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Journal of Child Neurology|September 9, 2010
Experience with hyperphenylalaninemia in a developing country: unusual clinical manifestations and a novel gene mutationPascale E Karam, Rose T Daher, Lisbeth B Moller, et al.Journal of Child Neurology|September 9, 2010
Depressed brainstem auditory function in children with cerebral palsyZe D Jiang, Yun Y Wu, Xian Y Liu, et al.Journal of Child Neurology|September 9, 2010
A clinical picture of Guillain-Barré syndrome in children in the United StatesCaitlin W Hicks, Benjamin Kay, Sarah E Worley, et al.Journal of Child Neurology|May 22, 2010
Trisomy 8 mosaicism and favorable outcome after treatment of infantile spasms: case reportAnita Datta, Jonathan Picker, Alexander RotenbergJournal of Child Neurology|July 1, 2010
Classification of the gait patterns of boys with Duchenne muscular dystrophy and their relationship to functionSusan Sienko Thomas, Cathleen E Buckon, Alina Nicorici, et al.Journal of Child Neurology|July 8, 2010
Torticollis as the only manifestation of acute disseminated encephalomyelitisMiki Har-Gil, Merav Evrani, Nathan WatembergJournal of Child Neurology|July 8, 2010
The examination of peer review and publication in neurologyVictoria S S WongJournal of Child Neurology|July 20, 2010
Hypoglycemia-occipital syndrome: a specific neurologic syndrome following neonatal hypoglycemia?Parvaneh Karimzadeh, Sepideh Tabarestani, Mohammad GhofraniJournal of Child Neurology|April 15, 2010
Bioelectrical impedance analysis can be a useful screen for excess adiposity in spinal muscular atrophyDouglas M Sproule, Jacqueline Montes, Sally L Dunaway, et al.Journal of Child Neurology|October 8, 2009
Mutation analysis of the ASPM gene in 18 Pakistani families with autosomal recessive primary microcephalyRizwana Kousar, Hira Nawaz, Maryam Khurshid, et al.Pageof 586