Kabra M - Search Results

1

Long-term daily high and low doses of azithromycin in children with cystic fibrosis: a randomized controlled trial.

Kabra SK, Pawaiya R, Lodha R, Kapil A, Kabra M, Vani AS, Agarwal G, Shastri SS. Kabra SK, et al. Among authors: kabra m. J Cyst Fibros. 2010 Jan;9(1):17-23. doi: 10.1016/j.jcf.2009.09.001. Epub 2009 Oct 8. J Cyst Fibros. 2010. PMID: 19818694 Free article. Clinical Trial.

2

Delta F 508 molecular mutation in Indian children with cystic fibrosis.

Kabra M, Ghosh M, Kabra SK, Khanna A, Verma IC. Kabra M, et al. Among authors: kabra sk. Indian J Med Res. 1996 Dec;104:355-8. Indian J Med Res. 1996. PMID: 8996936 Clinical Trial.

3

Cystic fibrosis--an Indian perspective on recent advances in diagnosis and management.

Kabra SK, Kabra M, Ghosh M, Verma IC. Kabra SK, et al. Among authors: kabra m. Indian J Pediatr. 1996 Mar-Apr;63(2):189-98. doi: 10.1007/BF02845243. Indian J Pediatr. 1996. PMID: 10829988 Review.

4

Is the spectrum of mutations in Indian patients with cystic fibrosis different?

Kabra M, Kabra SK, Ghosh M, Khanna A, Arora S, Menon PS, Verma IC, Wallace A. Kabra M, et al. Among authors: kabra sk. Am J Med Genet. 2000 Jul 17;93(2):161-3. doi: 10.1002/1096-8628(20000717)93:2<161::aid-ajmg15>3.0.co;2-l. Am J Med Genet. 2000. PMID: 10869121 No abstract available.

5

Idiopathic cranio-osteoarthropathy.

Kabra M, Kabra SK, Ghosh M, Gupta AK, Menon PS. Kabra M, et al. Among authors: kabra sk. Indian Pediatr. 2000 Jun;37(6):659-62. Indian Pediatr. 2000. PMID: 10869149 No abstract available.

6

Persistent hyperinsulinemic hypoglycemia with pyloric stenosis.

Dutta S, Lodha R, Kabra M, Deshpande V, Menon PS. Dutta S, et al. Among authors: kabra m. Indian Pediatr. 2000 Aug;37(8):890-3. Indian Pediatr. 2000. PMID: 10951639 No abstract available.

7

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

8

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

9

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

10

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

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

415 results

Search Page

Filters