The clinical and genetic spectrum in infants with (an) unprovoked cluster(s) of focal seizures
Self-limited (familial) infantile epilepsy (S(F)IE), formerly known as benign (familial) infantile convulsions (B(F)IC), is an infantile cluster epilepsy with in rule a complete recovery. This form of epilepsy is most often caused by variations in the PRRT2 gene (OMIM #605751).
Autor*in: |
van Roest, Aalt [verfasserIn] |
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Format: |
E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2020 |
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Schlagwörter: |
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Umfang: |
6 |
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Übergeordnetes Werk: |
Enthalten in: Biologically active vallesamine, strychnan, and rhazinilam alkaloids from - Lim, Jun-Lee ELSEVIER, 2015, ejpn : official journal of the European Paediatric Neurology Society, Burlington, Mass |
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Übergeordnetes Werk: |
volume:24 ; year:2020 ; pages:148-153 ; extent:6 |
Links: |
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DOI / URN: |
10.1016/j.ejpn.2019.12.003 |
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ELV049413058 |
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10.1016/j.ejpn.2019.12.003 doi /cbs_pica/cbs_olc/import_discovery/elsevier/einzuspielen/GBV00000000001051.pica (DE-627)ELV049413058 (ELSEVIER)S1090-3798(19)30423-4 DE-627 ger DE-627 rakwb eng 580 540 VZ BIODIV DE-30 fid 42.00 bkl van Roest, Aalt verfasserin aut The clinical and genetic spectrum in infants with (an) unprovoked cluster(s) of focal seizures 2020 6 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Self-limited (familial) infantile epilepsy (S(F)IE), formerly known as benign (familial) infantile convulsions (B(F)IC), is an infantile cluster epilepsy with in rule a complete recovery. This form of epilepsy is most often caused by variations in the PRRT2 gene (OMIM #605751). PRRT2 Elsevier Familial Elsevier Focal seizures Elsevier Infantile seizures Elsevier Clustered seizures Elsevier Self-limited Elsevier Van de Vel, Anouk oth Lederer, Damien oth Ceulemans, Berten oth Enthalten in Harcourt Lim, Jun-Lee ELSEVIER Biologically active vallesamine, strychnan, and rhazinilam alkaloids from 2015 ejpn : official journal of the European Paediatric Neurology Society Burlington, Mass (DE-627)ELV001176439 volume:24 year:2020 pages:148-153 extent:6 https://doi.org/10.1016/j.ejpn.2019.12.003 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U FID-BIODIV SSG-OLC-PHA 42.00 Biologie: Allgemeines VZ AR 24 2020 148-153 6 |
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10.1016/j.ejpn.2019.12.003 doi /cbs_pica/cbs_olc/import_discovery/elsevier/einzuspielen/GBV00000000001051.pica (DE-627)ELV049413058 (ELSEVIER)S1090-3798(19)30423-4 DE-627 ger DE-627 rakwb eng 580 540 VZ BIODIV DE-30 fid 42.00 bkl van Roest, Aalt verfasserin aut The clinical and genetic spectrum in infants with (an) unprovoked cluster(s) of focal seizures 2020 6 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Self-limited (familial) infantile epilepsy (S(F)IE), formerly known as benign (familial) infantile convulsions (B(F)IC), is an infantile cluster epilepsy with in rule a complete recovery. This form of epilepsy is most often caused by variations in the PRRT2 gene (OMIM #605751). PRRT2 Elsevier Familial Elsevier Focal seizures Elsevier Infantile seizures Elsevier Clustered seizures Elsevier Self-limited Elsevier Van de Vel, Anouk oth Lederer, Damien oth Ceulemans, Berten oth Enthalten in Harcourt Lim, Jun-Lee ELSEVIER Biologically active vallesamine, strychnan, and rhazinilam alkaloids from 2015 ejpn : official journal of the European Paediatric Neurology Society Burlington, Mass (DE-627)ELV001176439 volume:24 year:2020 pages:148-153 extent:6 https://doi.org/10.1016/j.ejpn.2019.12.003 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U FID-BIODIV SSG-OLC-PHA 42.00 Biologie: Allgemeines VZ AR 24 2020 148-153 6 |
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10.1016/j.ejpn.2019.12.003 doi /cbs_pica/cbs_olc/import_discovery/elsevier/einzuspielen/GBV00000000001051.pica (DE-627)ELV049413058 (ELSEVIER)S1090-3798(19)30423-4 DE-627 ger DE-627 rakwb eng 580 540 VZ BIODIV DE-30 fid 42.00 bkl van Roest, Aalt verfasserin aut The clinical and genetic spectrum in infants with (an) unprovoked cluster(s) of focal seizures 2020 6 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Self-limited (familial) infantile epilepsy (S(F)IE), formerly known as benign (familial) infantile convulsions (B(F)IC), is an infantile cluster epilepsy with in rule a complete recovery. This form of epilepsy is most often caused by variations in the PRRT2 gene (OMIM #605751). PRRT2 Elsevier Familial Elsevier Focal seizures Elsevier Infantile seizures Elsevier Clustered seizures Elsevier Self-limited Elsevier Van de Vel, Anouk oth Lederer, Damien oth Ceulemans, Berten oth Enthalten in Harcourt Lim, Jun-Lee ELSEVIER Biologically active vallesamine, strychnan, and rhazinilam alkaloids from 2015 ejpn : official journal of the European Paediatric Neurology Society Burlington, Mass (DE-627)ELV001176439 volume:24 year:2020 pages:148-153 extent:6 https://doi.org/10.1016/j.ejpn.2019.12.003 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U FID-BIODIV SSG-OLC-PHA 42.00 Biologie: Allgemeines VZ AR 24 2020 148-153 6 |
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The clinical and genetic spectrum in infants with (an) unprovoked cluster(s) of focal seizures |
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Self-limited (familial) infantile epilepsy (S(F)IE), formerly known as benign (familial) infantile convulsions (B(F)IC), is an infantile cluster epilepsy with in rule a complete recovery. This form of epilepsy is most often caused by variations in the PRRT2 gene (OMIM #605751). |
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Self-limited (familial) infantile epilepsy (S(F)IE), formerly known as benign (familial) infantile convulsions (B(F)IC), is an infantile cluster epilepsy with in rule a complete recovery. This form of epilepsy is most often caused by variations in the PRRT2 gene (OMIM #605751). |
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Self-limited (familial) infantile epilepsy (S(F)IE), formerly known as benign (familial) infantile convulsions (B(F)IC), is an infantile cluster epilepsy with in rule a complete recovery. This form of epilepsy is most often caused by variations in the PRRT2 gene (OMIM #605751). |
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The clinical and genetic spectrum in infants with (an) unprovoked cluster(s) of focal seizures |
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