867 results on '"Boileau C"'
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2. Involvement of U2-spliceosome in autosomal dominant hypercholesterolemia
3. Sexual and marital trajectories and HIV infection among ever-married women in rural Malawi
4. Retour au travail après un accident coronarien aigu
5. Family history of aortic dissection in patients with a FBN1 pathogenic variant
6. Les pneumopathies interstitielles diffuses de la polyarthrite rhumatoïde sont associées à une taille plus courte des télomères et un excès de variants rares au sein de gènes impliqués dans les téloméropathies
7. High prevalence of ventricular repolarization abnormalities in people carrying TGFβR2 mutations
8. La connaissance des facteurs de risque cardiovasculaire est-elle meilleure après la survenue d’un évènement ischémique majeur ? Enquête auprès de 135 cas et 260 témoins
9. From fatty streaks to culprit lesions, the impact of PCSK9 on human atherosclerotic lesions through smooth muscle cells functions
10. Whole exome/genome sequencing joint analysis in a family with oligogenic familial hypercholesterolemia
11. Growth rings show limited evidence for ungulates’ potential to suppress shrubs across the Arctic
12. POS0062 A RISK SCORE TO DETECT SUBCLINICAL RHEUMATOID ARTHRITIS-ASSOCIATED INTERSTITIAL LUNG DISEASE
13. Un score prédictif de la survenue de pneumopathie interstitielle diffuse préclinique au cours de la polyarthrite rhumatoïde
14. First heterozygous NOP10 mutation in familial pulmonary fibrosis
15. Family history of aortic dissection is not a risk factor in Marfan syndrome with a FBN1 gene mutation
16. Genotype-phenotype correlations in Marfan syndrome patients with FBN1 mutations: a cohort study on 1575 patients
17. Plasma PCSK9 levels increase following percutaneous coronary interventions
18. Looking for somatic mutations in fibrosing interstitial lung diseases
19. The revised ghent nosology; reclassifying isolated ectopia lentis
20. The BMP antagonists follistatin and gremlin in normal and early osteoarthritic cartilage: an immunohistochemical study
21. O.20A - Fond génétique partagé entre la pneumopathie interstitielle diffuse associée à la polyarthrite rhumatoïde et la fibrose pulmonaire idiopathique
22. PCSK9 in the development of human atherosclerosis
23. Molecular spectrum of PCSK9-based FH in FRANCE, The French P.(SER127ARG) founder variant
24. Histone deacetylase inhibitors suppress interleukin-1β-induced nitric oxide and prostaglandin E 2 production in human chondrocytes
25. Identification of opticin, a member of the small leucine-rich repeat proteoglycan family, in human articular tissues: a novel target for MMP-13 in osteoarthritis
26. A novel splice site mutation of the LDL receptor gene in a Tunisian hypercholesterolemic family
27. POS0095 DEVELOPPING A SCORE TO PREDICT PRECLINICAL INTERSTITIAL LUNG DISEASE IN PATIENTS WITH RHEUMATOID ARTHRITIS – A CROSS-SECTIONAL STUDY FROM THE ESPOIR COHORT
28. AB0205 A NOVEL METHOD FOR PREDICTING 1-YEAR RETENTION OF ABATACEPT USING MACHINE LEARNING TECHNIQUES: DIRECTIONALITY AND IMPORTANCE OF PREDICTORS
29. Clinical relevance of genotype–phenotype correlations beyond vascular events in a cohort study of 1500 Marfan syndrome patients with FBN1 pathogenic variants
30. Systematic molecular and cytogenetic screening of 100 patients with marfanoid syndromes and intellectual disability
31. Plasma proprotein-convertase-subtilisin/kexin type 9 (PCSK9) and cardiovascular events in type 2 diabetes
32. Effect of mutation type and location on clinical outcome in 1,013 probands with marfan syndrome or related phenotypes and FBN1 mutations: an international study
33. Identification de nouveaux marqueurs biologiques de la sarcopénie par l’analyse protéomique de sérum
34. The U2-spliceosome and its interactors regulate the levels and activity of the LDL receptor in humans
35. Prévalence de la pneumopathie interstitielle diffuse associée à la polyathrite rhumatoïde dans la cohorte Espoir et intérêt du génotypage de rs35705950
36. What do French patients and geneticists think about prenatal and preimplantation diagnoses in Marfan syndrome?
37. Mutational heterogeneity in low-density lipoprotein receptor gene related to familial hypercholesterolemia in Morocco
38. The new Ghent criteria for Marfan syndrome: what do they change?
39. S.12.1 Is H1N1 influenza vaccine safe and effective in patients with SSc?
40. Bone Mineral Density in Sixty Adult Patients with Marfan Syndrome
41. Evidence of the Contribution of the X Chromosome to Systemic Sclerosis Susceptibility: Association With the Functional Irak1 196Phe/532Ser Haplotype
42. Association of the CD226 Ser307variant with systemic sclerosis: Evidence of a contribution of costimulation pathways in systemic sclerosis pathogenesis
43. NLRP1 influences the systemic sclerosis phenotype: a new clue for the contribution of innate immunity in systemic sclerosis-related fibrosing alveolitis pathogenesis
44. Electrocardiographic and echocardiographic abnormalities associated with mitral valve prolapse in patients with Marfan syndrome
45. OP0036 METHOTREXATE AND RHEUMATOID ARTHRITIS ASSOCIATED INTERSTITIAL LUNG DISEASE
46. A Case of Follicular Lymphoma Presenting as Severe Interstitial Pneumonia
47. Clinical, electrical and morphological cardiac disorders in Marfan patients with FBN1 mutations
48. Association of the TNFAIP3 rs5029939 variant with systemic sclerosis in the European Caucasian population
49. Association of a KCNA5 gene polymorphism with systemic sclerosis–associated pulmonary arterial hypertension in the European Caucasian population
50. BANK1 is a genetic risk factor for diffuse cutaneous systemic sclerosis and has additive effects with IRF5 and STAT4
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