Early and severe indirect hyperbilirubinemia as a manifestation of galactosemia.

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Galactosaemia: an unusual cause of chronic bilirubin encephalopathy.A rare galactosemia complication: vitreous hemorrhage.

P2860

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P2860

Early and severe indirect hyperbilirubinemia as a manifestation of galactosemia.

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2010 nî lūn-bûn

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2010年の論文

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2010年学术文章

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2010年学术文章

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2010年学术文章

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2010年学术文章

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2010年学术文章

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2010年学术文章

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2010年學術文章

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2010年學術文章

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name

Early and severe indirect hyperbilirubinemia as a manifestation of galactosemia.

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Early and severe indirect hyperbilirubinemia as a manifestation of galactosemia.

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Early and severe indirect hyperbilirubinemia as a manifestation of galactosemia.

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Early and severe indirect hyperbilirubinemia as a manifestation of galactosemia.

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prefLabel

Early and severe indirect hyperbilirubinemia as a manifestation of galactosemia.

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Early and severe indirect hyperbilirubinemia as a manifestation of galactosemia.

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P1476

Early and severe indirect hyperbilirubinemia as a manifestation of galactosemia.

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P2093

A R Laptook

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C Phornphutkul

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H C Woo

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P2860

The human galactose-1-phosphate uridyltransferase gene

Analysis of common mutations in the galactose-1-phosphate uridyl transferase gene: new assays to increase the sensitivity and specificity of newborn screening for galactosemia

Inborn errors of metabolism in infancy: a guide to diagnosis.

Newborn screening fact sheets.

Introduction to the newborn screening fact sheets.

Conjugated hyperbilirubinemia: screening and treatment in older infants and children.

Some disturbances of erythrocyte metabolism in galactosaemia.

Mutations at the galactose-1-p-uridyltransferase gene in infants with a positive galactosemia newborn screening test.

P2888

jp.2009.136

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295-297

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scholarly article

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10.1038/JP.2009.136

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P921

bilirubin metabolic disorder

galactosemia

Early and severe indirect hyperbilirubinemia as a manifestation of galactosemia.

about

P2860

P2860

Early and severe indirect hyperbilirubinemia as a manifestation of galactosemia.

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