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

3. MAPT H2 haplotype and risk of Pick's disease in the Pick's disease International Consortium: a genetic association study

7. MAPT H2 haplotype and risk of Pick's disease in the Pick's disease International Consortium: a genetic association study

8. Novel antivirals for severe enterovirus infection in immunocompromised hosts; a case series

9. Multisite Assessment of Aging-Related Tau Astrogliopathy (ARTAG).

10. Seizure outcome and use of antiepileptic drugs after epilepsy surgery according to histopathological diagnosis: a retrospective multicentre cohort study

12. Aging-related tau astrogliopathy (ARTAG): harmonized evaluation strategy

13. Neurological features and progression in a large cohort with xeroderma pigmentosum

14. Desmoplastic myxoid tumor, SMARCB1-mutant: clinical, histopathological and molecular characterization of a pineal region tumor encountered in adolescents and adults

19. Neurological disease in xeroderma pigmentosum: prospective cohort study of its features and progression.

20. Inter-dural spinal cyst with acute thoracic compressive myelopathy: anatomical aspects of spinal dura, case report and literature review.

21. Intracranial dural based marginal zone MALT-type B-cell lymphoma: a case -- Based update and literature review.

22. Creating the Pick’s disease International Consortium: Association study ofMAPTH2 haplotype with risk of Pick’s disease

23. IgG4-related hypertrophic pachymeningitis with chronic subdural haematoma.

28. MGMT Promoter Methylation: Prognostication beyond Treatment Response.

32. The need to unify neuropathological assessments of vascular alterations in the ageing brain: Multicentre survey by the BrainNet Europe consortium

34. Neuropathological assessments of the pathology in frontotemporal lobar degeneration with TDP43-positive inclusions: an inter-laboratory study by the BrainNet Europe consortium

38. Novel phosphopantothenoylcysteine synthetase (PPCS) mutations with prominent neuromuscular features: Expanding the phenotypical spectrum ofPPCS‐related disorders

41. A novel case of paravertebral glomangiomyomatosis

45. EPG5-related Vici syndrome: a paradigm of neurodevelopmental disorders with defective autophagy

48. Do All Notochordal Lesions Require Proton Beam Radiotherapy? A Proposed Reclassification of Ecchordosis Physaliphora as Benign Notochord Cell Tumor.

49. Novel phosphopantothenoylcysteine synthetase (PPCS) mutations with prominent neuromuscular features: Expanding the phenotypical spectrum of PPCS‐related disorders.

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