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3. A Clinical Conundrum with Diagnostic and Therapeutic Challenge: a Tale of Two Disorders in One Case

5. Clinical, immunological and genomic characteristics of children with X-linked agammaglobulinemia from Kerala, South India

10. Diagnosis and Management of Infections in Patients with Mendelian Susceptibility to Mycobacterial Disease.

12. Expanding the clinical phenotype of FADD deficiency with a novel mutation and its role in Fas‐mediated apoptotic pathway

13. Clinical, immunological and molecular findings of patients with DOCK‐8 deficiency from India

14. Normative data for paediatric lymphocyte subsets: A pilot study from western India

15. Poliovirus Excretion in Children with Primary Immunodeficiency Disorders, India

16. Utility of HLA‐DR in screening panel for inborn errors of immunity

19. Utility of HLA‐DR in screening panel for inborn errors of immunity.

20. Clinical and Genetic Spectrum of Inborn Errors of Immunity in a Tertiary Care Center in Southern India

21. FADD Deficiency Mimicking ALPS-FAS: An Expanding Phenotype.

22. Whole genome sequencing identifies novel structural variant in a large Indian family affected with X-linked agammaglobulinemia

23. The Spectrum of Clinical, Immunological, and Molecular Findings in Familial Hemophagocytic Lymphohistiocytosis: Experience From India

24. Clinical Profile of Hyper-IgE Syndrome in India

25. Clinical and Molecular Findings in Mendelian Susceptibility to Mycobacterial Diseases: Experience From India

26. Clinical, Immunological, and Molecular Features of Severe Combined Immune Deficiency: A Multi-Institutional Experience From India

27. Clinical and Genetic Profile of X-Linked Agammaglobulinemia: A Multicenter Experience From India

28. Spectrum of Inborn errors of immunity in a cohort of 90 patients presenting with complications to BCG vaccination in India

29. Clinical and Genetic Spectrum of a Large Cohort of Patients With Leukocyte Adhesion Deficiency Type 1 and 3: A Multicentric Study From India

30. Prenatal Diagnosis for Primary Immunodeficiency Disorders—An Overview of the Indian Scenario

31. Whole Genome Sequencing identifies novel structural variant in a large Indian family affected with X - linked agammaglobulinemia

33. A Novel Splice Site Mutation in IFNGR2 in Patients With Primary Immunodeficiency Exhibiting Susceptibility to Mycobacterial Diseases

34. Natural Clearance of Prolonged VDPV Infection in a Child With Primary Immunodeficiency Disorder

36. Clinical, Immunological, and Molecular Findings in 57 Patients With Severe Combined Immunodeficiency (SCID) From India

37. A STUDY OF ENGLISH CREATIVE WRITING SKILLS AND ACADEMIC PERFORMANCE OF C.B.S.E. AND STATE BOARD SCHOOL CHILDREN

38. Clinical, Immunological, and Molecular Findings in Four Cases of B Cell Expansion With NF-κB and T Cell Anergy Disease for the First Time From India

41. HLA‐DR covers Bare Lymphocyte Syndrome.

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