33 results on '"Fieschi, Claire"'
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2. Pregnancy in primary immunodeficiency diseases: The PREPI study
3. The efficacy and safety of systemic corticosteroids as first line treatment for granulomatous lymphocytic interstitial lung disease
4. Genetic Diagnosis Guides Treatment of Autoimmune Enteropathy
5. Allogeneic stem cell transplantation compared to conservative management in adults with inborn errors of immunity
6. Immune thrombocytopenia and pregnancy: an exposed/nonexposed cohort study
7. Autoimmune hypoglycemia expands the biological spectrum of HHV8+ multicentric Castleman disease
8. Synergistic convergence of microbiota-specific systemic IgG and secretory IgA
9. Mutations in the SRP54 gene cause severe congenital neutropenia as well as Shwachman-Diamond–like syndrome
10. Genetic screening of male patients with primary hypogammaglobulinemia can guide diagnosis and clinical management
11. iNKT and memory B-cell alterations in HHV-8 multicentric Castleman disease
12. Exclusion of Patients with a Severe T-Cell Defect Improves the Definition of Common Variable Immunodeficiency
13. Rituximab decreases the risk of lymphoma in patients with HIV-associated multicentric Castleman disease
14. Common variable immunodeficiency disorders: division into distinct clinical phenotypes
15. A role for interleukin-12/23 in the maturation of human natural killer and CD56+ T cells in vivo
16. Intensive chemotherapy regimen (LMB86) for St Jude stage IV AIDS-related Burkitt lymphoma/leukemia: a prospective study
17. Romidepsin is an effective and well-tolerated therapy in CD3−CD4+ lymphocyte-variant hypereosinophilic syndrome: A case report
18. Genetic diagnosis of primary immunodeficiencies: A survey of the French national registry
19. Campylobacter infection in adult patients with primary antibody deficiency
20. A novel form of complete IL-12/IL-23 receptor β1 deficiency with cell surface-expressed nonfunctional receptors
21. DIAGNOSIS AND MANAGEMENT OF INHERITABLE DISORDERS OF INTERFERON-γ–MEDIATED IMMUNITY
22. Outcome of Immune Thrombocytopenia in Pregnancy: A French Nationwide Prospective Multicenter Observational Case-Control Study
23. How Many Patients Have Congenital Neutropenia? a Population-Based Estimation from the Nationwide French Severe Chronic Neutropenia Registry
24. Impact and Dynamics of TP53 Mutated Clones in Shwachman Diamond Syndrome in a Series of 80 Patients
25. Risk Factors of Neonatal Immune Thrombocytopenia in Pregnant Women Previously Diagnosed with ITP: Results from a French Nationwide Prospective Study
26. Congenital Neutropenia Is Also Associated with a High Cancer Risk: A Study from the French Severe Chronic Neutropenia Registry
27. Mutations in SRP54 Gene Cause Severe Primary Neutropenia As Well As Shwachman-Diamond-like Syndrome
28. FAS-L, IL-10, and double-negative CD4−CD8− TCR α/β+ T cells are reliable markers of autoimmune lymphoproliferative syndrome (ALPS) associated with FAS loss of function
29. HHV-8 Related Castleman Disease in the Absence of HIV Infection
30. Rituximab, Fludarabine and Alkylating Agents in Peripheral Neuropathies Related to IgM Monoclonal Gammopathy with Autoantibody Activity against Myelin-Associated-Glycoprotein : a Retrospective Study of 15 Patients.
31. Cutaneous tumor lysis syndrome in a patient with HTLV-1 adult T-cell lymphoma/leukemia
32. Cranial Nerves Paralysis Revealing Two Cases of Histiocytic Sarcoma.
33. Intensive Chemotherapy (LMB-86 Regimen) for AIDS-Related Burkitt's Lymphoma/Leukemia.
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