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See Latest ArticlesImproving Accuracy of Tay Sachs Carrier Screening of the Non Jewish Population: Analysis of 34 Carriers and 6 late-onset Patients with HEXA Enzyme and DNA Sequence Analysis
Pediatric Research, 10/29/09
Park NJ et al. – Gene sequencing, is useful in identifying rare mutations in TSD patients and their families, in evaluating spouses of known carriers for TSD who have indeterminate enzyme analysis and negative for common mutation analysis, and in resolving ambiguous enzyme testing results.
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The role of inhaled corticosteriods and montelukast in children with mild-moderate asthma: results of a systematic review with meta-analysis
BMJ - Archives of Diseases in Childhood, 12/11/09
Probable trigeminal autonomic cephalgia in a 3-month-old male infant
Developmental Medicine & Child Neurology, 12/11/09
Predictors of Relapse and End Stage Kidney Disease in Proliferative Lupus Nephritis: Focus on Children, Adolescents, and Young Adults
Clinical Journal of the American Society of Nephrology, 12/11/09
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