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Recent related articles ( arpida enrols first patients quithea intravenous Oral):

Combined approach with doppler echocardiography and b-type natriuretic peptide to stratify prognosis of patients with decompensated systolic heart failure.
CONCLUSIONS: The complementary assessment of Doppler transmitral flow and plasma BNP concentration may be reliable in identifying the prognosis of patients with SHF. PMID: 19027600 [PubMed - in process] (Source: Journal of Cardiology) MedWorm Sponsored Message: Find out how you can get your message across here
Combined approach with doppler echocardiography and b-type natriuretic peptide to stratify prognosis of patients with decompensated systolic heart failure....

Cardiac Biomarker Soluble ST2 Shows Significant Clinical Value Over Natriuretic Peptide Markers In Monitoring Hospitalized Heart Failure Patients
Critical Diagnostics announced today the publication of a key research paper identifying the clinical value of the cardiac biomarker soluble ST2 (sST2) as a tool to monitor patients hospitalized for heart failure. The research paper, “Serial Sampling of ST2 Predicts 90-day Mortality Following Destabilized Heart
Cardiac Biomarker Soluble ST2 Shows Significant Clinical Value Over Natriuretic Peptide Markers In Monitoring Hospitalized Heart Failure Patients...

CVBT Doses First Patient in its Phase II Clinical Trial for Severe Coronary Heart Disease
CardioVascular BioTherapeutics, Inc. (BULLETIN BOARD: CVBT) , announced today that it has dosed the first patient in North America (NA) as part of its ACORD Phase II clinical trial to treat patients with severe coronary heart disease.
CVBT Doses First Patient in its Phase II Clinical Trial for Severe Coronary Heart Disease...

Arthritis Advisory Committee Recommends FDA Approval of Febuxostat for the Treatment of Hyperuricemia in Patients With Gout
Takeda Pharmaceutical Company Limited and its wholly-owned subsidiary, Takeda Global Research & Development Center, Inc., U.S., announced today that the Arthritis Advisory Committee of the U.S. Food and Drug Administration (FDA) recommended that the FDA approve febuxostat for the treatment of hyperuricemia in patients with gout.
Arthritis Advisory Committee Recommends FDA Approval of Febuxostat for the Treatment of Hyperuricemia in Patients With Gout...

CardioVascular BioTherapeutics doses first patient in trial for severe coronary heart disease
CardioVascular BioTherapeutics, Inc. , announced today that it has dosed the first patient in North America (NA) as part of its ACORD Phase II clinical trial to treat patients with severe coronary heart disease.
CardioVascular BioTherapeutics doses first patient in trial for severe coronary heart disease...

Diagnostic yield, interpretation, and clinical utility of mutation screening of sarcomere encoding genes in danish hypertrophic cardiomyopathy patients and relatives
The American Heart Association (AHA) recommends family screening for hypertrophic cardiomyopathy (HCM). We assessed the outcome of family screening combining clinical evaluation and screening for sarcomere gene mutations in a cohort of 90 Danish HCM patients and their close relatives, in all 451 persons. Index patients were screened
Diagnostic yield, interpretation, and clinical utility of mutation screening of sarcomere encoding genes in danish hypertrophic cardiomyopathy patients and relatives...

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