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Your search keyword '"Assistance publique - Hôpitaux de Paris (AP-HP) (APHP)-CHU Necker - Enfants Malades [AP-HP]"' showing total 387 results

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387 results on '"Assistance publique - Hôpitaux de Paris (AP-HP) (APHP)-CHU Necker - Enfants Malades [AP-HP]"'

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1. False-negative Results of Human Immunodeficiency Virus (HIV) Rapid Testing in HIV Controllers

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

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

4. Use of prostate systematic and targeted biopsy on the basis of multiparametric MRI in biopsy-naive patients (MRI-FIRST): a prospective, multicentre, paired diagnostic study

5. Targeted temperature management in the ICU: Guidelines from a French expert panel

6. Temporal trends in living kidney donation in France between 2007 and 2017

7. Lopinavir-Ritonavir Impairs Adrenal Function in Infants

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

9. Efficacy of phosphodiesterase type 5 inhibitors in univentricular congenital heart disease: the SV‐INHIBITION study design

10. Pediatric cardiac computed tomography angiography: Expert consensus from the Filiale de Cardiologie Pédiatrique et Congénitale (FCPC) and the Société Française d’Imagerie Cardiaque et Vasculaire diagnostique et interventionnelle (SFICV)

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

12. Aspergillus fumigatus Infection in Humans With STAT3-Deficiency Is Associated With Defective Interferon-Gamma and Th17 Responses

13. Long-term event-free survival, chimerism and fertility outcomes in 234 patients with sickle-cell anemia younger than 30 years after myeloablative conditioning and matched-sibling transplantation in France

14. Multimorbidity in Elderly Persons According to the Year of Diagnosis of Human Immunodeficiency Virus Infection: A Cross-sectional Dat’AIDS Cohort Study

15. Concomitant PIK3CD and TNFRSF9 deficiencies cause chronic active Epstein-Barr virus infection of T cells

16. The tetraspanin CD9 controls migration and proliferation of parietal epithelial cells and glomerular disease progression

17. Germline TIM-3 Mutations Characterize Sub-Cutaneous Panniculitis T-Cell Lymphomas with Hemophagocytic Lymphohistiocytic Syndrome

18. XPO1 regulates erythroid differentiation and is a new target for the treatment of β-thalassemia

19. One-Fifth of Children with Sickle Cell Anemia Show Exercise-Induced Hemoglobin Desaturation: Rate of Perceived Exertion and Role of Blood Rheology

20. Anakinra in children and adults with Still's disease

21. Soft tissue angiomatosis: another PIK3CA ‐related disorder

22. Basal exon skipping and nonsense-associated altered splicing allows bypassing complete CEP290 loss-of-function in individuals with unusually mild retinal disease

23. Circulating IL-17-producing mucosal-associated invariant T cells (MAIT) are associated with symptoms in children with asthma

24. Strains Responsible for Invasive Meningococcal Disease in Patients With Terminal Complement Pathway Deficiencies

25. Chronic Granulomatous Disease in Patients Reaching Adulthood: A Nationwide Study in France

26. 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

27. Diagnosis and phenotypic assessment of trimethylaminuria, and its treatment with riboflavin: 1 H NMR spectroscopy and genetic testing

28. TUBB1 mutations cause thyroid dysgenesis associated with abnormal platelet physiology

29. UCP2 Deficiency Increases Colon Tumorigenesis by Promoting Lipid Synthesis and Depleting NADPH for Antioxidant Defenses

30. Synthesis, 3D-structure and stability analyses of NRPa-308, a new promising anti-cancer agent

31. Europium labeled lactosylated albumin as a model workflow for the development of biotherapeutics

32. Neuraxial analgesia is not associated with an increased risk of post-partum relapses in MS

33. Loss of ARHGEF1 causes a human primary antibody deficiency

34. Dermatological manifestations in Noonan syndrome: a prospective multicentric study of 129 patients positive for mutation

35. Neurological Involvement in Childhood Evans Syndrome

36. B-ALL With t(5;14)(q31;q32); IGH-IL3 Rearrangement and Eosinophilia: A Comprehensive Analysis of a Peculiar IGH-Rearranged B-ALL

37. Reconstruction 3D en IRM du pelvis de l'enfant : segmentation des structures osseuses par intelligence artificielle

38. Genetic diagnosis of primary immunodeficiencies: A survey of the French national registry

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

40. Etude exploratoire du réseau nerveux pelvien par tractographie

41. PET-adapted treatment for newly diagnosed advanced Hodgkin lymphoma (AHL2011): a randomised, multicentre, non-inferiority, phase 3 study

42. GAPDH Expression Predicts the Response to R-CHOP, the Tumor Metabolic Status, and the Response of DLBCL Patients to Metabolic Inhibitors

43. Etude du développement du système nerveux périphérique pelvien : du foetus à l'enfant porteur de malformations et tumeurs pelviennes

44. Comparative performance of the Biocentric Generic Viral Load, Roche CAP/CTM v1.5, Roche CAP/CTM v2.0 and m2000 Abbott assays for quantifying HIV-1 B and non-B strains: Underestimation of some CRF02 strains

45. Intestinal dysbiosis in Inflammatory Bowel Disease associated with primary immunodeficiency

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

47. Association of Matched-Sibling Donor Hematopoietic Stem Cell Transplantation with Transcranial-Doppler Velocities in Children with Sickle Cell Anemia

48. A variant erythroferrone disrupts iron homeostasis in SF3B1 -mutated myelodysplastic syndrome

49. Ttc7a regulates haematopoietic stem cell functions while controlling the stress-induced response

50. Enhanced Renewal of Erythroid Progenitors in Myelodysplastic Anemia by Peripheral Serotonin

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