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Peter Freisinger

Eberhard Karls University of Tubingen
H指数:52
被引数:8,453

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Mitochondrial diabetes mellitus: real world insights from the GENOMIT registry–a multinational, longitudinal cohort study

线粒体糖尿病:来自GENOMIT登记研究的真实世界见解——一项多国、纵向队列研究

2026-09-010
OAAI
Does hyperphenylalaninemia induce brain glucose hypometabolism? Cerebral spinal fluid findings in treated adult phenylketonuric patients

高苯丙氨酸血症是否会导致脑葡萄糖代谢低下?接受治疗的成人苯丙酮尿症患者的脑脊髓液发现

2024-05-012
OAAI
Impact of genetic and non-genetic factors on phenotypic diversity in NBAS-associated disease

遗传和非遗传因素对NBAS相关疾病表型多样性的影响

2024-03-011
OAAI
Neurological outcome in long-chain hydroxy fatty acid oxidation disorders
2024-01-233
OA
Genetic landscape of pediatric acute liver failure of indeterminate origin
2023-11-168
OAAI
Ketogenic Diet Treatment of Defects in the Mitochondrial Malate Aspartate Shuttle and Pyruvate Carrier
2022-08-3115
OAAI
DNAJC30 defect: a frequent cause of recessive Leber hereditary optic neuropathy and Leigh syndrome

DNAJC30缺陷: 隐性Leber遗传性视神经病变和Leigh综合征的常见原因

BRAIN
IF11.7
2022-02-1125
OAAI
Variants in Mitochondrial ATP Synthase Cause Variable Neurologic Phenotypes
2022-01-2027
OAAI
Inactivity of Peptidase ClpP Causes Primary Accumulation of Mitochondrial Disaggregase ClpX with Its Interacting Nucleoid Proteins, and of mtDNA

肽酶ClpP的失活导致线粒体解聚酶ClpX及其相互作用的类核蛋白和mtDNA的主要积累

CELLS
IF5.2
2021-11-2910
OAAI
The biochemical subtype is a predictor for cognitive function in glutaric aciduria type 1: a national prospective follow-up study (vol 11, 19300, 2021)
2021-10-120
OAAI
The biochemical subtype is a predictor for cognitive function in glutaric aciduria type 1: a national prospective follow-up study
2021-09-2920
OAAI
Long-term efficacy and safety of sapropterin in patients who initiated sapropterin at <4 years of age with phenylketonuria: results of the 3-year extension of the SPARK open-label, multicentre, randomised phase IIIb trial

在4岁以下开始使用sopropterin的苯丙酮尿症患者中sopropterin的长期疗效和安全性: SPARK开放标签,多中心,随机IIIb期试验延长3年的结果

2021-08-0316
OAAI
Impaired complex I repair causes recessive Leber?s hereditary optic neuropathy Sarah L. Stenton, ... , Ilka Wittig, Holger Prokisch ...
2021-03-1551
OAAI
Phenylalanine Effects on Brain Function in Adult Phenylketonuria

苯丙氨酸对成人苯丙酮尿症脑功能的影响

2021-01-1935
OAAI
Hepatorenal Tyrosinaemia: Impact of a Simplified Diet on Metabolic Control and Clinical Outcome
2020-12-318
OAAI
Long-term Outcomes of Individuals With Metabolic Diseases Identified Through Newborn Screening

通过新生儿筛查确定的代谢性疾病个体的长期结果

2020-11-0146
PREAI
Mutations in ATP6V1E1 or ATP6V1A Cause Autosomal-Recessive Cutis Laxa (vol 100, pg 216, 2017)
2020-08-017
OAAI