Matches in Nanopublications for { ?s ?p "[Due to their highly differentiated, malformative nature and glioneuronal phenotype, FCD(IIb) share neuropathological characteristics with lesions observed in familial disorders such as cortical tubers present in patients with autosomal dominant tuberous sclerosis complex (TSC), related to mutations in the TSC1 or TSC2 genes, and dysplastic gangliocytomas of the cerebellum found in Cowden disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP529875.RABv2tDCL4SC2_avGrfg9G167Oz4B76SleuUT1La6SnmY130_assertion description "[Due to their highly differentiated, malformative nature and glioneuronal phenotype, FCD(IIb) share neuropathological characteristics with lesions observed in familial disorders such as cortical tubers present in patients with autosomal dominant tuberous sclerosis complex (TSC), related to mutations in the TSC1 or TSC2 genes, and dysplastic gangliocytomas of the cerebellum found in Cowden disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP529875.RABv2tDCL4SC2_avGrfg9G167Oz4B76SleuUT1La6SnmY130_provenance.
- NP203624.RAOiBWZO-rFY3JsOR_kDP8EsDrs0k_Rm4PFiVzsHONMrQ130_assertion description "[Due to their highly differentiated, malformative nature and glioneuronal phenotype, FCD(IIb) share neuropathological characteristics with lesions observed in familial disorders such as cortical tubers present in patients with autosomal dominant tuberous sclerosis complex (TSC), related to mutations in the TSC1 or TSC2 genes, and dysplastic gangliocytomas of the cerebellum found in Cowden disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP203624.RAOiBWZO-rFY3JsOR_kDP8EsDrs0k_Rm4PFiVzsHONMrQ130_provenance.
- NP572285.RAQLpLW4jZct9Iz40u9W3TxzgKv0F2466M82A3S9Z2mWA130_assertion description "[Due to their highly differentiated, malformative nature and glioneuronal phenotype, FCD(IIb) share neuropathological characteristics with lesions observed in familial disorders such as cortical tubers present in patients with autosomal dominant tuberous sclerosis complex (TSC), related to mutations in the TSC1 or TSC2 genes, and dysplastic gangliocytomas of the cerebellum found in Cowden disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP572285.RAQLpLW4jZct9Iz40u9W3TxzgKv0F2466M82A3S9Z2mWA130_provenance.
- NP810152.RAMjMDKtA5GX4iMQHVtKqFlS6Wh072B03uck52xvfcGqI130_assertion description "[Due to their highly differentiated, malformative nature and glioneuronal phenotype, FCD(IIb) share neuropathological characteristics with lesions observed in familial disorders such as cortical tubers present in patients with autosomal dominant tuberous sclerosis complex (TSC), related to mutations in the TSC1 or TSC2 genes, and dysplastic gangliocytomas of the cerebellum found in Cowden disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP810152.RAMjMDKtA5GX4iMQHVtKqFlS6Wh072B03uck52xvfcGqI130_provenance.