The protein C pathway: implications for the design of the RESPOND study. - Wikidata - awgldk - TriplyDB

The protein C pathway: implications for the design of the RESPOND study.

The protein C pathway: implications for the design of the RESPOND study.

http://www.wikidata.org/entity/Q37082973

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Randomized trial evaluating serial protein C levels in severe sepsis patients treated with variable doses of drotrecogin alfa (activated).Protein C: a potential biomarker in severe sepsis and a possible tool for monitoring treatment with drotrecogin alfa (activated)Recombinant human activated protein C: current insights into its mechanism of action Protective mechanisms of activated protein C in severe inflammatory disorders.Therapeutic modulation of coagulation and fibrinolysis in acute lung injury and the acute respiratory distress syndrome Protein C as a surrogate end-point for clinical trials of sepsis Protein biomarker quantification by mass spectrometry.Alterations in the hemostatic profiles of dogs with naturally occurring septic peritonitis.Beyond single-marker analyses: mining whole genome scans for insights into treatment responses in severe sepsis.

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P2860

The protein C pathway: implications for the design of the RESPOND study.

http://www.wikidata.org/entity/Q37082973

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 January 2007

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

@cs

name

The protein C pathway: implications for the design of the RESPOND study.

@en

The protein C pathway: implications for the design of the RESPOND study.

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type

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The protein C pathway: implications for the design of the RESPOND study.

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The protein C pathway: implications for the design of the RESPOND study.

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prefLabel

The protein C pathway: implications for the design of the RESPOND study.

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The protein C pathway: implications for the design of the RESPOND study.

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The protein C pathway: implications for the design of the RESPOND study.

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P2093

Andrew F Shorr

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

Burkhard Vangerow

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

David R Nelson

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

Duncan Wyncoll

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

Jonathan Janes

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

Konrad Reinhart

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

P2860

Universal changes in biomarkers of coagulation and inflammation occur in patients with severe sepsis, regardless of causative micro-organism [ISRCTN74215569]

The cytoprotective protein C pathway

Efficacy and safety of recombinant human activated protein C for severe sepsis

Changes in the blood coagulation system associated with septicemia.

Epidemic meningococcemia and purpura fulminans with induced protein C deficiency.

Drotrecogin alfa (activated) for adults with severe sepsis and a low risk of death.

From evidence to clinical practice: effective implementation of therapeutic hypothermia to improve patient outcome after cardiac arrest.

New insights into the protein C pathway: potential implications for the biological activities of drotrecogin alfa (activated).

Relation between cytokines and routine laboratory data in children with septic shock and purpura.

Drotrecogin alfa (activated) in children with severe sepsis: a multicentre phase III randomised controlled trial.

P2888

P304

S4

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scholarly article

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10.1186/CC6155

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P478

11 Suppl 5

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2007-01-01T00:00:00Z

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5581809

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1051858916

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P698

18269691

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P921

protein precursor

biomedical investigative technique

P932

2230608

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