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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. Among authors: gupta n. 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
Neuroimaging in mental retardation.
Pandey A, Phadke SR, Gupta N, Phadke RV. Pandey A, et al. Among authors: gupta n. Indian J Pediatr. 2004 Mar;71(3):203-9. doi: 10.1007/BF02724269. Indian J Pediatr. 2004. PMID: 15080405
Unbalanced X; autosome translocation.
Gupta N, Goel H, Phadke SR. Gupta N, et al. Indian J Pediatr. 2006 Sep;73(9):840-2. doi: 10.1007/BF02790399. Indian J Pediatr. 2006. PMID: 17006048
Maffucci syndrome.
Gupta N, Kabra M. Gupta N, et al. Indian Pediatr. 2007 Feb;44(2):149-50. Indian Pediatr. 2007. PMID: 17351310 Free article. No abstract available.
Pyle metaphyseal dysplasia.
Gupta N, Kabra M, Das CJ, Gupta AK. Gupta N, et al. Among authors: gupta ak. Indian Pediatr. 2008 Apr;45(4):323-5. Indian Pediatr. 2008. PMID: 18451455 Free article.
8,613 results