Ghosh K - Search Results

1

Autoimmune lymphoproliferative syndrome caused by a homozygous null FAS ligand (FASLG) mutation.

Magerus-Chatinet A, Stolzenberg MC, Lanzarotti N, Neven B, Daussy C, Picard C, Neveux N, Desai M, Rao M, Ghosh K, Madkaikar M, Fischer A, Rieux-Laucat F. Magerus-Chatinet A, et al. Among authors: ghosh k. J Allergy Clin Immunol. 2013 Feb;131(2):486-90. doi: 10.1016/j.jaci.2012.06.011. Epub 2012 Jul 31. J Allergy Clin Immunol. 2013. PMID: 22857792 Free PMC article.

2

Advances in autoimmune lymphoproliferative syndromes.

Madkaikar M, Mhatre S, Gupta M, Ghosh K. Madkaikar M, et al. Among authors: ghosh k. Eur J Haematol. 2011 Jul;87(1):1-9. doi: 10.1111/j.1600-0609.2011.01617.x. Eur J Haematol. 2011. PMID: 21447005 Review.

3

Comprehensive report of primary immunodeficiency disorders from a tertiary care center in India.

Madkaikar M, Mishra A, Desai M, Gupta M, Mhatre S, Ghosh K. Madkaikar M, et al. Among authors: ghosh k. J Clin Immunol. 2013 Apr;33(3):507-12. doi: 10.1007/s10875-012-9829-2. Epub 2012 Oct 31. J Clin Immunol. 2013. PMID: 23108471

4

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. Madkaikar M, et al. Among authors: ghosh k. J Clin Immunol. 2015 May;35(4):431-4. doi: 10.1007/s10875-015-0155-3. Epub 2015 Apr 16. J Clin Immunol. 2015. PMID: 25876705

5

Rapid Flow cytometric prenatal diagnosis of primary immunodeficiency (PID) disorders.

Mishra A, Gupta M, Dalvi A, Ghosh K, Madkaikar M. Mishra A, et al. Among authors: ghosh k. J Clin Immunol. 2014 Apr;34(3):316-22. doi: 10.1007/s10875-014-9993-7. Epub 2014 Feb 18. J Clin Immunol. 2014. PMID: 24535004

6

Spectrum of perforin gene mutations in familial hemophagocytic lymphohistiocytosis (FHL) patients in India.

Mhatre S, Madkaikar M, Desai M, Ghosh K. Mhatre S, et al. Among authors: ghosh k. Blood Cells Mol Dis. 2015 Mar;54(3):250-7. doi: 10.1016/j.bcmd.2014.11.023. Epub 2014 Dec 23. Blood Cells Mol Dis. 2015. PMID: 25577959

7

X-linked hyper IgM syndrome: clinical, immunological and molecular features in patients from India.

Madkaikar M, Gupta M, Chavan S, Italia K, Desai M, Merchant R, Radhakrishnan N, Ghosh K. Madkaikar M, et al. Among authors: ghosh k. Blood Cells Mol Dis. 2014 Sep;53(3):99-104. doi: 10.1016/j.bcmd.2014.05.008. Epub 2014 Jun 11. Blood Cells Mol Dis. 2014. PMID: 24929972

8

Purine nucleoside phosphorylase deficiency with a novel PNP gene mutation: a first case report from India.

Madkaikar MR, Kulkarni S, Utage P, Fairbanks L, Ghosh K, Marinaki A, Desai M. Madkaikar MR, et al. Among authors: ghosh k. BMJ Case Rep. 2011 Dec 8;2011:bcr0920114804. doi: 10.1136/bcr.09.2011.4804. BMJ Case Rep. 2011. PMID: 22669887 Free PMC article.

9

Prenatal diagnosis of LAD-I on cord blood by flowcytometry.

Madkaikar MR, Gupta M, Rao M, Ghosh K. Madkaikar MR, et al. Among authors: ghosh k. Indian J Pediatr. 2012 Dec;79(12):1605-9. doi: 10.1007/s12098-012-0737-5. Epub 2012 Apr 4. Indian J Pediatr. 2012. PMID: 22477041

10

Diagnostic approach to primary immunodeficiency disorders.

Madkaikar M, Mishra A, Ghosh K. Madkaikar M, et al. Among authors: ghosh k. Indian Pediatr. 2013 Jun 8;50(6):579-86. doi: 10.1007/s13312-013-0171-4. Indian Pediatr. 2013. PMID: 23942400 Free article. Review.

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