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2009 AUG 10 ... symptoms with several other disorders, including autism, cerebral palsy, epilepsy, Rett Syndrome, and Prader-Willi Syndrome, any progress toward treating and curing symptoms has the ...
2009 SEP 28 ... or severely limited activities and interests. Other ASDs include Asperger syndrome, Rett syndrome, childhood disintegrative disorder, and pervasive developmental disorder not otherwise ...
2009 JUL 6 ... "Mutations in the methyl-CpG-binding protein 2 (MeCP2) cause Rett syndrome, a severe neurodevelopmental disease associated with ataxia and other post-natal ...
2009 OCT 20 ... in the United States that specializes in the diagnosis and care of girls and women with Rett Syndrome. Jeffrey L. Noebels, M.D., Ph.D. is Professor of Neurology, Neuroscience, ...
2009 SEP 21 ... Delphi technique. To develop guidelines for the clinical management of scoliosis in Rett syndrome through evidence review and consensus expert panel opinion," scientists writing in the ...
2009 NOV 9 ... Inspired by recent breakthroughs in research, today the International Rett Syndrome Foundation (IRSF) announced a major fundraising initiative entitled Research to Reality: ...
2009 OCT 19 ... intractable seizures with infantile spasms (IS), severe hypotonia and atypical Rett syndrome (RTT) features. So far, 48 deleterious alleles have been reported in the literature," ...
2009 SEP 7 ... 'Enhanced dense core granule function and adrenal hypersecretion in a mouse model of Rett syndrome,' have been published. "Rett syndrome (RTT) is a ...
2009 JUN 22 ... "Methyl-CpG-binding protein 2 (MECP2) gene mutations have been identified in girls with Rett syndrome and in boys with heterogeneous neuropsychiatric disorders. Because of the limited or ...
2009 SEP 7 ... psychiatric disorders such as schizophrenia, Tourette's syndrome, epilepsy, and Rett syndrome, an autism spectrum disorder. Until this paper, it had not been known how ...
2009 JUN 29 ... and drug resistance. We screened a population of 92 patients with classic/atypical Rett syndrome, 17 Angelman/Angelman-like patients and six idiopathic autistic patients for CDKL5 ...
2009 JUL 6 ... According to recent research from Perth, Australia, "Rett syndrome (RTT) is a rare genetic disorder within the autistic spectrum. This study compared ...
2009 OCT 19 ... ASD and ASD characteristics was conducted in the following syndrome groups: Fragile X, Rett, Tuberous Sclerosis Complex, Down, Angelman, CHARGE and Phenylketonuria." ...
2009 JUL 20 ... with neurodegenerative and neurodevelopmental disorders such as Alzheimer's disease and Rett syndrome indicated that epigenetic mechanisms and chromatin remodeling need to be tightly ...
2009 JUL 6 ... The researchers concluded: "Finally, we used EOS selection to establish Rett syndrome-specific mouse and human iPS cell lines with known mutations in MECP2." ...
2009 JUN 30 ... in the gene encoding methyl-CpG-binding protein 2 (MECP2). Loss of MeCP2 function causes Rett syndrome (RTT), whereas increased copy number of the gene causes MECP2 duplication or ...
2009 AUG 10 ... dysfunction of the UPS may also underlie cognitive disorders such as Angelman syndrome, Rett syndrome and autism, and muscle and nerve diseases, e.g., inclusion body myopathy and giant axon ...
2009 SEP 1 ... hyperpnoeic episodic breathing, widely reported in pre-term neonates, young girls with Rett's syndrome, patients with Joubert syndrome and adults with Cheyne-Stokes respiration," ...