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355 results on '"Imagine - Institut des maladies génétiques (IMAGINE - U1163)"'

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1. Polymorphisme des gènes HLA et KIR et l’impact sur le devenir de la greffe et le choix du donneur non apparenté de cellules souche hématopoïétiques : recommandations de la Société francophone de greffe de moelle et de thérapie cellulaire (SFGM-TC)

2. Resilience and Life Expectations of Perinatally HIV-1 Infected Adolescents in France

3. Similar outcome of allogeneic stem cell transplantation after myeloablative and sequential conditioning regimen in patients with refractory or relapsed acute myeloid leukemia: A study from the Société Francophone de Greffe de Moelle et de Thérapie Cellula

4. Recessive loss of function PIGN alleles, including an intragenic deletion with founder effect in La Réunion Island, in patients with Fryns syndrome

5. Systemic inflammatory and autoimmune manifestations associated with myelodysplastic syndromes and chronic myelomonocytic leukaemia: a French multicentre retrospective study

6. Yeast as a system for modeling mitochondrial disease mechanisms and discovering therapies

7. Subcutaneous Panniculitis-like T-cell Lymphoma: Immunosuppressive Drugs Induce Better Response than Polychemotherapy

8. Antifungal therapy for patients with proven or suspected Candida peritonitis: Amarcand2, a prospective cohort study in French intensive care units

9. Mutations in DCC cause isolated agenesis of the corpus callosum with incomplete penetrance

10. De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal development

11. VLITL is a major cross-beta-sheet signal for fibrinogen A alpha-chain frameshift variants

12. Do the Side Effects of BRAF Inhibitors Mimic RASopathies?

13. Shared genetic predisposition in rheumatoid arthritis-interstitial lung disease and familial pulmonary fibrosis

14. Trichodysplasia spinulosa polyomavirus infection occurs during early childhood with intra-familial transmission, especially from mother to child

15. Complementary Roles of Nod2 in Hematopoietic and Nonhematopoietic Cells in Preventing Gut Barrier Dysfunction Dependent on MLCK Activity

16. Bendamustine for the treatment of relapsed or refractory peripheral T cell lymphomas: A French retrospective multicenter study

17. Profiling olfactory stem cells from living patients identifies miRNAs relevant for autism pathophysiology

18. Adult T cell leukemia aggressivenness correlates with loss of both 5-hydroxymethylcytosine and TET2 expression

19. Evidence of innate lymphoid cell redundancy in humans

20. Contactin-Associated Protein 1 (CNTNAP1) Mutations Induce Characteristic Lesions of the Paranodal Region

21. Mast cells' involvement in inflammation pathways linked to depression: evidence in mastocytosis

22. Severe Pulmonary Fibrosis as the First Manifestation of Interferonopathy (TMEM173 Mutation)

23. A Tumor Profile in Edwards Syndrome (Trisomy 18)

24. Seizures in dominantly inherited Alzheimer disease

25. Impact of Thymoglobulin by Stem Cell Source (Peripheral Blood Stem Cell or Bone Marrow) After Myeloablative Stem Cell Transplantation From HLA 10/10-Matched Unrelated Donors. A Report From the Société Française de Greffe de Moelle et de Thérapie Cellulaire

26. NAP1L1-MLLT10 is a rare recurrent translocation that is associated with HOXA activation and poor treatment response in T-cell acute lymphoblastic leukaemia

27. Post-paralysis tyrosine kinase inhibition with masitinib abrogates neuroinflammation and slows disease progression in inherited amyotrophic lateral sclerosis

28. Mycobacterial disease in patients with chronic granulomatous disease: A retrospective analysis of 71 cases

29. Screening of dementia genes by whole-exome sequencing in early-onset Alzheimer disease: input and lessons

30. Brentuximab vedotin in refractory or relapsed peripheral T-cell lymphomas: the French named patient program experience in 56 patients

31. Decreased tryptophan and increased kynurenine levels in mastocytosis associated with digestive symptoms

32. An early thymic precursor phenotype predicts outcome exclusively in HOXA-overexpressing adult T-cell acute lymphoblastic leukemia: a Group for Research in Adult Acute Lymphoblastic Leukemia study

33. Epilepsy in young Tsc1+/− mice exhibits age-dependent expression that mimics that of human tuberous sclerosis complex

34. Antimony to Cure Visceral Leishmaniasis Unresponsive to Liposomal Amphotericin B

35. Pediatric-Like Acute Lymphoblastic Leukemia Therapy in Adults With Lymphoblastic Lymphoma: The GRAALL-LYSA LL03 Study

36. Tuning Eye-Gaze Perception by Transitory STS Inhibition

37. Autosomal Dominant STAT3 Deficiency and Hyper-IgE Syndrome

38. Utility of whole exome sequencing for the early diagnosis of pediatric-onset cerebellar atrophy associated with developmental delay in an inbred population

39. Genetic basis of dominant dystrophic epidermolysis bullosa in tunisian families and co-occurrence of dominant and recessive mutations

40. In primary effusion lymphoma cells, MYB transcriptional repression is associated with v-FLIP expression during latent KSHV infection while both v-FLIP and v-GPCR become involved during the lytic cycle

41. Latent Tuberculosis Infection Screening and 2-Year Outcome in Antiretroviral-Naive HIV-Infected Patients in a Low-Prevalence Country

42. Relevance of EORTC Criteria for the Diagnosis of Invasive Aspergillosis in HIV-Infected Patients, and Survival Trends Over a 20-Year Period in France

43. Gastrointestinal Disorder Associated with Olmesartan Mimics Autoimmune Enteropathy

44. C-Nap1 mutation affects centriole cohesion and is associated with a Seckel-like syndrome in cattle

45. Submicroscopic Deletions at 13q32.1 Cause Congenital Microcoria

46. Spectrum and Prognosis of Noninfectious Renal Mixed Cryoglobulinemic GN

47. Adult T-Cell Leukemia/Lymphoma in a Caucasian Patient After Sexual Transmission of Human T-Cell Lymphotropic Virus Type 1

48. Human regulator of telomere elongation helicase 1 (RTEL1) is required for the nuclear and cytoplasmic trafficking of pre-U2 RNA

49. L’IRIS : une réaction inflammatoire paradoxale chez les patients traités simultanément pour une tuberculose et une infection par le VIH

50. Biological Description of 109 Cases of Blastic Plasmacytoid Dendritic Cell Neoplasm (BPDCN) from the French Network of BPDCN

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