174 results on '"Solé G"'
Search Results
2. Anti-SARS-CoV-2 (COVID-19) vaccination efficacy in patients with severe neuromuscular diseases
3. Current clinical management of CIDP with immunoglobulins in France: An expert opinion
4. Dropped head syndrome in severe hypotension
5. Reducing the Risk of Falls by 78% with a New Generation of Slip Resistant Winter Footwear
6. Guidance for the care of neuromuscular patients during the COVID-19 pandemic outbreak from the French Rare Health Care for Neuromuscular Diseases Network
7. Analyse rétrospective des patients porteurs d’anticorps anti-TIF1gamma, anti-NXP2 et anti-SAE1/2 au CHU de Bordeaux de novembre 2014 à février 2017
8. Maladie de Charcot-Marie-Tooth associée au gène de la périaxine (CMT4F) : description clinique, électrophysiologique et génétique de 24 patients
9. Miopatie dei cingoli
10. Diagnostic des dystrophies musculaires progressives des ceintures de type 2A ou calpaïnopathies : étude des patients du centre de référence des maladies neuromusculaires de Bordeaux (France)
11. Rechallenge de l’immunothérapie après toxicités sévères : expérience d’une RCP immunoTox
12. The ‘Glass shoulder’: individuals’ perspectives of living with at traumatic glenohumeral dislocation – a qualitative study
13. La mujer en la Edad Media: una aproximación historiográfica
14. Long-term benefit of enzyme replacement therapy with alglucosidase alfa in adults with Pompe disease: prospective analysis from the French Pompe Registry
15. DMD – BIOMARKERS & OUTCOME MEASURES
16. An extraordinary ‘sunburn’ in a black patient
17. P.335Phenotypic and genomic characterization as predictors of DMD 45 to 55 multi-exon skipping therapy
18. Bilateral periventricular nodular heterotopia in France: frequency of mutations in FLNA, phenotypic heterogeneity and spectrum of mutations
19. Current French Pompe Prevalence Study (French PoPS)
20. CHANNELOPATHIES AND RELATED DISORDERS: EP.221 Diagnostic delay and atypical phenotypes in a French cohort of Andersen-Tawil syndrome
21. Instantaneous mapping of ionospheric characteristics using 5-minute measurements for the day of the total solar eclipse of 11 August 1999
22. COST 251 recommended instantaneous mapping model of ionospheric characteristics — PLES
23. Novel mutations in DNAJB6 cause LGMD1D and distal myopathy in French families
24. Prevalence of low levels of fecal elastase in decompensated cirrhotic patients
25. Onchocerca volvulus DNA Probe Classification Correlates with Epidemiologic Patterns of Blindness
26. Maggots Dyed With Chrysoidine: A Possible Risk To Anglers
27. Hypnotherapy For Incontinence Caused By The Unstable Detrusor
28. Long-term exposure to Myozyme results in a decrease of anti-drug antibodies in late-onset Pompe disease patients
29. Overcoming fear of re-injury after anterior cruciate ligament reconstruction: a qualitative study
30. Joint loading asymmetry is associated with the asymmetry in muscle strength in people with anterior cruciate ligament reconstruction
31. Muscle involvement in limb-girdle muscular dystrophy with GMPPB deficiency (LGMD2T)
32. Effect of enzyme replacement therapy with alglucosidase alfa (Myozyme®) in 12 patients with advanced late-onset Pompe disease
33. Population trends and survival of nesting green sea turtles Chelonia mydas on Aves Island, Venezuela
34. Charcot–Marie–Tooth type 4B1 (MTMR2 gene): Confounding clinical presentation and report of 5 original mutations
35. Association non fortuite d’une neutropénie chronique et d’une maladie de Charcot-Marie-Tooth en rapport avec une mutation de la dynamine 2
36. P.329 - Efficiency of next generation sequencing of a large panel of genes for diagnosis of children with myopathies and muscular dystrophies, especially for early and/or typical cases
37. P.245 - Efficiency of targeted NGS on myopathies and muscular dystrophy genes: Importance of an optimized strategy of capture, sequencing, bioinformatic analyses and multidisciplinary approach for variants detection and interpretation
38. P.170 - OPALE: A patient registry for laminopathies and emerinopathies in France
39. P.67 - Effect of enzyme replacement therapy with alglucosidase alfa (Myozyme®) in 12 patients with advanced late-onset Pompe disease
40. 10 - Glassflake coatings for corrosion protection
41. G.P.332 - Charcot–Marie–Tooth type 4B1 (MTMR2 gene): Confounding clinical presentation and report of 5 original mutations
42. La Conferencia de Pekín
43. Association non fortuite d’une neutropénie chronique et d’une maladie de Charcot-Marie-Tooth en rapport avec une mutation de la dynamine 2
44. P270 Une neuropathie périphérique sévère grabatérisante après une sleeve gastrectomie
45. Résultats d’une étude évaluant la tolérance de Tégéline® administrée à domicile chez des patients atteints de maladie auto-immune
46. Myopathies des ceintures
47. Discovery and preclinical evaluation of anti-miR-17 oligonucleotide RGLS4326 for the treatment of polycystic kidney disease
48. Comprehensive RNA-Sequencing Analysis in Serum and Muscle Reveals Novel Small RNA Signatures with Biomarker Potential for DMD
49. M - 17 Dystrophie musculaire par mutation du gène VCP avec anomalies osseuses atypiques
50. Dynamics of cellular states of fibro-adipogenic progenitors during myogenesis and muscular dystrophy
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