250 results on '"Lemonnier L"'
Search Results
2. 9. Piroplasmose équine : portage asymptomatique et diversité génétique des deux parasites responsables
3. Uncovering cystic fibrosis patient profiles and exposome associations through unsupervised multidimensional phenotyping
4. Detection of fungi in the airways of horses according to the sample site: a methodological study
5. WS10.01 The French Compassionate Programme of elexacaftor/tezacaftor/ivacaftor in people with cystic fibrosis with advanced lung disease and no F508del CFTR variant
6. High-flow cannula for frail patients with SARS-CoV-2 infection non-eligible for intensive care unit management
7. Comparison of analog and digitally evaluated volume of the female breast in reconstructive breast surgery. Validation of a noninvasive measurement method with 3D camera1
8. The multi-faceted nature of 15 CFTR exonic variations: Impact on their functional classification and perspectives for therapy
9. Phospholipase C-Coupled Receptors and Activation of TRPC Channels
10. Incidence et prévalence des cancers chez les patients atteints de mucoviscidose : données issues du chainage entre le Système national des données de santé (SNDS) et le registre français de la mucoviscidose
11. Comparison of analog and digitally evaluated volume of the female breast in reconstructive breast surgery. Validation of a noninvasive measurement method with 3D camera1.
12. Comparison of analog and digitally evaluated volume of the female breast in reconstructive breast surgery. Validation of a noninvasive measurement method with 3D camera1.
13. 36: International comparison of survival in cystic fibrosis between Canada, France, and Australia
14. PSA reduces prostate cancer cell motility by stimulating TRPM8 activity and plasma membrane expression
15. Digital Breast Surgery: Validierung einer nicht-invasiven Volumetrie der Brust mit 3D-Kamera.
16. Facteurs de risque de l’aspergillose bronchopulmonaire allergique chez des patients atteints de mucoviscidose : analyse du registre français
17. P126 Health care resource use (HCRU) and associated costs preceding lung transplantation (LT) in Cystic Fibrosis patients
18. WS03.04 Survival of people with cystic fibrosis: complete overview in France and first evaluation of the impact of modulators
19. WS08.2 Cancer incidence and prevalence among patients with cystic fibrosis: data from the National French Cystic Fibrosis Registry
20. Appariement probabiliste des données du Registre français de la mucoviscidose aux données du Système national des données de santé
21. ePS2.04 Gastrointestinal surgery in adult patients with cystic fibrosis: observational French prospective study over 11 years
22. WS23.6 Impact of the French high emergency program in cystic fibrosis: survival comparison between France and Canada
23. WS21.3 Overview of shared benefits from the 6-year long collaboration between the French Cystic Fibrosis Registry and the CFTR-France genetics database
24. P058 Follow-up before and after lung transplantation for cystic fibrosis: state of the French practices between 2011 and 2017 based on the French Registry
25. Appariement probabiliste des données du Registre français de la mucoviscidose aux données du Système national des données de santé
26. Phospholipase C-Coupled Receptors and Activation of TRPC Channels
27. 2-APB inhibits volume-regulated anion channels independently from intracellular calcium signaling modulation
28. Store-operated Ca 2+ channels in prostate cancer epithelial cells: function, regulation, and role in carcinogenesis
29. A new human gene KCNRG encoding potassium channel regulating protein is a cancer suppressor gene candidate located in 13q14.3
30. P064 Comparison of the characteristics of patients enrolled in the 2016 French Cystic Fibrosis Registry according to the value of their sweat test
31. P017 Update of CFTR-France: toward a more relevant dataset for predicting the impact of rare CFTR variants
32. Direct modulation of volume-regulated anion channels by Ca 2+ chelating agents
33. Pregnancy outcome in women with cystic fibrosis and poor pulmonary function
34. EPS5.02 Estimation of survival of cystic fibrosis patients in France by two different methods
35. WS17.1 The multi-faceted nature of CFTR exonic mutations: impact on their functional classification
36. WS05.5 Pregnancy outcome in women with cystic fibrosis and poor pulmonary function
37. EPS7.5 Long-term effects of azithromycin in cystic fibrosis
38. 413 Outcome in children diagnosed with cystic fibrosis via newborn screening 2003–2014
39. WS14.2 PYOnever study: characteristics of cystic fibrosis adults never colonized by Pseudomonas aeruginosa
40. WS11.3 Cystic fibrosis survival and socioeconomic status across Europe
41. Volume-regulated chloride conductance in the LNCaP human prostate cancer cell line
42. Étude PYOnever : caractéristiques des adultes atteints de mucoviscidose indemnes de colonisation pulmonaire par Pseudomonas aeruginosa
43. Impact du diabète pendant et après la grossesse : données issues du Registre français de la mucoviscidose
44. ePS05.1 CF deaths in France often occurred in the intensive care unit: always justified?
45. 26 Retrospective observational study of French patients with cystic fibrosis and a G551D mutation after 1 and 2 years of treatment with ivacaftor
46. WS11.1 The French CF newborn screening: optimization of the programme by a centralized tracking process
47. 4 Valuable collaboration between a molecular CFTR database and a national CF registry: the French experience
48. TRP channel-associated factors are a novel protein family that regulates TRPM8 trafficking and activity.
49. WS09.8 End-of-life care in CF patients: France, 2007–2010
50. 302 MucoDoméos: An electronic medical record (SMR) dedicated to the CF patients
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