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23. Neonatal seizures and subsequent epilepsy. Watanabe K; Kuroyanagi M; Hara K; Miyazaki S Brain Dev; 1982; 4(5):341-6. PubMed ID: 7137512 [TBL] [Abstract][Full Text] [Related]
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25. [Autosomal dominant cerebral seizures in the 6th month of life with benign outcome]. Kurlemann G; Vossschulte P; Weglage J; Palm DG Klin Padiatr; 1995; 207(1):17-8. PubMed ID: 7885012 [TBL] [Abstract][Full Text] [Related]
26. [Electroencephalographic diagnosis of the idiopathic generalized epilepsies of childhood]. Bauzano-Poley E; Rodríguez-Barrionuevo AC Rev Neurol; 2001 Feb 16-28; 32(4):365-72. PubMed ID: 11333394 [TBL] [Abstract][Full Text] [Related]
27. [Phenotype study of SCN2A gene related epilepsy]. Zeng Q; Zhang YH; Yang XL; Zhang J; Liu AJ; Liu XY; Jiang YW; Wu XR Zhonghua Er Ke Za Zhi; 2018 Jul; 56(7):518-523. PubMed ID: 29996185 [No Abstract] [Full Text] [Related]
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29. Benign familial neonatal convulsions; psychosocial adjustment to the threat of recurrent seizures. Psenka TM; Holden KR Seizure; 1996 Sep; 5(3):243-5. PubMed ID: 8902929 [TBL] [Abstract][Full Text] [Related]
30. Summary of recommendations for the management of infantile seizures: Task Force Report for the ILAE Commission of Pediatrics. Wilmshurst JM; Gaillard WD; Vinayan KP; Tsuchida TN; Plouin P; Van Bogaert P; Carrizosa J; Elia M; Craiu D; Jovic NJ; Nordli D; Hirtz D; Wong V; Glauser T; Mizrahi EM; Cross JH Epilepsia; 2015 Aug; 56(8):1185-97. PubMed ID: 26122601 [TBL] [Abstract][Full Text] [Related]
33. The syndrome of benign familial neonatal seizures. Christodorescu D Neurol Psychiatr (Bucur); 1985; 23(3):207-9. PubMed ID: 4048807 [No Abstract] [Full Text] [Related]
34. Benign familial and non-familial infantile seizures: a study of 64 patients. Caraballo RH; Cersósimo RO; Espeche A; Fejerman N Epileptic Disord; 2003 Mar; 5(1):45-9. PubMed ID: 12773296 [TBL] [Abstract][Full Text] [Related]
35. Autosomal dominant benign neonatal seizures. Cunniff C; Wiedlin N; Jones KL Am J Med Genet; 1988 Aug; 30(4):963-6. PubMed ID: 3189416 [TBL] [Abstract][Full Text] [Related]
36. Neonatal nonepileptic myoclonus is a prominent clinical feature of KCNQ2 gain-of-function variants R201C and R201H. Mulkey SB; Ben-Zeev B; Nicolai J; Carroll JL; Grønborg S; Jiang YH; Joshi N; Kelly M; Koolen DA; Mikati MA; Park K; Pearl PL; Scheffer IE; Spillmann RC; Taglialatela M; Vieker S; Weckhuysen S; Cooper EC; Cilio MR Epilepsia; 2017 Mar; 58(3):436-445. PubMed ID: 28139826 [TBL] [Abstract][Full Text] [Related]
37. Seizure characteristics in chromosome 20 benign familial neonatal convulsions. Ronen GM; Rosales TO; Connolly M; Anderson VE; Leppert M Neurology; 1993 Jul; 43(7):1355-60. PubMed ID: 8327138 [TBL] [Abstract][Full Text] [Related]
38. [Clinical characteristics and genetic features of benign infantile epilepsy with PRRT2 mutation]. Chen CH; Wu HS; Wang XH; Wang HM; Zhang S; Lyu JL; Ren XT; Fang F; Chen GH Zhonghua Er Ke Za Zhi; 2018 Nov; 56(11):818-823. PubMed ID: 30392205 [No Abstract] [Full Text] [Related]
39. Benign familial neonatal convulsions followed by benign epilepsy with centrotemporal spikes in two siblings. Maihara T; Tsuji M; Higuchi Y; Hattori H Epilepsia; 1999 Jan; 40(1):110-3. PubMed ID: 9924911 [TBL] [Abstract][Full Text] [Related]
40. Benign infantile familial convulsions: natural history of a case and clinical characteristics of a large Italian family. Giordano L; Accorsi P; Valseriati D; Tiberti A; Menegati E; Zara F; Vignoli A; Vigevano F Neuropediatrics; 1999 Apr; 30(2):99-101. PubMed ID: 10401694 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]