Kabra M - Search Results

1

Do polymorphisms in MDR1 and CYP3A5 genes influence the risk of cytogenetic relapse in patients with chronic myeloid leukemia on imatinib therapy?

Harivenkatesh N, Kumar L, Bakhshi S, Sharma A, Kabra M, Velpandian T, Gogia A, Shastri SS, Gupta YK. Harivenkatesh N, et al. Among authors: kabra m. Leuk Lymphoma. 2017 Sep;58(9):1-9. doi: 10.1080/10428194.2017.1287359. Epub 2017 Apr 3. Leuk Lymphoma. 2017. PMID: 28367681

2

Prenatal diagnosis of Duchenne muscular dystrophy.

Maheshwari M, Vijaya R, Kabra M, Arora S, Shastri SS, Deka D, Kriplani A, Menon PS. Maheshwari M, et al. Among authors: kabra m. Natl Med J India. 2000 May-Jun;13(3):129-31. Natl Med J India. 2000. PMID: 11558111

3

Prenatal diagnosis of haemoglobinopathies.

Arora S, Kabra M, Maheshwari M, Shastri S, Kaur D, Deka D, Kriplani A, Menon PS. Arora S, et al. Among authors: kabra m. Natl Med J India. 2001 Nov-Dec;14(6):340-2. Natl Med J India. 2001. PMID: 11804364

4

An indigenously developed method for sweat collection and estimation of chloride for diagnosis of cystic fibrosis.

Kabra SK, Kabra M, Gera S, Lodha R, Sreedevi KN, Chacko S, Mathew J, Shastri S, Ghosh M. Kabra SK, et al. Among authors: kabra m. Indian Pediatr. 2002 Nov;39(11):1039-43. Indian Pediatr. 2002. PMID: 12466575

5

Screening of families with autosomal recessive non-syndromic hearing impairment (ARNSHI) for mutations in GJB2 gene: Indian scenario.

Maheshwari M, Vijaya R, Ghosh M, Shastri S, Kabra M, Menon PS. Maheshwari M, et al. Among authors: kabra m. Am J Med Genet A. 2003 Jul 15;120A(2):180-4. doi: 10.1002/ajmg.a.20014. Am J Med Genet A. 2003. PMID: 12833397

6

Clinical profile and frequency of delta f508 mutation in Indian children with cystic fibrosis.

Kabra SK, Kabra M, Lodha R, Shastri S, Ghosh M, Pandey RM, Kapil A, Aggarwal G, Kapoor V. Kabra SK, et al. Among authors: kabra m. Indian Pediatr. 2003 Jul;40(7):612-9. Indian Pediatr. 2003. PMID: 12881616 Free article.

7

Thrombocytopenic purpura as a presenting manifestation of tubercular lymphadenitis.

Bakhshi S, Kabra M, Iyer VK, Arya LS. Bakhshi S, et al. Among authors: kabra m. Indian J Pediatr. 2003 Dec;70(12):993-4. doi: 10.1007/BF02723827. Indian J Pediatr. 2003. PMID: 14719790

8

Glucose-6-phosphate dehydrogenase deficiency with bilateral cataract.

Bakhshi S, Kabra M. Bakhshi S, et al. Among authors: kabra m. Indian Pediatr. 2004 Jun;41(6):630-1. Indian Pediatr. 2004. PMID: 15235179 Free article. No abstract available.

9

Novel missense mutation in the coagulation factor IX catalytic domain associated with severe haemophilia B--Factor IXDelhi.

Mahajan A, Sharma A, Chavali S, Kabra M, Chowdhury MR, Srinivasan N, Bharadwaj D. Mahajan A, et al. Among authors: kabra m. Haemophilia. 2004 Sep;10(5):550-2. doi: 10.1111/j.1365-2516.2004.00948.x. Haemophilia. 2004. PMID: 15357782

10

Carrier frequency of F508del mutation of cystic fibrosis in Indian population.

Kapoor V, Shastri SS, Kabra M, Kabra SK, Ramachandran V, Arora S, Balakrishnan P, Deorari AK, Paul VK. Kapoor V, et al. Among authors: kabra m, kabra sk. J Cyst Fibros. 2006 Jan;5(1):43-6. doi: 10.1016/j.jcf.2005.10.002. Epub 2005 Nov 28. J Cyst Fibros. 2006. PMID: 16311077 Free article.

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