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See Latest ArticlesDeafness Genes in Israel: Implications for Diagnostics in the Clinic
Pediatric Research, 07/22/09
Brownstein Z et al. – The authors review the current status of deafness genes in Israel and report one known mutation in a syndromic form of deafness, Usher syndrome, described in the Jewish Israeli population for the first time. In the future, the identification of specific mutations may be relevant for specific types of treatment.
Today in Basic Science/Genetics...keeping you current
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Neonatal seizures and Long QT Syndrome: A cardiocerebral channelopathy
Epilepsia, 11/10/09
Genetic forms of hypopituitarism and their manifestation in the neonatal period
Early Human Development, 10/30/09
BTNL2 gene polymorphisms may be associated with susceptibility to Kawasaki disease and formation of coronary artery lesions in Taiwanese children
European Journal of Pediatrics, 11/05/09
Today in Pediatric Otolaryngology...keeping you current
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Propranolol treatment for infantile hemangiomas
Current Opinion in Otolaryngology and Head & Neck Surgery, 11/13/09
Bilateral cochlear implantation: Current concepts, indications, and results
The Laryngoscope, 11/09/09
Vocal cord paralysis in children
Current Opinion in Otolaryngology and Head & Neck Surgery, 11/19/09
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