29 results on '"LeDeist F"'
Search Results
2. Physical mapping by FISH of the DiGeorge critical region (DGCR): Involvement of the region in familial cases
3. Rituximab therapy for childhood Evans syndrome
4. Anémie hémolytique auto-immune et dysérythropoïèse révélatrices d'un déficit de l'apoptose Fas chez 3 enfants
5. Adoptive Immunotherapy with Donor Allodepleted T Cells.
6. A non-XLA primary deficiency causes the earliest known defect of B cell differentiation in humans: a comparison with an XLA case
7. A human non-XLA immunodeficiency disease characterized by blockage of B cell development at an early pro-B cell stage
8. Patterns of changes in neutrophil adhesion molecules during normothermic cardiopulmonary bypassA clinical study
9. Treatment of familial hemophagocytic lymphohistiocytosis with antithymocyte globulins, steroids, and cyclosporin A
10. Unusual T cell clones in a patient with Nijmegen breakage syndrome.
11. Pearson's marrow-pancreas syndrome. A multisystem mitochondrial disorder in infancy.
12. An embryonic-like methylation pattern of classical satellite DNA is observed in ICF syndrome.
13. Anémie hémolytique auto-immune et déficit de l'apoptose Fas
14. Heterogeneity of immunologic and enzymatic deficiencies in the familial reticuloendotheliosis syndrome
15. Physical mapping by FISH of the DiGeorge critical region (DGCR): involvement of the region in familial cases
16. Idiopathic disseminated bacillus Calmette-Guérin infection: a French national retrospective study
17. INHERITED DEFICIENCIESCAN AFFECT SEPARATELY THE PLATELET MEMBRANE GLYCOPROTEIN Ilb-IIIa COMPLEX AND THE LEUKOCYTE LFA-1, Mac-1 and pl50,95 COMPLEXES
18. Very Early-Onset Inflammatory Manifestations of X-Linked Chronic Granulomatous Disease.
19. Clinical features of cytotoxic CD8+ T-lymphocyte deficiency in chronic rhinosinusitis patients: a demographic and functional study.
20. A systematic analysis of recombination activity and genotype-phenotype correlation in human recombination-activating gene 1 deficiency.
21. ORAI1 deficiency and lack of store-operated Ca2+ entry cause immunodeficiency, myopathy, and ectodermal dysplasia.
22. STIM1 mutation associated with a syndrome of immunodeficiency and autoimmunity.
23. [Auto-immune hemolytic anemia and dyserythropoïesis as the presenting signs of Fas-deficient condition in 3 children].
24. Dyserythropoiesis associated with a fas-deficient condition in childhood.
25. Molecular cytogenetic analysis of a series of 23 DiGeorge syndrome patients by fluorescence in situ hybridization.
26. Major histocompatibility complex class II deficiency: clinical manifestations, immunologic features, and outcome.
27. Physical mapping by FISH of the DiGeorge critical region (DGCR): involvement of the region in familial cases.
28. Multibranched chromosomes in the ICF syndrome: immunodeficiency, centromeric instability, and facial anomalies.
29. [Omenn's reticuloendotheliosis].
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