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Lissencephaly presenting with congenital hypothyroidism.
Kumar S, Suthar R, Panigrahi I, Marwaha RK. Kumar S, et al. Among authors: suthar r. J Pediatr Endocrinol Metab. 2013;26(11-12):1175-7. doi: 10.1515/jpem-2013-0102. J Pediatr Endocrinol Metab. 2013. PMID: 23751382
Niemann-Pick Disease: An Underdiagnosed Lysosomal Storage Disorder.
Panigrahi I, Dhanorkar M, Suthar R, Kumar C, Baalaaji M, Thapa BR, Kalra J. Panigrahi I, et al. Among authors: suthar r. Case Rep Genet. 2019 Apr 21;2019:3108093. doi: 10.1155/2019/3108093. eCollection 2019. Case Rep Genet. 2019. PMID: 31139477 Free PMC article.
Identification of novel pathogenic variants in the GCDH gene and assessment of neurodevelopmental outcomes in 24 children with glutaric aciduria type 1.
Paria P, Saini AG, Attri S, Kaur R, Malhi P, Didwal G, Kasinathan A, Bhatia P, Sahu JK, Suthar R, Saini L, Vyas S, Panigrahi I, Sankhyan N. Paria P, et al. Among authors: suthar r. Eur J Paediatr Neurol. 2022 Jul;39:49-58. doi: 10.1016/j.ejpn.2022.05.005. Epub 2022 May 24. Eur J Paediatr Neurol. 2022. PMID: 35662016
196 results