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3. Phenotype-driven genomics enhance diagnosis in children with unresolved neuromuscular diseases

5. Mutations of GEMIN5 are associated with coenzyme Q10 deficiency: long-term follow-up after treatment

6. Correction: Phenotype-driven genomics enhance diagnosis in children with unresolved neuromuscular diseases

8. Advancing the Understanding of Vesicle-Associated Membrane Protein 1-Related Congenital Myasthenic Syndrome: Phenotypic Insights, Favorable Response to 3,4-Diaminopyridine, and Clinical Characterization of Five New Cases

10. Prophylaxis

11. Geospatial and Spatio-Temporal Models

12. Management of COVID-19 Data for the FASSSTER Platform

13. Variants in DTNA cause a mild, dominantly inherited muscular dystrophy

15. Clinical, genetic, epidemiologic, evolutionary, and functional delineation of TSPEAR-related autosomal recessive ectodermal dysplasia 14

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

18. Systematic Collaborative Reanalysis of Genomic Data Improves Diagnostic Yield in Neurologic Rare Diseases

20. Inferring disease course from differential exon usage in the wide titinopathy spectrum.

21. Éléments de données communs pour l'arthrogrypose multiple congénitale: Un cadre international.

22. Elementos de datos comunes para la artrogriposis múltiple congénita: Un marco internacional.

23. Common data elements for arthrogryposis multiplex congenita: An international framework.

26. Congenital LMNA-Related Muscular Dystrophy in Paediatrics: Cardiac Management in Monozygotic Twins

27. Effects of HMGCR deficiency on skeletal muscle development

28. Improving Diagnostic Precision: Phenotype-Driven Analysis Uncovers a Maternal Mosaicism in an Individual with RYR1-Congenital Myopathy

30. Safety and efficacy of avalglucosidase alfa versus alglucosidase alfa in patients with late-onset Pompe disease (COMET): a phase 3, randomised, multicentre trial

31. A Novel Missense Variant in the NKX2-1 Homeodomain Prevents Transcriptional Rescue by TAZ.

32. The recurrent deep intronic pseudoexon-inducing variant COL6A1 c.930+189C>T results in a consistently severe phenotype of COL6-related dystrophy: Towards clinical trial readiness for splice-modulating therapy

36. Assessing the optimality of a three-part pricing policy for an asset-sharing platform in the Philippines.

40. Epilepsy in Duchenne and Becker muscular dystrophies.

41. The emerging spectrum of neurodevelopmental comorbidities in early-onset Spinal Muscular Atrophy

42. Full-Length SMN Transcript in Extracellular Vesicles as Biomarker in Individuals with Spinal Muscular Atrophy Type 2 Treated with Nusinersen

44. Expanding the phenotypic spectrum ofTRAPPC11-related muscular dystrophy: 25 Roma individuals carrying a founder variant

45. The emerging spectrum of foetal acetylcholine receptor antibody-associated disorders (FARAD)

47. Clinical, genetic, epidemiologic, evolutionary, and functional delineation of TSPEAR-related autosomal recessive ectodermal dysplasia 14

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

49. Twist exome capture allows for lower average sequence coverage in clinical exome sequencing

50. Innovative computerized dystrophin quantification method based on spectral confocal microscopy

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