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7. Neonatal Hyperekplexia: Is It Still a Diagnostic Challenge? Evidence From a Systematic Review. Falsaperla R; Sortino V; Giacchi V; Saporito MAN; Marino S; Tardino LG; Marino L; Gennaro A; Ruggieri M; Barberi C; Polizzi A J Child Neurol; 2024 Oct; 39(11-12):415-424. PubMed ID: 39223854 [TBL] [Abstract][Full Text] [Related]
8. Hyperekplexia in the first year of life. Koning-Tijssen MA; Brouwer OF Mov Disord; 2000 Nov; 15(6):1293-6. PubMed ID: 11104232 [No Abstract] [Full Text] [Related]
9. Hyperekplexia, a cause of neonatal apnea: a case report. Gherpelli JL; Nogueira AR; Troster EJ; Deutsch AD; Leoné CR; Brotto MW; Diament A; Ramos JL Brain Dev; 1995; 17(2):114-6. PubMed ID: 7625544 [TBL] [Abstract][Full Text] [Related]
10. Sporadic major hyperekplexia in neonates and infants: clinical manifestations and outcome. Shahar E; Raviv R Pediatr Neurol; 2004 Jul; 31(1):30-4. PubMed ID: 15246489 [TBL] [Abstract][Full Text] [Related]
11. Hyperekplexia and other startle syndromes. Saini AG; Pandey S J Neurol Sci; 2020 Sep; 416():117051. PubMed ID: 32721683 [TBL] [Abstract][Full Text] [Related]
12. Hyperekplexia: pedigree studies in two families. Hayashi T; Tachibana H; Kajii T Am J Med Genet; 1991 Aug; 40(2):138-43. PubMed ID: 1897565 [TBL] [Abstract][Full Text] [Related]
13. Persisting hyperekplexia after idiopathic, self-limiting brainstem encephalopathy. van de Warrenburg BP; Cordivari C; Brown P; Bhatia KP Mov Disord; 2007 May; 22(7):1017-20. PubMed ID: 17415799 [TBL] [Abstract][Full Text] [Related]
15. Two Japanese families with hyperekplexia who have a Arg271Gln mutation in the glycine receptor alpha 1 subunit gene. Kimura M; Taketani T; Horie A; Isumi H; Sejima H; Yamaguchi S Brain Dev; 2006 May; 28(4):228-31. PubMed ID: 16478653 [TBL] [Abstract][Full Text] [Related]
16. Sinus node paucity in hyperekplexia. Ozkiraz S; Gokmen Z; Orün UA; Alehan F Indian Pediatr; 2010 Dec; 47(12):1066-8. PubMed ID: 21220806 [TBL] [Abstract][Full Text] [Related]
18. Abnormal neurodevelopment outcome in case of neonatal hyperekplexia secondary to missense mutation in Gupta NP; Verma V; Chopra S; Choudhury V BMJ Case Rep; 2020 Dec; 13(12):. PubMed ID: 33323420 [TBL] [Abstract][Full Text] [Related]
19. Hyperekplexia and trismus due to brainstem encephalopathy. Kellett MW; Humphrey PR; Tedman BM; Steiger MJ J Neurol Neurosurg Psychiatry; 1998 Jul; 65(1):122-5. PubMed ID: 9667574 [TBL] [Abstract][Full Text] [Related]
20. [Clinical and genetic analysis of hyperekplexia in a Chinese child and literature review]. Li H; Yang ZX; Xue J; Qian P; Liu XY Zhonghua Er Ke Za Zhi; 2017 Feb; 55(2):120-124. PubMed ID: 28173650 [No Abstract] [Full Text] [Related] [Next] [New Search]