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2009 MAR 16 ... adulthood.
Led by Dr Mohammad Hajihosseini, the UEA scientists focused on Apert Syndrome - the most severe of the craniosynostosis range of diseases that is caused by mutations ...
2009 OCT 27 ... According to a study from the United States, "Apert syndrome is almost always caused by a spontaneous mutation of paternal origin in one of two ...
2009 FEB 25 ... and aesthetic (Whitaker score) outcomes were assessed at follow-up. Diagnoses included Apert syndrome, Crouzon syndrome, Pfeiffer syndrome, Saethre-Chotzen syndrome, and nonsyndromic. Early ...
2009 APR 13 ... According to a study from Oxford, the United Kingdom, "Apert syndrome (AS) is a severe disorder, characterized by craniosynostosis and complex syndactyly of ...
2009 JUL 7 ... identify and describe the nature of dysphagia and nutrition difficulties in infants with Apert syndrome. The study comprised a review of the medical, nutrition, and feeding records of 13 ...
2009 NOV 9 ... fibroblast growth factor receptor 2 (FGFR2)-mediated craniosynostosis syndromes, such as Apert syndrome. However, there is little information on the frequency of palatal clefts in the ...
2009 MAY 12 ... cause. Discussed in detail are type 2 thanatophoric dysplasia, type 2 Pfeiffer syndrome, Apert syndrome, amniotic bands, Say-Poznanski syndrome, and COH syndrome," wrote M.M. Cohen and ...
2009 MAR 17 ... in 'Evidence that Fgf10 contributes to the skeletal and visceral defects of an apert syndrome mouse model' have been presented. "Apert syndrome ...
2009 JUL 14 ... USA. Keywords: United States, St. Louis, Acrocephalosyndactylia, Apert Syndrome, Pathology, Polydactyly, Surgery, Syndactyly, Washington University, Medical Department. ...
2009 JUL 27 ... has been proposed to be involved in acne pathogenesis and explains acne lesions in Apert syndrome and unilateral acneiform nevus associated with gain-of-function point mutations of ...
2009 NOV 9 ... on corotial gap was demonstrated by 68.2% of those with Crouzon and 54.5% of those with Apert syndrome. In contrast, 85.7% of those with Pfeiffer syndrome had ''poor'' or ''absent'' ...
2009 MAY 12 ... treatment for the deformity associated with craniofacial dysostoses (e.g., Crouzon, Apert, and Pfeiffer syndromes). The technical and physiological principles of osteogenesis ... scans. The CT scans of 25 patients (11 with Crouzon, 6 with Apert, and 8 with Pfeiffer syndrome) were analyzed. Eleven individual areas along the osteotomy lines were assessed for ...
2008 SEP 2 ... over conventional surgery, with less morbidity. We present a case of a patient with Apert syndrome who underwent monobloc advancement using the Rigid External Device (RED) device and who ...
2008 JUL 29 ... basis for the advantage in the testis.
Keywords: Acrocephalosyndactylia, Apert Syndrome, DNA, Genetic Diseases, Genetic Disorders, Genetics, Genomics, University of Southern ...
2008 AUG 12 ... Seven children with Crouzon syndrome underwent monobloc distraction and three with Apert syndrome underwent facial bipartition distraction using the rigid external distractor frame. The ...
2008 DEC 2 ... "Raised intracranial pressure is a well-known complication of Apert syndrome. The current policy in the authors' unit is to monitor these patients and only perform ...
2008 SEP 1 ... According to recent research from the United States, "Apert syndrome is a congenital condition characterized by craniosynostosis, syndactyly, and maxillary ...
2008 OCT 14 ... human FGFR2 gene (C755G or C758G) are responsible for virtually all sporadic cases of Apert syndrome. This condition is 100-1,000 times more common than genomic mutation frequency data ...
