Search

Your search keyword '"Norma B Romero"' showing total 413 results

Search Constraints

Start Over You searched for: Author "Norma B Romero" Remove constraint Author: "Norma B Romero"
413 results on '"Norma B Romero"'

Search Results

1. Caveolae and Bin1 form ring-shaped platforms for T-tubule initiation

2. QIL1 mutation causes MICOS disassembly and early onset fatal mitochondrial encephalopathy with liver disease

3. Generation of iPSC lines from three Laing distal myopathy patients with a recurrent MYH7 p.Lys1617del variant

4. An integrated diagnosis strategy for congenital myopathies.

5. Generation of two iPSC lines from patients with inherited central core disease and concurrent malignant hyperthermia caused by dominant missense variants in the RYR1 gene

6. Generation of two iPSC lines from adult central core disease patients with dominant missense variants in the RYR1 gene

7. Generation of two induced pluripotent stem cell lines from a 33-year-old central core disease patient with a heterozygous dominant c.14145_14156delCTACTGGGACA (p.Asn4715_Asp4718del) deletion in the RYR1 gene

8. A recurrent RYR1 mutation associated with early-onset hypotonia and benign disease course

9. In vivo RyR1 reduction in muscle triggers a core-like myopathy

10. rAAV-related therapy fully rescues myonuclear and myofilament function in X-linked myotubular myopathy

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

12. 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

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

14. 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

16. Cuando el continente LatinoAmericano empezó a involucrarse más activamente en el tema neuromuscular …

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

18. Human light meromyosin mutations linked to skeletal myopathies disrupt the coiled coil structure and myosin head sequestration

19. Diagnostic work-up and phenotypic characteristics of a family with variable severity of distal arthrogryposis type 2B (Sheldon-Hall syndrome) and TNNT3 pathogenic variant

20. LAMA2-Related Muscular Dystrophy: The Importance of Accurate Phenotyping and Brain Imaging in the Diagnosis of LGMD

21. Muscle MRI as a Diagnostic Challenge in Emery-Dreifuss Muscular Dystrophy

22. L’Atlas du Muscle : une banque d’images de biopsies musculaires

23. Severe ACTA1-related nemaline myopathy: intranuclear rods, cytoplasmic bodies, and enlarged perinuclear space as characteristic pathological features on muscle biopsies

24. Clinical phenotype and loss of the slow skeletal muscle troponin T in three new patients with recessive TNNT1 nemaline myopathy

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

26. Heterozygous frameshift variants in HNRNPA2B1 cause early-onset oculopharyngeal muscular dystrophy

27. Generation of two isogenic induced pluripotent stem cell lines from a 1-month-old nemaline myopathy patient harbouring a homozygous recessive c.121C T (p.Arg39Ter) variant in the ACTA1 gene

28. Congenital Nemaline Myopathy with Dense Protein Masses

29. [JAG2-related muscular dystrophy: When differential diagnosis matters]

30. [AcadeMYO, a successful bet]

31. A recurrent RYR1 mutation associated with early-onset hypotonia and benign disease course

32. 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

33. ASC‐1 Is a Cell Cycle Regulator Associated with Severe and Mild Forms of Myopathy

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

35. Epidemiology and natural history of cutaneous squamous cell carcinoma in recessive dystrophic epidermolysis bullosa patients: 20 years’ experience of a reference centre in Spain

36. Generation of an induced pluripotent stem cell line from a 3-month-old nemaline myopathy patient with a heterozygous dominant c.515C > A (p.Ala172Glu) variant in the ACTA1 gene

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

38. 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

39. Missense mutations in small muscle protein X-linked (SMPX) cause distal myopathy with protein inclusions

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

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

42. rAAV-related therapy fully rescues myonuclear and myofilament function in X-linked myotubular myopathy

43. In vivo RyR1 reduction in muscle triggers a core-like myopathy

44. Physiological impact and disease reversion for the severe form of centronuclear myopathy linked to dynamin

45. Lamin-related congenital muscular dystrophy alters mechanical signaling and skeletal muscle growth

46. SH3KBP1 scaffolds endoplasmic reticulum and controls skeletal myofibers architecture and integrity

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

48. Clathrin plaques and associated actin anchor intermediate filaments in skeletal muscle

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

50. Asymmetric muscle weakness due to

Catalog

Books, media, physical & digital resources