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2. Progressive encephalopathy with edema, hypsarrhythmia, and optic nerve atrophy (PEHO)-like syndrome: what diagnostic characteristics are defining? D'Arrigo S; Grazia BM; Faravelli F; Riva D; Pantaleoni C J Child Neurol; 2005 May; 20(5):454-6. PubMed ID: 15968934 [TBL] [Abstract][Full Text] [Related]
3. PEHO and PEHO-like syndromes: report of five Australian cases. Field MJ; Grattan-Smith P; Piper SM; Thompson EM; Haan EA; Edwards M; James S; Wilkinson I; Adès LC Am J Med Genet A; 2003 Sep; 122A(1):6-12. PubMed ID: 12949965 [TBL] [Abstract][Full Text] [Related]
4. Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy (PEHO syndrome) in two Japanese siblings. Fujimoto S; Yokochi K; Nakano M; Wada Y Neuropediatrics; 1995 Oct; 26(5):270-2. PubMed ID: 8552220 [TBL] [Abstract][Full Text] [Related]
5. Low insulin-like growth factor (IGF-1) in the cerebrospinal fluid of children with progressive encephalopathy, hypsarrhythmia, and optic atrophy (PEHO) syndrome and cerebellar degeneration. Riikonen R; Somer M; Turpeinen U Epilepsia; 1999 Nov; 40(11):1642-8. PubMed ID: 10565594 [TBL] [Abstract][Full Text] [Related]
6. [Progressive encephalopathy with oedema, hypsarrhythmia and optic atrophy (PEHO syndrome). A case report]. Nieto-Barrera M; Nieto-Jiménez M; Díaz-Fernandez F; Campaña-Marchal C; Candau Fernández-Mensaque R Rev Neurol; 2003 Jun 1-15; 36(11):1044-6. PubMed ID: 12808501 [TBL] [Abstract][Full Text] [Related]
7. CCDC88A mutations cause PEHO-like syndrome in humans and mouse. Nahorski MS; Asai M; Wakeling E; Parker A; Asai N; Canham N; Holder SE; Chen YC; Dyer J; Brady AF; Takahashi M; Woods CG Brain; 2016 Apr; 139(Pt 4):1036-44. PubMed ID: 26917597 [TBL] [Abstract][Full Text] [Related]
8. PEHO syndrome (progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy): neuroradiologic findings. Somer M; Salonen O; Pihko H; Norio R AJNR Am J Neuroradiol; 1993; 14(4):861-7. PubMed ID: 8352158 [TBL] [Abstract][Full Text] [Related]
9. Diagnostic criteria and genetics of the PEHO syndrome. Somer M J Med Genet; 1993 Nov; 30(11):932-6. PubMed ID: 8301648 [TBL] [Abstract][Full Text] [Related]
10. [A case of PEHO (progressive encephalopathy with edema, hypsarrhythmia and optic atrophy) syndrome: changes in clinical and neuroradiological findings]. Tanaka M; Tanaka Y; Hamano S; Nara T; Imai M No To Hattatsu; 1997 Nov; 29(6):488-93. PubMed ID: 9394605 [TBL] [Abstract][Full Text] [Related]
11. PEHO syndrome: the endpoint of different genetic epilepsies. Chitre M; Nahorski MS; Stouffer K; Dunning-Davies B; Houston H; Wakeling EL; Brady AF; Zuberi SM; Suri M; Parker APJ; Woods CG J Med Genet; 2018 Dec; 55(12):803-813. PubMed ID: 30287594 [TBL] [Abstract][Full Text] [Related]
12. Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy (PEHO syndrome) in a Turkish child. Tekgül H; Tütüncüoğlu S Turk J Pediatr; 2000; 42(3):246-9. PubMed ID: 11105628 [TBL] [Abstract][Full Text] [Related]
13. Serial MR imaging, diffusion tensor imaging, and MR spectroscopic findings in a child with progressive encephalopathy, edema, hypsarrhythmia, and optic atrophy (PEHO) syndrome. Huisman TA; Klein A; Werner B; Straube T; Boltshauser E AJNR Am J Neuroradiol; 2006 Aug; 27(7):1555-8. PubMed ID: 16908579 [TBL] [Abstract][Full Text] [Related]
14. Epilepsy and the electroencephalogram in progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy (the PEHO syndrome). Somer M; Sainio K Epilepsia; 1993; 34(4):727-31. PubMed ID: 8330584 [TBL] [Abstract][Full Text] [Related]
15. Dutch patients with progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy (PEHO) syndrome. Vanhatalo S; Somer M; Barth PG Neuropediatrics; 2002 Apr; 33(2):100-4. PubMed ID: 12075493 [TBL] [Abstract][Full Text] [Related]
16. Clinical and genetic features of PEHO and PEHO-Like syndromes: A scoping review. Sabaie H; Ahangar NK; Ghafouri-Fard S; Taheri M; Rezazadeh M Biomed Pharmacother; 2020 Nov; 131():110793. PubMed ID: 33152950 [TBL] [Abstract][Full Text] [Related]
17. The PEHO syndrome. Riikonen R Brain Dev; 2001 Nov; 23(7):765-9. PubMed ID: 11701291 [TBL] [Abstract][Full Text] [Related]
18. Infantile cerebello-optic atrophy. Neuropathology of the progressive encephalopathy syndrome with edema, hypsarrhythmia and optic atrophy (the PEHO syndrome). Haltia M; Somer M Acta Neuropathol; 1993; 85(3):241-7. PubMed ID: 8460530 [TBL] [Abstract][Full Text] [Related]
19. De novo dominant variants affecting the motor domain of KIF1A are a cause of PEHO syndrome. Langlois S; Tarailo-Graovac M; Sayson B; Drögemöller B; Swenerton A; Ross CJ; Wasserman WW; van Karnebeek CD Eur J Hum Genet; 2016 Jun; 24(6):949-53. PubMed ID: 26486474 [TBL] [Abstract][Full Text] [Related]
20. PEHO Syndrome May Represent Phenotypic Expansion at the Severe End of the Early-Onset Encephalopathies. Gawlinski P; Posmyk R; Gambin T; Sielicka D; Chorazy M; Nowakowska B; Jhangiani SN; Muzny DM; Bekiesinska-Figatowska M; Bal J; Boerwinkle E; Gibbs RA; Lupski JR; Wiszniewski W Pediatr Neurol; 2016 Jul; 60():83-7. PubMed ID: 27343026 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]