52 results on '"Bakker E"'
Search Results
2. Detection of osteoarthritis in dogs by metabolic, pro-inflammatory and degenerative synovial fluid biomarkers and traditional radiographic screening: A pilot study
3. Traduction française de la terminologie commune de l’International Urogynecological Association (IUGA) et de l’International Continence Society (ICS) relative à la prise en charge conservatrice et non pharmacologique des troubles pelvi-périnéaux de la femme
4. Assessment of specific muscle tension in dogs through functional electrical stimulation of the gastrocnemius muscle
5. Rééducation pelvi-périnéale et troubles de la statique pelvienne de la femme
6. Évaluation de l’activité électromyographique des muscles du plancher pelvien pendant des exercices posturaux à l’aide du jeu vidéo virtuel Wii Fit Plus©. Analyses et perspectives en rééducation
7. Sickle cell anemia and α-thalassemia: A modulating factor in homozygous HbS/S patients in Oman
8. Molecular diagnostics of the HBB gene in an Omani cohort using bench-top DNA Ion Torrent PGM technology
9. Accuracy and precision of pseudo-continuous arterial spin labeling perfusion during baseline and hypercapnia: A head-to-head comparison with 15O H2O positron emission tomography
10. The use of the HiSPECT bone scan in canine flexor enthesopathy and coronoid pathology
11. Relationship between DHA status at birth and child problem behaviour at 7 years of age
12. Like being hit by a truck; pain metaphors in osteoarthritis patients’ narratives
13. The human genome project and the future of diagnostics, treatment, and prevention
14. “False positive” or true paternity: Investigating one or two STR mismatches by detailed SNP analyses
15. Cardiac involvement in carriers of Duchenne and Becker muscular dystrophy
16. Signs and symptoms of Duchenne muscular dystrophy and Becker muscular dystrophy among carriers in the Netherlands: a cohort study
17. Calpainopathy—A Survey of Mutations and Polymorphisms
18. PV-0201 Development and validation of prediction models for salivary dysfunction in HN cancer patients
19. Small-airways deposition of dornase alfa in children with asthma and persistent airway obstruction
20. Recommandations de bonnes pratiques pour l’incontinence urinaire. Analyse critique du guidelines EAU pour les physiothérapeutes francophones
21. 161P - DKK1 stabilization as a new malignant pleural mesothelioma therapeutic avenue
22. Becker muscular dystrophy patients with deletions around exon 51; a promising outlook for exon skipping therapy in Duchenne patients
23. Efficacy of platelet-rich plasma injections in osteoarthritis of the knee: an updated systematic review and meta-analysis
24. PSY13 - The Burden of Obesity in Mexico: Prevalence, Comorbidities, and Associations With Quality of Life, Resource Utilization and Productivity
25. PSY12 - Weight Loss Treatment Patterns in Mexico
26. A 6 Mb deletion in band 2q22 due to a complex chromosome rearrangement associated with severe psychomotor retardation, microcephaly and distinctive dysmorphic facial features
27. Rapid and accurate diagnosis of facioscapulohumeral muscular dystrophy
28. Somatic mosaicism of a point mutation in the dystrophin gene in a patient presenting with an asymmetrical muscle weakness and contractures
29. P4.10 Duchenne/Becker in the family: are women aware of the potential risks?
30. G.P.13.06 Clinical phenotype of Becker muscular dystrophy patients with deletions of exons 45–51 and 50–51
31. FP59-FR-05 Genetic factors in myasthenia gravis and Lambert-Eaton myasthenic syndrome
32. G.P.14.02 MLPA analysis of the CAPN3 gene detects large deletions in LGMD2A patients
33. G.P.12.01 Epidemiology of the dystrophinopathies in the Netherlands
34. G.P.9.01 Impact of prenatal diagnosis on the incidence of DMD in the Netherlands
35. Clinical diagnosis of heterozygous dystrophin gene deletions by fluorescence in situ hybridization
36. Application of in vitro myo-differentiation of non-muscle cells to enhance gene expression and facilitate analysis of muscle proteins
37. Optodes in clinical chemistry: potential and limitations
38. A deletion hot spot in the Duchenne muscular dystrophy gene
39. 242 Breakpoints in the 200-kb deletion-prone P20 region of the DMD gene are widely spread
40. Long-range genomic map of the Duchenne muscular dystrophy (DMD) gene: Isolation and use of J66 (DXS268), a distal intragenic marker
41. New polymorphic DNA marker close to the fragile site FRAXA
42. The DNA fingerprint
43. PRENATAL DIAGNOSIS AND CARRIER DETECTION OF DUCHENNE MUSCULAR DYSTROPHY WITH CLOSELY LINKED RFLPs
44. Infectivity of blood seropositive for hepatitis C virus antibodies
45. A physical map of 4 million bp around the Duchenne muscular dystrophy gene on the human X-chromosome
46. K+-transport Protein TrkA of Escherichia coli Is a Peripheral Membrane Protein That Requires other trk Gene Products for Attachment to the Cytoplasmic Membrane
47. Progressive dementia, without cerebral hemorrhage, in a patient with hereditary cerebral amyloid angiopathy
48. Borderline repeat expansion in Huntington's disease
49. Different positively charged amino acids have similar effects on the topology of a polytopic transmembrane protein in Escherichia coli.
50. Diagnostics and carrier testing in DMD/BMD
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