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85 results on '"Centre Hospitalier Universitaire de Nice (CHU Nice)-Hôpital l'Archet"'

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1. An unusual Staphylococcus saccharolyticus spondylodiscitis post kyphoplasty: a case report

2. Tanning practice, perception, and sunburn among Emirati youth

3. Risk for Major Bleeding in Patients Receiving Ticagrelor Compared With Aspirin After Transient Ischemic Attack or Acute Ischemic Stroke in the SOCRATES Study (Acute Stroke or Transient Ischemic Attack Treated With Aspirin or Ticagrelor and Patient Outcomes)

4. Biologics in myelodysplastic syndrome-related systemic inflammatory and autoimmune diseases: French multicenter retrospective study of 29 patients

5. Acquiring procedural skills in ICUs: a prospective multicenter study*

6. Toxoplasmosis and horse meat, France

7. Ostéonécroses aseptiques, une revue générale des ostéonécroses de la hanche, et au-delà

8. PW02-012 - First clinical description of an infant with DITRA

9. Case Report: A New Mycobacterium ulcerans Genotype Causing Buruli Ulcer in Côte d’Ivoire

10. Bone disorders associated with diabetes mellitus and its treatments

11. Novel Approach to Estimate Osteoarthritis Progression: Use of the Reliable Change Index in the Evaluation of Joint Space Loss

12. Late clinical failure associated with cytochrome b codon 268 mutation during treatment of falciparum malaria with atovaquone–proguanil in traveller returning from Congo

13. Bed bug bites

14. Assessment of structural lesions, synovitis and bone marrow lesions in erosive hand osteoarthritis on MRI (0.3T) compared to the radiographic anatomical Verbruggen-Veys score

15. Seawater drowning-associated pneumonia: a 10-year descriptive cohort in intensive care unit

16. Strategy for suspected myositis

17. Newly diagnosed and growing subependymal giant cell astrocytoma in adults with tuberous sclerosis complex: results from the international TOSCA study

18. Clinical Characteristics of Subependymal Giant Cell Astrocytoma in Tuberous Sclerosis Complex

19. eKLIPse: a sensitive tool for the detection and quantification of mitochondrial DNA deletions from next-generation sequencing data

20. Is self-assessment by patients of disease activity acceptable over the long term in rheumatoid arthritis? A 3-year follow-up of 771 patients

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

22. Oxytocin Controls Chondrogenesis and Correlates with Osteoarthritis

23. Translocation of dead or alive bacteria from mucosa to joints and epiphyseal bone-marrow: facts and hypotheses

24. Early-onset encephalopathy with paroxysmal movement disorders and epileptic seizures without hemiplegic attacks: About three children with novel ATP1A3 mutations

25. Molecular diagnosis of inherited peripheral neuropathies by targeted next-generation sequencing: molecular spectrum delineation

26. Human cryptosporidiosis in immunodeficient patients in France (2015–2017)

27. Abnormal T-cell phenotype in episodic angioedema with hypereosinophilia (Gleich's syndrome): frequency, clinical implication and prognosis

28. Prevalence of pelvic Paget's disease of bone in France

29. Hypoxia Inhibits Cavin-1 and Cavin-2 Expression and Down-Regulates Caveolae in Adipocytes

30. Mechanical thrombectomy after intravenous thrombolysis for acute ischaemic stroke – Authors' reply

31. Efficacy of adalimumab in patients with Crohn's disease and symptomatic small bowel stricture: a multicentre, prospective, observational cohort (CREOLE) study

32. Bacterial infection in compensated viral cirrhosis impairs 5-year survival (ANRS CO12 CirVir prospective cohort)

33. Weakening osteopathies, chronic kidney disease, malabsorption, biological anomalies of calium/phosphorus metabolism: appropriate indications for a reasoned reimbursment of serum vitamin D measurement

34. French law: what about a reasoned reimbursement of serum vitamin D assays?

35. Psychiatric and substance use disorders in HIV/hepatitis C virus (HCV)-coinfected patients: does HCV clearance matter? [Agence Nationale de Recherche sur le SIDA et les Hépatites Virales (ANRS) HEPAVIH CO13 cohort]

36. Screening for and management of comorbidities after a nurse-led program: results of a 3-year longitudinal study in 769 established rheumatoid arthritis patients

37. Reproducibility of radiographic hip measurements in adults

38. Inactivation of Pif1 helicase causes a mitochondrial myopathy in mice

39. Sex-specific autophagy modulation in osteoblastic lineage: a critical function to counteract bone loss in female

40. SNP Array Profiling of Childhood Adrenocortical Tumors Reveals Distinct Pathways of Tumorigenesis and Highlights Candidate Driver Genes

41. CHCHD10 mutations promote loss of mitochondrial cristae junctions with impaired mitochondrial genome maintenance and inhibition of apoptosis

42. The Clinical Variability of Maternally Inherited Diabetes and Deafness Is Associated with the Degree of Heteroplasmy in Blood Leukocytes

43. Changes in Causes of Death Among Adults Infected by HIV Between 2000 and 2005: The 'Mortalité 2000 and 2005' Surveys (ANRS EN19 and Mortavic)

44. Oxytocin Controls Differentiation of Human Mesenchymal Stem Cells and Reverses Osteoporosis

45. Nephroblastoma Overexpressed/Cysteine-Rich Protein 61/Connective Tissue Growth Factor/Nephroblastoma Overexpressed Gene-3 (NOV/CCN3), a Selective Adrenocortical Cell Proapoptotic Factor, Is Down-Regulated in Childhood Adrenocortical Tumors

46. High Cure Rate With 24 Weeks of Daclatasvir-Based Quadruple Therapy in Treatment-Experienced, Null-Responder Patients With HIV/Hepatitis C Virus Genotype 1/4 Coinfection: The ANRS HC30 QUADRIH Study

47. Reply: CHCHD10 mutations in Italian patients with sporadic amyotrophic lateral sclerosis

48. Impact of a nurse-led programme on comorbidity management and impact of a patient self-assessment of disease activity on the management of rheumatoid arthritis: results of a prospective, multicentre, randomised, controlled trial (COMEDRA)

49. Long-term outcome of AIDS-associated cryptococcosis in the era of combination antiretroviral therapy

50. Reply: Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosis

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