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2. ‘Minimal symptom expression’ in patients with acetylcholine receptor antibody-positive refractory generalized myasthenia gravis treated with eculizumab

3. Consistent improvement with eculizumab across muscle groups in myasthenia gravis

4. INTEREST IN CD2, a global patient-centred study of long-term cervical dystonia treatment with botulinum toxin

5. Eculizumab in refractory generalized myasthenia gravis previously treated with rituximab:subgroup analysis of REGAIN and its extension study

6. Eculizumab Improves Fatigue in Refractory Generalized Myasthenia Gravis

7. ‘Minimal symptom expression’ in patients with acetylcholine receptor antibody-positive refractory generalized myasthenia gravis treated with eculizumab

8. How satisfied are cervical dystonia patients after 3 years of botulinum toxin type A treatment? Results from a prospective, long-term observational study

9. Correction to: Eculizumab improves fatigue in refractory generalized myasthenia gravis (Quality of Life Research, (2019), 28, 8, (2247-2254), 10.1007/s11136-019-02148-2)

11. Fourth meeting of the European Neurological Society 25–29 June 1994 Barcelona, Spain: Abstracts of Symposia and free communications

16. The effectiveness of physiotherapy for cervical dystonia: a systematic literature review

18. Dysphagia in a patient with giant osteophytes: case presentation and review of the literature

19. Normative data of computerized electronystagmography in a healthy population between 25 and 70 years of age

21. Value of somatosensory and motor evoked potentials in predicting arm recovery after a stroke.

22. Debulking of stage IVA thymoma

25. Highly heterogeneous nature of delta-aminolevulinate dehydratase (ALAD) deficiencies in ALAD porphyria

27. Hereditary Hepatic Porphyria Due To Homozygous Delta-aminolevulinic-acid Dehydratase Deficiency - Studies in Lymphocytes and Erythrocytes

32. Neurogenic scapuloperoneal syndrome in childhood.

33. Molecular analysis of d-aminolevulinate dehydratase deficiency in a patient with an unusual late-onset porphyria

34. Biochemical diagnosis of an hereditary aminolaevulinate dehydratase deficiency in a 63-year-old man.

36. Myoadenylate Deaminase Deficiency - Absence of Correlation With Exercise Intolerance in 452 Muscle Biopsies

37. Myoadenylate Deaminase Deficiency in a Patient With Facial and Limb Girdle Myopathy

38. Clinical Heterogeneity of Myo-adenylate Deaminase Deficiency

39. Patient homozygous for a recessive POLGmutation presents with features of MERRF

43. Scientific Meeting of the Flemish Society of Neurology-Psychiatry held in Aalst, May 9th 1987

48. Long-term safety and efficacy of eculizumab in generalized myasthenia gravis

49. Current management of myasthenia gravis in Belgium: a single-center experience.

50. Caspr2 autoantibody-associated Morvan syndrome predating thymoma relapse by 30 months.

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