Hepatocellular Carcinoma in Fanconi-Bickel Syndrome.

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Hepatocellular Carcinoma in Fanconi-Bickel Syndrome.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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2017年學術文章

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name

Hepatocellular Carcinoma in Fanconi-Bickel Syndrome.

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Hepatocellular Carcinoma in Fanconi-Bickel Syndrome.

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Item

label

Hepatocellular Carcinoma in Fanconi-Bickel Syndrome.

@en

Hepatocellular Carcinoma in Fanconi-Bickel Syndrome.

@nl

prefLabel

Hepatocellular Carcinoma in Fanconi-Bickel Syndrome.

@en

Hepatocellular Carcinoma in Fanconi-Bickel Syndrome.

@nl

P1476

Hepatocellular Carcinoma in Fanconi-Bickel Syndrome.

@en

P2093

Allison F O'Neill

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Antonio R Perez-Atayde

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Jennifer Pogoriler

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Robert C Shamberger

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Stephan D Voss

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P2860

The mutation spectrum of the facilitative glucose transporter gene SLC2A2 (GLUT2) in patients with Fanconi-Bickel syndrome

Development of hepatocellular adenomas and carcinomas in mice with liver-specific G6Pase-α deficiency

Fanconi-Bickel syndrome--the original patient and his natural history, historical steps leading to the primary defect, and a review of the literature.

Genetic variant SLC2A2 [corrected] Is associated with risk of cardiovascular disease – assessing the individual and cumulative effect of 46 type 2 diabetes related genetic variants.

Malignant Transformation of Hepatic Adenoma in Glycogen Storage Disease Type-1a: Report of an Exceptional Case Diagnosed on Surveillance Imaging

Fanconi-Bickel syndrome and autosomal recessive proximal tubulopathy with hypercalciuria (ARPTH) are allelic variants caused by GLUT2 mutations.

Hepatocellular carcinoma arising in adenoma: similar immunohistochemical and cytogenetic features in adenoma and hepatocellular carcinoma portions of the tumor.

Fanconi-Bickel syndrome versus osteogenesis imperfeeta: An Iranian case with a novel mutation in glucose transporter 2 gene, and review of literature.

Genetic risk score of 46 type 2 diabetes risk variants associates with changes in plasma glucose and estimates of pancreatic β-cell function over 5 years of follow-up.

Fanconi-Bickel syndrome as an example of marked allelic heterogeneity.

P304

84-90

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P31

scholarly article

P356

10.1177/1093526617693540

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P433

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P478

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P577

2017-01-01T00:00:00Z

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P698

28382841

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