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Page 1
GRIN2D variants in three cases of developmental and epileptic encephalopathy.
Tsuchida N, Hamada K, Shiina M, Kato M, Kobayashi Y, Tohyama J, Kimura K, Hoshino K, Ganesan V, Teik KW, Nakashima M, Mitsuhashi S, Mizuguchi T, Takata A, Miyake N, Saitsu H, Ogata K, Miyatake S, Matsumoto N. Tsuchida N, et al. Among authors: ganesan v. Clin Genet. 2018 Dec;94(6):538-547. doi: 10.1111/cge.13454. Clin Genet. 2018. PMID: 30280376
Novel biallelic SZT2 mutations in 3 cases of early-onset epileptic encephalopathy.
Tsuchida N, Nakashima M, Miyauchi A, Yoshitomi S, Kimizu T, Ganesan V, Teik KW, Ch'ng GS, Kato M, Mizuguchi T, Takata A, Miyatake S, Miyake N, Osaka H, Yamagata T, Nakajima H, Saitsu H, Matsumoto N. Tsuchida N, et al. Among authors: ganesan v. Clin Genet. 2018 Feb;93(2):266-274. doi: 10.1111/cge.13061. Epub 2017 Sep 18. Clin Genet. 2018. PMID: 28556953
Quality of life of children with tuberous sclerosis complex.
Fong CY, Ng K, Kong AN, Ong LC, Rithauddin MA, Thong MK, Ganesan V, Heng HS, Teh CM, Yahya N. Fong CY, et al. Among authors: ganesan v. Arch Dis Child. 2019 Oct;104(10):972-978. doi: 10.1136/archdischild-2018-316394. Epub 2019 May 23. Arch Dis Child. 2019. PMID: 31122923
Advance care plan discussion among parents of children with cerebral palsy.
Khalid F, Ng Voon SI, Ong LC, Lim WK, Li L, Adnan A, Ganesan V, Teh CM, Fong CY. Khalid F, et al. Among authors: ganesan v. Dev Med Child Neurol. 2022 Aug;64(8):1025-1033. doi: 10.1111/dmcn.15184. Epub 2022 Feb 25. Dev Med Child Neurol. 2022. PMID: 35213736 Free article.
539 results