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1. Phenotypic Spectrum of Myopathies with Recessive Anoctamin-5 Mutations

2. A new congenital multicore titinopathy associated with fast myosin heavy chain deficiency

3. Generation of two isogenic induced pluripotent stem cell lines from a 10-year-old typical nemaline myopathy patient with a heterozygous dominant c.541G>A (p.Asp179Asn) pathogenic variant in the ACTA1 gene

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

5. X-linked Emery–Dreifuss muscular dystrophy manifesting with adult onset axial weakness, camptocormia, and minimal joint contractures

6. ACTN2 mutations cause 'Multiple structured Core Disease' (MsCD)

7. The first French case of MATR3-related distal myopathy: Clinical, radiological and histopathological characterization

8. Late-onset camptocormia caused by a heterozygous in-frame CAPN3 deletion

9. Generation of two isogenic induced pluripotent stem cell lines from a 4-month-old severe nemaline myopathy patient with a heterozygous dominant c.553C > A (p.Arg183Ser) variant in the ACTA1 gene

10. 251st ENMC international workshop: Polyglucosan storage myopathies 13–15 December 2019, Hoofddorp, the Netherlands

11. NEM6, KBTBD13-Related Congenital Myopathy: Myopathological Analysis in 18 Dutch Patients Reveals Ring Rods Fibers, Cores, Nuclear Clumps, and Granulo-Filamentous Protein Material

12. Clinical correlations and long-term follow-up in 100 patients with sarcoglycanopathies

13. Diagnostic des myopathies congénitales

14. Calpaïnopathies : état des lieux et perspectives thérapeutiques

15. The importance of an integrated genotype-phenotype strategy to unravel the molecular bases of titinopathies

16. New genotype-phenotype correlations in a large European cohort of patients with sarcoglycanopathy patients

17. Glycogenin-1 deficiency mimicking limb-girdle muscular dystrophy

18. Mild clinical presentation in KLHL40-related nemaline myopathy (NEM 8)

19. Pathogenic variants in the myosin chaperone UNC-45B cause progressive myopathy with eccentric cores

20. The clinical, histologic, and genotypic spectrum of SEPN1-related myopathy : A case series

21. KBTBD13 is an actin-binding protein that modulates muscle kinetics

22. GGPS1 Mutations Cause Muscular Dystrophy/Hearing Loss/Ovarian Insufficiency Syndrome

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

24. Biallelic mutations in Tenascin-X cause classical-like Ehlers-Danlos syndrome with slowly progressive muscular weakness

25. Novel ASCC1 mutations causing prenatal-onset muscle weakness with arthrogryposis and congenital bone fractures

26. Inclusion body myositis and human immunodeficiency virus type 1: A new case report and literature review

27. Dysfunctional sarcomere contractility contributes to muscle weakness in ACTA1 -related nemaline myopathy (NEM3)

28. An Integrated Clinical-Biological Approach to Identify Interindividual Variability and Atypical Phenotype-Genotype Correlations in Myopathies: Experience on A Cohort of 156 Families

29. Update on new muscle glycogenosis

30. RecessiveMYPNmutations cause cap myopathy with occasional nemaline rods

31. ORAI1 Mutations with Distinct Channel Gating Defects in Tubular Aggregate Myopathy

32. Tubular aggregate myopathy with features of Stormorken disease due to a new STIM1 mutation

33. Discordant manifestations in Italian brothers with GNE myopathy

34. Novel Phenotypes and Cardiac Involvement Associated With DNA2 Genetic Variants

35. Valosin-containing protein-related myopathy and Meige syndrome: Just a coincidence or not?

36. Deep morphological analysis of muscle biopsies from type III glycogenesis (GSDIII), debranching enzyme deficiency, revealed stereotyped vacuolar myopathy and autophagy impairment

37. Myoglobinopathy is an adult-onset autosomal dominant myopathy with characteristic sarcoplasmic inclusions

38. Sarcomeric disorganization and nemaline bodies in muscle biopsies of patients with EXOSC3-related type 1 pontocerebellar hypoplasia

39. Dusty core disease (DuCD): expanding morphological spectrum of RYR1 recessive myopathies

40. Severe asymmetric muscle weakness revealing glycogenin-1 polyglucosan body myopathy

41. Nemaline myopathies: State of the art

42. Mutation-specific effects on thin filament length in thin filament myopathy

43. CASQ1 mutations impair calsequestrin polymerization and cause tubular aggregate myopathy

44. Some DNM2 mutations cause extremely severe congenital myopathy and phenocopy myotubular myopathy

45. Loss of Sarcomeric Scaffolding as a Common Baseline Histopathologic Lesion in Titin-Related Myopathies

46. Rescue of GSDIII Phenotype with Gene Transfer Requires Liver- and Muscle-Targeted GDE Expression

47. Diseases of the skeletal muscle

48. Clinical heterogeneity and phenotype/genotype findings in 5 families with &ITGYG1&IT deficiency

49. A new titinopathy

50. Common and variable clinical, histological, and imaging findings of recessive RYR1-related centronuclear myopathy patients

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