Publications on PID

Congenital defects of phagocyte number, function, or both

Chronic granulomatous disease presenting with small bone osteomyelitis in a young child: A case report.

Approach to Molecular Diagnosis of Chronic Granulomatous Disease (CGD): an Experience from a Large Cohort of 90 Indian Patients.

Clinical, Immunological, and Molecular Findings of Patients with p47phox Defect Chronic Granulomatous Disease (CGD) in Indian Families.
Kulkarni M, Desai M, Gupta M, Dalvi A, Taur P, Terrance A, Bhat S, Manglani M, Raj R, Shah I, Madkaikar M.
J Clin Immunol. 2016 Nov;36(8):774-784. Epub 2016 Oct 3.

Leukocyte adhesion deficiency-I with a novel intronic mutation presenting with pyoderma gangrenosum- like lesions.
Madkaikar M, Italia K, Gupta M, Desai M, Aggarwal A, Singh S, Suri D, Mishra A, Chavan S, Ghosh K, Sarangal R, Dogra S.
J Clin Immunol. 2015 May;35(4):431-4. doi: 10.1007/s10875-015-0155-3. Epub 2015 Apr 16.

Molecular characterization of leukocyte adhesion deficiency-I in Indian patients: identification of 9 novel mutations.
Madkaikar M, Italia K, Gupta M, Chavan S, Mishra A, Rao M, Mhatre S, Desai M, Manglani M, Singh S, Suri D, Agrawal A, Ghosh K.
Blood Cells Mol Dis. 2015 Mar;54(3):217-23. doi: 10.1016/j.bcmd.2015.01.012. Epub 2015 Jan 23.

CGD In India, Amit Rawat et al.

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