Hyperinsulinemic hypoglycemia: clinical, molecular and therapeutical novelties.

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Hyperinsulinemic hypoglycemia: clinical, molecular and therapeutical novelties.

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2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年論文

@yue

2017年論文

@zh-hant

2017年論文

@zh-hk

2017年論文

@zh-mo

2017年論文

@zh-tw

2017年论文

@wuu

2017年论文

@zh

2017年论文

@zh-cn

name

Hyperinsulinemic hypoglycemia: clinical, molecular and therapeutical novelties.

@en

Hyperinsulinemic hypoglycemia: clinical, molecular and therapeutical novelties.

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type

Item

label

Hyperinsulinemic hypoglycemia: clinical, molecular and therapeutical novelties.

@en

Hyperinsulinemic hypoglycemia: clinical, molecular and therapeutical novelties.

@nl

prefLabel

Hyperinsulinemic hypoglycemia: clinical, molecular and therapeutical novelties.

@en

Hyperinsulinemic hypoglycemia: clinical, molecular and therapeutical novelties.

@nl

P1476

Hyperinsulinemic hypoglycemia: clinical, molecular and therapeutical novelties.

@en

P2093

Arianna Maiorana

http://www.w3.org/2001/XMLSchema#string

Carlo Dionisi-Vici

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P2860

Acute insulin responses to leucine in children with the hyperinsulinism/hyperammonemia syndrome

TRMT10A dysfunction is associated with abnormalities in glucose homeostasis, short stature and microcephaly

Long-term medical treatment in congenital hyperinsulinism: a descriptive analysis in a large cohort of patients from different clinical centers

Galactose supplementation in phosphoglucomutase-1 deficiency; review and outlook for a novel treatable CDG

Altered Phenotype of β-Cells and Other Pancreatic Cell Lineages in Patients With Diffuse Congenital Hyperinsulinism in Infancy Caused by Mutations in the ATP-Sensitive K-Channel.

Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism

Preoperative evaluation of infants with focal or diffuse congenital hyperinsulinism by intravenous acute insulin response tests and selective pancreatic arterial calcium stimulation

A novel syndrome of autosomal-dominant hyperinsulinemic hypoglycemia linked to a mutation in the human insulin receptor gene

Hyperinsulinism and hyperammonemia in infants with regulatory mutations of the glutamate dehydrogenase gene

Defective glucose transport across the blood-brain barrier as a cause of persistent hypoglycorrhachia, seizures, and developmental delay

P2888

s10545-017-0059-x

P304

531-542

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P31

scholarly article

P356

10.1007/S10545-017-0059-X

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P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

C Dionisi-Vici

Arianna Maiorana

P577

2017-06-27T00:00:00Z

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P698

28656511

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P921

hypoglycemia