1 Sinajon P, "The expanding phenotypic spectrum of female SLC9A6 mutation carriers : a case series and review of the literature" 135 : 841-850, 2016
2 Padmanabha H, "Syndrome of X linked intellectual disability, epilepsy, progressive brain atrophy and large head associated with SLC9A6 mutation" 2017 : 2017
3 Coorg R, "Successful treatment of electrographic status epilepticus of sleep with felbamate in a patient with SLC9A6mutation" 53 : 527-531, 2015
4 Gilfillan GD, "SLC9A6 mutations cause X-linked mental retardation, microcephaly, epilepsy, and ataxia, a phenotype mimicking Angelman syndrome" 82 : 1003-1010, 2008
5 Specchio N, "International League Against Epilepsy classification and definition of epilepsy syndromes with onset in childhood : position paper by the ILAE Task Force on Nosology and Definitions" 63 : 1398-1442, 2022
6 Tan WH, "If not Angelman, what is it? A review of Angelman-like syndromes" 164A : 975-992, 2014
7 Kessi M, "Genetic etiologies of the electrical status epilepticus during slow wave sleep : systematic review" 19 : 40-, 2018
8 Gong P, "Genetic etiologies in developmental and/or epileptic encephalopathy with electrical status epilepticus during sleep : cohort study" 12 : 607965-, 2021
9 Pescosolido MF, "Genetic and phenotypic diversity of NHE6 mutations in Christianson syndrome" 76 : 581-593, 2014
10 Parsons MP, "Extrasynaptic NMDA receptor involvement in central nervous system disorders" 82 : 279-293, 2014
1 Sinajon P, "The expanding phenotypic spectrum of female SLC9A6 mutation carriers : a case series and review of the literature" 135 : 841-850, 2016
2 Padmanabha H, "Syndrome of X linked intellectual disability, epilepsy, progressive brain atrophy and large head associated with SLC9A6 mutation" 2017 : 2017
3 Coorg R, "Successful treatment of electrographic status epilepticus of sleep with felbamate in a patient with SLC9A6mutation" 53 : 527-531, 2015
4 Gilfillan GD, "SLC9A6 mutations cause X-linked mental retardation, microcephaly, epilepsy, and ataxia, a phenotype mimicking Angelman syndrome" 82 : 1003-1010, 2008
5 Specchio N, "International League Against Epilepsy classification and definition of epilepsy syndromes with onset in childhood : position paper by the ILAE Task Force on Nosology and Definitions" 63 : 1398-1442, 2022
6 Tan WH, "If not Angelman, what is it? A review of Angelman-like syndromes" 164A : 975-992, 2014
7 Kessi M, "Genetic etiologies of the electrical status epilepticus during slow wave sleep : systematic review" 19 : 40-, 2018
8 Gong P, "Genetic etiologies in developmental and/or epileptic encephalopathy with electrical status epilepticus during sleep : cohort study" 12 : 607965-, 2021
9 Pescosolido MF, "Genetic and phenotypic diversity of NHE6 mutations in Christianson syndrome" 76 : 581-593, 2014
10 Parsons MP, "Extrasynaptic NMDA receptor involvement in central nervous system disorders" 82 : 279-293, 2014
11 Ikeda A, "Epilepsy in Christianson syndrome : two cases of Lennox-Gastaut syndrome and a review of literature" 13 : 100349-, 2019
12 Mathieu ML, "Electrical status epilepticus in sleep, a constitutive feature of Christianson syndrome" 22 : 1124-1132, 2018
13 Rim JH, "Efficient strategy for the molecular diagnosis of intractable early-onset epilepsy using targeted gene sequencing" 11 : 6-, 2018
14 Gardella E, "EEG features in encephalopathy related to status epilepticus during slow sleep" 21 (21): 22-30, 2019
15 van den Munckhof B, "Corticosteroids versus clobazam in epileptic encephalopathy with ESES: a European multicentre randomised controlled clinical trial (RESCUE ESES*)." 21 : 957-, 2020
16 Bosemani T, "Christianson syndrome : spectrum of neuroimaging findings" 45 : 247-251, 2014
17 Liu X, "Case report : novel SLC9A6 splicing variant in a Chinese boy with Christianson syndrome with electrical status epilepticus during sleep" 12 : 796283-, 2022
18 Zanni G, "A novel mutation in the endosomal Na+/H+ exchanger NHE6(SLC9A6)causes Christianson syndrome with electrical status epilepticus during slow-wave sleep(ESES)" 108 : 811-815, 2014
19 Masurel-Paulet A, "A new family with an SLC9A6 mutation expanding the phenotypic spectrum of Christianson syndrome" 170 : 2103-2110, 2016