4.4 Article

Fructose-1,6-bisphosphatase deficiency causes fatty liver disease and requires long-term hepatic follow-up

相关参考文献

注意:仅列出部分参考文献,下载原文获取全部文献信息。
Review Gastroenterology & Hepatology

Inborn errors of metabolism in the differential diagnosis of fatty liver disease

Yilmaz Yildiz et al.

TURKISH JOURNAL OF GASTROENTEROLOGY (2020)

Review Biochemistry & Molecular Biology

Gluconeogenesis in cancer cells - Repurposing of a starvation-induced metabolic pathway?

Gabriele Grasmann et al.

BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER (2019)

Review Genetics & Heredity

Genetic analysis of patients with fructose-1,6-bisphosphatase deficiency

Franciele Cabral Pinheiro et al.

Article Endocrinology & Metabolism

Exon 2 deletion represents a common mutation in Turkish patients with fructose-1,6-bisphosphatase deficiency

Mustafa Kilic et al.

METABOLIC BRAIN DISEASE (2019)

Review Gastroenterology & Hepatology

Paediatric fatty liver disease (PeFLD): All is not NAFLD - Pathophysiological insights and approach to management

Robert Hegarty et al.

JOURNAL OF HEPATOLOGY (2018)

Article Medicine, General & Internal

Novel fructose bisphosphatase 1 gene mutation presenting as recurrent episodes of vomiting in an Indian child

A. G. Sharma et al.

JOURNAL OF POSTGRADUATE MEDICINE (2018)

Review Biochemistry & Molecular Biology

Mechanisms of NAFLD development and therapeutic strategies

Scott L. Friedman et al.

NATURE MEDICINE (2018)

Article Biochemistry & Molecular Biology

Clinical and Molecular Characterization of Patients with Fructose 1,6-Bisphosphatase Deficiency

Niu Li et al.

INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (2017)

Article Endocrinology & Metabolism

Fructose-1,6-bisphosphatase deficiency caused by a novel homozygous Alu element insertion in the FBP1 gene and delayed diagnosis

Somashekara Hosaagrahara Ramakrishna et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM (2017)

Article Endocrinology & Metabolism

Genetic analysis of fructose-1,6-bisphosphatase (FBPase) deficiency in nine consanguineous Pakistani families

Sadaqat Ijaz et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM (2017)

Article Endocrinology & Metabolism

Fructose 1,6-bisphosphatase deficiency: clinical, biochemical and genetic features in French patients

Elise Lebigot et al.

JOURNAL OF INHERITED METABOLIC DISEASE (2015)

Article Multidisciplinary Sciences

Fructose-1,6-bisphosphatase opposes renal carcinoma progression

Bo Li et al.

NATURE (2014)

Article Gastroenterology & Hepatology

Molecular characterization of hepatocellular adenomas developed in patients with glycogen storage disease type I

Julien Calderaro et al.

JOURNAL OF HEPATOLOGY (2013)

Article Endocrinology & Metabolism

Recurrent infantile hypoglycemia due to combined fructose-1,6-diphosphatase deficiency and growth hormone deficiency

Dania Takagi et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM (2013)

Review Gastroenterology & Hepatology

Secondary causes of nonalcoholic fatty liver disease

Jacob M. Kneeman et al.

THERAPEUTIC ADVANCES IN GASTROENTEROLOGY (2012)

Article Emergency Medicine

Gluconeogenesis Defect Presenting With Resistant Hyperglycemia and Acidosis Mimicking Diabetic Ketoacidosis

Muhammet Sukru Paksu et al.

PEDIATRIC EMERGENCY CARE (2011)

Review Endocrinology & Metabolism

Glycogen storage disease type I and G6Pase-β deficiency: etiology and therapy

Janice Y. Chou et al.

NATURE REVIEWS ENDOCRINOLOGY (2010)

Article Pediatrics

Novel FBP1 gene mutations in Arab patients with fructose-1,6-bisphosphatase deficiency

Muhammad Faiyaz-Ul-Haque et al.

EUROPEAN JOURNAL OF PEDIATRICS (2009)