Long-standing mild hypertransaminasaemia caused by congenital disorder of glycosylation (CDG) type IIx.
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Persistent hypertransaminasemia in asymptomatic children: a stepwise approachTMEM199 Deficiency Is a Disorder of Golgi Homeostasis Characterized by Elevated Aminotransferases, Alkaline Phosphatase, and Cholesterol and Abnormal GlycosylationDefining the phenotype and diagnostic considerations in adults with congenital disorders of N-linked glycosylation.An update on factor XI structure and function.An Unexplained Congenital Disorder of Glycosylation-II in a Child with Neurohepatic Involvement, Hypercholesterolemia and Hypoceruloplasminemia.
P2860
Long-standing mild hypertransaminasaemia caused by congenital disorder of glycosylation (CDG) type IIx.
description
article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 09 December 2008
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Long-standing mild hypertransa ...... glycosylation (CDG) type IIx.
@en
Long-standing mild hypertransaminasaemia caused by congenital disorder of glycosylation
@nl
type
label
Long-standing mild hypertransa ...... glycosylation (CDG) type IIx.
@en
Long-standing mild hypertransaminasaemia caused by congenital disorder of glycosylation
@nl
prefLabel
Long-standing mild hypertransa ...... glycosylation (CDG) type IIx.
@en
Long-standing mild hypertransaminasaemia caused by congenital disorder of glycosylation
@nl
P2093
P2860
P50
P1476
Long-standing mild hypertransa ...... f glycosylation (CDG) type IIx
@en
P2093
L Sturiale
S Pagliardini
T Vinciguerra
P2860
P2888
P304
P356
10.1007/S10545-008-1004-9
P478
31 Suppl 2
P577
2008-12-09T00:00:00Z