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Severe neurodevelopmental disease caused by a homozygous TLK2 variant.
Töpf A, Oktay Y, Balaraju S, Yilmaz E, Sonmezler E, Yis U, Laurie S, Thompson R, Roos A, MacArthur DG, Yaramis A, Güngör S, Lochmüller H, Hiz S, Horvath R. Töpf A, et al. Among authors: hiz s. Eur J Hum Genet. 2020 Mar;28(3):383-387. doi: 10.1038/s41431-019-0519-x. Eur J Hum Genet. 2020. PMID: 31558842 Free PMC article.
Severe neurologic involvement of Degos disease in a pediatric patient.
Karaoğlu P, Topçu Y, Bayram E, Yis U, Akarsu S, Atalay E, Koroğlu T, Cakmakçi H, Ozer E, Hız S. Karaoğlu P, et al. Among authors: hiz s. J Child Neurol. 2014 Apr;29(4):550-4. doi: 10.1177/0883073812474692. Epub 2013 Feb 11. J Child Neurol. 2014. PMID: 23400246
Williams Syndrome with Infantile Spasms.
Polat İ, Karaoglu P, Ayanoglu M, Yis U, Hiz S. Polat İ, et al. Among authors: hiz s. Indian J Pediatr. 2015 Aug;82(8):757-8. doi: 10.1007/s12098-015-1740-4. Epub 2015 Mar 14. Indian J Pediatr. 2015. PMID: 25772942 No abstract available.
Life-Threatening and Rare Adverse Effects of Phenytoin.
Polat I, Karaoglu P, Ayanoglu M, Yis U, Hiz S. Polat I, et al. Among authors: hiz s. Pediatr Emerg Care. 2015 Jul;31(7):e3. doi: 10.1097/PEC.0000000000000495. Pediatr Emerg Care. 2015. PMID: 26148111 No abstract available.
44 results