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See Latest ArticlesCompound heterozygous HAX1 mutations in a Swedish patient with severe congenital neutropenia and no neurodevelopmental abnormalities
Pediatric Blood & Cancer, 06/17/09
Carlsson G et al. - The authors describe a patient with a compound heterozygous HAX1 mutation consisting of a nonsense mutation and a frame-shift mutation resulting in a premature stop codon. The patient has a history of neutropenia and a propensity for infections, but has shown no signs of neurodevelopmental abnormalities.
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Thyroid lymphoma and airway obstruction – is there a rationale for surgical management?
International Journal of Clinical Practice, 10/19/09
Prospective, Observational Study of Outcomes in Neonates With Severe Thrombocytopenia
Pediatrics, 10/28/09
Role of Antiplatelet Agents in Hematoma Expansion During The Acute Period of Intracerebral Hemorrhage
Neurocritical Care , 10/23/09
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Diclofenac for acute pain in children
Cochrane Reviews, 10/08/09
Management of acute appendicitis: an imaging strategy in children
Pediatric Surgery International, 10/27/09
Rapid viral diagnosis for acute febrile respiratory illness in children in the Emergency Department
Cochrane Reviews, 10/26/09
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