Barrier: Cause or Consequence of Epileptic Seizures or Both?

26. Chronic Pain in Peripheral Neuropathy

27. Principles of Peripheral Nerve Surgery

28. Cranial Nerves

30. Autonomic Neuropathies

31. Radiculopathies

33. New Neuromuscular Therapies

34. Imaging

35. Tools

36. Motor Neuron Diseases

38. Muscle and Myotonic Diseases

39. Polyneuropathies

40. Mononeuropathies

41. A Prospective Comparison of Subjective Symptoms and Neurophysiological Findings in the Assessment of Neuropathy in Cancer Patients.

44. Small fiber involvement is independent from clinical pain in late-onset Pompe disease

45. Serum neurofilament light chain in distinct phenotypes of amyotrophic lateral sclerosis: A longitudinal, multicenter study

46. Safety and efficacy of cipaglucosidase alfa plus miglustat versus alglucosidase alfa plus placebo in late-onset Pompe disease (PROPEL): an international, randomised, double-blind, parallel-group, phase 3 trial

47. Safety and efficacy of oral levosimendan in people with amyotrophic lateral sclerosis (the REFALS study): a randomised, double-blind, placebo-controlled phase 3 trial

50. Commonalities in epileptogenic processes from different acute brain insults: Do they translate?

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