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

4. P192 The open-access treatabolome platform enhances the visibility of treatable and actionable genes in RD-connect's GPAP and other clinical diagnosis support tools

7. VP429 Impaired skeletal muscle strength in adult patients with laminopathies

8. P158 Heterozygous SPTAN1 frameshift mutations cause distal myopathy with neurogenic features

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

13. Cardiac arrhythmia and late-onset muscle weakness caused by a myofibrillar myopathy with unusual histopathological features due to a novel missense mutation in FLNC

14. Myofibrillar myopathies: State of the art, present and future challenges

15. VP.70 OPALE: a patient registry for laminopathies and emerinopathies in France

18. Objective evaluation of clinical actionability for genes involved in myopathies: 63 genes with a medical value for patient care

20. 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. DISTAL MYOPATHIES

22. NEW GENES AND DISEASES

29. Nuclear lamins: laminopathies and their role in premature ageing

30. OMICs AND AI APPROACHES FOR MUSCLE DISEASES

32. The NOx-HNO3 system in the lower stratosphere: Insights from in situ measurements and implications of J(sub HNO3)-[OH] relationship

34. 5164New risk prediction score for life-threatening ventricular tachyarrhythmias in laminopathies

35. P.256Steroid treatment may change natural history in young children with LMNA mutations and dropped head syndrome

36. P.252LGMD, exercise intolerance, ptosis, ophthalmoplegia and dermatologic features: the phenotypic pleiotropy of plectinopathies in 8 French families

37. P.143Correlation between dystrophin espression and clinical phenotype using high-throughput digital immunoanalysis in Duchenne and Becker muscular dystrophy patients

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

41. Evaluation of missense and splicing in silico predictions tools and implementation of an efficient SNV prioritization NGS pipeline for molecular diagnosis of Myopathies and Muscular Dystrophies

48. Inorganic Chlorine Partitioning in the Summer Lower Stratosphere: Modeled and Measured [ClONO2/HCl] During POLARIS

49. The NO(x)-HNO3 System in the Lower Stratosphere: Insights from In Situ Measurements and Implications of the J(HNO3)-[OH] Relationship

50. An Examination of the Inorganic Chlorine Budget in the Lower Stratosphere

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