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1. Poster session Friday 13 December - PM: 13/12/2013, 14:00-18:00 * Location: Poster area

2. Club 35 Poster Session Thursday 6 December: Intracardiac flows and pressures

3. Poster Session 2: Thursday 8 December 2011, 14:00-18:00 * Location: Poster Area

4. Poster session II * Thursday 9 December 2010, 14:00-18:00

5. Automatic Analysis in Electromyography

7. EFNS task force on molecular diagnosis of neurologic disorders Guidelines for the molecular diagnosis of inherited neurologic diseases First of two parts

8. Evaluation of MUAP shape irregularity-a new concept of quantification

9. Muscle stiffness and continuous electromyographic activity in old rats; An animal model for spasticity?

10. Chronic acquired demyelinating motor neuropathy

11. Circulating autoantibodies to troponin I in Emery-Dreifuss muscular dystrophy

12. Looking for disease being a model of human aging

13. Autosomal recessive axonal form of Charcot-Marie-Tooth Disease caused by compound heterozygous 3'-splice site and Ser130Cys mutation in the GDAP1 gene

14. Expression of emerin and lamins in muscle of patients with different forms of Emery-Dreifuss muscular dystrophy

15. Focally folded myelin in Charcot-Marie-Tooth type 1B disease is associated with Asn131Lys mutation in myelin protein zero gene: short report

16. Phenotype and genotype correlation in childhood spinal muscular atrophy

17. Spinal muscular atrophy of childhood at the edge of the centuries

18. Controversies about the function of dystrophin in muscle

20. Dystrophinopathies in females

21. [Detecting carriers of a deletion in the dystrophin gene in families with a single case of Duchenne/Becker muscular dystrophy]

23. Macroemg in manifesting carriers of Duchenne muscular dystrophy

24. Diagnostic value of satellite potentials in clinical EMG

25. [Detection of dystrophin gene mutation carrier state]

27. [Conduction bloc in peripheral nerves. Facts and hypotheses]

28. [Diagnostic yield of electrophysiological and immunological studies in inflammatory myopathies]

29. [Clinical-genetic studies of infantile and juvenile proximal spinal muscular atrophy]

30. Features of motor control in patients with proximal childhood spinal muscle atrophy (pilot study)

31. MU firing characteristics in human dystrophic muscle

32. Interrelationship between gene, its product and phenotype in Duchenne and Becker muscular dystrophy

35. Dystrophinopathy in isolated cases of myopathy in females

36. Role of electromyography in the diagnosis of motor neuron disorders

37. Quantitative evaluation of the motor unit potential complexity

39. Disintegration of the motor unit in post-polio syndrome. Part II. Electrophysiological findings in patients with post-polio syndrome

40. Fiber density in congenital muscle fiber type disproportion. I. Congenital myopathies

41. Disintegration of the motor unit in post-polio syndrome. Part I. Electrophysiological findings in patients after poliomyelitis

42. [A trial of cronassial use in late postpoliomyelitis syndrome]

43. Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q11.2-13.3

49. International federation of societies for electroencephalography and clinical neurophysiology1,2. Proceedings of the general assembly, September 17, 1981

50. Serum cholinesterase activity in infantile and juvenile spinal muscular atrophy

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