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3. P156 Muscle biopsy findings in a large cohort of patients affected by valosin containing protein disease: preliminary analysis of the international multicentric VCP study

4. P338 Clinical, morphological, and proteomic features of patients suspected of X-linked myopathy with excessive autophagy (XMEA)

5. O09 Bi-allelic variants of FILIP1 cause congenital myopathy, dysmorphism and neurological defects

6. P203 Proven interoperability of five neuromuscular rare disease registries

7. Molecular characterization of congenital myasthenic syndromes in Spain

9. A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing

11. Treatabolome DB: linking gene and variants with treatments for rare diseases

13. MYO-xIA : Quantification de marqueurs pathologiques sur coupes histologiques et exploitation de rapport de biopsie par intelligence artificielle explicative pour le diagnostic de myopathies congénitales

14. FP.05 From the Muscle Atlas to an AI-based diagnostic tool

15. From the Muscle Atlas to an AI-based diagnostic tool

17. Treatabolome database: current state and new developments towards enhancing rare disease treatment visibility

18. Correction: Solving unsolved rare neurological diseases—a Solve-RD viewpoint (European Journal of Human Genetics, (2021), 29, 9, (1332-1336), 10.1038/s41431-021-00901-1)

21. 525P Management of seizures in patients with primary mitochondrial diseases: consensus statement from the inter-ERNs mitochondrial working group.

23. CHANNELOPATHIES AND RELATED DISORDERS

24. OTHER NMDs

25. REGISTRIES AND CARE OF NMD

26. DMD - BIOMARKERS

27. OTHER NMDs

28. COVID-19 AND NEUROMUSCULAR DISEASES

29. CONGENITAL MYOPATHIES – NEMALINE MYOPATHIES

30. REGISTRIES AND CARE OF NMD

31. Treatabolome database: towards enhancing Rare Diseases’ treatment visibility

32. Specific heterozygous frameshift variants in hnRNPA2B1 cause early-onset oculopharyngeal muscular dystrophy

33. 1st FSHD European Trial Network workshop:Working towards trial readiness across Europe

34. Yield and physicochemical characteristics of west indian cherry genotypes grown in the semi-arid region

35. Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases

38. Treatabolome: a rare diseases treatment awareness project

41. FSHD / OPMD / MYOTONIC DYSTROPHY

43. Morphological, ultrastructural and western blot analysis in adult and child with PLEC1-related myopathy

45. SMCHD1 mutation spectrum for facioscapulohumeral muscular dystrophy type 2 (FSHD2) and Bosma arhinia microphthalmia syndrome (BAMS) reveals disease-specific localisation of variants in the ATPase domain

46. 1st ENMC European meeting: The EURO-NMD pathology working group Recommended Standards for Muscle Pathology Amsterdam, The Netherlands, 7 December 2018

47. CONGENITAL MYOPATHIES: RYR1 AND TITIN

48. P.245Morphological, ultrastructural and western blot analysis in adult and child with PLEC1-related myopathy

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