Rama Devi AR - Search Results

1

Neuro-fuzzy model of homocysteine metabolism.

Naushad SM, Rama Devi AR, Nivetha S, Lakshmitha G, Stanley AB, Hussain T, Kutala VK. Naushad SM, et al. Among authors: rama devi ar. J Genet. 2017 Dec;96(6):919-926. doi: 10.1007/s12041-017-0856-x. J Genet. 2017. PMID: 29321350 Free article.

2

In silico analysis of the structural and functional implications of SLC19A1 R27H polymorphism.

Naushad SM, Rama Devi AR, Hussain T, Alrokayan SA, Janaki Ramaiah M, Kutala VK. Naushad SM, et al. Among authors: rama devi ar. J Genet. 2019 Sep;98:85. J Genet. 2019. PMID: 31544789 Free article.

3

Relationship between methionine synthase, methionine synthase reductase genetic polymorphisms and deep vein thrombosis among South Indians.

Naushad SM, Jain Jamal MN, Prasad CK, Rama Devi AR. Naushad SM, et al. Among authors: rama devi ar. Clin Chem Lab Med. 2008;46(1):73-9. doi: 10.1515/CCLM.2008.021. Clin Chem Lab Med. 2008. PMID: 18034637

4

Identification and in Silico Characterization of a Novel CASK c.2546T>C (p.V849A) Mutation in a Male Infant with Pontocerebellar Hypoplasia.

Rama Devi AR, Lingappa L, Naushad SM. Rama Devi AR, et al. Ann Indian Acad Neurol. 2019 Oct-Dec;22(4):523-524. doi: 10.4103/aian.AIAN_2_19. Epub 2019 Oct 25. Ann Indian Acad Neurol. 2019. PMID: 31736593 Free PMC article. No abstract available.

5

Newborn screening in India.

Rama Devi AR, Naushad SM. Rama Devi AR, et al. Indian J Pediatr. 2004 Feb;71(2):157-60. doi: 10.1007/BF02723099. Indian J Pediatr. 2004. PMID: 15053381

6

Spectrum of SMPD1 mutations in Asian-Indian patients with acid sphingomyelinase (ASM)-deficient Niemann-Pick disease.

Ranganath P, Matta D, Bhavani GS, Wangnekar S, Jain JM, Verma IC, Kabra M, Puri RD, Danda S, Gupta N, Girisha KM, Sankar VH, Patil SJ, Ramadevi AR, Bhat M, Gowrishankar K, Mandal K, Aggarwal S, Tamhankar PM, Tilak P, Phadke SR, Dalal A. Ranganath P, et al. Am J Med Genet A. 2016 Oct;170(10):2719-30. doi: 10.1002/ajmg.a.37817. Epub 2016 Jun 24. Am J Med Genet A. 2016. PMID: 27338287

7

De novo pericentric inversion of chromosome 4, inv(4)(p16q12) in a boy with piebaldism and mental retardation.

Ramadevi AR, Naik U, Dutta U, Srikanth, Prabhakara K. Ramadevi AR, et al. Am J Med Genet. 2002 Nov 22;113(2):190-2. doi: 10.1002/ajmg.10739. Am J Med Genet. 2002. PMID: 12407711

8

Partial 15q22 trisomy due to segregation of maternal 10;15 reciprocal translocation.

Prabhakara K, Dutta U, Ramadevi AR. Prabhakara K, et al. Indian Pediatr. 2002 Nov;39(11):1050-4. Indian Pediatr. 2002. PMID: 12466578 No abstract available.

9

Molecular genetic analysis of patients from India with hypohidrotic ectodermal dysplasia reveals novel mutations in the EDA and EDAR genes.

RamaDevi AR, Reddy EC, Ranjan S, Bashyam MD. RamaDevi AR, et al. Br J Dermatol. 2008 Jan;158(1):163-7. doi: 10.1111/j.1365-2133.2007.08231.x. Epub 2007 Oct 26. Br J Dermatol. 2008. PMID: 17970812 No abstract available.

10

Familial (11;21)(p13;q22)pat balanced reciprocal translocation in a female child with regression of milestones.

Ramadevi AR, Prabhakara K, Dutta U. Ramadevi AR, et al. Ann Genet. 2002 Jan-Mar;45(1):13-5. doi: 10.1016/s0003-3995(02)01099-7. Ann Genet. 2002. PMID: 11934384

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