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155 results on '"Assistance publique - Hôpitaux de Paris (AP-HP) (APHP)-CHU Trousseau [APHP]"'

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1. Control of TLR7-mediated type I IFN signaling in pDCs through CXCR4 engagement—A new target for lupus treatment

2. Chromosomal rearrangements in the 11p15 imprinted region: 17 new 11p15.5 duplications with associated phenotypes and putative functional consequences

3. Does neonatal pain management in intensive care units differ between night and day? An observational study

4. Optimized gene transfer into human primary leukemic T cell with NOD-SCID/leukemia-initiating cell activity

5. Use of ruxolitinib in COPA syndrome manifesting as life-threatening alveolar haemorrhage

6. Development and Validation of a New Risk Prediction Score for Life-Threatening Ventricular Tachyarrhythmias in Laminopathies

7. Pediatric Evans syndrome is associated with a high frequency of potentially damaging variants in immune genes

8. Successful in utero stem cell transplantation in X-linked severe combined immunodeficiency

9. Correlation between work impairment, scores of rhinitis severity and asthma using the MASK-air ® App

10. Intensity of perinatal care for extremely preterm babies and outcomes at a higher gestational age: evidence from the EPIPAGE-2 cohort study

11. Two-hybrid screening of FAM13A protein partners in lung epithelial cells

12. Human C-terminal CUBN variants associate with chronic proteinuria and normal renal function

13. A cadaveric validation of a method based on impact analysis to monitor the femoral stem insertion

14. Maternal diet before and during pregnancy and risk of asthma and allergic rhinitis in children

15. Impact of mutations within the [Fe-S] cluster or the lipoic acid biosynthesis pathways on mitochondrial protein expression profiles in fibroblasts from patients

16. Risk of autoimmune diseases and human papilloma virus (HPV) vaccines: Six years of case-referent surveillance

17. Postoperative Complications after Ileocecal Resection in Crohn’s Disease: A Prospective Study From the REMIND Group

18. Anti-Factor B and Anti-C3b Autoantibodies in C3 Glomerulopathy and Ig-Associated Membranoproliferative GN

19. Real-Life Safety and Effectiveness of Lumacaftor-Ivacaftor in Patients with Cystic Fibrosis

20. Long-term clinical outcome and HAVCR2 mutations in 70 patients with subcutaneous panniculitis-like T-cell lymphoma: a study from the French Cutaneous Lymphoma Group

21. Follow-Up and Management of Chronic Rhinosinusitis in Adults with Primary Ciliary Dyskinesia: Review and Experience of Our Reference Centers

22. EFL1 mutations impair eIF6 release to cause Shwachman-Diamond syndrome

23. A Novel Intelligent Scan Assistant System for Early Pregnancy Diagnosis by Ultrasound: Clinical Decision Support System Evaluation Study

24. Author Correction: A framework to identify contributing genes in patients with Phelan-McDermid syndrome

25. Detection of complicated ectopic pregnancies in the hospital discharge database: A validation study

26. Head to pelvis alignment of adolescent idiopathic scoliosis patients both in and out of brace

27. Exome sequencing in congenital ataxia identifies two new candidate genes and highlights a pathophysiological link between some congenital ataxias and early infantile epileptic encephalopathies

28. A large multicenter study of pediatric myotonic dystrophy type 1 for evidence-based management

29. Regulator of telomere length 1 ( RTEL1 ) mutations are associated with heterogeneous pulmonary and extra-pulmonary phenotypes

30. Revealing the potential of capillary electrophoresis/mass spectrometry: the tipping point

31. Prenatal parental involvement in decision for delivery room management at 22-26 weeks of gestation in France - The EPIPAGE-2 Cohort Study

32. Ontogenic changes in hematopoietic hierarchy determine pediatric specificity and disease phenotype in fusion oncogene-driven myeloid leukemia

33. Planned delivery route of preterm breech singletons and neonatal and 2-year outcomes: a population-based cohort study

34. Associations of black carbon with lung function and airway inflammation in schoolchildren

35. Diversity and evolution of the emerging $Pandoraviridae$ family

36. Unexpected macrophage-independent dyserythropoiesis in Gaucher disease

37. Systematic MRI in NF1 children under six years of age for the diagnosis of optic pathway gliomas. Study and outcome of a French cohort

38. H4K44 Acetylation Facilitates Chromatin Accessibility during Meiosis

39. Metabolic risk factors in young adults infected with HIV since childhood compared with the general population

40. MASK 2017: ARIA digitally-enabled, integrated, person-centred care for rhinitis and asthma multimorbidity using real-world-evidence

41. Chronic interstitial lung diseases in children: diagnosis approaches

42. Prenatal therapy with pyrimethamine + sulfadiazine vs spiramycin to reduce placental transmission of toxoplasmosis: a multicenter, randomized trial

43. Association of Intraventricular Hemorrhage and Death With Tocolytic Exposure in Preterm Infants

44. Functional assessment of newly identified SFTPA1 and SFTPA2 mutations in patients with idiopathic interstitial pneumonia (IIP) and lung cancer28th International Congress of the European-Respiratory-Society (ERS)

45. Chromosome 14q32.2 Imprinted Region Disruption as an Alternative Molecular Diagnosis of Silver-Russell Syndrome

46. Mutations involving the SRY-related gene SOX8 are associated with a spectrum of human reproductive anomalies

47. Clinical and genetic heterogeneity in familial steroid-sensitive nephrotic syndrome

48. Novel Intergenically Spliced Chimera, NFATC3-PLA2G15 , Is Associated with Aggressive T-ALL Biology and Outcome

49. Transfer of innovation on allergic rhinitis and asthma multimorbidity in the elderly (MACVIA-ARIA) - EIP on AHA Twinning Reference Site (GARD research demonstration project)

50. Intensity of perinatal care, extreme prematurity and sensorimotor outcome at 2 years corrected age: evidence from the EPIPAGE-2 cohort study

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