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2. Imaging mass cytometry analysis of Becker muscular dystrophy muscle samples reveals different stages of muscle degeneration

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

4. Analysis of muscle magnetic resonance imaging of a large cohort of patient with VCP-mediated disease reveals characteristic features useful for diagnosis

5. Disease-associated comorbidities, medication records and anthropometric measures in adults with Duchenne muscular dystrophy

7. Correction to: Analysis of muscle magnetic resonance imaging of a large cohort of patient with VCP‑mediated disease reveals characteristic features useful for diagnosis

8. Genotype-phenotype correlations in valosin-containing protein disease: a retrospective muticentre study.

13. Decoding the transcriptome of Duchenne muscular dystrophy to the single nuclei level reveals clinical-genetic correlations

14. Muscle magnetic resonance imaging of a large cohort of distal hereditary motor neuropathies reveals characteristic features useful for diagnosis

17. Diagnostic interest of whole-body MRI in early- and late-onset LAMA2 muscular dystrophies: a large international cohort

20. Expanding the clinical-pathological and genetic spectrum of RYR1-related congenital myopathies with cores and minicores: an Italian population study

21. NEB mutations disrupt the super-relaxed state of myosin and remodel the muscle metabolic proteome in nemaline myopathy

23. Muscle diffusion tensor imaging in facioscapulohumeral muscular dystrophy.

25. Familial childhood onset, slowly progressive myopathy plus cardiomyopathy expands the phenotype related to variants in the TTN gene

26. 272nd ENMC international workshop: 10 Years of progress - revision of the ENMC 2013 diagnostic criteria for inclusion body myositis and clinical trial readiness. 16–18 June 2023, Hoofddorp, The Netherlands

27. Functional abilities, respiratory and cardiac function in a large cohort of adults with Duchenne muscular dystrophy treated with glucocorticoids

28. Models of practice and training in psychotherapy: cross-national perspectives from Italy and Canada

31. Hospital admissions from the emergency department of adult patients affected by myopathies

32. Familial childhood onset, slowly progressive myopathy plus cardiomyopathy expands the phenotype related to variants in the TTN gene

33. Single cell RNA sequencing of human FAPs reveals different functional stages in Duchenne muscular dystrophy.

34. RareACTN2Frameshift Variants Resulting in Protein Extension Cause Distal Myopathy and Hypertrophic Cardiomyopathy through Protein Aggregation

35. Hospital admissions from the emergency department of adult patients affected by myopathies

36. Genotype–phenotype correlations in recessive titinopathies

37. Mediators and moderators of change in mindfulness-based stress reduction for painful diabetic peripheral neuropathy

38. MRI patterns of muscle involvement in type 2 and 3 spinal muscular atrophy patients

39. European muscle MRI study in limb girdle muscular dystrophy type R1/2A (LGMDR1/LGMD2A)

47. Introduction.

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