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Buket Dalgıç

Gazi University
H指数:27
被引数:3,556

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Correction to: Clinical, laboratory and molecular features of glycogen storage disease type 1a and 1b patients from Turkey: novel mutations and phenotypes

更正:来自土耳其的糖原贮积症1a型和1b型患者的临床、实验室及分子特征:新发突变和表型

2025-09-050
PRE
Clinical, laboratory and molecular features of glycogen storage disease type 1a and 1b patients from Turkey: novel mutations and phenotypes

土耳其糖原贮积症1型和1b型患者的临床、实验室及分子特征:新发突变和表型

2025-08-090
PRE
GIMAP5 deficiency reveals a mammalian ceramide-driven longevity assurance pathway (vol 25, pg 282, 2024)

GIMAP5缺陷揭示了哺乳动物神经酰胺驱动的长寿保证途径 (第25卷,282页,2024页)

2024-02-120
OA
Genetic landscape of pediatric acute liver failure of indeterminate origin
2023-11-168
OAAI
Interim results from an ongoing, open-label, single-arm trial of odevixibat in progressive familial intrahepatic cholestasis

正在进行的odevixibat治疗进行性家族性肝内胆汁淤积症的开放标签单臂试验的中期结果

2023-08-0112
OAAI
Odevixibat treatment in progressive familial intrahepatic cholestasis: a randomised, placebo-controlled, phase 3 trial

Odevixibat治疗进行性家族性肝内胆汁淤积症: 一项随机,安慰剂对照,3期试验

2022-09-0172
OAAI
GIMAP5 maintains liver endothelial cell homeostasis and prevents portal hypertension
2021-05-0621
OAAI
Deep mining of oxysterols and cholestenoic acids in human plasma and cerebrospinal fluid: Quantification using isotope dilution mass spectrometry
2021-04-0111
OAAI
Broadly effective metabolic and immune recovery with C5 inhibition in CHAPLE disease
2021-01-0436
OAAI