日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

A Case of Early Infantile Epileptic Encephalopathy Due to KCNQ2 Gene Mutation Presenting With Episodes of Hiccups

一例因KCNQ2基因突变引起的早期婴儿癫痫性脑病,表现为呃逆发作

Alan, Serdar; Vural, Sevde Nur; Aliefendioglu, Didem; Senbil, Nesrin

Novel Mutations in the PC Gene in Patients with Type B Pyruvate Carboxylase Deficiency

B型丙酮酸羧化酶缺乏症患者PC基因的新突变

Ostergaard, Elsebet; Duno, Morten; Møller, Lisbeth Birk; Kalkanoglu-Sivri, H Serap; Dursun, Ali; Aliefendioglu, Didem; Leth, Helle; Dahl, Marianne; Christensen, Ernst; Wibrand, Flemming

Mutation spectrum of fumarylacetoacetase gene and clinical aspects of tyrosinemia type I disease

延胡索酰乙酰乙酸酶基因突变谱及I型酪氨酸血症的临床表现

Dursun, A; Ozgül, R K; Sivri, S; Tokatlı, A; Güzel, A; Mesci, L; Kılıç, M; Aliefendioglu, D; Ozçay, F; Gündüz, M; Coşkun, T

Endothelin 1 concentrations in infants with meconium stained amniotic fluid

胎粪污染羊水中内皮素-1浓度

Yigit, S; Tekinalp, G; Oran, O; Yurdakok, M; Aliefendioglu, D; Gurgey, A