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Sirenomelia: case reports and current concepts of pathogenesis.
Pillay M, Yesodharan D, Narayanan DL, Jojo A, Luiz N, Nampoothiri S. Pillay M, et al. Among authors: narayanan dl. Pediatr Dev Pathol. 2012 Sep-Oct;15(5):403-6. doi: 10.2350/12-05-1199-CC.1. Epub 2012 Jul 20. Pediatr Dev Pathol. 2012. PMID: 22816558
Eight years experience from a skeletal dysplasia referral center in a tertiary hospital in Southern India: a model for the diagnosis and treatment of rare diseases in a developing country.
Nampoothiri S, Yesodharan D, Sainulabdin G, Narayanan D, Padmanabhan L, Girisha KM, Cathey SS, De Paepe A, Malfait F, Syx D, Hennekam RC, Bonafe L, Unger S, Superti-Furga A. Nampoothiri S, et al. Among authors: narayanan d. Am J Med Genet A. 2014 Sep;164A(9):2317-23. doi: 10.1002/ajmg.a.36668. Epub 2014 Jul 14. Am J Med Genet A. 2014. PMID: 25044831
Infantile Systemic Hyalinosis with Mutation in ANTXR2.
Narayanan DL, Phadke SR. Narayanan DL, et al. Indian J Pediatr. 2016 Nov;83(11):1356-1357. doi: 10.1007/s12098-015-1990-1. Epub 2016 Jan 25. Indian J Pediatr. 2016. PMID: 26806203 No abstract available.
Metatropic Dysplasia with a Novel Mutation in TRPV4.
Narayanan DL, Bhavani GS, Girisha KM, Phadke SR. Narayanan DL, et al. Indian Pediatr. 2016 Aug 8;53(8):735-7. doi: 10.1007/s13312-016-0921-1. Indian Pediatr. 2016. PMID: 27567651 Free article.
Hotspots in PTPN11 Gene Among Indian Children With Noonan Syndrome.
Narayanan DL, Pandey H, Moirangthem A, Mandal K, Gupta R, Puri RD, Patil SJ, Phadke SR. Narayanan DL, et al. Indian Pediatr. 2017 Aug 15;54(8):638-643. doi: 10.1007/s13312-017-1125-z. Epub 2017 Jun 4. Indian Pediatr. 2017. PMID: 28607217 Free article.
230 results