These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
349 related articles for article (PubMed ID: 26677014)
41. PRRT2 mutation in Japanese children with benign infantile epilepsy. Okumura A; Shimojima K; Kubota T; Abe S; Yamashita S; Imai K; Okanishi T; Enoki H; Fukasawa T; Tanabe T; Dibbens LM; Shimizu T; Yamamoto T Brain Dev; 2013 Aug; 35(7):641-6. PubMed ID: 23131349 [TBL] [Abstract][Full Text] [Related]
42. Emergence of lingual dystonia and strabismus in early-onset SCN8A self-limiting familial infantile epilepsy. Ancora C; Ortigoza-Escobar JD; Valletti MA; Furia F; Nielsen JEK; Møller RS; Gardella E Epileptic Disord; 2024 Apr; 26(2):219-224. PubMed ID: 38436508 [TBL] [Abstract][Full Text] [Related]
43. Atypical course in individuals from Spanish families with benign familial infantile seizures and mutations in the PRRT2 gene. Guerrero-López R; Ortega-Moreno L; Giráldez BG; Alarcón-Morcillo C; Sánchez-Martín G; Nieto-Barrera M; Gutiérrez-Delicado E; Gómez-Garre P; Martínez-Bermejo A; García-Peñas JJ; Serratosa JM Epilepsy Res; 2014 Oct; 108(8):1274-8. PubMed ID: 25060993 [TBL] [Abstract][Full Text] [Related]
44. Mutations in PRRT2 result in paroxysmal dyskinesias with marked variability in clinical expression. Liu Q; Qi Z; Wan XH; Li JY; Shi L; Lu Q; Zhou XQ; Qiao L; Wu LW; Liu XQ; Yang W; Liu Y; Cui LY; Zhang X J Med Genet; 2012 Feb; 49(2):79-82. PubMed ID: 22209761 [TBL] [Abstract][Full Text] [Related]
45. A Girl with PRRT2 Mutation Presenting with Benign Familial Infantile Seizures Followed by Autistic Regression. Zhang L; Wan ZX; Zhu JY; Liu HJ; Sun J; Zou XH; Zhang T; Li Y Case Rep Pediatr; 2024; 2024():5539799. PubMed ID: 38406554 [TBL] [Abstract][Full Text] [Related]
46. PRRT2 benign familial infantile seizures (BFIS) with atypical evolution to encephalopathy related to status epilepticus during sleep (ESES). Cossu A; Santos JL; Galati G; Nikanorova M; Costa P; Mang Y; Silahtaroglu A; Rubboli G; Tommerup N; Dalla Bernardina B; Møller RS; Cantalupo G; Gardella E Neurol Sci; 2023 Jun; 44(6):2173-2176. PubMed ID: 36913149 [TBL] [Abstract][Full Text] [Related]
47. Novel familial cases of ICCA (infantile convulsions with paroxysmal choreoathetosis) syndrome. Rochette J; Roll P; Fu YH; Lemoing AG; Royer B; Roubertie A; Berquin P; Motte J; Wong SW; Hunter A; Robaglia-Schlupp A; Ptacek LJ; Szepetowski P Epileptic Disord; 2010 Sep; 12(3):199-204. PubMed ID: 20716510 [TBL] [Abstract][Full Text] [Related]
48. Penetrance estimation of PRRT2 variants in paroxysmal kinesigenic dyskinesia and infantile convulsions. Chen Y; Chen D; Zhao S; Liu G; Li H; Wu ZY Front Med; 2021 Dec; 15(6):877-886. PubMed ID: 34825340 [TBL] [Abstract][Full Text] [Related]
49. Benign infantile convulsion as a diagnostic clue of paroxysmal kinesigenic dyskinesia: a case series. Matsumoto N; Takahashi S; Okayama A; Araki A; Azuma H J Med Case Rep; 2014 Jun; 8():174. PubMed ID: 24886244 [TBL] [Abstract][Full Text] [Related]
