Bone

Phase I clinical trial of DFMO initiated to treat children with neuroblastoma

A new Phase I clinical trial sponsored by the Vermont Cancer Center at the University of Vermont and Fletcher Allen Health Care has opened to test the investigational drug DFMO, or alpha-difluoromethy

Submited in: on: Thu, 04/15/2010 - 05:06

New cardiac CT technology promises low radiation exposure and improved image quality

Cardiovascular disease is the leading cause of death globally and a tremendous burden on the healthcare system.

Submited in: on: Thu, 04/15/2010 - 04:18

Investigational treatment with IGIV reduces brain atrophy in Alzheimer's patients

An investigational intervention using naturally ocurring antibodies in human blood has preserved the thinking abilities of a group of mild- to moderate-stage Alzheimer's patients over 18 months and si

Submited in: on: Thu, 04/15/2010 - 04:08

Successful stem cell therapy performed on CHF patients in Mexico

Bioheart, Inc.

Submited in: on: Thu, 04/15/2010 - 03:56

Targeted therapy MDV3100 is effective for patients with CRPC: Study

An experimental drug is showing promise for the treatment of men with an aggressive form of advanced prostate cancer.

Submited in: on: Thu, 04/15/2010 - 02:55

New iVAS inflatable vertebral augmentation system released for VCFs

Stryker's Interventional Spine business unit today announced the release of its iVAS inflatable vertebral augmentation system, a minimally invasive device cleared for use in treating vertebral compres

Submited in: on: Thu, 04/15/2010 - 02:18

Phase II GAMMAGARD clinical study for Alzheimer's disease: 18-month results announced

Baxter International Inc.

Submited in: on: Thu, 04/15/2010 - 01:12

biospace med raises $18M for accelerating market expansion of EOS ultra-low-dose 2D/3D imaging system

biospace med announced today that it has raised $18 million to accelerate market expansion in North America and Europe of the company's FDA-cleared EOS ultra-low-dose 2D/3D imaging system.

Submited in: on: Thu, 04/15/2010 - 01:06

Tel Aviv University is bioengineering tissues as an alternative to animal testing

It's illegal for health products with medical formulations to be accepted by the U.S.

Submited in: on: Thu, 04/15/2010 - 00:02

ConforMIS' iUni G2 patient-specific knee replacement system receives CE Mark certification

ConforMIS, Inc. announced today that the iUni® G2 has received CE Mark certification, providing regulatory approval for ConforMIS to begin the sale of this products throughout the European Union.

Submited in: on: Wed, 04/14/2010 - 23:46

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