Case report: perioperative management of caesarean section for a parturient with mitochondrial myopathy - Test2 - elhamkhani - TriplyDB

Case report: perioperative management of caesarean section for a parturient with mitochondrial myopathy

Case report: perioperative management of caesarean section for a parturient with mitochondrial myopathy

http://www.wikidata.org/entity/Q33901000

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Case report: perioperative management of caesarean section for a parturient with mitochondrial myopathy

http://www.wikidata.org/entity/Q33901000

description

2017 nî lūn-bûn

@nan

2017 թուականի Յուլիսին հրատարակուած գիտական յօդուած

@hyw

2017 թվականի հուլիսին հրատարակված գիտական հոդված

@hy

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

name

Case report: perioperative man ...... nt with mitochondrial myopathy

@ast

Case report: perioperative man ...... nt with mitochondrial myopathy

@en

type

label

Case report: perioperative man ...... nt with mitochondrial myopathy

@ast

Case report: perioperative man ...... nt with mitochondrial myopathy

@en

prefLabel

Case report: perioperative man ...... nt with mitochondrial myopathy

@ast

Case report: perioperative man ...... nt with mitochondrial myopathy

@en

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S12871-017-0385-4

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BMC Anesthesiology

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Case report: perioperative man ...... nt with mitochondrial myopathy

@en

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Fucheng Ji

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

Haipeng Zhou

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

Jinfeng Zhou

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

Penghui Wei

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

Qiang Zheng

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

Wenxi Tang

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

P2860

Mutations in the UQCC1-interacting protein, UQCC2, cause human complex III deficiency associated with perturbed cytochrome b protein expression

A Comprehensive Genomic Analysis Reveals the Genetic Landscape of Mitochondrial Respiratory Chain Complex Deficiencies

Deleterious mutation in FDX1L gene is associated with a novel mitochondrial muscle myopathy

Mitochondrial myopathies and the role of the pathologist in the molecular era.

Characteristic cardiac phenotypes are detected by cardiovascular magnetic resonance in patients with different clinical phenotypes and genotypes of mitochondrial myopathy.

Clinical implications of mitochondrial disease.

Anesthetic considerations in mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes syndrome: a case series.

Perioperative management of the paediatric patient with coexisting neuromuscular disease.

Anesthetic considerations in patients with mitochondrial defects.

Diagnosis of mitochondrial myopathies.

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10.1186/S12871-017-0385-4

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1

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cesarean section

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