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2020 | 1 |
2023 | 2 |
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Page 1
Electroclinical Features of Epilepsy in Kleefstra Syndrome.
Neuropediatrics. 2023 Dec;54(6):433-438. doi: 10.1055/s-0043-1775977. Epub 2023 Oct 6.
Neuropediatrics. 2023.
PMID: 37802085
Quantitative MRI-Based Analysis Identifies Developmental Limbic Abnormalities in PCDH19 Encephalopathy.
Lenge M, Marini C, Canale E, Napolitano A, De Masi S, Trivisano M, Mei D, Longo D, Rossi Espagnet MC, Lucenteforte E; PCDH19 Clinical Study Group; Barba C, Specchio N, Guerrini R.
Lenge M, et al. Among authors: canale e.
Cereb Cortex. 2020 Oct 1;30(11):6039-6050. doi: 10.1093/cercor/bhaa177.
Cereb Cortex. 2020.
PMID: 32582916
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Exome Analysis Reveals Novel Missense and Deletion Variants in the CC2D2A Gene as Causative of Joubert Syndrome.
Cabrita Pinto RL, Viaggi S, Canale E, Martinez Popple M, Capra V, Conteduca G, Testa B, Coviello D, Covone AE.
Cabrita Pinto RL, et al. Among authors: canale e.
Genes (Basel). 2023 Mar 28;14(4):810. doi: 10.3390/genes14040810.
Genes (Basel). 2023.
PMID: 37107568
Free PMC article.
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