50. The evolving spectrum of PRRT2-associated paroxysmal diseases. Ebrahimi-Fakhari D; Saffari A; Westenberger A; Klein C Brain; 2015 Dec; 138(Pt 12):3476-95. PubMed ID: 26598493 [TBL] [Abstract][Full Text] [Related]
52. The clinical and genetic spectrum in infants with (an) unprovoked cluster(s) of focal seizures. van Roest A; Van de Vel A; Lederer D; Ceulemans B Eur J Paediatr Neurol; 2020 Jan; 24():148-153. PubMed ID: 31901402 [TBL] [Abstract][Full Text] [Related]
54. PRRT2 mutations are the major cause of benign familial infantile seizures. Schubert J; Paravidino R; Becker F; Berger A; Bebek N; Bianchi A; Brockmann K; Capovilla G; Dalla Bernardina B; Fukuyama Y; Hoffmann GF; Jurkat-Rott K; Anttonen AK; Kurlemann G; Lehesjoki AE; Lehmann-Horn F; Mastrangelo M; Mause U; Müller S; Neubauer B; Püst B; Rating D; Robbiano A; Ruf S; Schroeder C; Seidel A; Specchio N; Stephani U; Striano P; Teichler J; Turkdogan D; Vigevano F; Viri M; Bauer P; Zara F; Lerche H; Weber YG Hum Mutat; 2012 Oct; 33(10):1439-43. PubMed ID: 22623405 [TBL] [Abstract][Full Text] [Related]
55. Girl with a PRRT2 mutation and infantile focal epilepsy with bilateral spikes. Torisu H; Watanabe K; Shimojima K; Sugawara M; Sanefuji M; Ishizaki Y; Sakai Y; Yamashita H; Yamamoto T; Hara T Brain Dev; 2014 Apr; 36(4):342-5. PubMed ID: 23768507 [TBL] [Abstract][Full Text] [Related]
56. PRRT2 gene mutations: from paroxysmal dyskinesia to episodic ataxia and hemiplegic migraine. Gardiner AR; Bhatia KP; Stamelou M; Dale RC; Kurian MA; Schneider SA; Wali GM; Counihan T; Schapira AH; Spacey SD; Valente EM; Silveira-Moriyama L; Teive HA; Raskin S; Sander JW; Lees A; Warner T; Kullmann DM; Wood NW; Hanna M; Houlden H Neurology; 2012 Nov; 79(21):2115-21. PubMed ID: 23077024 [TBL] [Abstract][Full Text] [Related]
57. [Familial and non-familial benign infantile seizures: A homogeneous entity?]. Bourel-Ponchel E; Le Moing AG; Delignières A; De Broca A; Wallois F; Berquin P Rev Neurol (Paris); 2011; 167(8-9):592-9. PubMed ID: 21592539 [TBL] [Abstract][Full Text] [Related]
58. Mutations in PRRT2 are not a common cause of infantile epileptic encephalopathies. Heron SE; Ong YS; Yendle SC; McMahon JM; Berkovic SF; Scheffer IE; Dibbens LM Epilepsia; 2013 May; 54(5):e86-9. PubMed ID: 23566103 [TBL] [Abstract][Full Text] [Related]
59. Paroxysmal kinesigenic dyskinesia and generalized seizures: clinical and genetic analysis in a Spanish pedigree. Cuenca-Leon E; Cormand B; Thomson T; Macaya A Neuropediatrics; 2002 Dec; 33(6):288-93. PubMed ID: 12571782 [TBL] [Abstract][Full Text] [Related]
60. Clinical and polygraphic study of familial paroxysmal kinesigenic dyskinesia with PRRT2 mutation. Fabbri M; Marini C; Bisulli F; Di Vito L; Elia A; Guerrini R; Mei D; Tinuper P Epileptic Disord; 2013 Jun; 15(2):123-7. PubMed ID: 23771590 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]