42 results on '"Dalvi, Aparna"'
Search Results
2. Double Trouble: Novel Digenic CD19-RABEP2 Deletion in Predominantly Antibody Deficiency with Syndromic Features
3. A Clinical Conundrum with Diagnostic and Therapeutic Challenge: a Tale of Two Disorders in One Case
4. Clinical Utility of Flow-Cytometry for Diagnosis and Genotype Phenotype Correlation in a Cohort of X-linked Agammaglobulinemia Patients
5. Clinical, immunological and genomic characteristics of children with X-linked agammaglobulinemia from Kerala, South India
6. Clinical and Genetic Spectrum of Inborn Errors of Immunity in a Tertiary Care Center in Southern India
7. CD8 + T Cells Exhibit an Exhausted Phenotype in Hemophagocytic Lymphohistiocytosis
8. Novel CD3Z and CD3E Deficiency in Two Unrelated Females
9. Lymphopenia and Severe Combined Immunodeficiency (SCID) - Think Before You Ink
10. Diagnosis and Management of Infections in Patients with Mendelian Susceptibility to Mycobacterial Disease.
11. Approach to Molecular Diagnosis of Chronic Granulomatous Disease (CGD): an Experience from a Large Cohort of 90 Indian Patients
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
17. Clinical, Immunological, and Molecular Findings of Patients with p47phox Defect Chronic Granulomatous Disease (CGD) in Indian Families
18. Rapid Flow Cytometric Prenatal Diagnosis of Primary Immunodeficiency (PID) Disorders
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
32. HLA‐DR covers Bare Lymphocyte Syndrome
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
35. Application of Flow Cytometry in Primary Immunodeficiencies: Experience From India
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
39. Clinical, Immunological, and Molecular Findings in Five Patients with Major Histocompatibility Complex Class II Deficiency from India
40. Low T cell receptor excision circles (TRECs) in a case of ZAP 70 deficient severe combined immunodeficiency (SCID) with a novel mutation from India
41. HLA‐DR covers Bare Lymphocyte Syndrome.
42. Normative data for paediatric lymphocyte subsets: A pilot study from western India.
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