Kabra M - Search Results

1

Late onset Pompe Disease in India - Beyond the Caucasian phenotype.

Puri RD, Setia N, N V, Jagadeesh S, Nampoothiri S, Gupta N, Muranjan M, Bhat M, Girisha KM, Kabra M, Verma J, Thomas DC, Biji I, Raja J, Makkar R, Verma IC, Kishnani PS. Puri RD, et al. Among authors: kabra m. Neuromuscul Disord. 2021 May;31(5):431-441. doi: 10.1016/j.nmd.2021.02.013. Epub 2021 Feb 16. Neuromuscul Disord. 2021. PMID: 33741225

2

Group B meningococcal meningitis in India.

Suri M, Kabra M, Singh S, Rattan A, Verma IC. Suri M, et al. Among authors: kabra m. Scand J Infect Dis. 1994;26(6):771-3. doi: 10.3109/00365549409008652. Scand J Infect Dis. 1994. PMID: 7747107

3

Poland anomaly with unusual associated anomalies: case report of an apparent disorganized defect.

Kabra M, Suri M, Jain U, Verma IC. Kabra M, et al. Am J Med Genet. 1994 Oct 1;52(4):402-5. doi: 10.1002/ajmg.1320520403. Am J Med Genet. 1994. PMID: 7747752

4

Blepharophimosis, telecanthus, microstomia, and unusual ear anomaly (Simosa syndrome) in an infant.

Suri M, Kabra M, Verma IC. Suri M, et al. Among authors: kabra m. Am J Med Genet. 1994 Jul 1;51(3):222-3. doi: 10.1002/ajmg.1320510309. Am J Med Genet. 1994. PMID: 8074148

5

A clinical and cytogenetic study of Turner syndrome.

Suri M, Kabra M, Jain U, Sanders V, Saxena R, Shukla A, Singh GV, Verma IC. Suri M, et al. Among authors: kabra m. Indian Pediatr. 1995 Apr;32(4):433-42. Indian Pediatr. 1995. PMID: 8635807

6

Denys-Drash syndrome.

Suri M, Kabra M, Kataria A, Singh GR, Sharma S, Gupta AK, Menon PS, Verma IC. Suri M, et al. Among authors: kabra m. Indian Pediatr. 1995 Dec;32(12):1310-3. Indian Pediatr. 1995. PMID: 8772891 No abstract available.

7

Karyotyping of at risk fetuses by cordocentesis in advanced gestation.

Kabra M, Saxena R, Chinnappan D, Sanders V, Deka D, Buckshee K, Verma IC. Kabra M, et al. Indian J Med Res. 1996 Nov;104:288-91. Indian J Med Res. 1996. PMID: 8979519

8

Clinical and biochemical studies in homocystinuria.

Kaur M, Kabra M, Das GP, Suri M, Verma IC. Kaur M, et al. Among authors: kabra m. Indian Pediatr. 1995 Oct;32(10):1067-75. Indian Pediatr. 1995. PMID: 8984043

9

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.

10

Clinical and enzyme studies in Gaucher disease.

Kaur M, Kabra M, Kher A, Naik G, Bharucha BA, Verma IC. Kaur M, et al. Among authors: kabra m. Indian Pediatr. 1996 Sep;33(9):735-8. Indian Pediatr. 1996. PMID: 9057400

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