Wernicke's Encephalopathy in a Patient with Peptic Ulcer Disease.

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Wernicke's encephalopathy: expanding the diagnostic toolbox.Thiamine pyrophosphokinase deficiency in encephalopathic children with defects in the pyruvate oxidation pathway Elevated Lactate Secondary to Gastrointestinal Beriberi

P2860

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P2860

Wernicke's Encephalopathy in a Patient with Peptic Ulcer Disease.

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http://www.wikidata.org/entity/Q42797992

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2011 nî lūn-bûn

@nan

2011年の論文

@ja

2011年論文

@yue

2011年論文

@zh-hant

2011年論文

@zh-hk

2011年論文

@zh-mo

2011年論文

@zh-tw

2011年论文

@wuu

2011年论文

@zh

2011年论文

@zh-cn

name

Wernicke's Encephalopathy in a Patient with Peptic Ulcer Disease.

@en

Wernicke's Encephalopathy in a Patient with Peptic Ulcer Disease.

@nl

type

Item

label

Wernicke's Encephalopathy in a Patient with Peptic Ulcer Disease.

@en

Wernicke's Encephalopathy in a Patient with Peptic Ulcer Disease.

@nl

prefLabel

Wernicke's Encephalopathy in a Patient with Peptic Ulcer Disease.

@en

Wernicke's Encephalopathy in a Patient with Peptic Ulcer Disease.

@nl

P1476

Wernicke's Encephalopathy in a Patient with Peptic Ulcer Disease.

@en

P2093

Akinori Uruha

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

Shiro Matsubara

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

Tomoji Katoh

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

Toshio Shimizu

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

Yasushi Yamasaki

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

P2860

Cloning of human transketolase cDNAs and comparison of the nucleotide sequence of the coding region in Wernicke-Korsakoff and non-Wernicke-Korsakoff individuals

Abnormality of a thiamine-requiring enzyme in patients with Wernicke-Korsakoff syndrome

Direct genomic PCR sequencing of the high affinity thiamine transporter (SLC19A2) gene identifies three genetic variants in Wernicke Korsakoff syndrome (WKS)

Wernicke's encephalopathy: new clinical settings and recent advances in diagnosis and management.

The natural history and pathophysiology of Wernicke's Encephalopathy and Korsakoff's Psychosis.

The power of the 3' UTR: translational control and development.

Expression and promoter analysis of SLC19A2 in the human intestine.

Wernicke-Korsakoff syndrome in monozygotic twins: a biochemical peculiarity.

P304

156104

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scholarly article

case report

P356

10.1155/2011/156104

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P478

2011

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P577

2011-06-28T00:00:00Z

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51499027

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21765841

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3135057

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Wernicke's Encephalopathy in a Patient with Peptic Ulcer Disease.

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P2860

P2860

Wernicke's Encephalopathy in a Patient with Peptic Ulcer Disease.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P478

P577

P5875

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P478

P577

P5875

P698

P932