Matches in Nanopublications for { ?s ?p "[Three cases with deletion of the whole sodium channel gene cluster (SCN3A, SCN2A, SCN1A, SCN9A, and SCN7A) exhibited a complex epilepsy phenotype that was atypical for Dravet syndrome and suggestive of migrating partial seizures of infancy: early seizure onset (before 2 months of age), severe developmental delay from seizure onset, multifocal interictal spikes, polymorphous focal seizures, and acquired microcephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP1249536.RAjZWOfDhT5qFpITqxDMj9nrZge2OmPS5aw_GXv5vh-BQ130_assertion description "[Three cases with deletion of the whole sodium channel gene cluster (SCN3A, SCN2A, SCN1A, SCN9A, and SCN7A) exhibited a complex epilepsy phenotype that was atypical for Dravet syndrome and suggestive of migrating partial seizures of infancy: early seizure onset (before 2 months of age), severe developmental delay from seizure onset, multifocal interictal spikes, polymorphous focal seizures, and acquired microcephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1249536.RAjZWOfDhT5qFpITqxDMj9nrZge2OmPS5aw_GXv5vh-BQ130_provenance.
- NP1249528.RAEATMb7CUCdTxB5J3ojnjijrOP3HzIhszLuOrMnd57DA130_assertion description "[Three cases with deletion of the whole sodium channel gene cluster (SCN3A, SCN2A, SCN1A, SCN9A, and SCN7A) exhibited a complex epilepsy phenotype that was atypical for Dravet syndrome and suggestive of migrating partial seizures of infancy: early seizure onset (before 2 months of age), severe developmental delay from seizure onset, multifocal interictal spikes, polymorphous focal seizures, and acquired microcephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1249528.RAEATMb7CUCdTxB5J3ojnjijrOP3HzIhszLuOrMnd57DA130_provenance.
- NP1249533.RAPWVaFDwMazY1rHKTeUoINiMjal2IcaHuTlyEs2XOUY0130_assertion description "[Three cases with deletion of the whole sodium channel gene cluster (SCN3A, SCN2A, SCN1A, SCN9A, and SCN7A) exhibited a complex epilepsy phenotype that was atypical for Dravet syndrome and suggestive of migrating partial seizures of infancy: early seizure onset (before 2 months of age), severe developmental delay from seizure onset, multifocal interictal spikes, polymorphous focal seizures, and acquired microcephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1249533.RAPWVaFDwMazY1rHKTeUoINiMjal2IcaHuTlyEs2XOUY0130_provenance.
- NP1249525.RA7DrX_NfW820FzgCoPD_d_aYzQEi5yl-lhMAuU__PCFo130_assertion description "[Three cases with deletion of the whole sodium channel gene cluster (SCN3A, SCN2A, SCN1A, SCN9A, and SCN7A) exhibited a complex epilepsy phenotype that was atypical for Dravet syndrome and suggestive of migrating partial seizures of infancy: early seizure onset (before 2 months of age), severe developmental delay from seizure onset, multifocal interictal spikes, polymorphous focal seizures, and acquired microcephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1249525.RA7DrX_NfW820FzgCoPD_d_aYzQEi5yl-lhMAuU__PCFo130_provenance.
- NP1249526.RA0pBaDOV6Y33C0i93JnVmc0VhFaBcI8IbzkPLAGq0JSc130_assertion description "[Three cases with deletion of the whole sodium channel gene cluster (SCN3A, SCN2A, SCN1A, SCN9A, and SCN7A) exhibited a complex epilepsy phenotype that was atypical for Dravet syndrome and suggestive of migrating partial seizures of infancy: early seizure onset (before 2 months of age), severe developmental delay from seizure onset, multifocal interictal spikes, polymorphous focal seizures, and acquired microcephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1249526.RA0pBaDOV6Y33C0i93JnVmc0VhFaBcI8IbzkPLAGq0JSc130_provenance.
- NP1249532.RA249EqGDGnDZEFqV2Fo4tzn3WTo4Q-813Vpnx75BTcNQ130_assertion description "[Three cases with deletion of the whole sodium channel gene cluster (SCN3A, SCN2A, SCN1A, SCN9A, and SCN7A) exhibited a complex epilepsy phenotype that was atypical for Dravet syndrome and suggestive of migrating partial seizures of infancy: early seizure onset (before 2 months of age), severe developmental delay from seizure onset, multifocal interictal spikes, polymorphous focal seizures, and acquired microcephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1249532.RA249EqGDGnDZEFqV2Fo4tzn3WTo4Q-813Vpnx75BTcNQ130_provenance.