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2009 NOV 24 ... is the International Hyperhidrosis Society (IHHS). IHHS knows that many hereditary skin conditions like hyperhidrosis (excessive sweating) are often passed on within ...
2009 NOV 23 ... a leading cause of blindness in dogs with approximately 100 breeds affected by primary hereditary forms. Despite the large number of breeds affected with...
2009 NOV 24 ... "Cystic fibrosis is one of the most common autosomal recessive hereditary diseases in the Caucasian population, with an incidence of 1:2000 to 1:3500 liveborns. ...
2009 NOV 23 ... is increasing," scientists in Madrid, Spain report. "A proportion show a hereditary component, as in Lynch syndrome and Familial Adenomatous Polyposis, and a recently ...
2009 NOV 23 ... dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a hereditary cerebral microangiopathy linked to mutations in the Notch3 gene. The cerebral ...
2009 NOV 23 ... those with ''equivocal carcinoma'' did. Mutations in HRPT2, the gene responsible for hereditary hyperparathyroidism with jaw-tumor syndrome, were strongly associated with sporadic ...
2009 NOV 23 ... breast and ovarian cancers. We analyzed a family fulfilling classical criteria of hereditary breast/ovarian cancer." "After complete sequencing of coding regions and ...
2009 NOV 23 ... According to a study from Toronto, Canada, "Hereditary haemorrhagic telangiectasia (HHT) is an autosomal dominant disease characterised by ...
2009 NOV 23 ... 'Expression of metalloproteinases and their tissue inhibitors in gingiva affected by hereditary gingival fibromatosis: analysis of three cases within a family,' have been published. ...
2009 NOV 23 ... were found. The mutations of six of these residues have already been known to cause hereditary elliptocytosis or hereditary pyropoikilocytosis. ...
2009 NOV 23 ... "Turcot syndrome (TS), a rare variant of hereditary non-polyposis colorectal cancer (HNPCC), is characterized by familial clustering of ...
2009 NOV 24 ... myasthenic syndromes are a clinically and genetically heterogeneous group of hereditary disorders affecting neuromuscular transmission. We have identified mutations within the ...
2009 NOV 24 ... tip links have shed new light on the molecular basis of MET and the mechanisms causing hereditary deafness, noise-induced hearing loss and presbycusis." Sakaguchi and ...
2009 NOV 23 ... monoclonal B-cell disorders producing amyloidogenic immunoglobulin light chains, and the hereditary and ''senile systemic'' (ATTR) variants from mutant and wild-type transthyretin ...
2009 NOV 27 ... concluded: "They also help current understanding of the mechanisms of certain forms of hereditary hearing loss." Mistrik and colleagues published their study in Current ...
2009 NOV 23 ... According to recent research published in the Journal of Neurology, "Hereditary spastic paraplegia with thin corpus callosum (HSP-TCC) is one of the most common ...
2009 NOV 24 ... integrated product solutions for genetic testing of the mutations that underlie human hereditary diseases. The combination of TessArae's expertise in microarray-based resequencing with ...
